Midterm 2 Flashcards

1
Q

What determines the contractility?

isotonic tension

isometric tension

maximum isometric tension, maximum contraction speed

contraction speed

A

maximum isometric tension, maximum contraction speed

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2
Q

What influences the efficiency of the working fibers in the heart?

parasympathetic stimulation
sympathetic inhibition
direct electrical stimulation
sympathetic stimulation

A

Sympathetic stimulation

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3
Q
How does the cardiac output change during the direct stimulation of the heart?
the C.O. doesn`t change
the C.O. decreases slightly
the C.O. increases significantly
the C.O. decreases significantly
A

The C.O. doesn’t change

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4
Q

How does the cardiac output change if we stimulate the heart through its sympathetic nerve?

the C.O. decreases continuously
the C.O. increases continuously
the C.O. doesn’t change
the C.O. increases slightly

A

The C.O. increases continuously

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5
Q

How does the systole/diastole rate change with direct stimulation of the heart?

systole and diastole decrease
systole increases, diastole decreases
systole doesn’t change, diastole decreases
systole decreases, diastole increases

A

systole doesn’t change, diastole decreases

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6
Q

How does the systole/diastole ratio change if we stimulate the heart through its sympathetic nerve?

it increases
it decreases
it increases the muscle force only
the ratio doesn’t change too much

A

The ratio doesn’t change too much

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7
Q
How can we measure the cardiac output?
on the basis of the Ficks-principle
on the basis of the Van`t Hoff law
on the basis of the Laplace law
on the basis of Henderson- Hasselbalch equation
A

On the basis of the Ficks-principle

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8
Q
What formula can be used to calculate the cardiac output?
C.O.=QtO2x(CaO2- CvO2)
C.O.=QtO2/(CaO2- CvO2)
C.O.=QtO2/(CvO2- CaO2)
C.O.=QtO2/ (CaO2xCvO2)
A

C.O. = QtO2/(CaO2-CvO2)

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9
Q

Can we apply the Stewart-principle for the determination of the cardiac output?
yes, because we measure the volume
yes, when we inject tritiated water
yes, but modified, instead of volume we measure volume flow
no

A

Yes, but modified, instead of volume we measure volume flow

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10
Q
What efficiency does the heart have?
80 %
30-40%
4%
10-20%
A

10-20%

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11
Q

What is the external work of the heart?
The product of systolic volume and the mean arterial pressure
The quotient of pulse pressure and the circulatory mid- pressure
The product of cardiac output and the arterial mid-pressure
the difference of the pressure-work and the kinetic-work

A

The product of systolic volume and the mean arterial pressure

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12
Q

What can we show with the help of the Rushmer-diagram?
the ratio of external and internal work
the ratio of the active and passive component of the external work of the heart
the difference between the external and internal work of the heart
the efficiency of the work of the heart

A

The ratio of the active and passive component of the external work

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13
Q

What does the passive work of the heart derive from?

from the tension during the isovolumetric contraction
from the isovolumetric relaxation
from the energy stored in the elastic components
from the tension of the aortic wall

A

From the energy stored in the elastic components

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14
Q

How do the pressure and volume of the left ventricle change during the fast ejection phase of systole?

the pressure does not change, the volume decreases significantly
the pressure drops, the volume decreases
the pressure increases, the volume does not change
the pressure increases, the volume decreases

A

The pressure increases, the volume decreases

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15
Q

How does the efficiency of the heart change with increasing ventricular volume?

It decreases
It increases
It does not change
It decreases, since the oxygen consumption is less

A

It decreases

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16
Q
What happens when we stimulate the heart muscle to the threshold potential?
Cl and Ca influx
K outflow, Na inflow
Na influx
Ca and Na influx
A

Na influx

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17
Q
What happens at a potential of +25 mV?
Na inflow stops, K inflow, Cl outflow
Ca inflow, Na outflow
Na inflow continues, K outflow stops
Na inflow stops; Cl inflow begins
A

Na inflow stops: Cl inflow begins

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18
Q
What influx happens during the plateau-phase of the heart muscle's AP?
slow Ca inflow, slow K outflow
quick Ca inflow, slow K outflow
slow Ca outflow, quick K inflow
quick Na inflow, slow Ca inflow
A

Slow Ca inflow, slow K outflow

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19
Q
What is going on in the phase leading to the total repolarization of the heart muscle?
slow Ca inflow, slow K outflow
rapid K outflow, Ca inflow stops
Ca inflow, slow K outflow
Na inflow, slow Ca inflow
A

rapid K outflow, Ca inflow stops

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20
Q

How does the potassium conductance change during phase 3 of the AP of the working fibers of the heart?
it decreases
it does not change
it increases
its change is parallel to the sodium conductance

A

It increases

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21
Q
Which ion flux causes the plateau phase in the AP of the heart muscle?
potassium
chloride
sodium
mainly calcium
A

Mainly calcium

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22
Q
How does the sodium conductance change in phase 1 of the AP of the working fibers of the heart?
it ceases suddenly
it increases
it decreases continuously
it does not change
A

It ceases suddenly

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23
Q

What is the most important difference between the action potential of the heart muscle and that of the skeletal muscle?

the AP of the heart muscle is shorter
the AP of the skeletal muscle has no plateau phase
the contraction of the heart muscle starts after the AP
the AP of the skeletal muscle overlaps its mechanogram

A

The AP of the skeletal muscle has no plateau phase

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24
Q

What answer is produced when the stimulus is given during the absolute refractory phase?
a new AP is generated
a new AP is produced when the stimulus is strong enough
no AP can be produced
AP is generated about 300 msecs later

A

No AP can be produced

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25
Q

Which statement is correct for the relative refractory period?
Only a slight stimulus may elicit a new AP
no stimulus can elicit an AP
a normal stimulus causes an AP
only a very strong stimulus can elicit an AP

A

Only a very strong stimulus can elicit an AP

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26
Q

Which statement is correct for the supernormal phase?
a very slight stimulus can provoke an AP
only a strong stimulus elicits an AP
AP cannot be elicited at all in this phase
only serial stimuli elicit a new AP

A

A very slight stimulus can provoke an AB

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27
Q
In which phase of the AP can a stimulus cause life threatening ventricular fibrillation?
absolute refractory period
supernormal phase
relative refractory period
immediately after the diastole
A

Supernormal phase

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28
Q
What is the center of the nomotopic stimulus formation?
septum
Purkinje fibers
sinoatrial node
bundle of His
A

Sinoatrial node

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29
Q

Which formation generates the pacemaker activity in the heart?
large round cells of the SA node
elongated cells of the sinoauricular node
sympathetic fibers
parasympathetic fibers

A

Large round cells of the SA node

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30
Q
Which formation synchronizes and delays the pacemaker signal?
large round cells of the SA node
elongated cells of the SA node
pacemaker cells of the SA node
working muscle fibers
A

Elongated cells of the SA node

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31
Q
The depolarisation of the pacemaker cells begins at what potential?
-90 mV
-35 mV
-55 mV
\+35 mV
A

-55 mV

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32
Q
What kind of ion channels function in the period of spontaneous diastolic depolarisation?
Ih channels, slow Na- channels
slow Na-channels
fast Na-channels
Ih channels, T and L-type channels
A

LH channels, T and L type channels

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33
Q
Which channels determine the 0 phase of the action potential of the pacemaker cells?
fast Na-channels
slow Na-channels
Ih channels
T and L-type Ca- channels
A

Fast Na-channels

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34
Q

What are the characteristics of the subendocardial conduction?
the specialized fibre system projects deep into the ventricular muscle
The specialized fibre system does not project deep into the ventricular muscle
it occurs in large animals
elongates the heart cycle

A

The specialized fibre system does not project deep into the ventricular muscle

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35
Q

What are the characteristics of the epicardial conduction?
it occurs in small animals
the specialized fibre system is on the surface of the ventricle
the specialized fibre system projects deep into the muscles of the ventricle
elongates the heart cycle

A

the specialized fibre system projects deep into the muscles of the ventricle

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36
Q

What is the function of the sinoatrial node?
ventricular activation
synchronizes atrial and ventricular contraction
delays the conduction time
nomotopic excitation

A

nomotopic excitation

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37
Q

What is the function of the atrioventricular node?
delays the excitation
synchronizing the contraction of the two ventricles
nomotopic excitation
fast ventricular activation

A

delays the excitation

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38
Q
What is the function of the annulus fibrosus?
ventricular activation
synchronization
nomotopic stimulus generation
heterotopic stimulus generation
A

Synchronization

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39
Q

What is the function of the His-bundle?

delays the conduction of the stimulus
nomotopic stimulus generation
fast ventricular activation
synchronization atrial and ventricular activity

A

Fast ventricular activation

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40
Q

Where is the conduction the slowest in the heart?

in the ventricle
in the His-bundle and the Tawara-stalk
in the SA node
in the AV node

A

In the AV node

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41
Q

Where is the conductance the fastest in the heart?

in the His and Tawara bundles
in the working muscle fibres
in the ventricles
in the atriovenrticular node

A

In the His and Tawara bundles

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42
Q

How does sympathetic stimulation affect the frequency of the heart?

it decreases the frequency
it increases the frequency
there is no change
first it increases, later it decreases

A

It increases its frequency

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43
Q

How does parasympathetic stimulation affect the frequency of the heart?

it increases the frequency
there is no change
it decreases the frequency
first it increases, later it decreases

A

It decreases the frequency

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44
Q

What mediates the sympathetic effect in the heart?

cAMP concentration decreases
inhibiting of the beta-1 receptor
stimulating the nicotinic acetylcholine receptor
stimulating the beta-1 receptor

A

Stimulating the beta-1 receptor

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45
Q
How does the AP of the heart change during sympathetic stimulation?
the steepness of the SDD increases
the MDP lowers
the steepness of the SDD decreases
the MDP does not change
A

The steepness of the SDD increases

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46
Q

How does the parasympathetic effect act in the heart?

via beta-1 receptor stimulation
via acetylcholine receptor stimulation
by inhibiting the beta-1 receptors
increasing the cAMP concentration

A

Via acetylcholine receptor stimulation

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47
Q

What nerval effect determines the heart function at rest?

sympathetic inhibition
sympathetic stimulation
parasympathetic stimulation
parasympathetic inhibition

A

Parasympathetic inhibition

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48
Q

What neural effects act on the heart in case of increased physical activity?

increased sympathetic stimulation, reduced parasympathetic activity

increased parasympathetic activity

reduced sympathetic activity

increased vagal stimulation

A

Increased sympathetic stimulation, reduced parasympathetic activity

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49
Q

What is the bathmotrop effect?

an effect influencing frequency
an effect influencing threshold
an effect influencing force generation
an effect influencing contractility

A

An effect influencing treshold

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50
Q

What is the dromotrop effect?

an effect influencing frequency
an effect influencing threshold
an effect influencing conductance
an effect influencing SDD

A

An effect influencing conductance

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51
Q
What is the inotrop effect?
an effect influencing frequency
an effect influencing threshold
an effect influencing force generation
an effect influencing SDD
A

An effect influencing force generation

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52
Q
What is the chronotrop effect?
an effect influencing frequency
an effect influencing force generation
an effect influencing conductance
an effect influencing threshold
A

An effect influencing frequency

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53
Q

How does the parasympathetic nervous system alter the activity of the heart?

negative inotrop, chronotrop, positive dromotrop, bathmotrop effect

negative inotrop, chronotrop, dromotrop, bathmotrop effect

positive inotrop, chronotrop, dromotrop, bathmotrop effect

positive inotrop, chronotrop, negative dromotrop, bathmotrop effect

A

Negative inotrop, chonotrop, dromotrop, bathmotrop effect

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54
Q

How does sympathetic nervous system alter the activity of the heart?

negative inotrop, chronotrop, positive dromotrop, bathmotrop effect.

negative inotrop, chronotrop, dromotrop, bathmotrop effect

positive inotrop, chronotrop, dromotrop, bathmotrop effect

positive inotrop, chronotrop, negative dromotrop, bathmotrop effect

A

Positive inotrop, chronotrop, dromotrop, bathmotrop effect

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55
Q

What is characteristic of the electro-mechanical coupling in the heart muscle?

its main element is the voltage sensitive channel on the membrane of the SR

the process is started by the opening of the Na-dependent Ca channel

its basis is the increase of the IC potassium level

the stimulation of the DHP sensitive proteins

A

The stimulation of the DHP sensitive proteins

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56
Q

What directly starts the cross bridge cycling in the heart muscle?

the calcium signal
conformation change of the voltage dependent DHP receptor and T-tubulus
opening of DHP-type Ca channels on the SP membrane
pumping of the calcium into the SR

A

The calcium signal

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57
Q

What mechanisms make calcium flow out of the IC?

