ANS pharmacology & pathophysiology 5 Flashcards

1
Q

Direct-acting vasodilators exert

A

an arterial relaxing effect without interfering with systemic or local constrictor mechanisms or Ca2+ channels

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2
Q

The primary action of nitroglycerin is

A

venodilator with reduced preload

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3
Q

The primary action of nitroprusside is

A

reduces afterload and preload

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4
Q

The primary action of hydralazine is

A

arterial smooth muscle dilator

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5
Q

The vasodilatory effect of NTG is greater on

A

venules than arterioles

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6
Q

Nitroglycerin exerts its action via the

A

liberation of nitric oxide, a vascular dilator

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7
Q

Nitroglycerin improves the balance of

A

myocardial O2 supply and demand due to its direct coronary artery vasodilator and systemic effects

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8
Q

____________ is an excellent first-line treatment of cardiac ischemia

A

Nitroglycerin

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9
Q

Cautioned should be used when using nitroglycerin in the setting of

A

a patient with myocardial ischemia who is hypovolemic–> risk of severe hypotension
when using nitric oxide liberation drug like sildenafil d/t risk of severe hypotension

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10
Q

Unlike nitroglycerin, nitroprusside is NOT used in _____

A

MI b/c it will induce “coronary steal”

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11
Q

Sodium nitroprusside is an ultra-short-acting

A

nitric oxide donor with potent venous and arteriolar vasodilator activity decreasing preload and afterload

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12
Q

____________ may be seen more so with sodium nitroprusside than nitroglycerine.

A

reflex tachycardia

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13
Q

_____________ is produced in sodium nitroprusside metabolism inhibiting aerobic metabolism

A

Cyanide

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14
Q

Cyanide also binds with hemoglobin forming

A

methemoglobin and binding to sulfur to form thiocyanate

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15
Q

The direct vasodilating activity of hydralazine is a result of

A

activation of KATP channels reducing intracellular Ca2+

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16
Q

____________ can be seen with hydralazine

A

Reflex tachycardia

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17
Q

Hydralazine preserves ___________ as it does not dilate

A

LV preload; venous capacitance vessels

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18
Q

Minoxidil’s strong, direct vasodilating effect is limited by

A

reflex-mediated tachycardia, necessitating co-administration of a beta antagonist

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19
Q

Use of minoxidil is uncommon due to

A

causing hypertrichosis (hair growth), salt and water retention, and rare reports of pericardial effusion

20
Q

Phosphodiesterase 5 inhibitors include

A

sildenafil
tadalafil
vardenafil

21
Q

PDE5 inhibitors work by

A

increasing levels of cGMP and targeting the lungs and penis (viagra)
induce smooth muscle relaxation and increase blood flow

22
Q

PDE4 inhibitors include

A

roflumilast
apremilast
ibudilast

23
Q

PDE4 inhibitors work by

A

increasing levels of cAMP, targeting the airways, skin, and immune system

24
Q

PDE4 inhibitors are used for

A

airway smooth muscle relaxation in those with hyperreactive airways
useful in inflammatory states that affect the skin, bowel, and joints

25
Q

PDE3 inhibitors include

A

milrinone and cilostazol

26
Q

PDE3 inhibitors work by

A

increasing the levels of cAMP and cGMP and are used in those with CV disease

27
Q

Uses of PDE3 inhibitors include

A

prevent platelet aggregation for thrombosis prophylaxis
promote vasodilation in peripheral vessels to treat intermittent claudication
increased inotropy and relaxation of vascular and airway smooth muscle

28
Q

________ is a positive inotrope and is frequently used in weaning the patient from cardiopulmonary bypass.

A

Milrinone

29
Q

Vasopressin acts on

A

V1, V2 and V3 cellular receptors

30
Q

What is the function of V1 receptors?

A

mediate CV effects such as increased SVR

31
Q

What is the function of V2 receptors?

A

function in the kidney as an antidiuretic hormone

32
Q

What is the function of V3 receptors?

A

found in the pituitary gland and modulate autocoids

33
Q

Vasopressin is indicated for those in

A

vasodilatory shock states who are resistant or refractory to catecholamine fluid therapy

34
Q

The dry cough associated with an ACE-inhibitor is MOST likely due to:
a. paradoxical effect of drug-induced pulmonary vasoconstriction
b. accumulation of bradykinin
c. direct irritant effects of the ACE-inhibitor
d. dysregulation of catecholamines in the lung

A

b. accumulation of bradykinin

35
Q

The ___________ is essential in cardiovascular homeostasis.

A

renin-angiotensin-aldosterone system (RAAS)

36
Q

Lidocaine is a ______________

A

Class 1B antiarrhythmic

37
Q

Class 1B antiarrhythmics suppress automaticity by

A

increasing the electrical stimulation threshold of the ventricle and His-Purkinje system & inhibiting spontaneous depolarization during diastole

38
Q

ARBs have a greater affinity for the

A

AT1 receptor, impeding angiotensin 2’s effect at the AT1 receptor

39
Q

ACE inhibitors imapir the activity of

A

both AT1 and AT2 receptors

40
Q

Side effects of ARBs are

A

similar to ACEi but are milder and without the dry cough

41
Q

ARBs are indicated for the treatment of

A

HTN, CHF, and coronary disease

42
Q

ACE-inhibitors are best suited for

A

hypertension d/t increased renin production and are first-line therapy for HTN, CHF, mitral regurgitation, and LV dysfunction

43
Q

ACE inhibitors decreasethe

A

generation of angiotensin, reduce arterial tone, and reduce left ventricular afterload

44
Q

ACE inhibitors exert __________ in diabetic patients

A

renal protective effects

45
Q

Important side effects of ACE-inhibitors include

A

dry cough d/t blockade of ACE-induced degradation of bradykinin
angioedema d/t inhibition of bradykinin breakdown
profound hypotension with GA