Cardiovascular Physiology Lecture 3 Flashcards

1
Q

What are the two types of AP’s in the heart?

A

Fast and slow

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2
Q

Where are fast AP’s found?

A

Found in contractile myocytes in the atrial myocardium, ventricular myocardium, bundle of His, Bundle branches (left and right) and Purkinje fibres

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3
Q

Where are slow response action potentials found?

A

Conducting myocytes of the:

  • Sinoatrial node
  • Atrioventricular node
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4
Q

What do the terms fast and slow refer to in types of action potentials?

A

How quickly the membrane potential changes during the depolarization phase of the AP

  • Fast:
    • Rapid rate of depolarization in which the membrane potential rises very quickly from the threshold pot. to the new transiently positive potential
  • Slow:
    • Slower rate of depolarization, in which the membrane potential take more time to m=reach the new potential
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5
Q

Why do action potentials have different rates of depolarization?

A

Depends on the ions and ion channels involved in the depolarization phase

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6
Q

Phases of the cardiac AP are associated with changes in the permeability of the cell membrane mainly to which 3 ions?

A

Na+

K+

Ca2+

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7
Q

What happens during a Cardiac AP in regards to K+, Ca2+ and Na+

A

[K+] inside cell is higher than outside (will leave cell)

[Ca2+] is higher outside the cell than inside the cell (will enter cell)

[Na+] is higher outside the cell than inside (will enter cell)

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8
Q

What are the 3 phases of a slow action potential (as with the SA node AP)

A
  1. Pacemaker potential
  2. Depolarization
  3. Repolarization
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9
Q

it is not a steady or true resting potential but a slow depolarization to threshold; gradual depolarization of the membrane potential to threshold

A

Pacemaker potential

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10
Q

Pacemaker potential allows the SA Nodal cells to generate spontaneous ________

A

Pacemaker potential allows the SA Nodal cells to generate spontaneous action potentials without any external influence from nerves or hormones

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11
Q

What three ionic conductances are involved with bringing a pacemaker potential to a spontaneous AP?

A
  1. Progressive reduction in K+ permeability (K+ channels that opened during the repolarization phase of the previous AP gradually close due tot he return of the membrane to negative potential)
  2. F-type channels (depolarizing Na+ current; Na+ moves into cell)
  3. T-Type channels (Ca2+ channels; T=transient; opens only transiently (briefly); contributes to inward Ca2+ current; provides a final depolarization to bring the membrane to threshold)
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12
Q

What is the depolarization phase of a slow action potential?

A
  • L-type channels (Ca2+ channel; L=long lasting; channels open more slowly and remain open for a prolonged period
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13
Q

Why does the rising phase of an action potential occur slower in slow AP?

A

Ca2+ currents depolarize the membrane more slowly than voltage-gated Na+ channels, so the rising phase occurs slower than if Na+ was responsible (as they are in nerve/muscle AP)

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14
Q

What is the repolarization phase of the slow AP?

A

Opening of voltage gated K+ channels. K+ leaves the cell

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15
Q

______ _______ of the pacemaker potential allows SA Node to generate AP

A

Gradual Depolarization of the pacemaker potential allows SA Node to generate AP

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16
Q

In slow AP which ion is responsible for the depolarization phase?

A

Ca2+ (not Na+)

17
Q

If the SA node becomes damaged, the ______ may generate Ap’s to drive the ventricles, but at a slower rate (40-60 bpm)

A

If the SA node becomes damaged, the AV node may generate Ap’s to drive the ventricles, but at a slower rate (40-60 bpm)

18
Q

Various _____ channels are involved in the resting phase, the notch and the repolarization phase of Ventricular Muscle Cell AP

A

Various K+ channels are involved in the resting phase, the notch and the repolarization phase of Ventricular Muscle Cell AP

19
Q

What is the P-wave of an ECG?

A
  • First wave on ECG
  • Represents depolarization of the atria
  • Upward deflection in the trace
  • approximately 25ms after the P-wave the atria will contract
20
Q

What is the QRS complex?