ATP dependent calcium pump towards the EC, Na/Ca antiporter towards SR

ATP dependent calcium pump towards the SR, Na/ Ca antiporter towards EC

Na/Ca antiporter towards EC and SR

ATP dependent Ca pump towards the SR and EC

A

ATP dependent calcium pump towards the SR, Na/Ca antiporter towards EC

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58
Q

Which of the following statements is false?

regarding its function, the heart can be considered as an electric dipole

a dipole can be described by a vector

depolarization vector points from the positive to the negative direction

an electrical signal has direction, measure and polarity

A

Depolarization vector points from the positive to the negative direction

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59
Q
Who constructed the first ECG equipment?
A. L. Lavoisier.
G. R. Kirchhoff.
C. Bernard.
W. Einthoven.
A

W. Einthoven

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60
Q

Which of the following statements is true?

the sum of the voltage differences measured between the vertices of the equilateral triangle around the dipole is always zero.

the sum of voltage differences measured between the vertices of the triangle around the dipole equals unity

the Einthoven’s lead is a unipolar lead

the depolarization wave causes an upward defelction on the ECG

A

The sum of the voltage differences measured between the vertices of the equilateral triangle around the dipole is always zero

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61
Q

What is the principle of the bipolar lead?

potential difference between two electrodes is compared to a third reference point

potential difference between two electrodes placed on the surface of a dipol is measured

potential difference between two electrodes is compared to a third neutral point

potential difference between two electrodes is compared to standard voltage value

A

Potential difference between two electrodes placed on the surface of a dipole is measured

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62
Q

What can be seen in the oscilloscope during full depolarization?

an upwards deflection

a downwards deflection

an isoelectric line - no deflection

an irregular line

A

An isoelectric line - no deflection

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63
Q

What is the Einthoven’s first lead?

reference electrode on right arm, measuring electrode on left leg

reference electrode on left arm, measuring electrode on left leg

reference electrode on right arm, measuring electrode on right leg

reference electrode on right arm, measuring electrode on left arm

A

Reference electrode on right arm, measuring electrode on left arm

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64
Q

What is the Einthoven’s second lead?

reference electrode on right arm, measuring electrode on left leg

reference electrode on left arm, measuring electrode on left leg

reference electrode on right arm, measuring electrode on right leg

reference electrode on right arm, measuring electrode on left arm

A

Reference electrode on right arm, measuring electrode on left leg

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65
Q

What is the Einthoven’s third lead?

reference electrode on right arm, measuring electrode on left leg

reference electrode on left arm, measuring electrode on left leg

reference electrode on right arm, measuring electrode on right leg

reference electrode on right arm, measuring electrode on left arm

A

Reference electrode on left arm, measuring electrode on left leg

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66
Q

Why is the integral vector of the heart not zero?

the measurement points do not form an exact triangle

the stimulus passing between the atrium and the ventricle is slowing down

the heart is asymmetric it has altering width of wall and the SA node is not in the middle

speed of conduction is different in all directions

A

The heart is asymmetric it has altering width of wall and the SA node is not in the middle

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67
Q

With which state of the atrial activity does the ventricular depolarization coincide?

depolarization
activated state
repose state
repolarization

A

Repolarization

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68
Q

What does the T- wave describe on the ECG?

atrial depolarization
SA node depolarization
ventricular repolarization
atrial repolarization

A

Ventricular repolarization

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69
Q

What does the PQ segment describe on the ECG?

SA node depolarization
atrio-ventricular conduction
ventricular depolarization
atrial repolarization

A

Atrio-ventricular conduction

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70
Q

What does the QRS complex describe on the ECG?

full atrial depolarization
full repolarization
ventricular depolarization, atrial repolarization
ventricular repolarization, atrial depolarization

A

Ventricular depolarization, atrial repolarization

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71
Q

What makes the Q wave point downwards?

ventricular depolarization spreads to the vertex of the heart
repolarization of the right ventricle
atrial repolarization
ventricular depolarization spreads toward the base of the heart

A

Ventricular depolarization spreads toward the base of the heart

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72
Q

What does the S-T segment describe?

full ventricular depolarization
ventricle is fully repolarized
atrium is depolarized, ventricle is repolarized
full repolarization of the atria

A

Full ventricular depolarization

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73
Q

What does the T wave represent?

atrial repolarization
ventricular repolarization
atrial depolarization
ventricular depolarization

A

Ventricular repolarization

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74
Q

What does the T-P segment represent?

complete atrial depolarization
the beginning of ventricular repolarization
complete repolarization, state of rest
complete ventricular depolarization

A

Complete repolarization, state of rest

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75
Q

What is the essence of the unipolar lead?

to measure the voltage fluctuation between a point of the chest and a limb

to connect electrodes placed on the chest, and registers the integrated voltage fluctuations

to measure the voltage of a single conduction point only

to measure the voltage fluctuation between the examining electrode and a place of 0 potential

A

To measure the voltage fluctuation between the examining electrode and a place of 0 potential

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76
Q

Which type of ECG gives precise information about the heart’s anatomical position?

vector cardiography
esophageal ECG
His-Bundle ECG
unipolar ECG

A

Vector cardiography

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77
Q

What causes heartsound I?

Closure of semilunar valves
Closure of cuspidal valves
Sound of sudden ventricular filling
Turbulent flow following atrial systole

A

Closure of cuspidal valves

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78
Q
What causes heartsound II?
Closure of cuspidal valves
Sound of sudden ventricular filling
Closure of semilunar valves
Turbulent flow following atrial systole
A

Closure of semilunar valves

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79
Q
Which wave cannot be registered on v. jugularis during the heart-cycle?
Wave V
Wave C
Wave A
Wave P
A

Wave P

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80
Q
How long is a complete heart- cycle in dogs?
800 msec
270 msec
530 msec
220 msec
A

800 msec

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81
Q
What percent of the ventricular volume gets to the periphery during the fast ejection phase of ventricular systole?
60 %
80 %
90 %
50 %
A

80%

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82
Q

Of the following elements of the heart-cycle which is the longest in time?

isovolumetric relaxation
isovolumetric relaxation
ventricular systole
atrial systole

A

Ventricular systole

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83
Q
Which is the shortest element of the heart-cycle?
isovolumetric relaxation
atrial systole
fast phase of auxotonic contraction
isovolumetric contraction
A

Isovolumetric contraction

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84
Q
Where is there no valve in the blood flow?
v.cava - right atrium
right atrium - right ventricle
left atrium - left ventricle
left atrium - aorta
A

Vena cava - right atrium

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85
Q
Where you could find tricuspid valves in the heart?
left atrium - left ventricle
right atrium - right ventricle
left ventricle - aorta
right ventricle - a. pulmonalis
A

Right atrium - right ventricle

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86
Q
Where you could find bicuspid valves in the heart?
right atrium - right ventricle
left ventricle - aorta
left atrium - left ventricle
right ventricle - a. pulmonalis
A

Left atrium - left ventricle

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87
Q

What vessel carries venous blood?

a. radialis
a. carotis communis
v. pulmonalis
a. pulmonalis

A

A. pulmonalis

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88
Q

What vessel carries arterial blood?

v. pulmonalis
a. pulmonalis
v. cava cranialis
v. portae

A

V. pulmonalis

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89
Q

How is the mechanical performance of the heart controlled by the nervous system tone?

parasympathethic increases
sympathethic increases
sympathethic decreases
no effect on the mechanical performance

A

Sympathetic increases

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90
Q
How does the nervous system influence the heart basal activity?
sympathethic predominance
parasympathethic inhibition
parasympathethic dominance
no effect on the basal activity
A

Parasympathetic dominance

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91
Q

What is typical for the serial elastic component?
inhibits overextension of muscle
it is linked parallel with the contractile elements
it is stretched in diastole
it is relaxed in diastole and stretched in systole

A

It is relaxed in diastole and stretched in systole

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92
Q

What is typical for the parallel elastic component?
energy is stored in it due to the tension which is created by the blood flow-in

it is relaxed in diastole and stretched in systole

it is linked serial to the contractile elements

inhibits over extension of muscle

A

Energy is stored in it due to the tension which is created by the blood flow-in

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93
Q

What is typical for the collagen-fiber system?

it is linked serial to the contractile elements
inhibits over extension of muscle
it is stretched in diastole and relaxed in systole
it has a fiber-mass value = 1

A

Inhibits over-extension of muscle

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94
Q

What is typical for the isometric phase of the heart activity?

movement at the same tension

SEC and PEC elements are tensed during this phase

there is tension but no movement

contractile elements are not contracting but are tensing

A

There is tension but no movement

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95
Q

What is typical for the isotonic phase of the heart activity?

sudden tension of the collagen fibers

no change in contraction of the contracting components during this phase

there is tension but no movement

there is movement but no change in tension

A

There is movement but no change in tension

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96
Q

What happens at the maximal loading of the heart?

collagen fibers extend and display maximal resistance

collagen fibers relax and reduce their resistance to minimal

tension of contractile elements increase

SEC and PEC components contract maximal

A

Collagen fibers extend and display maximal resistance

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97
Q

What conditions allow isotonic contraction?

muscle can not move the load
muscle can freely move the load
muscle works against a spring
muscle is supported to a certain length

A

Muscle can freely move the load

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98
Q

What condition is needed for isometric contraction?

muscle can freely move the load
muscle works against a spring
muscle can not move the load
muscle is supported to a certain length

A

Muscle can not move the load

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99
Q

What condition is needed for auxotonic contraction?

muscle is supported to a certain length
muscle can not move the load
muscle can freely move the load
muscle works against a spring

A

Muscle works against a spring

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100
Q

What type of muscle contraction can be demonstrated in the preload experiment?

two components: first isometric, then isotonic
two components: first isotonic, then isometric
one component: isometric
one component: isotonic

A

Two components: first isometric, then isotonic

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101
Q

What do we demonstrate in the “afterload” experiment?

two different type of contractions: first isometric, then isotonic
two different type of contractions: first isotonic, then isometric
the isometric contraction
the isotonic contraction

A

Two different types of contractions: first isotonic, then isometric

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102
Q

What physiological situation can we demonstrate with the preload experiment?

heart keeps the balance with the peripheral resistance at the end of the contraction

heart muscle reaches a certain length at the end of the systole, then is starts to constrict

at the end of the diastole heart starts to constrict

at the end of the diastole the heart keeps balance with the peripheral resistance

A

At the end of the diastole heart starts to constrict

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103
Q

What is the difference between the mechanogram of skeletal and heart muscle?

