Lecture 7 Flashcards

1
Q

Know anatomy of the heart including chambers, valves and pathway of blood

A

See figure.

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2
Q

Describe histology of cardiac muscle tissue and compare the skeletal muscle tissue

A

Sarcomeric Arrangement (striated)

Mononucleated

Central nuclei

Syncytium

Intercalated discs

Cells may branch

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3
Q

Compare the skeletal muscle fibers with cardiac muscle fibers with regard to the T-tubules and sarcoplasmic reticulum

A

SKELETAL Muscle Fibers:

T-tubules are at the ends of Thick Filaments

Two Cisternae per T-Tubule

T-Tubules form triads with the SR.

SR is MORE extensive in skeletal muscle fibers.

Motor unit arrangement (one 1 nerve fiber synapses with one or more skeletal muscle fiber)

CARDIAC Muscle Fibers:

T-Tubules are found along the Z-line

One Cisterna per T-tubule

T-Tubules form Diads with SR.

SR is LESS extensive

Cardiac Muscle cells form a Synctium

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4
Q

Compare the physiology of fast and slow cardiac muscle action potentials

A

FAST:Due to changes in conductance of Potassium, Sodium, and Calcium ions.

Conductance pattern is due to Voltage dependent gates.

Faster conductance: Greater AP amplitude, More rapid rate of rise of phase 0, Larger Cell Diameter.

SLOW:NO fast Sodium ion gates

Upstroke (negative to positive) of AP is due to CALCIUM (so it goes slow)

Resting phase potential 4 is -60mV (rather than -90mV)

Change in potential (Amplitude) is less than that for fast APs

SA & AV nodal tissue will spontaneously depolarize slowly to reach threshold during phase 4 (resting phase)

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5
Q

Describe the activities that occur during each of the five phases of a cardiac muscle potential

A

Phase 0: Depolarization

Fast Sodium Channels open and allow Sodium Ions to rapidly flow into the cell. Membrane Potential reaches +20mV.

(L-type Calcium Channels open up)

Phase 1: Initial Repolarization

Fast Sodium Channels close and cell begins to repolarize.

Potassium channels open and Potassium leaves cell.

(L-Type Calcium channels open up)

Phase 2: Plateau

Calcium Channels open and [fast] Potassium channels close.

Brief initial repolarization occurs and AP plateaus because of Increase Calcium Ion permeability & Decreased Potassium Ion Permeability.

(Calcium Ion channels open slowly during phases 1 & 0)

Phase 3: Rapid Repolarization

Calcium Channels Close and Slow Potassium Channels Open

Closure of Calcium Channels & Potassium Ions exiting the cell ends the plateau

Cell membrane return to resting level

Phase 4:

Resting Membrane Potential

-90mV.

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6
Q

Describe fast cardiac action potentials

A

Fast: • Found in atria, ventricles and conduction system • Very rapidly conducting but non-contractile in Purkinje fibers • Rapidly conducting and contractile in atrial and ventricular fibers • High amplitude (100 mV) • Fast action potentials are due to changes in conductance of potassium, sodium, and calcium ions. • Conductance pattern is mostly due to voltage dependent gates• Greater AP amplitude, • More rapid rate of rise of phase 0 • Larger cell diameter

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7
Q

Describe slow cardiac action potentials

A

Slow: • Found in SA and AV nodal tissues • Conducts slowly • Automatically depolarizes during resting phase: • More rapidly in SA node than in AV node • Low amplitude (60 mV)• No fast sodium ion gates • Upstroke (negative to positive) of action potential is due to calcium (therefore it proceeds slowly). • Resting phase potential 4 is close to -60 mV rather than -90 mV characteristic of fast action potentials. • Change in potential (amplitude) is less than that for fast action potentials. • SA and AV nodal tissue will spontaneously depolarize slowly to reach threshold during phase 4 (resting phase).

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8
Q

3 Characteristics of fast type contractile myocytes

A

• Large diameter • High amplitude • Rapid onset of action potential

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9
Q

What are 2 Characteristics of fast type non-contractile myocytes

A

• Very large diameter • Very rapid upstroke

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10
Q

3 Characteristics of slow type non-contractile myocytes

A

• Small diameter • Low amplitude • Slow rate of depolarization

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11
Q

Explain the role of Ca2+, Na+ and K+ in the creation of cardiac muscle action potential plateau

A

• In skeletal muscle, the sodium channels close rapidly. • In cardiac muscle the sodium channels also close rapidly, but the calcium channels open slowly and stay open for a longer period of time. • In cardiac muscle there is also a delay in the opening of the potassium channels. • The large concentration of both calcium ions and potassium ions is responsible for the plateau.

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12
Q

Describe role of SA node as the heart’s pacemaker

A

Resting membrane potential of SA node fiber: • -55 to -60 mV (Threshold ≈ -40 mv) • Fast sodium channels are already inactivated (blocked). • Inactivation gates close when membrane potential is less negative than -55 mV. • Therefore, only slow sodium-calcium channels can open. • Therefore, atrial nodal action potential is slower to develop. • Therefore, repolarization is also slower. • There is a slow leak of sodium ions back into the cells. • Membrane potential becomes more positive. • At -40 mV, sodium-calcium channels become activated. • Sodium-calcium channels are inactivated within 100-150 msec after opening

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13
Q

Compare a sinus rhythm with an ectopic focus

A

• Action potentials that originate anywhere else are said to be from an ectopic focus or pacemaker.