A
  • Wave consisting of 3 peaks labelled Q, R, and S
  • represents depolarization of the ventricles
  • When the ventricles are depolarizing, the atria repolarize
21
Q

Which wave would you see approximated 25ms before the atria contract?

A

P-wave

22
Q

What would you see on the ECG if the ventricles were contracting?

A

QRS complex

23
Q

What is the T-Wave on the ECG?

A
  • upward deflection
  • represents repolarization of the ventricles
24
Q

What is an AV node block?

A

Type of heart block in which the conduction between the atria and ventricles is impaired; partial or complete interruption of the impulse from the atria to the ventricles

25
Q

plasma/cell membrane of a cardiac cell =

A

sarcolemma

26
Q

Special type of smooth ER that stores and pumps Ca2+ in the heart:

A

Sarcoplasmic reticulum

27
Q

What is the contractile unit of heart muscle (contains filaments actin and myosin)

A

Sarcomeres (make up myofibrils)

28
Q

What are invaginations of the sarcolemma that surround myofibrils and transmit AP’s?

A

T-Tubules

29
Q

T-Tubules lie in close proximity to the ________ and contain many _______ channels

A

T-Tubules lie in close proximity to the sarcoplasmic reticulum and contain many L-type Ca2+ channels

30
Q

What is excitation-contraction coupling?

A

process by which the arrival of an AP at the cell membrane leads to contraction of the muscle cell

31
Q

What are the steps involved in ECC (excitation-contraction coupling)

  1. __\_ levels control contraction of the cardiac muscle
    • normally found in low concentrations in the _____\_and in high concentration sin the ____\_
    • During the plateau phase of the AP, extracellular Ca2+ enter the cytoplasm of the cardiac muscle cell through the ______\_
      • not enough to cause contraction of myocytes
    • Ca2+ that enters binds to _____\_and their channels open allowing release of Ca2+ from the ______ ____\_ into the cytoplasm
A

What are the steps involved in ECC (excitation-contraction coupling)

  1. Ca2+ levels control contraction of the cardiac muscle
    • normally found in low concentrations in the cytoplasm of the cell and in high concentration sin the ECF
    • During the plateau phase of the AP, extracellular Ca2+ enter the cytoplasm of the cardiac muscle cell through the L-type Ca2+ channels
      • not enough to cause contraction of myocytes
    • Ca2+ that enters binds to ryanodine receptors and their channels open allowing release of Ca2+ from the sarcoplasmic reticulum into the cytoplasm
32
Q

How does Ca2+ cause its own release from the sarcoplasmic reticulum?

A

By binding to the ryanodine receptor = calcium dependent calcium release or calcium-induced calcium release

33
Q

Excitation spreads along the sarcolemma (plasma membrane) from ventricular myocyte to ventricular myocyte via ______

Excitation spreads down the interior of the myocyte via ______

A

Excitation spreads along the sarcolemma (plasma membrane) from ventricular myocyte to ventricular myocyte via gap junctions

Excitation spreads down the interior of the myocyte via t-tubules

34
Q

What are L-Type calcium channels?

A

voltage gated Ca2+ channels

Type of modified Dihydropyridine (DHP) receptor

35
Q

Why is diastole (ventricle relaxation) important?

A

Because ventricles only fill with blood when they are relaxed

36
Q

How is a contraction ended in Cardiac muscle?

Must reduce Ca2+ levels:

  • _____ channels close to reduce influx of Ca2+ into the cell
  • SR no longer stimulated to release Ca2+ into cytoplasm as Ca2+ is not longer entering to bind to _____
  • SR contains _____ to pump Ca2+ in the cytosol back into the Sr
  • Ca2+ is removed form the myocyte by a _____ in the sarcolemma
A

Must reduce Ca2+ levels:

  • L-type ca2+ channels close to reduce influx of Ca2+ into the cell
  • SR no longer stimulated to release Ca2+ into cytoplasm as Ca2+ is not longer entering to bind to ryanodine
  • SR contains Ca2+ ATPases to pump Ca2+ in the cytosol back into the Sr
  • Ca2+ is removed form the myocyte by a Na+/Ca2+ exchanger in the sarcolemma