The maximal tension in the heart muscle is at 1.9-2.6 micrometer sarcomere length

The optimal sarcomere length is optimal for actin-myosin bridging at 1.9-2.6 micrometer sarcomere length

Stretching skeletal muscle has significant energy reserves

The heart muscle shows maximal tension at long sarcomeric length (2.5 micrometer)

A

The heart muscle shows maximal tension at long sarcomeric length (2.5 micrometer)

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104
Q

Why is there no maximal tension in the heart muscle at 2 micrometer sarcomere length?

calcium is only sufficient for maximal tension at 2.5 micrometer sarcomere length
calcium binding sites are 100% saturated below 2.5 micrometer sarcomere length
below 2 micrometer not all the possible bridges can be formed
there is not enough calcium due to maximal sarcomere length

A

Calcium is only sufficient for maximal tension at 2.5 micrometer sarcomere length

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105
Q

Which of the below is the sarcomere length of the heart at default function?

2.2 micrometers
1.9 micrometers
2.5 micrometers
between 2-2.5 micrometers

A

1.9 micrometers

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106
Q

What is the reason for the difference between the length- tension diagram of heart and skeletal muscle?

the sarcomere structure is different

there is only a small amount of calcium in the skeletal muscle after stimulation

calcium might enter the IC space in proportion to the extension of the heart muscle

2.5 micrometer sarcomere length is optimal for the heart to work

A

Calcium might enter the IC space in proportion to the extension of the heart muscle

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107
Q

What does the EDV stand for?

stroke volume
cardiac output
volume at the end of systole
volume at the end of diastole

A

Volume at the end of diastole

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108
Q

What does the ESV stands for?

volume at the end of systole
volume at the end of diastole
cardiac output
stroke volume

A

Volume at the end of systole

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109
Q

What does the SV stands for?

volume at the end of diastole
stroke volume
volume at the end of systole
cardiac output

A

Stroke volume

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110
Q

How can the stroke volume be calculated?

End systolic volume - end diastolic volume

(end diastolic volume - end systolic volume) x heart frequency

end diastolic volume - end systolic volume

end diastolic volume + end systolic volume

A

End diastolic volume - end systolic volume

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111
Q

Which of the parameters below describes the work of the heart?

end systolic volume
heart frequency
stroke volume
cardiac output

A

Cardiac output

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112
Q

Which equation describes the Cardiac Output?

C.O. = (end diastolic volume - end systolic volume) x frequency

C.O. = (end systolic volume - end diastolic volume) x frequency

C.O. = (end diastolic volume - end systolic volume) / frequency

C.O. = (end diastolic volume + end systolic volume) x frequency

A

C.O. = (end diastolic volume - end systolic volume) x frequency

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113
Q
Who formulated the "law of the heart"?
C. Bernard
H. Starling
A. L. Lavoisier
W. Einthoven
A

H. Starling

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114
Q

Which are the most important components of the Starling’s preparations?

Intact systemic circulation, denervated heart, peripheral resistance instead of lung circulation

Intact lung circulation, denervated heart, intact systemic circulation

Intact lung circulation, denervated heart, peripheral resistance instead of systemic circulation, reservoir instead of venous system

Intact lung circulation, intact heard, peripheral resistance instead of systemic circulation, reservoir instead of venous system

A

Intact lung circulation, denervated heart, peripheral resistance instead of systemic circulation, reservoir instead of venous system

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115
Q

What happens when you increase the venous return in the Starling’s preparation?

Stroke volume does not change, frequency increases, cardiac output increases

Stroke volume and frequency increase, cardiac output increases

End diastolic volume increases, stroke volume and frequency do not change

End diastolic volume increases immediately, then stroke volume and cardiac output increases, while frequency does not change

A

End diastolic volume increaes immediately, then stroke volume and cardiac output increases, while frequency does not change

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116
Q

What happens when you increase the peripheral resistance in the Starling preparation?

End diastolic volume increases immediately, but stroke volume, frequency, and cardiac output do not change

End diastolic volume increases immediately, stroke volume and frequency do not change, cardiac output increases

Stroke volume does not change, frequency and cardiac output increases

Stroke volume, frequency and cardiac output increases

A

End diastolic volume increases immediately, but stroke volume, frequency and cardiac output do not change

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117
Q

How does the Starling law apply in case of change in posture?

The peripheral resistance changes when the animal stands up, or lies down

Venous return changes when the animal stands up, or lies down

Changing posture the altered frequency provides the immediate capability to adapt

The systolic reserve provides the background of the higher heart performance

A

Venous return changes when the animal stands up or lies down

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118
Q

What is the heterometric autoregulation?

During one cycle the same amount of blood is pumped out from the left and right heart

The different blood volumes entering the left and right side of the heart requires no compensation

Higher amount of blood pumped out from one side of the heart dilates the other side, as well, which makes the heart able to pump more blood

increased venous return decreases the work of the heart

A

Higher amount of blood pumped out from one side of the heart dilates the other side as well, which makes the heart able to pump more blood

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119
Q

What does the Starling “heart law” tell us?

The performance of the heart is equal even in changing conditions

Increased venous return does not alter the performance of the heart

Increased expansion of the heart muscle increases the performance of the heart slightly

Increased expansion of the muscle increases the performance of the heart significantly

A

Increased expansion of the muscle increases the performance of the heart significantly

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120
Q

What does the compliance of the heart depend on?

the inherent abilities of the heart muscle to dilate

the end systolic pressure

only the peripheral blood pressure

the peripheral blood pressure has no effect

A

The inherent abilities of the heart muscle to dilate

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121
Q

What is the correlation between EDV and SV values?

Negative correlation
Positive correlation
Logarithmic correlation
no correlation

A

Positive correlation

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122
Q

Which parameters influence the end diastolic volume?

diastolic filling time, contractility, aortic pressure
ventricular compliance, diastolic filling time, contractility
ventricular compliance, ventricular preload, diastolic filling time
ventricular compliance, aortic pressure, diastolic filling time

A

Ventricular compliance, ventricular preload, diastolic filling time

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123
Q

Which parameters influence the end systolic volume?

Venous blood pressure, duration of the systole, contractility

ventricular compliance, contractility, duration of the systole

contractility, duration of the systole

contractility, aortic pressure

A

Contractility, aortic pressure

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124
Q

How does age affect the compliance?

Decreases with age
Increases with age
Compliance curve is shifted to the right in old age
Ventricular compliance is not altered by age

A

Decreases with age

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125
Q
What is the ratio of adult and young EVDP to reach the same EVD?
1.5 to 1
2 to 1
3 to 1
4 to 1
A

2 to 1

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126
Q
Which formula can be used to derive the peripheral resistance?
Q = delta P / R
Q = C.O. / R
Q=R/C
Q = delta P x R
A

Q = delta P / R

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127
Q

What is the critical closing pressure?

the pressure at which muscles of vessels relax

the pressure at which vessels collapse due to their tone

the pressure at which resistance of vessels decrease

the pressure at which the myogenic tone of vessels increase

A

The pressure at which vessels collapse due to their tone

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128
Q

What does the Laplace-law state?

The pressure is a function of wall tension
The pressure is determined by the radius of the hollow organ
keeping a given pressure inside a spherical container is influenced by the radius
Q = delta P x R

A

Keeping a given pressure inside a spherical container is influenced by the radius

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129
Q

How does the viscosity of the blood change with the increase of the hematocrit value?

the change is determined by the diameter of the red blood cells
it does not change
it decreases
it increases

A

It increases

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130
Q

What is characteristic of laminar flow?

liquid layers slide over each other smoothly

the maximum velocity of the flow occurs close to the wall of the tube

vortex development

the flow is determined by the velocity, density and viscosity of the fluid, and the diameter of the tube

A

Liquid layers slide over each other smoothly

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131
Q

Which of the following is not true for turbulent flow?

it can be described by the Reynold’s number

liquid layers slide over each other smoothly

when the Reynold’s number is over 3000 the flow is turbulent

liquid layers mix due to vortex formation

A

Liquid layers slide over each other smoothly

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132
Q

What is the physiological importance of laminar flow?

while moving in the parietal stream blood cells
decrease their resistance

it stimulates heart work

the slow flow rate alongside the walls of the vessels enables material exchange

due to the faster flow rate alongside the walls of vessels the blood cells do not stick to the wall

A

The slow flow rate alongside the walls of the vessels enables material exchange

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133
Q

What is the function of the arterial section of the circulation?

enhances the capacity of the circulation

acts as a reserve for blood

forms an exchange surface

builds up resistance

A

Builds up resistance

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134
Q

What is the function of the capillary section of the circulation?

enhances the capacity of the circulation

acts as a reserve for blood

forms an exchange surface
builds up resistance

A

Forms an ion exchange surface

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135
Q

Which units belong to the serially attached elements of the circulation?

Arteries, veins
Capillaries of separate organs
Arteries, capillaries, veins
Arteries of separate organs

A

Arteries, capillaries, veins

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136
Q

With which formula can you calculate the total resistance of the serially attached elements of the circulatory bed?

sum of the reciprocal resistance of the elements

the difference of the smallest and largest resistance

resistance of the elements should be multiplied by each other

sum of elementary resistances

A

Sum of elementary resistances

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137
Q

What is the role of the Windkessel function?

it insures a continuous flow of blood

it stabilizes the blood pressure in the aorta

keeps the pressure constant during systole/ diastole in the large arteries

during diastole the aorta can actively pump blood to the periphery

A

It insures a continuous flow of blood

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138
Q

What determines the tone of resistance vessels?

myogenic tone

myogenic and sympathetic vasoconstrictor tone

myogenic and sympathetic vasodilator tone

sympathetic vasoconstrictor tone

A

Myogenic and sympathetic vasoconstrictor tone

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139
Q
Where is the highest number of elastic elements?
arterial end of capillary
muscular arteries
aorta
arterioles
A

Aorta

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140
Q
Which blood vessels are the most important resistance segments?
aorta
muscular arteries
capillaries
arterioles
A

Arterioles

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141
Q
In which vessels can resistance be adjusted?
in muscular arteries
in capillaries
in the aorta
in veins
A

In muscular arteries

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142
Q

Where can continuous capillaries be found?

in liver and hemopoietic tissues

in muscle, skin, central nervous system and the lungs

in the mucosa of intestines and endocrine glands

in renal glomeruli

A

In muscle, skin, central nervous system and the lungs

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143
Q

Where can fenestrated capillaries be found?

in liver and hemopoietic tissues
in muscle, skin, central nervous system and the lungs
in the mucosa of intestines and endocrine glands
in renal glomeruli

A

In the mucosa of intestines and endocrine glands

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144
Q

Where can porous capillaries be found?

in liver and hemopoietic tissues
in muscle, skin, central nervous system and the lungs
in the mucosa of intestines and endocrine glands
in renal glomeruli

A

In renal glomeruli

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145
Q

Where can sinusoid capillaries be found?

in liver and hemopoietic tissues

in muscle, skin, central nervous system and the lungs

in the mucosa of intestines and endocrine glands

in renal glomeruli

A

In the liver and hemopoietic tissues

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146
Q

What characterizes the capillaries of the skin?

lamina basalis serves as a barrier for ions
single-layered, continuous endothelium
ability of contraction
lack of pore-like intracellular channels

A

Single-layered continuous endothelium

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147
Q

What characterizes the capillaries of the intestinal mucosa?

thin endothel layer
free transport of substances
small and large pores
reflection of all proteins

A

Small and large pores

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148
Q

What characterizes the capillaries of the kidney?

small and large pores

lamina densa has a strong positive charge

lamina basalis serves as a barrier for ions

the large round gaps in it enable free transport of substances

A

The large round gaps in it enable free transport of substances

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149
Q

What characterizes the capillaries of the hemopoietic organs?

