Muscle Flashcards

1
Q

What are the characteristics of skeletal muscle?

A

Voluntary control
Striated
Single long cylindrical cells
Multiple peripheral nuclei

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2
Q

What are the characteristics of caridac muscle?

A
Only in heart
Striated
Branched with 1 - 3 central nuclei (variable)
Connected via intercalated discs
Involuntary control
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3
Q

What are the characteristics of smooth muscle?

A
Involuntary
Found the wall of internal organs
Spindle shaped (fat middle, thin ends)
Uni-nucleated
Not striated
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4
Q

What is the structure of skeletal muscle?

A
Attached to bones via tendons
The fibres can be long (up to 35cm)
Reasonably wide (.1mm)
Composed of fibrils containing highly organised contractile filaments
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5
Q

What are the components of a sarcomere (myofibril)?

A

Thin actin filaments
Thick myosin filaments
Z discs (anchoring point)

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6
Q

What are the areas of a sarcomere?

A
H zone (Exclusively thick filaments)
M line (Thick filaments are joined)
A band (thick and thin filaments)
I band (thin filaments)
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7
Q

What is the T tubule?

A

Tunnels continuous with the sarcolemma into the cell at A and I bands, full of extracellular fluid, exposing the fibres to APs etc.

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8
Q

What is the Sarcoplasma Reticulum?

A

Calcium storage site, the terminal cisternae lie close to the T tubules.

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9
Q

What is the Sarcolemma?

A

Surrounds the cell, has holes for T tubules

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10
Q

Structure of thick filaments?

A

Myosin
Made out of two subunits
Has a head and a tail, the two tails form a helix
Heads having a binding site for actin
The head is an enzyme that hydrolyses ATP

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11
Q

Thin filaments

A

Primarily globular actin proteins
Filaments are a double stranded helical actin chain
Troponin and tropomyosin are regulatory proteins associated with actin in cardiac and skeletal muscle

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12
Q

What is the sliding filament theory?

A

The sarcomere shortens as the thin filaments are pulled over the thick filaments.
Z-line is pulled towards the M-line
The I band and the H zone become narrower

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13
Q

Which areas don’t change in contraction?

A

M line and A band

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14
Q

Which areas change during contraction?

A

Z discs and I band

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15
Q

What are the steps of the cross bridge cycle?

A
  1. Cross-bridge formation (Actin-Myosin)
  2. Power stroke (ADP and Pi released)
  3. Detachement (New ATP)
  4. Energisation of mysoin head (ATP to ADP + Pi)
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16
Q

Why must calcium be present?

A

It binds with troponin to move tropomyosin allowing access to myosin binding sites on the actin.

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17
Q

What happens during the power stroke?

A

Both Pi and ADP released
Mysoin rotates to low energy state (45 degrees to actin).
Pulls the thin filaments

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18
Q

What happens during detachment?

A

New ATP binds to myosin head and it detaches from actin.

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19
Q

What happens during energisation of myosin head?

A

Hydrolysis of ATP to ADP and Pi
Myosin head cocks to it’s high energy confirmation
(90 degrees to actin)

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20
Q

Why is calcium important?

A

Calcium ions provide the “on” switch for the cross cycle

The cycle will continue as long as Ca levels remain above the critical threshold. (.001 - .01 mM).

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21
Q

How is calcium regulated?

A

Calcium channels in the SR open and calcium flows into cytosol/t tubules
Active Ca ATPase pumps are constantly moving calcium back into the SR.

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22
Q

What is isometric contraction?

A

No shortening
Length constant
Tension variable

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23
Q

What is Isotonic contraction?

A

Shortening
Tension constant
Velocity variable

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24
Q

Why determines the the maximum force in isometric contraction?

A

The degree of myosin and actin overlap

2.2 um is optimum

25
Q

At what stage do the filaments start overlapping too much?

26
Q

At what length does the force start decreasing due to stretch?

27
Q

What are the steps of a motor neuron action potential?

