Cardiac Flashcards

1
Q

Pacemaker cells are located in what 2 nodes?

A

SA and AV

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2
Q

These depolarize only when electrical impulses (APs) initiated by the SA or AV node are transmitted to them.

A

Non-pacemaker Cells

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3
Q

What is a cellular mechanism that allows pacemaker cells to depolarize spontaneously?

A

There is no true resting membrane potential

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4
Q

What is the primary transport mechanism responsible for the generation of the action potentials of pacemaker cells?

A

Passive diffusion of ions

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5
Q

Nodal or pacemaker cells exhibit an unstable RMP during ____ which begins at maximal value of about -65mv and slowly becomes less negative towards 0 mv until threshold is reached.

A

Phase 4

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6
Q

In phase 4 as the maximum diastolic potential is reached three changes (2 early and 1 late in the phase) occurring causing the membrane to slowly depolarize toward threshold, what are they?

A
  1. An influx of Na+ through “funny” cation channels
  2. A decrease in membrane permeability of K+ (not as much K+ can exit the cell)
  3. Late in phase 4, transient “T” type Ca++ channels open
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7
Q

In phase 0, when the membrane potential reaches threshold (~-40 mv), ____ open allowing Ca++ to enter the cell and generate an AP.

A

Long lasting “L” type Ca++ channels open

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8
Q

In phase 3, when does repolarization occur?

A

when the membrane permeability to K+ increase. Consequently, K+ leave the cell and the membrane potential moves toward the equilibrium potential for K+.

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9
Q

If a drug increase the K+ leak rate of a pacemaker cell, what effect does it have on the maximal diastolic potential?

A

It is more negative (Hyperpolarization)

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10
Q

If a drug increases the Ca++ permeability of the L-type calcium channels in a pacemaker cell, what effect does it have on the amplitude of phase 0 of the action potential?

A

It increases

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11
Q

Is the action potential of non-pacemaker cells similar to the action potential of pacemaker cells?

A

No; phase 4 is more of a true resting membrane potential

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12
Q

Why are the shapes of the non-pacemaker cell and the pacemaker cell action potentials so different?

A

There are different/other ion channels involved

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13
Q

The cardiac cell RMP in a non-pacemaker cell is established principally by:

  1. The difference in the concentrations of individual ions across the cell membrane established mainly by the _____.
  2. The difference in the cell membrane permeability to _____.
A
  1. Na+/K+ ATPase exchange pump

2. sodium and potassium ions

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14
Q

In the resting state, the cell membrane is more than 100 times more permeable to ___ than to ____.

A

Potassium than to sodium

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15
Q

During phase 1 of the action potential, a … is activated when the inside of the cell becomes positive.

A

Transient Potassium Efflux Channel (Ito)

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16
Q

The opening of this channels returns the membrane potential from about +20 mV to a value near 0 mV. This channel conducts potassium OUT of the cell.

17
Q

During the plateau (phase 2), another …. becomes active, permitting potassium to be conducted out of the cell.

A

Potassium Channel (Ik)

18
Q

This channel is responsible for Repolarization (Phase 3) and establishing the RMP.

19
Q

Fast sodium influx channel has a voltage threshold of about … and when activated, sodium ions diffuse along their concentration and electrical gradients.

A

-70 mV (voltage-gated)

20
Q

Fast sodium influx channel is responsible for phase ___ and is activated and inactivated very rapidly (time dependent).

21
Q

The fast sodium channel is blocked by the drug, …

A

tetrodotoxin

22
Q

Calcium influx channel has an activation threshold voltage of about … and when activated, the membrane permeability to calcium ions increases, allowing these ions to diffuse along their electrochemical gradient.

23
Q

Calcium influx channel is primarily responsible for phase ___.

24
Q

The calcium channel is blocked by voltage-gated calcium channel blockers like

25
Q

What is the permeability status of K+ in early phase 2?

A

First a K+ spike, then decreasing K+ (Ito)

26
Q

What is the permeability status of Ca+ in early phase 2?

A

increasing Ca++

27
Q

What is the permeability status of Ca++ in late phase 2?

A

decreasing Ca++

28
Q

What is the permeability status of K+ in phase 3?

A

increasing K+ (Ik)

29
Q

What channels open during phase 0 of the action potential, but due to their slow influx they don’t contribute towards the amplitude (positive voltage) of phase 0.

A

Calcium channels