place of transport is the Disse-space

thin endothel layer

ability of contraction

lamina densa has a strong negative charge

A

Place of transport is the Disse-space

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150
Q
Which type of capillary is the most common in the body?
porous
continuous
fenestrated
sinusoid
A

Continuous

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151
Q
From the following, which is not a venule type?
postcapillary
collecting
elastic
muscular
A

Elastic

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152
Q

What is the peculiarity of veins?

they are not all able to contract actively

veins only with a diameter larger than 5 cm can store significant amount of blood

they have an important role in maintaining blood pressure

they expand without resistance, and then suddenly they resist

A

They expand without resistance and then suddenly they resist

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153
Q

What is true for the parallelly connected sections of the circulation?

the total resistance of the elements is smaller than that of the individual organs

the total resistance is equal to that of the organs

the total resistance is hardly greater than that of the organs

the total resistance is equal to 1/Rt = (1/ R1 + 1/R2 +… 1/Rn) xn

A

The total resistance of the elements is smaller than that of the individual organs

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154
Q

Which units are part of the parallelly connected parts of circulation?

arteries, capillaries and veins
the circulatory bed of the individual organs
arteries, veins
capillaries of different organs

A

The circulatory bed of the individual organs

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155
Q

How does the diameter of the individual vessels change in the different sections?

diameter of vessels decrease to arterioles, then radically increase to capillaries, then continuously grows up to the big veins

the diameter of vessels continuously decrease from the aorta to the capillaries, then it does not change

diameter of vessels radically decrease from the aorta to the capillaries, while from the capillaries to the vena cava the change is in the opposite direction

diameter of arteries and veins is the order of cm, while that of the capillaries is the order of mm

A

Diameter of vessels radically decrease from the aorta to the capillaries while from the capillaries to the vena cava the change is in the opposite direction

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156
Q

How does the total diameter of the vessels change in the different sections?

total diameter of arteries and veins is hardly smaller than that of capillaries

total diameter of capillaries is 600-1000 times greater than the total diameter of large arteries

total diameter of capillaries is 100 times greater than the diameter of the aorta

total diameter of capillaries is 600-1000 times greater than the diameter of the aorta

A

Total diameter of capillaries is 600-1000 times greater than the diameter of the aorta

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157
Q
In which section can the most blood be found?
in veins
in capillaries
in arteries
in arterioles
A

In veins

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158
Q
What percentage of the circulating blood can be found in capacity vessels?
90 %
79 %
11 %
60 %
A

79%

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159
Q

What percentage of the circulating blood can be found in resistance vessels?

2%
79 %
11 %
30 %

A

11%

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160
Q
What percentage of the circulating blood can be found in the heart?
40 %
1%
22 %
10 %
A

10%

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161
Q

What maintains blood pressure?

work of the heart and the resistance of peripheral system

the work of the heart solely

the Windkessel function of the aorta

the myogenic and sympathetic vasoconstrictor tone of arterioles

A

Work of the heart and the resistance of peripheral system

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162
Q

Which of the following factors is not significant in maintaining blood pressure?

elasticity of vessels
hemoglobin content of the blood
cardiac output
peripheral resistance

A

Hemoglobin content of the blood

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163
Q
What is the value of the systolic blood pressure?
10.7 kPa
6 kPa
16 kPa
12 kPa
A

16 kPa

164
Q
How much is the value of diastolic blood pressure?
12 kPa
6 kPa
16 kPa
10.7 kPa
A

10.7 kPa

165
Q

What is pulse- pressure?

difference between diastolic and systolic pressure
simple average of systolic and diastolic pressure
quotient of systolic and diastolic pressure
static pressure on the vessels

A

Difference between diastolic and systolic pressure

166
Q

What is mid- pressure?
difference between diastolic and systolic pressure
corrected average of systolic and diastolic pressure
quotient of systolic and diastolic pressure
static pressure on the vessels

A

Corrected average of systolic and diastolic pressure

167
Q

What is ordinary respiratory pressure?

difference between diastolic and systolic pressure

simple average of systolic and diastolic pressure

static pressure on the walls of the vessels

quotient of systolic and diastolic pressure

A

Static pressure on the walls of the vessels

168
Q

What determines the value of mid- pressure the most?

static pressure of blood
circulating quantity of blood
elasticity of the vessels
cardiac output and the peripherial resistance

A

Cardiac output and peripheral resistance

169
Q

What determines most the pulse- pressure?

cardiac output and arterial compliance

total quantity of circulating blood

cardiac output

static pressure of blood

A

Cardiac output and arterial compliance

170
Q

How does the increase of heart rate influence blood pressure?

it decreases blood pressure

it has no effect on blood pressure

it increases blood pressure

it becomes fluctuating

A

It increases blood pressure

171
Q

How does the increase of peripheral resistance influence peripheral effusion?

it decreases it continuously, then effusion increases after some minutes

it has no effect on peripheral effusion

it increases peripheral effusion

it decreases peripheral effusion, then after some cycles of the heart the original cardiac output is restored

A

It decreases peripheral effusion, then after some cycles of the heart the original cardiac output is restored

172
Q

How does the increase of arterial blood volume influence blood pressure?

pulse pressure and mid-pressure increase
systolic pressure increases
diastolic pressure increases
static pressure on the vessels increases

A

Pulse pressure and mid-pressure increase

173
Q

How does expansion of blood- vessels change in the elderly?

in a healthy individual age does not influence the elasticity of the vessels

pulse-pressure increases, compliance decreases

compliance increases

elasticity decreases

A

Pulse-pressure increases, compliance decreases

174
Q

Where can the highest value of blood pressure be measured?

in the arteries
in the a. pulmonalis
in the left ventricle and in the aorta
in the right ventricle

A

In the left ventricle and in the aorta

175
Q

Where can the lowest value of blood pressure be measured?

in the right ventricle
venous side of the capillary
in the left atrium
in the right atrium

A

In the right atrium

176
Q

What causes the notch on the descending side of the arterial pulse wave?

reflection pressure

static pressure

the difference in the pressure between two points of the artery

dimmed effect of systolic pressure

A

Reflection pressure

177
Q
How much is the velocity of pulse- wave?
40 cm/sec
7 m/sec
0.3 mm/sec
1.2 m/sec
A

7 m/sec

178
Q

How does the value of pressure-pulse change towards the periphery?

it decreases
first it increases, then later it decreases
it increases
it does not change

A

It increases

179
Q

How does the value of flow-pulse change from the aorta towards the small arteries?

it does not change

first it increases, then it decreases

it increases

it decreases

A

It decreases

180
Q

On which section of the circulation does pulse-wave attenuate?

in the metarterioles
in the capillaries
in the small arteries
in the venule

A

In the metarterioles

181
Q

How does the value of mid-pressure change towards periphery?

it increases
it decreases continuously
first it decreases, then it increases
it does not change

A

It decreases continuously

182
Q

On which section of the circulation does blood flow become continuous?

in the capillaries
in the small arteries
after the metarterioles
in the venule

A

In the metarterioles

183
Q

Which process is dominant in the material exchange?

transcytosis
resorption
filtration
diffusion

A

Diffusion

184
Q

What process determines the interstitial volume?

filtration/resorption
diffusion
filtration
filtration, diffusion

A

Filtration/resorption

185
Q

On which interface do we find single muscle sphincter?

small arterioles - metarteriola

metarterioles - capillary

small arterioles - capillary

capillary - venule

A

Metarterioles - capillary

186
Q
What is the percentage of capillaries that are open during resting state?
1-2 %
10-20 %
5-10 %
50 %
A

5-10%

187
Q

How much time does the total gas exchange in capillaries during resting state take?

400-500 msec
1 sec
20-30 msec
200-300 msec

A

200-300 msec

188
Q

Which of the following factors does not influence the measurement of diffusion?

number of red blood cells
concentration gradients
permeability
surface area

A

Number of red blood cells

189
Q

How large is the water transport by diffusion?

0.6 ml/ sec/ 100 g of tissue

300 ml/ sec/ 100 g of tissue

0.06 ml/ sec/ 1 g of tissue

30 ml/ sec/ 100 g of tissue

A

300 ml/sec/100g of tissue

190
Q

How large is the water transport with filtration and resorption?

0.6 ml/ sec/ 1 g of tissue

300 ml/ sec/ 100 g of tissue

0.06 ml/ sec/ 100 g of tissue

30 ml/ sec/ 1 g of tissue

A

0.06ml/sec/100g of tissue

191
Q

Which of the following substances do not move by diffusion?

small molecular weight metabolites
the small molecular weight nutrients
gases
proteins

A

Proteins

192
Q

Which of the following substance exchange is limited by its diffusion capability?

proteins
glucose
gases
small molecular nutrients

A

Proteins

193
Q

How does the the oxygen diffusion change in the capillaries?

the partial pressure of the O2 linearly decreases as it flows towards the veins

the partial pressure of the O2 rapidly decreases as it flows towards the veins

the partial pressure of the O2 slightly decreases as it flows towards the veins

the partial pressure of the O2 increases as it flows towards the veins

A

The partial pressure of the O2 rapidly decreases as it flows towards the veins

194
Q

What is typical of the flow dependent material exchange?

the concentration increases in a small degree toward the venous side of capillaries

the concentration in the capillaries increases significantly towards the venous capillaries

it has a crucial importance in the case of easily diffusing substances

the growing flow rate reduces the substance deposition toward the tissues

A

It has crucial importance in the case of easily diffusing substances

195
Q

What is typical of the diffusion limited transport?

the concentration does not change alongside the capillaries

the concentration rapidly increases in the tissue toward the venous side of the capillaries

it is typical of the transport of the easily diffusing substances

capillary transit time influences the rate of transport of large molecules

A

Capillary transit time influences the rate of transport of large molecules

196
Q

What do we call Starling forces?

all the forces that play a role in the formation of the effective filtration pressure

all the forces that affect the oncotic pressure

all the facts that regulate the capillary permeability

all the facts that affect the effective hydrostatic pressure

A

All the forces that play a role in the formation of the effective filtration pressure

197
Q

What is typical for capillaries?

in the arterial capillaries filtration, in the venous resorption occurs

in some of the capillaries filtration, in others resorption happens

because of the loss of fluid the hydrostatic pressure decreases towards the venous side of the capillary

the effective filtration pressure is constant alongside the capillaries

A

In some of the capillaries filtration, in others resorption happens

198
Q

How can we calculate the effective filtration pressure?

on the basis of the difference between the oncotic pressure in the capillary and the blood pressure

on the basis of the difference between the effective hydrostatic pressure and oncotic pressure

on the basis of the difference between the effective hydrostatic pressure and the effective oncotic pressure

it is the product of the effective hydrostatic pressure and the effective oncotic pressure

A

On the basis of the difference between the effective hydrostatic pressure and the effective oncotic pressure

199
Q

What determines the filtration rate?

the oncotic pressure of the plasma
the hydrostatic pressure of the interstitium
the hydrostatic pressure of the plasma
the effective filtration pressure and the capillary permeability

A

The effective filtration pressure and the capillary permeability

200
Q

Which formula describes filtration rate?

Q= P effective x filtration coefficient of the capillary

Q= P hydrostatic x coefficient of the capillary filtration

Q= P effective / coefficient of the capillary filtration

Q= (P onc.- P hidr.) x coefficient of the capillary filtration

A

Q = P effective x filtration coefficient of the capillary

201
Q

How much surplus filtrate is produced normally?