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14
Q

Describe the mechanism of calcium release during the contraction of a cardiomyocyte with regard to DHP and ryanodine channels and compare with calcium release in skeletal muscle fibers

A

Calcium floods in the SR and completes the electromechanical coupling process.

Far FEWER Calcium-Induced Calcium Release Channels in Cardiac Muscle compared to skeletal muscle.

This allows Fine control over Sarcoplasmic Calcium concentration and contractility.

In Skeletal Muscle, the excitation always triggers the MAXIMUM release of Calcium from the SR.

After the AP travels along the sarcolemma of cardiac myocytes, it enters the T-Tubules

Calcium then enters from the Extracellular Fluid through the Dihydropyridine Receptor Channels of the T-tubules.

Elevated cytoplasmic Calcium triggers more Calcium to enter from the Cisternae of Sarcoplasmic Tubules through Ryanodine Receptors.

Elevated Cytoplasmic Calcium binds to Troponin and Myofilament Contraction occurs.

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15
Q

Describe the role of two Ca2+ transporters involved in cardiac muscle relaxation

A

SERCA: Sarcoplasmic Reticulum Calcium ATPase

Stimulated by the Phosphorylation via an integral SR protein called “Phospholambian”, reduces its ability to inhibit SERCA pump when phosphorylated.

Returns Calcium to SR during DIASTOLE

This will allow for an even greater Calcium release on the next beat.

Also allows for Fast Clearance of Calcium form the Sarcoplasm.

Sodium-Calcium Exchanger in Sarcolemma:

Transports Calcium out of the Cell.

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16
Q

Atria act as what?

A

Primer Pumps because 80% of blood flows from the Atria to the Ventricles BEFORE Atria Contract

Atria add 20% more blood by contraction

17
Q

What happens during Ventricular Systole?

A

AV Valves close during systole.

18
Q

What happens at the End of Ventricular Systole?

A

AV valves open at the end of systole because of Increase Pressured on the Atria.

19
Q

What is this Valve?

A

Mitral Valve

20
Q

What is this valve?

A

Aortic Valve

21
Q

What Happens during the First 1/3 of Diastole?

A

Rapid Filling

22
Q

What happens during the Middle Third of Diastole (diastasis)?

A

Small amount of blood flows into the ventricles.

23
Q

What happens during the last third of Diastole?

A

Atria contract to push last 20% of blood into ventricles

24
Q

What happens during Isometric (Isovolumic) contraction?

A

Ventricles contract, but Semilunar Valves do NOT open for .02-.03 seconds.

25
Q

What happens during the Period of Rapid Ejection and when does it occur?

A

Occurs when LEFT Ventricular pressure is above 80mmHg and RIGHT Ventricular Pressure is slightly above 8mmHg

The Semilunar Valves open so that 70% of blood ejected and occurs during the 1st third of ejction.

26
Q

What happens during the Period of Slow Ejection and when does it occur?

A

Remaining 30% of blood is ejected from ventricles and occurs during the Last 2/3s of Ejection.

27
Q

What does the Frank-Sterling Law of The Heart describe?

A

The greater the Heart muscle is stretched during filling, the Greater the force of contraction and thus the greater the quantity of blood pumped into the Aorta.

28
Q

How is the Force of Contraction Altered and How does it Affect Stroke Volume?

A

Stroke Volume output can be increased by Incresing EDV

and Decresing ESV

29
Q

How do You Calculate Ejection Fraction?

A

Stroke Volume/ End Diastolic Volume

*SV= 70mL*

30
Q

What happens during each of these 4 phases?

A

Phase I: Period of Filling

Phase II: Isovolumic Contraction

Phase III: Period of Ejection

Phase IV: Isovolumic relaxation

31
Q

How fast does blood flow in the Proximal Aorta and what type of Flow is it?

A

Reaches a mean speed of 40 cm/s

The Flow is Phasic

Velocity can range from 120 cm/s (systole) to negative bfore aortic valves close in diastole.

32
Q

What happens to the blood in the Distal Aorta/Arteries and when is the Velocity greater?

A

Forward flow is continuous because the vessel walls during Diastole

and Velocity is greater in Systole

33
Q

What are the “Forces Altering Flow?

A
  • Rate of blood flow to tissue is precisly controlled in relation to tissue need
  • Active Tissues may need up to 30x more blood flow than at rest
  • Cardiac output CANNOT exceed 4-7x greater than at rest
  • Needs of Tissue Act Directly on local blood vessels
  • NS and Hormones help control tissue blood flow
34
Q

What happens to the Heart during Sympathetic NS stimulation?

A

Cardiac Output INCREAES

35
Q

What Happens to Cardiac Output during Parasympathetic NS stimulation?

A

Cardiac Output DECREASES

36
Q

What two Changes related to ANS lead to a Greater or Less Cardiac Output?

A

Heart Heart and Contractile Strength