Conduction Flashcards

(15 cards)

1
Q

What is the funny current?

A

sodium and potassium ionic currents allow for a steady increase in the resting membrane potential of the myocyte. Once the threshold potential is reached, an action potential is generated

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2
Q

What are the two unique features of pacemaker cells which serve to initiate sinus activity?

A

The funny current and calcium-induced calcium release

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3
Q

What is calcium-induced calcium release?

A

calcium influx through voltage-gated calcium channels causes and increase in intracellular calcium which trigger calcium release from the sarcoplasmic reticulum

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4
Q

What is the main ion responsible for maintaining the resting state?

A

Potassium through the inward rectifier current (IK1) - the predominant channel open at rest.

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5
Q

Where are the fast response tissues located?

A

Atria, Bundle of His, Fascicles and bundles branches, terminal Purkinje fibres, Ventricles and AV bypass tracts

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6
Q

Which ions are responsible for the 4 stages of the cardiac AP?

A

phase 0: Na+ influx

Phase 1:

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7
Q

Which ions are responsible for the 4 stages of the cardiac AP?

A

phase 0: cell membrane reaches threshold and voltage- gated Na+ channels open - Na+ influx - rapid depolarisation
Phase 1: slowing of Na+ influx + efflux of K+ - depolarisation “notch”
Phase 2: calcium influx balances K+ efflux causing plateau phase
Phase 3: Ca influx ceases and K+ efflux continues with resolution back to the resting potential

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8
Q

What is the function of gap junctions?

A

low resistance structures that allow ions to flow from one cell to another causing sequential depolarisation from cell to cell - cardiac impulse propagation

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9
Q

How does the action potential in the SA and AV nodes differ from other myocardial cells?

A

Phase 0 depolarisation depends on influx of Ca (not Na+) via L-type calcium channels and funny channels. This depolarisation occurs more slowly than other myocardial cells

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10
Q

What is the funny current?

A

Na+ channels which open when the voltage is more negative, immediately after the end of a previous action potential.
This allows for a steady increase in the resting membrane potential of the myocyte until it reaches . threshold potential which triggers the action potential

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11
Q

How do Class 1 antiarrhythmics work, name some.

A

modulate or block Na+ channels, inhibiting phase 0 depolarisation thereby slowing conduction
1A: intermediate speed of binding and dissociation from receptor
- Quinidine, Procainamide
1B: rapid
- Lidocaine, Mexiletine
1C: slow
- Flecainide, Propafenone

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12
Q

How do class II antiarrhythmics work

A

inhibit sympathetic activity through beta blockade

- slow the rate of discharge of the sinus node

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13
Q

How do class III antiarrhythmics work, name some.

A

Block K+ channels thereby prolonging depolarisation

- Sotalol (also beta blocking effect), Amiodarone (also blocks Na+ and Ca channels)

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14
Q

How do class IV antiarrhythmics work, name some.

A

Calcium channel blockers

  • Verapamil - more effect on the SA and AV nodes than Diltiazem
  • Dihydropyridines (felodipine, Amlodipine) have few electrophysiologic effects
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15
Q

How do class IV antiarrhythmics work, name some.

A

Calcium channel blockers

  • Verapamil - more effect on the SA and AV nodes than Diltiazem
  • Dihydropyridines (felodipine, Amlodipine) have few electrophysiologic effects
  • NOTE DILTIAZEM AND VERAPIL DEPRESS LV FUNCTION
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