Cardiac Physiology and Pharmacology Flashcards

1
Q

Interaction between actin and myosin in myocytes is inhibited by what protein

A

Tropomyosin (effect of tropomyosin disinhibition is mediated by intracellular Ca+)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Medications that exert their effects by altering intracellular Na currents

A
  • Lidocaine
  • Procainamide
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Medications that exert their effects by altering intracellular K currents

A
  • Amiodarone
  • Sotolol
  • Ibutilide
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Medications that exert their effects by altering intracellular Ca currents

A
  • Diltiazem
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Impact and MOA of decreased ATP, acidosis, and elevated lactate levels on vascular tone

A

Decrease vascular tone MOA: increased permeability of the ATP–sensitive K+ channel, resulting in hyperpolarization of the cell membrane that inhibits Ca entry into the cell.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Pharmacologic agents that act via cyclic GMP

A
  • Nitric Oxide
  • Nitroglycerine
  • Na Nitroprusside
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Pharmacologic agents that regulate intramyocyte Ca levels via cyclic AMP

A

Catecholamines with beta activity (epi, norepi, dobutamine)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe ion fluxes at each point of the cardiac action potential

A
  • 0: Depolarization with overshoot (inward Na influx)
  • 1: Recovery (ceaseing of Na influx)
  • 2: Plateau (inward Ca influx)
  • 3: Repolarization (outward K efflux)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Vaughn Williams Anti-arrhythmiac Classification

A
  • Class I (Na channel blockers)
  • Class II (Beta blockers)
  • Class III (Prolong AP)
  • Class IV (Block Ca entry)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Class I Anti-arrhythmics

A
  • Class Ia (long time constant for disassocatio from Na channel > drug accumulation in channel > slowed conduction/prolonged AP)
    • Procainamide
    • Quinidine
    • Disopyramide
  • Class Ib (short time constant for disaccoation from Na channel)
    • Lidocaine
    • Mexiletine
  • Class Ic (long time constant for disassocatio from Na channel > drug accumulation in channel > slowed conduction/prolonged AP)
    • Encainide
    • Flecainide
    • Propafenone
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Na channel blocker class that markedly decrease conduction velocity

A

Class Ic

  • CAST study demonstrated higher incidence of sudden death with encainide and flecainide (not used commonly)
  • Propafenone may be used for both atrial and venticular dysrhythmias.
    • beta-blocking and Na channel blocking effects
    • lengthens PR, QRS and QT intervals
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Na channel blocker that has little effect on conduction velocity in normal myocardial but slows conduction in ischemic myocardium

A

Lidocaine

  • little effect on atrial tissue
  • not recommended for shock resistent VT/VF
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Class III antiarrhythmics that are approved for the treatment of atrial fibrillation

A
  • ibutilide (iv)
  • dofetilide (po)

(carry risk of torsade de pointes)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Class III antiarrhythmic that has both beta-blocker and K-channel blocker activity

A

Sotolol

(life threatening ventricular arrhythmias)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What explains the effectivness of Class IV antiarrhythmics (verapimil and diltiazem) in treatment of supraventricular tachycardia

A

In SA and AV nodal tissue Ca channels contribute sinificantly to phase 0 depolarization, then the AV nodal refractory period is prolonged by Ca entry blockade.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Drug that inhibits Na,K ATPase pump, leading to reduced intracelllular K

A