1-2 ml / 100 kg
10-15 ml / 100 kg
3-4 ml / 100 kg
30-40 ml / 100 kg

A

3-4 ml/100kg

202
Q

What happens with the filtrate surplus at the interstitium?

the veins carry it away

it increases the oncotic pressure in the interstitium

it increases the hydrostatic pressure in the interstitium

the lymph vessels carry it away

A

The lymph vessels carry it away

203
Q

What is the most important fact which plays a role in the maintenance of the venous circulation?

the work of the heart
the presence of the valves
the peripheral resistance
the gravitation

A

The work of the heart

204
Q

How does the venous blood pressure change?

it is low in the small veins and the venules but grows toward the right atrium

it decreases constantly from the venules toward the right atrium

it increases constantly from the venules toward the right atrium

it does not change between the venules and the big veins but then it decreases suddenly

A

It decreases constantly from the venules toward the right atrium

205
Q

What is the most important factor in the extrinsic regulation of the circulation?

local autoregulation

nutritive demand of the tissues

the regulated contractile state of resistance and capacitance vessels

the effects of the parasymphatetic tone on the blood vessels

A

The regulated contractile state of resistance and capacitance vessels

206
Q

What happens when the blood pressure drops in an organ of high metabolic rate?

the tissue is damaged

nutrient supply to the cells decrease

vessel contraction compensates this change

normal perfusion is restored by adaptive vessel relaxation

A

Normal perfusion is restored by adaptive vessel relaxation

207
Q

What happens if the blood pressure increases in a given organ of steady metabolic rate?

because of the compensatory contraction of the vessels the normal perfusion is restored

because of the relaxation of the vessels the blood pressure decreases

the metabolic rate increases in the tissues

oedema evolves

A

Because of the compensatory contraction of the vessels the normal perfusion is restored

208
Q

In which range can the autoregulation restore normal perfusion?

90-110 Hgmm
40-140 Hgmm
80-120 Hgmm
20-240 Hgmm

A

40-140 Hgmm

209
Q

What is the Bayliss- effect?

the circulation is under endocrine control

the constant midpressure of the arteries ensures microcirculation

increase of heart frequency in case of atrial expansion

the vessels reply to the decrease of pressure with relaxation

A

Increase of heart frequency in case of atrial expansion

210
Q

What plays a role in the local adjustment of perfusion?

simply the laws of physics

parasymphathetic neural regulation

symphathetic neural regulation

myogenic answer

A

Myogenic answer

211
Q

What role does the endothel layer have in the regulation of perfusion?

the factors produced by it influence contraction state of the muscular layer of the vessels

the NO produced by it contracts the vessels

the EDCF produced by it increases the blood flow

ERDF production of smooth muscles is stimulated

A

The factors produced by it influence contraction state pf the muscular layer of the vessels

212
Q

How do smooth muscle elements react to acetylcholine in the walls of blood- vessels with a continuous endothel?

contraction
indirect relaxation
direct relaxation
EDCF mediated contraction

A

Indirect relaxation

213
Q

What determines the diameter of blood-vessels?

the quantity of acetylcholine and other factors in the plasma

hormone producing ability of the endothel cell

the equilibrium of the sympathetic vasomotor tone and NO production

the metabolic state of the smooth muscle of the blood vessel

A

The equilibrium of the sympathetic vasomotor tone and NO production

214
Q

What stimulates NO synthesis?

release of endothelins
decreased bradikinin, histamine levels
decreased adenosine concentration
increased adenosine concentration

A

Increased adenosine concentration

215
Q

Which substance is not part of the EDCF-family?

substance P
cyclooxigenase dependent factors
endothelins
angiotensin-II

A

Substance P

216
Q

What changes take place in the tissues when their metabolic rate increases?

partial pressure of oxygen increases in the tissue
due to the indirect effect of EC metabolites perfusion increases
concentration of EC metabolites decreases perfusion
with their humoral signals enothel cells decrease perfusion

A

Due to the indirect effect of EC metabolites perfusion increases

217
Q

What is hyperaemia?

susceptibility to bleeding
increased hematocrit value
local increase of perfusion
high blood pressure

A

Local increase of perfusion

218
Q

When can we speak of active hyperaemia?

when increased perfusion is generated locally to compensate the decrease of systemic blood pressure

when increased perfusion is due to the increase of systemic blood pressure

when increased perfusion is a secondary effect

when perfusion increases parallelly with the increase of local metabolic rate

A

When perfusion increases parallelly with the increase of local metabolic rate

219
Q

In what ways can the decreased partial pressure of O2 influence perfusion?

primarily by stimulating NO release

decreased partial pressure of O2 acts only indirectly on smooth muscle

mediated by an increased partial pressure of CO2

by increasing hydrogen concentration

A

Primarily by stimulating NO release

220
Q

Where is the pressor center located?

in the caudal region of the reticular formation

in the dorsolateral region of the reticular formation

in the caudomedial region of the reticular formation

in the lateral region of hypothalamus

A

In the dorsolateral region of the reticular formation

221
Q

Where is the depressor center located?

in the caudal region of the reticular formation

in the dorsolateral region of reticular formation

in the ventromedial region of the reticular formation

in the medial region of hypothalamus

A

In the ventromedial region of the reticular formation

222
Q

What is true for depressor effect?

it causes vasoconstiction in the periphery

has a positive chronotrop and dromotrop effect

has spontaneous activity which decreases heart rate

it is mediated by n.vagus

A

It is mediated by n.vagus

223
Q

What is true for pressor effect?

has spontaneous activity, and it is mediated by the thoracolumbar sympathetic neurons

it causes vasodilatation

has a negative chronotrop and dromotrop effect

it is mediated by n.vagus

A

Has spontaneous activity and it is mediated by the thoracolumbar sympathetic neurons

224
Q

What is the effect of sympathetic nervous system on the resistance vessels?

general vasoconstriction

vasodilatation in skeletal muscle, vasoconstriction in the splanchnic region

general vasodilatation

vasoconsriction in skeletal muscle, vasodilatation in the splanchnic region

A

Vasodilatation in skeletal muscle, vasocontriction in the splanchnic region

225
Q

What is the effect of sympathetic nervous system on the capacitance vessels?

vasodilatation

mild vasoconstriction

a little increase in sympathetic tone evokes immediate strong contraction

has little or no effect

A

A little increase in sympathetic tone evokes immediate strong contraction

226
Q

Of the following organs which is under parasympathetic control?

resistance vessels
skeletal muscle arterioles
skin vessels
heart

A

Heart

227
Q

What is the role of parasympathetic system in the adjustment of the diameter of blood vessels?

no significant effect
strong vasodilator effect
mild vasoconstrictor effect
strong vasoconstrictor effect

A

No significant effect

228
Q

In which organ can indirect parasympathetic vasodilatation be found?

corpora cavernosa
salivary gland
uterus
pancreas

A

Salivary gland

229
Q

In which organ can direct parasymathetic vasodilatation be found?

salivary gland
skin
uterus
liver

A

Uterus

230
Q

What is the effect of a small quantity of epinephrine on the blood vessels?

general constriction

coronary constriction

dilatation in skin, constriction in skeletal muscle and splanchnic regions

dilatation in skeletal muscle, constriction in skin and splanchnic regions

A

Dilatation in skeletal muscle, constriction in skin and splanchnic regions

231
Q

What is the effect of a large quantity of epinephrine on the blood vessels?

generalized vasoconstriction

dilatation in skeletal muscle, constriction in skin and splanchnic regions

dilatation in skin, constriction in skeletal muscle and splanchnic regions

coronary constriction

A

Generalized vasoconstriction

232
Q

What is the effect of norepinephrine on the blood vessels?

beta-adrenergic constriction

alpha-adrenergic constriction

alpha-adrenergic dilatation

beta-adrenergic dilatation

A

Alpha-adrenergic constriction

233
Q

What did the Heymans experiment prove?

the presence of volume receptors

the presence of osmotic receptors

the presence of baroreceptors

the presence of gas receptors

A

The presence of baroreceptors

234
Q

How does blood pressure change after the destruction of baroreceptors?

blood pressure does not change substantially

blood pressure increases beyond 180 mmHg

blood pressure decreases below 80 mmHg

blood pressure fluctuates between 40-170 mmHg

A

Blood pressure fluctuates between 40-170 mmHg

235
Q

In case of what blood pressures does baroreceptor reflex regulate?

between 50-170 mmHg
below 80 mmHg
over 120 mmHg
between 80-120 mmHg

A

Between 50-170 mmHg

236
Q

What defensive processes act below 50 mmHg blood pressure?

maximal parasympathetic effect, ceasing sympathetic activity

continuous maximal sympathetic and ceasing parasympathetic activity

in different parts of the organism simultaneously either increased parasympathetic or increased sympathetic activity can be observed

slow increase in sympathetic activity

A

Continuous maximal sympathetic and ceasing parasympathetic activity

237
Q

What kind of protecting processes begin above 17O mmHg blood pressure?

continuous maximal sympathetic and discontinued parasympathetic activity

mixed sympathetic and parasympathetic activities

maximal parasympathetic effect, discontinued sympathetic activity

slight parasympathetic increase

A

Maximal parasympathetic effect, discontinued sympathetic activity

238
Q

Where are baroreceptors located?

glomus caroticum
a. pulmonalis
glomus aorticum
arcus aortae

A

Arcus aortae

239
Q

Where are oxygen sensitive receptors located?

glomus aotricum
a. pulmonalis
sinus caroticus
arcus aortae

A

Glomus aotricum

240
Q
What kind of effects are responsible for vasodilation?
increasing parasympathetic effect
decreasing sympatethic effect
increased tissue oxygen concentration
decreased tissue CO2 level
A

Decreasing sympathetic effect

241
Q

In which animal do we find sympathetic cholinergic vasodilatation?

in birds
in ruminants
in dog and cat
in horse and pig

A

In dog and cat

242
Q

What mechanism acts against hypervolemia?

a peptide that is produced in the left ventricle

increases sodium excretion
ANP is produced and it decreases sodium excretion

ADH is produced and increases water loss

decreased ADH and increased ANP production

A

Decreased ADH and increased ANP production

243
Q

What is the Bainbridge reflex?

increasing volume of the atria increases heart frequency if it was low previously

increasing volume of the atria decreases heart frequency

it is the same as the Starling mechanism

it is a depressor reflex

A

Increasing volume of the atria increases heart frequency if it was low previously

244
Q

How is cardiovascular and respiratory interrelated?

the decrease of the pO2 in the medulla causes significant sympathetic activation

the increase of the pCO2 in the medulla causes significant sympathetic activation

the increase of the pCO2 in the glomus caroticum causes significant sympathetic activation

the decrease of the pO2 in the medulla causes significant parasympathetic activation

A

The increase of the pCO2 in the medulla causes significant sympathetic activation

245
Q

In the long run what is the most important regulator of coronary circulation?

the actual stage of the heart cycle

the aortic pressure change

the metabolic state of the heart

the arterial mean pressure

A

The metabolic state of the heart

246
Q

In which phase of heart cycle does the blood flow backward in the coronary artery?

never
slow ejection
fast ejection
fast filling

A

Fast filling

247
Q

what phase of the heart cycle gets more blood into the coronary artery?

diastole
systole
slow filling
fast ejection

A

Diastole

248
Q

What characterizes the regulation of brain circulation?

the perfusion is kept constant in different regions of the brain

the intravasal / EC volume is kept constant

mostly the sympathetic innervation regulates the ampleness of vessel

the principal local regulator is the pO2

A

The intravasal / EC volume is kept constant

249
Q

In which range of mean pressure is the brain circulation constant?

