Cardiac Ion Channels & Action Potentials Flashcards

1
Q

T or F: Electrical activity propagates within myocardium AND via specialized conductive pathways

A

True

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2
Q

What cardiac structure serves as the main control for HR?

A

pacemaker cells in the sinoatrial node (SA node).

  • fire intrinsically at ~100/min.
  • Rate modulated by ANS.
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3
Q

What slows down the intrinsic HR of the SA node?

A

Parasympathetic tone slows rate to 60-80/min.

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4
Q

T of F: AV node is also capable of spontaneous activity

A

True

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5
Q

What is overdrive suppression?

A

Describes how the AV node is driven by action potentials originating in the SA node since their firing frequency is less than the SA node.

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6
Q

What are ectopic pacemakers?

A

Self firing cells that (or others, especially cells in damaged regions of the myocardium) can take over initiation of the heartbeat Under abnormal circumstances

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7
Q

How does cell-to-cell conduction take place?

A

gap junctions

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8
Q

How is the direction of electricl propagation controlled?

A

by gap junction position and by connective tissue “insulation” (e.g., between the atria and ventricles).

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9
Q

T of F: The AV node is the only place where action potentials can propagate from the SA node to the ventricles.

A

True

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10
Q

Which structures are characterized as having a fast action potential?

A
  • Atrial and ventricular muscle

- Purkinje fibers

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11
Q

Which structures are characterized as having a slow action potential?

A

SA & AV nodes

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12
Q

Direction of current flow depends on what?

A
  • membrane potential (Vm) and

- ion gradient (Nernst Potential, Eion)

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13
Q

T or F: If Vm<Eion, current flows into cell

A

True

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14
Q

T or F: If Vm>Eion, current flows out of cell

A

True

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15
Q

What causes depolarization?

A

Current flowing into cell causes depolarization

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16
Q

What causes hyperpolarization?

A

Current flowing out of cell causes hyperpolarization

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17
Q

T or F: ion channels serve as gates; open upon depolarization and close upon repolarization

A

True

18
Q

T of F: Current is constant with voltage

A

True

19
Q

T of F: If we keep the voltage positive inactivation gate closes with time

A

True

20
Q

What is the characteristic subunit in cardiac sodium channels?

A

NaV1.5 , cardiac Na channels show Voltage-dependent inactivation

21
Q

What are the types of Ca++ channels in the heart?

A

L & T types. Also, Ryanodine Receptors (intracellular- SR)

22
Q

What are the characteristics of the L type Ca++ channels

A

-L-type current; dihydropyridine receptor (DHPR)
-(CaV1.2, CaV1.3)

23
Q

What are the characteristics of the T type Ca++ channels

A
  • T-type current
  • (CaV3.1, CaV3.2)
  • Low-Voltage Activated (LVA)
  • Voltage-dependent Inactivation
24
Q

List the Time-dependent potassium currents

A

-IKto (Kv4.3 tetramer + KChiP2): voltage-dependent inactiv.
-IKr (HERG tetramer + miRP1): “rapid” delayed rectifier
-IKs (KvLQT1 tetramer + minK):“slow” delayed rectifier
Depolarization causes activation of IKr and IKs

25
Q

What are the characteristics of the time dependent cation current?

A

If (or Ih) (HCN tetramer)
Evoked by hyperpolarization
Na+ & K+ permeable, Erev  -30 mV

26
Q

What are the characteristics of the Inward Rectifier potassium current

A
IK1 (Kir tetramer)
IKACh (GIRK tetramer)
  Increased by activation of
   muscarinic receptors; 
   slows pacemaking
27
Q

The categorization of cardiac action potentials as fast or slow is based on _________

A

on whether the initial upstroke is rapid or slow

28
Q

Phase 0, fast

A

rapid depolarization caused by the entry of sodium ions (INa) through voltage- activated sodium channels

29
Q

Phase 1, fast

A

partial repolarization produced by inactivation of sodium current and activation of a transient potassium current IKto.

30
Q

Phase 2, fast

A

prolonged plateau, voltage-activated, L-type calcium channels are open. influx of calcium = efflux of potassium ions (IKr and IKs) so that membrane potential remains at a roughly constant level (near 0 mV)

31
Q

phase 3, fast

A

rapid repolarization due to inactivation of (ICa) and increasing activation of IKr and IKs causes termination of the plateau

32
Q

Phase 4, fast

A

IKr and IKs are de-activated, and inactivation of INa and ICa is removed; the cell is held near EK (phase 4) by the inward rectifier (IK1).

33
Q

What are the notable difference b/t currents in myocardial cells and the nodes?

A
  • pacemaker cells have reduced INa and little IK1;

- pacemaker cells express If and ICa-T which are essentially absent in myocardial cells

34
Q

T of F: there is no stable resting potential in pacemaker cells

A

True

35
Q

Phase 0, slow

A

upstroke due to activation of ICa-T and ICa-L and is relatively slow owing to the absence of INa

36
Q

Phase 3, slow

A

repolarization occurs shortly after the peak of the action potential due to balance between ICa and delayed rectifier current (IKr and IKs)

37
Q

Phase 4, slow

A

repolarization is followed by a slow depolarization (the “pacemaker potential”)

38
Q

What induced pacemaker potential?

A

funny current (If) which is induced by hyperpolarization

39
Q

HERG produces what?

A

IKr, Impt. for duration of slow and fast action potentials

40
Q

Reducing IKr can result in?

A

arrhythmias