A
  1. ACh released into neurotransmitter junction
  2. Activation of ACh receptors
  3. A muscle AP is triggered
  4. Calcium is released from the SR
  5. Calcium binds with troponin
  6. Cross bridge formation
  7. Power stroke
  8. De tatchment
  9. Re-energisation
  10. Contracation ends when Ca levels fall
28
Q

What happens when an Action potenital hits the end plate?

A

Ca+ enters axon terminal, which trigggers the ACh vesicles fusing with membrane

29
Q

What does the binding of ACh allow?

A

The movement of Na+ into the muscle cell (end plate potential)

30
Q

What is ACh broken down by?

A

Acytelcholieesterase

31
Q

What happens when enough ligand gated channels open?

A

Voltage gated channels open and propagate down the sacrolemma

32
Q

What is the typical resting potential for motor neurons?

33
Q

What is the excitation-contraction coupling?

A

Action potentials run down the sarcolemma and the t tubules.
AP reaches the voltage sensitive protein which then releases the voltage gated channel in the sarcoplasmic reticulum into the sarcoplasm.

34
Q

What does creatine phophate do?

A

It can hold a phosphate and donate it to an ADP. (under 15 seconds only)
Anaerobic process

35
Q

What are the charateristics of anaerobic glycolysis?

A

Fast but efficient.

Leads to a build uo of lactic acid and H+ limits duration to 30-40s

36
Q

What are the characterisics of aerobic metabolism?

A

Efficient but slow
Only about 300 W
Cna run for a long time

37
Q

What are type one muscle fibres?

A

Slow oxidative

38
Q

What are type IIB muscle fibres?

A

Fast glycolyitc

39
Q

What are type IIA muscles?

A

Fast oxidative (not in humans)

40
Q

What regulates force?

A
  1. Rate of stimulation of individual motor unit

2. The number of motor units used.

41
Q

What muscle fibres do we usually recruit first?

42
Q

What is another name for involuntary movement?

43
Q

What is another name for voluntary movement?

A

Neurogenic

44
Q

Is cardiac muscle electrically isolated like skeletal?

45
Q

What’s the difference in T tubules between skeletal an cardia?

A

The T-tubules are at the Z disks in cardiac and there is only one per sarcomere instead of 2 at the …

46
Q

What are the two types of cardiac action potential?

A

Ventricular myocyte

Sinoatrial node

47
Q

In Ventricular myocyte AP, what ion flows do we have?

A

Out:
Na+
Ca2+

In:
K+

48
Q

How long is a vetricular monocyte AP?

A

300 - 400 ms

49
Q

What are the steps of calcium-induced calcium release?

A
  1. Excittion
  2. Opeing of voltage-sensative plasma membrane
  3. Flow of C into cell
  4. Stimulation of CA from SR
  5. Cytosolic concentration inrease
  6. Contraction
50
Q

What is a DHPR channel?

A

L type Calcium channel

51
Q

How do we increase the CO?

A

Increased stretch of ventricles
Increased rate of firing
Certain hormones

52
Q

What is the cardiac output equation?

A

Cardiac output = Stroke volume * Heart rate

53
Q

Why does the heart beat spontaneously?

A

Because the SA node is spontaneously depolarizing

54
Q

What is the ion flow in Sinoatrial Node APs?

A

In:
CaL
CaT
If(funny)

Out:
K

55
Q

What is the spontaneous depolarisation commonly called?

A

Pacemaker potential

56
Q

What are ways to control thr heart rate?

A
  1. Decrease the threrhold
  2. Making the maximum diastolic potential more postive (less hyperpolarised)
  3. Increasing the rate of spontaneous deploarisation
57
Q

What does the Vagus nerve do?

A

It is part of the parasympathetic system
Activates SA node
DereaSes heart rate
Release Acetyl Choline

58
Q

What does the Sympathetic nerve do?

A

Increases heart rate
Releases noradrenaline
Activates AV Node

59
Q

What is intrinsic heart rate?

A

100-110 bpm