90-110 mmHg
80-120 mmHg
30-200 mmHg
60-160 mmHg

A

60-160 mmHp

250
Q

What is the most important role of the skin circulation?

supporting heat balance

blood storing function

covering the high oxygen and nutrient demand of this organ

enlarging the resistance segment of the circulation

A

Supporting heat balance

251
Q

What characterizes the splanchnic circulation?

extensive metabolic autoregulation

low capacity

double circulation, portal system

myogenic autoregulation

A

Double circulation, portal system

252
Q

Among the following statements which is true for the splanchnic circulation?

low capacity

the liver has no significant reservoir function

the autoregulation has primary role

main regulator is the vasoconstrictor tone

A

The main regulator is the vasoconstrictor tone

253
Q

What characterizes the fetal circulation?

the left ventricle pumps 20% larger volumes than the right ventricle

two-thirds of blood flows to cranial areas from the aorta

the pressure of the pulmonary artery is 5 mmHg higher than the pressure of the aorta

O2 saturation of the a. umbilica is 85%

A

The left ventricle pumps 20% larger volumes than the right ventricle

254
Q

Which are the structural proteins of the muscle?

actin and myosin

actin, myosin, micro and intermediary filaments

contractile proteins

microfilaments

A

Actin, myosin, micro and intermediary filaments

255
Q

What is the primary energy store for the muscle?

creatinphosphate
ATP
glycogen
lipids

A

Creatinphosphate

256
Q

Which muscle has the biggest quantity of creatinphosphate?

heart muscle
smooth muscle and striated muscle
skeletal muscle
smooth muscle

A

Skeletal muscle

257
Q

What are the functions of elastic elements in the muscle?

decrease heat loss

decrease resistance

they prevent excess shortening

they support the work of the muscle passively

A

They support the work of the muscle passively

258
Q

What kind of stripes and zones are in the sarcomere?

Z-stripe, H-zone, M- stripe
A-stripe, Z-stripe
H-zone, M-stripe, I- stripe
A-stripe,M-zone, Z- stripe

A

Z-stripe, H-zone, M-stripe

259
Q

What is the fibrillum?

unit part of the sarcomere
muscle fibres in a muscle
elementary contraction unit
muscle cells

A

Muscle fibres in a muscle

260
Q

In which list do you find a protein which is not a component of a sacromere?

actin, titin, nebulin

meromyosin, actinin, titin

titin, nebulin, alpha-actinin, actin, myosin, troponin, tropomyosin

alpha-actinin, nebulin, troponin, albumin

A

Alpha-actinin, nebulin, troponin, albumin

261
Q

What is the function of the tropomyosin?

stimulates the myosin ATP-ase enzyme
covers the active surface of actin
it has Ca binding capaticy
gides the actin fibre

A

Covers the active surface of actin

262
Q

What is the troponin complex?

complex protein which stimulates the myosin ATP-ase enzyme

a single protein which have Ca binding capacity

complex protein which fixes myosin

complex protein which sets the position of tropomyosin

A

Complex protein which sets the position of tropomyosin

263
Q

What do the myosin isotypes determine?

The efficiency of sarcomere
The angle of moving
The power of muscle
What thickens the muscle fibre

A

The efficiency of sarcomere

264
Q

What does the crossbridge cycle start?

The tropomyosin is slipped
The calcium signal
The activity of myosin ATPase
The magnesium

A

The calcium signal

265
Q
How many times does the intracytoplasmic calcium level grow during activation?
10 x
1000 x
200 - 600 x
50 x
A

200-600 x

266
Q

What is the calcium transient?

Ca influx

Ca outflux

Ca influx, plateau, pumping out of the intracytoplasmic space

Ca outflux induced by decreasing calcium level

A

Ca influx, plateau, pumping out of the intracytoplasmic space

267
Q

What happens if the ATP is taken away from the system?

The muscle stops in relaxed state

The head of myosin can not bind to the actin

Permanent, inactive contraction

The myosin moves and separates from actin

A

Permanent, inactive contraction

268
Q

What happens if the calcium is taken away from the intracytoplasmic space?

Muscle relaxation

The head of myosin links to the actin

Permanent, inactivate contraction happens

The myosin does not separate from actin

A

Muscle relaxation

269
Q

What occurs in the sarcomere, when the ATP-ase cleaves the bound ATP?

The head of myosin binds to the actin

Energy discharge, the head of the myosin moves

The tropomyosin is moved from activate points of actin

The myosin separates from actin

A

Energy discharge, the head of the myosin moves

270
Q

What binds to the TnC non-specific binding site?

Calcium
Tropomyosin
Magnesium
Sodium

A

Magnesium

271
Q

What links to the TnC specific binding site?

Calcium
Tropomyosin
Magnesium
Sodium

A

Calcium

272
Q

What happens if a calcium signal is present?

The myosin separates from actin

The head of myosin bends to 55 degrees

The head of myosin detaches from actin

The TnC binds calcium and the myosin binding site of the actin is exposed

A

The TnC binds calcium and the myosin binding site of the actin is exposed

273
Q

What happens when ADP and Pi is released from the acto-myosin complex?

a two-step bending of the myosin head (40 plus 5 degrees)

a three-step bending of the myosin head (40 plus 5 plus 15 degrees)

a one-step bending of the myosin head (55 degrees)

a two-step bending of the myosin head ensuring altogether a 15 nm sliding

A

A two-step bending of the myosin head (40 plus 5 degrees)

274
Q

What’s the physiological background of rigor mortis?

there is too much ATP present

ATP is not available

there is too much calcium present

calcium is missing

A

ATP is not available

275
Q

What is true for cross bridge cycling?

a lot of heads are moving in synchronized form

repetitive pendular movement is present for all myosin heads

an asynchronous movement of thousands of myosin heads occur

synchronous ATP cleavage is present in all light chains of myosins

A

An asynchronous movement of thousands of myosin heads occur

276
Q

What is true for electromechanic coupling?

it lasts from the arrival of muscle AP to the development of a twitch

it is the generation AP in the myoneural junction

it is the calcium release through effect of the AP

it is the depolarization of the myolemma

A

It lasts from the arrival of muscle AP to the development of a twitch

277
Q

What happens with the intracytoplasmic calcium level when a twitch occurs?

the calcium level is increased continuously

the calcium level is constantly high

the calcium level increases, reaches a plateau and then decreases

the calcium level is increased and then stays constant until the next AP

A

The calcium level increases, reaches a plateau and then decreases

278
Q

What is the connection between the AP and the calcium maximum?

The maximum of calcium level coincides with AP

The maximum of calcium level preceeds the AP

The calcium level is not influenced by AP

The maximum of calcium level is reached after AP

A

The maximum of calcium level is reached after AP

279
Q

In which muscle type can we find a “diad”?

In the heart muscle
In the skeletal muscle
In the smooth muscle
in all types of muscles

A

In the heart muscle

280
Q

What happens in the triads?

Chemical signal is transformed to electrical signal

Electrical signal is transformed to chemical signal

Ca efflux from the cell

Release of ryanodin as a transmitter

A

Electrical signal is transformed to chemical signal

281
Q

What type of channel can we find on the membrane of the terminal cysternae?

Voltage dependent calcium channel

L-type calcium channel

Ryanodine sensitive calcium channel

There is no channel, but a voltage dependent membrane protein on this membrane

A

Ryanodin sensitive calcium channel

282
Q

What happens if the ryanodine sensitive calcium canal is opened?

Ca influx from EC to cells
Ca influx into the SR
Ca influx from EC to IC
Ca influx from SR to IC

A

Ca influx from the SR to IC

283
Q

How can the calcium signal attenuate its own effect?

positive feedback: it opens the calcium pumps to EC and SR

negative feedback: it opens more sodium channels

it stimulates the Ca-Na symporter

it inhibits the ATPase depedent pumps

A

Positive feedback: it opens the calcium pumps to EC and SR

284
Q

What is aequorin?

Reaction of this material with calcium forms a visible precipitate

Reaction of this material with a calcium channel emmits a light signal

a ryanodine receptor blocking agent

a protein channel for calcium

A

Reaction of this material with a calcium channel emmits a light signal

285
Q

What are “sequesters”?

Cell organelles that pump calcium into the EC

Transport proteins

Intracellular calcium storing sites

Voltage dependent channels

A

Intracellular calcium storing sites

286
Q

What pumps calcium back into the SR?

Ryanodin sensitive calcium channels

Carrier proteins

Voltage dependent calcium channels

ATP dependent calcium channels

A

ATP dependent calcium channels

287
Q

What pumps calcium into the EC?

Ryanodin sensitive calcium channels

Na-Ca symporter

Voltage dependent calcium channels

Sodium/calcium antiporter proteins

A

Sodium/calcium antiporter proteins

288
Q

During long-term muscle work energy for the muscle is provided by:

anaerobic glycolysis or aerobic glycose oxidation

anaerobic glycolysis and aerobic glycose oxidation

fat oxidation

protein decomposition

A

Anaerobic glycolysis or aerobic glycose oxidation

289
Q

How long is sufficient for the energy to be stored in form of ATP?

for 2-3 hours
for 2-3 seconds
for 2-3 minutes
for 20-30 seconds

A

For 2-3 seconds

290
Q

How long is sufficient the energy stored as creatinine-phosphate?

for 2-3 hours
for 2-3 seconds
for 20-30 seconds
for 2-3 minutes

A

20-30 sec

291
Q

Why does anaerobic glycolysis have to cover the sudden, intensive energy requirement?

because enzymes of aerobic glucose oxidation are not present

because aerobic glucose oxidation produces less energy

because aerobic glucose oxidation is initially inhibited

because aerobic glucose oxidation is a very slow process

A

Because aerobic glucose oxidation is a very slow process

292
Q

What is the source of anaerobic glycolysis in case of excessive stress?

glycogen
fat
glucose and later fats
lactic acid

A

Glucose and later fats

293
Q

What will be the fate of lactic acid produced during glycolysis?

it will be burnt in aerobic processes

it will be excreted through liver

it will be stored in the muscle

it will be entering the Cori-cycle in the liver

A

It will be entering the Con-cycle in the liver

294
Q

What is the disadvantage of oxidative processes?

the rate of ATP production is very low

too much CO2 is produced

toxic materials are released

insufficient amount of ATP is produced

A

The rate of ATP production is very low

295
Q

What kind of muscle tissue is especially suitable for FFA burning?

skeletal-muscle

heart muscle

smooth muscle and skeletal-muscle

skeletal-muscle and heart muscle

A

Heart muscle

296
Q

What is meant by paying back the oxygen debt?

muscle consumes less oxygen in resting state

fast twitch muscles consume more energy after external work stops

oxygen consumption of all muscle types is in direct proportion to their working intensity

fast twitch muscle fibres do not utilize oxygen at all and so they accumulate oxygen

A

Fast twitch muscles consume more energy after external work stops

297
Q

What kind of muscle accumulates a great oxygen debt?

red muscle
smooth muscle
white muscle
heart muscle

A

White muscle

298
Q

What is the effect of lactic acid in the muscle?

it is an energy storing compound

it is the final product of aerobic glucose oxidation

it is that final product of anaerobic glycolysis which stimulates sarcomeric activity

it is that final product of anaerobic glycolysis which has a direct inhibiting effect on sarcomeric activity

A

It is that final product of anaerobic glycolysis which has a direct inhibiting effect on sarcomeric activity

299
Q

What are the characteristic properties of white fibres?

quick, powerful contraction, anaerobic glycolysis

slow, permanent contraction, anaerobic glycolysis

quick, powerful contraction, aerobic oxidation processes

slow, permanent contraction, aerobic oxidation processes

A

Quick, powerful contraction, anaerobic glycolysis

300
Q

What are the characteristic properties of red fibres?

quick, powerful contraction, anaerobic glycolysis

quick, powerful contraction, aerobic oxidation processes

slow, permanent contraction, anaerobic glycolysis

slow, permanent contraction, aerobic oxidation processes

A

Slow, permanent contraction, aerobic oxidation processes

301
Q

How can you tell whether a whole muscle fibre belongs to the white or red group?

by measuring the strength of the muscle

by counting the ratio of white and red filaments in muscle

by measuring the length of the whole muscle

by counting the number of sympathetic fibers innervating the whole muscle

A

By counting the ratio of white and red filaments in the muscle

302
Q

What types of fibers exist in skeletal muscle?

pink and red
red
pink and white
red and white

A

Pink and white

303
Q

What is the color of slow twitch fibers?

pink and red
pink and white
red
red and white

A

Red

304
Q

What is the ratio between myoneural junction/filaments in fast twitch fibers?

many filaments one nerve

some filaments(2-3) one nerve

grape like

near to one filament/one nerve ratio

A

Near to one filament/one nerve ratio

305
Q

What is the ratio between myoneural junction/filaments of red fibers?

many filaments, one nerve

some filaments(2-3), one nerve

many filaments, one nerve with grape-bunch like innervation

one filament, one nerve

A

Many filaments, one nerve with grape-bunch like innervation

306
Q
What is the contraction time of red fibers?
2 ms
20 ms
10 ms
200 ms
A

200 ms

307
Q

What is the contraction time of pink fast fibers?

20 ms
2 ms
200 ms
10 ms

A

20 ms

308
Q

what is the contraction time of the quickest white fibers?

2-3 ms
10 ms
20 ms
200 ms

A

2-3 ms

309
Q

What is true for the fatigue of fast twitch fibers?

slow
there is no fatigue
quick
medium

A

Quick

310
Q

What is true for the fatigue of slow twitch fibers?

there is almost no fatigue
quick
medium
slow

A

There is almost no fatigue

311
Q

What type of metabolism do you find in red muscles?

anaerobic
oxidative
mixed
only fat burning exists

A

Oxidative

312
Q

What do we mean by “quantal summation”?

the increase of tension is given by the intracytoplasmic calcium level increase

the increase of tension is given by the sum of the contractions of many fibres

the increase in the power of contraction is the consequence of the fact that the calcium has no time to leave the cytoplasm after the previous contractions

the maximal contraction and the summation which caused this contraction

A

The increase of tension is given by the sum of the contractions of many fibres

313
Q

What do we mean by “contraction summation”?

the increase of tension is given by the sum of the contraction of many fibres

the increase in the power of contraction is the consequence of the fact that the calcium has no time to leave the cytoplasm after the previous contractions

the increase of tension is determined by the increased calcium level

the maximal contraction and the summation forms which caused this contraction

A

The increase of tension is determined by the increased calcium level

314
Q

What do we mean by “Treppe”?

the increase of tension is given by the sum of the contraction of many fibres

the increase of tension is given by the intracytoplasmic calcium level decrease

the maximal contraction and the summation forms which caused this contraction

the increase in the power of contraction is the consequence of the fact that the calcium has no time to leave the cytoplasm after the previous contractions

A

The increase in the power of contraction is the consequence of the fact that the calcium has no time to leave the cytoplasm after the previous contractions

315
Q

What can we learn from the the speed-tension diagram?

the working power of the muscle

the measure of the stretch of the muscle

the output of the muscle

the length of the maximal stretch of the muscle

A

The output of the muscle

316
Q

What can we learn from the length-tension diagram?

the working power of the muscle

the measure of the stretch of the muscle

the output of the muscle

the length of the maximal stretch of the muscle

A

The working power of the muscle

317
Q

What is the physiological role of the heat production of the muscle?

it has no significant role, it mainly means a loss

it has significant role in maintaining the coat temperature

only heat production through shivering has a significant role

it has a physiological role in maintaining core temperature

A

It has a physiological role in maintaining core temperature

318
Q
How many main components make up the total work of the muscle?
3
1
4
2
A

2

319
Q

What is the contraction/length domain of the optimal muscle workload?

medium tension/rest length
medium tension/ minimal length
maximal tension/rest length
minimal length/ maximal tension

A

Medium tension/rest length

320
Q

When do phasic fast fibres produce a great quantity of heat?

under restitution
under active contraction
under passive tension
only under “Treppe”

A

Under restitution

321
Q

When do red slow tonic fibres produce a great quantity of heat?

under restitution
under passive tension
under active contraction
only in relation with the initial heat production

A

Under active contraction

322
Q

What type of metabolism is there in white phasic fibres?

oxidative
mixed
anaerobic
there is only fat oxidation

A

Anaerobic

323
Q

What type of metabolism is there in pink phasic fibres?

oxidative
anaerobic
there is only fat oxidation
mixed

A

Mixed

324
Q

How long is a fibre in pink phasis fibres?

very long
middle sized
very short
short

A

Middle sized

325
Q
What is the length of a fibre in white phasic fibres?
middle sized
very short
very long
short
A

Very long

326
Q

What is the fibre-length in red tonic fibre?

very long
middle sized
short
varying

A

shorty

327
Q

Which muscle type contains the most collagen fibres?

the heart muscle
the skeletal muscle
the plain muscle
the skeletal and the heart muscle

A

The heart muscle

328
Q

What is a “twitch”?

muscle relaxation
muscle tremor
continuous muscle contraction
the refractory state of the muscle

A

Muscle tremor

329
Q

Which statements below is correct?

the calcium transient occurs concurrently with AP, there is no biological delay

the calcium transient follows an AP, the biological delay does not occur here

the calcium transient does not directly follow AP, there is biological delay

AP is followed by calcium transient with no delay

A

The calcium transient follows an AP, the biological delay does not occur here

330
Q

What is isometric contraction?

only the length of the muscle changes, but the tension does not

both the length and tension change

the muscle overstretches

only the tension changes, the length of the muscle does not

A

Only the tension changes, the length of the muscle does not

331
Q

What is isotonic contraction?

only the length of the muscle changes, but the tension does not
only the tension changes, the length of the muscle does not
both the length and tension change
the muscle overstretches

A

Only the length of the muscle changes, but the tension does not

332
Q

What is auxotonic contraction?

only the length of the muscle changes, but the tension does not

both the length and tension change

only the tension changes, the length of the muscle does not

the muscle overstretches

A

Both the length and tension change

333
Q

What arrangement suits the “preload” circumstances?

a load is put on the muscle

a load is put on the muscle and free movement of muscle is restricted with the use of a frame

a load is put on the muscle, passive flexing is allowed to a certain degree, then the load is proped up

free movement of muscle is hindered with a load

A

A load is put on the muscle, passive flexing is allowed to a certain degree, then the load is proped up

334
Q

Which arrangement suits the “afterload” circumstances?

A load is put on the muscle

a load is put on the muscle and we the passive stretching is hindered with a support

free movement of muscle hindered with a load

a load is put on the muscle and free contraction is hindered with a buffer

A

A load is put on the muscle and free contraction is hindered with a buffer

335
Q

What do we mean by “all-or-none” law?

in a single fiber maximal contraction is caused by an adequate stimulus, a smaller stimulus does not produce contraction

all muscle fibre contractions are caused by one single stimulus

the stimulus does not produce answer in all cases

the total muscle either contracts maximally or does not respond at all

A

In a single fiber maximal contraction is caused by an adequate stimulus, a smaller stimulus does not produce contraction

336
Q

Does the muscle produce heat in rest?

Not at all

Yes, this heat is a small contribution to the total heat production

Yes, this is the BMR

Yes, this heat production makes most of the BMR

A

Yes, this heat production makes most of the BMR

337
Q

BMR

A

Basic metabolic rate

  • the rate of energy expenditure per unit time by endothermic animals at rest
338
Q

the activation heat belongs to which stage of heat production?

to the initial heat production
to the resting heat production
to the delayed heat production
to the BMR of muscle

A

To the initial heat production

339
Q

Where does the activating heat production originate from?

calcium pump and cross bridge cycling

electromechanical coupling

onset of stimulus

replenishment of used up energy

A

Electromechanical coupling

340
Q

Which is larger in the fast glycolytic fiber?

The initial heat production is larger than activating heat production

The delayed heat production is larger than activating heat production

The initial heat production is larger than delayed heat production

Contraction heat production is larger than activating heat production

A

The initial heat production is larger than delayed heat production

341
Q
What is the efficiency of the skeletal muscle?
30 %
15 %
7%
20 %
A

20%

342
Q
What is the maximal speed of frame muscle?
7 m/sec
30 m/sec
15 m/sec
20 m/sec
A

7 m/sec

343
Q

Why do the muscles get tired in physiological circumstances?

Result of transmitter deficiency

Metabolic by-products accumulate

The oxygen supply is not adequate

Capacity of oxidative enzymes is not enough

A

Metabolic by-products accumulate

344
Q

What is the first sign of fatigue on the mechanogram?

The muscle does not relax

Reduced amplitude of contractions

The muscle only react on bigger stimulus

The muscle does not react on any stimulus

A

Reduced amplitude of contractions

345
Q

What is happening when the muscle is working in an oxygenated atmosphere in vitro?

After the muscle gets tired, it needs a long time to recover

The muscle does not recover from exhaustion

restitution is quick after the muscle gets tired

The muscle can not be exhausted

A

Restitution is quick after the muscle gets tired

346
Q

What is happening when the muscle is working in a nitrogen atmosphere in vitro?

After the muscle gets tired, it needs a long time to recover

Restitution is quick after the muscle gets tired

The muscle gets never tired

The muscle cannot recover after fatigue

A

The muscle cannot recover after fatigue

347
Q

Which type of muscles get tired the most easily?

White muscle
Whole muscle
Smooth muscle
Red muscle

A

White muscle

348
Q

Which type of muscles get tired least easily?

White muscle
Red muscle
Whole muscle
Smooth muscle

A

Red muscle

349
Q

What mediates the effect of acetylcholine on the muscle membrane?

Muscarinic receptor
G-protein receptor
Nicotinic receptor
Transmembrane enzyme

A

Nicotinic receptor

350
Q

what occurs when acetylcholine binds?

sodium-channel closes
Ligand-dependent cation channel closes
sodium-channel opens
Ligand-dependent cation channel opens

A

Ligand-dependent cation channel opens

351
Q

What does opening of cation channel cause after the binding of acetylcholine?

It induces the generation of End Plate Potential
Hyperpolarization
Cation outflow
Closure of thesodium-channel

A

It induced the generation of End Plate Potential

352
Q
What does the rate of muscle fiber and nerve fiber depend on?
Length of muscle
Exercise of muscle
Number of muscle fibres
The working ability of muscle fiber
A

Exercise of muscle

353
Q

What is happening right after the nervous AP arrives at the myoneural junction?

acetylcholine is filling the synaptic junction

The muscle fiber is contracting

Calcium enters the synaptic knob from the EC

The ligand- dependent cation channel is opening on the muscle fiber’s membrane

A

Calcium enters the synaptic know from the EC

354
Q

Where is acetylcholine produced?

On the post synaptic membrane
In the axon
In nerve cell body
In the synaptic junction

A

In the synaptic junction

355
Q

How many subunits does the ligand-dependent acetylcholine receptor make in the muscle?

5
4
3
2

A

5

356
Q

What kind of subunits does the acetylcholine-dependent receptor have in the muscle?

2 alpha, 3 beta
2 alpha, 2 beta, 1 delta
5 alpha
4 beta, 1 alpha

A

2 alpha, 2 beta, 1 delta

357
Q

What kind of subunits does the acetylcholine-dependent receptor have in the CNS?

2 alpha, 3 delta
2 alpha, 3 beta
5 alpha
4 beta, 1 alpha

A

2 alpha, 3 beta

358
Q

What is the difference between the nicotinic acetylcholine receptor of muscle and central nervous system?

There is no difference

The muscle has got 4 and the nerve has got 5 subunits

The nerve has no delta subunit

Only the nerve receptor is sensitive to the curare

A

The nerve has no delta subunit

359
Q

What is happening right after the calcium enters the synaptic knob?

Calcium causes IP3 increase

The acetylcholine is released to the synaptic split

Calcium activates the vesicles

Calcium activates the protein system which binds the vesicula to the presynaptic membranes binding sites

A

Calcium activates the protein system which binds the vesicula to the presynaptic membranes binding sites

360
Q

What is the MEPP?

One quantum of acetylcholine induces 1 mV End Plate Potential

One type of AP

Voltage dependent channel’s opening induces the potential changing

Maximal End Plate Potential

A

One quantum of acetylcholine induces 1mV End Plate Potential

361
Q

What kind of AP is generated, when the muscle fiber membrane’s voltage dependent sodium channels is open?

Amplitude fluctuates, frequency is equal to growing amount of acetylcholine

Amplitude is permanent, frequency is proportional to the amount of acetylcholine released from the presynaptic knob

Amplitude is uniformly decreasing

Amplitude is uniformly increasing

A

Amplitude is permanent, frequency is proportional to the amount of acetylcholine released from the presynaptic knob

362
Q

What degrades acetylcholine?

acetylcholine- hydrolase
acetylcholine-lyase
acetylcholine-esterase
acetylcholine- hydroxylase

A

Acetylcholine-esterase

363
Q

What happens to choline after acetylcholine release?

It is used up by the nerve cell during its energy producing processes

it is eliminated from the organism

it is further metabolized

after presynaptic reuptake it is used for acetylcholine synthesis

A

After presynaptic reuptake it is used for acetylcholine synthesis

364
Q

What inhibits the binding of acetylcholine?

the high extracellular magnesium level
the low extracellular magnesium level
the high intracellular calcium level
the low intracellular calcium level

A

The high extracellular magnesium level

365
Q

How can you inhibit acetylcholine- esterase activity?

curare
eserine
bungarotoxin
magnesium

A

Eserine

366
Q

What does curare inhibit?

the acetycholine- esterase

the excretion of acetylcholine

the generation of the end plate potential

the binding of acetylcholine to the receptor

A

The generation of the end plate potential

367
Q

What has an effect similar to curare?

eserine
the high EC magnesium level
the high intracytoplasmic calcium level
botuline and bungarotoxin

A

Botuline and bungarotoxin

368
Q

What causes myasthenia gravis?

there aren’t or there are only a few acetylcholine receptors, or they don’t work because of autoimmune processes

too many acetylcholine receptors

too much acetylcholine- release

the function of voltage-dependent sodium channels is defective

A

there aren’t or there are only a few acetylcholine receptors or they don’t work because of autoimmune processes

369
Q

How can you cure myasthaenia gravis?

with curare
with acetylcholine- esterase inhibitors
with infusion of magnesium
with bungarotoxin

A

with acetylcholine-esterase inhibitors

370
Q

What composes the motor unit?

motor unit = myoneural junction

the axon ending on the muscle fibre’s membrane

the nerves supplying the muscle and the muscle itself

the nerves supplying the muscle

A

The nerves supplying the muscle and the muscle itself

371
Q

What belongs to the large motor unit?

tonic fibres
tonic fibres and nerves
the red muscle
fast fibers

A

fast fibres

372
Q

What belongs to the small motor unit?

slow twitch fibres
fast fibres
fast and slow twitch fibres
the white muscle fibres

A

slow twitch fibres

373
Q

How can you describe the conductivity of the small motor unit’s nerves?

slow
fast
very fast
average

A

fast

374
Q

How can you describe the conductivity of the large motor unit’s nerves?

slow
fast
very fast
average

A

very fast

375
Q

How can you describe the excitability of the large motor unit’s nerves?

very difficult to stimulate
average
easy to stimulate
difficult to stimulate

A

Difficult to stimulate

376
Q

How can you describe the excitability of the small motor unit’s nerves?

easy to stimulate
very difficult to stimulate
average
difficult to stimulate

A

Easy to stimulate

377
Q

What is not true regarding the small motor unit’s muscles?

their metabolism is oxidative
their stretchability is good
they are slow
they don’t get tired

A

Their stretchability is good

378
Q

What is not true regarding the large motor unit’s muscles?

their metabolism is anaerobic

they are quick

their fibre length is small

they get tired easily

A

Their fibre length is small

379
Q

On what level do the small and the large motor unit differ?

They already differ at the level of the truncus cerebri

they don’t differ

only at the level of the fibres

both at the level of the spinal alfa motor neurons and at the level of the fibres

A

Both at the level of the spinal alfa motor neurons and at the level of the fibres

380
Q

What is true for the intrafusal fibre?

It is a specialized, stretch sensitive, and to some extent, contractile fibre

it accounts for the main mass of the skeletal muscle

it is tendon receptor

it is a pain sensitive fibre

A

It is a specialized, stretch sensitive, and to some extent, contractile fibre

381
Q

What is true regarding extrafusal fibres?

They exist as a few, muscle-stretch sensitive fibres

working muscle fibres, which give the main mass of skeletal muscle

they are tendon receptors

they are pain sensitive fibre-types

A

working muscle fibres, which give the main mass of skeletal muscle

382
Q

What kind of receptor is found in the tendon?

extrafusal fibre
intrafusal fibre
Golgi-receptor
Meissner-receptor

A

Golgi receptor

383
Q

What kind of afferents start from the nuclear chain receptor?

dynamic
dynamic and static
special
static

A

Static

384
Q

Where are the nuclear bag and nuclear chain receptors?

in the intrafusal fibres
in the extrafusal fibres
in the tendon
in the axon endings

A

In the intrafusal fibres

385
Q

What is the servo- mechanism of the muscle?

it is a spinal feedback mechanism, which prevents contraction

it is a reflex ensuring smooth muscle movement at the spinal level

it is a reflex of the extrafusal fibres

it is a cerebellar reflex

A

It is a reflex ensuring smooth muscle movement at the spinal level

386
Q

What is coactivation?

it is a reflex exclusively governed by the spinal cord

it is a reflex exclusively governed by the sensory cortex

the concurrent activation of alpha and gamma motoneurons

it is a reflex exclusively governed by the alpha motoneurons

A

The concurrent activation of alpha and gamma motoneurons

387
Q

Which receptor discharges more frequent afferent AP when the muscle is overstretched?

Intrafusal fiber
Extrafusal fiber
Nuclear chain receptor
Golgi receptor

A

Golgi receptor

388
Q

What discharges more frequent afferent AP with increasing load of the muscle?

Intrafusal fibres
Only the Golgi receptor
Extrafusal fibres
None of them

A

Intrafusal fibres

389
Q

What happens when the contraction exactly follows the motor command?

Intrafusal and extrafusal fibres contract with the same strength but not the same speed

Intrafusal and extrafusal fibres contract with same speed and same strength

Intrafusal and extrafusal fibres contract with the same speed but not with the same strength

Intrafusal and extrafusal fibres contract with differing speed and strength

A

Intrafusal and extrafusal fibres contract with same speed and same strength

390
Q

What’s the main function served by the smooth muscle?

Moving the skeleton

Moving the skeleton and setting the volume of hollow organs

Moving inner organs and setting the volume of hollow organs

they can be found in sphincters only

A

Moving inner organs and setting the volume of hollow organs

391
Q

What is not typical of single-unit smooth muscles?

There are no gap junctions connecting the fibres to each other

Each fibre or small group of fibres has its direct innervation

Fast and exact movements

They form a functional syncytium

A

They form a functional syncytium

392
Q

What is not typical of multiple - unit smooth muscle?

There are no gap junctions connecting the fibres to each other

Just a very few nerves are going to the functional syncytium

It is present in m. Ciliaris

they form a functional syncytium

A

There are no gap junctions connecting the fibres to each other

393
Q

What is MLCK (myosin light chain kinase) enzyme responsible for in smooth muscle?

For relaxation

For starting the cross - bridge cycle and for sustained contraction

For energy supply of the muscle

For mobilization of energy stored in glycogen

A

For starting the cross-bridge cycle and for sustained contraction

394
Q

What is myosin phosphatase enzyme responsible for in smooth muscle?

For starting the cross - bridge cycle and for contraction

For contraction

For producing relaxation

For binding ATP to myosin

A

For producing relaxation

395
Q

What happens in smooth muscle when myosin phosphatase is inhibited?

Muscle relaxes immediately

Muscle contracts maximally

Muscle relaxes after a short contraction

Muscle remains in a contracted state

A

Muscle remains in a contracted state

396
Q

What does “latch” mechanism mean in connection with the function of smooth muscle?

Immediate relaxation of the muscle in case of overstraining

Muscle’s reaction to a strong stimulus is not relaxation but contraction

Muscle relaxes after a short contraction

Muscle contracts without energy investment because of the MLCK mechanism

A

Muscle contracts without energy investment because of the MLCK mechanism

397
Q

What is the function of myosin phosphatase in smooth muscle?

It expels calcium from the IC compartment and causes relaxation this way

Dissociates the phosphoryl group from actomyosin thereby producing relaxation

It activates the sliding filament mechanism
sustains continuous cross bridge cycling

A

Dissociates the phosphoryl group from actomyosin thereby producing relaxation

398
Q

Is the “all-or-none” law true for smooth muscle?

No, because smooth muscle functions as a syncytium

Yes

No, because smooth muscle is in a continuous, slight contraction

Yes, just like skeletal muscle

A

No, because smooth muscle is in a continuous, slight contraction

399
Q

What adjusts the ratio of active MLCK/MP?

EC calcium level
IC magnesium level
Energy-supply of the muscle
IC calcium level

A

IC calcium level

400
Q

What increases the MLCK enzyme activity in smooth muscle?

Saturation of calmodulin by the rising calcium level

Calcium concentration of EC

Calcium concentration of IC

Increasing irritability of the muscle

A

Saturation of calmodulin by the rising calcium level

401
Q

What does a myogenic answer mean?

Stretching of an extensor causes relaxation of a flexor muscle

Straining of the smooth muscle causes automatic contraction in some of the organs

Relatively slight stimulus can cause contraction

it is the same as the reflex relaxation

A

Straining of the smooth muscle causes automatic contraction in some of the organs

402
Q

What is reflex relaxation?

Stretching of the smooth muscle is followed by decreased tension in some of the organs

Relatively slight stimulus can cause contraction

Straining the smooth muscle causes visceral pain

Straining causes a gradually rising contraction

A

Stretching of the smooth muscle is followed by decreased tension in some of the organs

403
Q

What does not elicit contraction in smooth muscle?

Effect of a neural AP

Chemical ligands

Beta-2 receptor stimulation and NO release

Calcium release from sequesters

A

Beta-2 receptor stimulation and NO release

404
Q

What doesn’t induce relaxation in smooth muscle?

Phosphorylation by MLCK

Chemical ligand binding to ligand- dependent calcium channel

Beta-2 receptor stimulation and NO release

Increasing MP (Myosin Phosphatase) activity

A

Chemical ligand binding to ligand dependent calcium channel

405
Q

What kind of receptor is not present in the single-unit smooth muscle?

Muscarinic ACh- receptor
Nicotinic ACh- receptor
Beta-2 receptor
Beta-1 receptor

A

Nicotinic ACh-receptor

406
Q

Which one of these muscles is not a single-unit smooth muscle?

Bronchial muscles
m. ciliaris
Gastrointestinal muscles
Muscles of the blood vessels

A

M.ciliaris

407
Q

Which ligand causes smooth muscle contraction?

Acetylcholine
NO
Adenosine
ATP

A

Acetylcholine