All the Drugs for Midterm 1 Flashcards

1
Q

what are thiazide diuretics?

A

drugs that increase water loss and have a direct vasodilatory effect

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2
Q

what is the mechanism of action of thiazide diuretics?

A

they inhibit the sodium chloride cotransporter, preventing sodium reabsorption, increasing water in the urine

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3
Q

a commonly used thiaziade

A

bendroflumethiazide

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4
Q

what are beta blockers?

A

competitive antagonists of adrenergic receptors

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5
Q

propranolol

A

non-selective beta blocker (competitive antagonist), can cause bronchospasm/vasoconstriction as a side effect of targetting beta-2 receptors

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6
Q

adrenolol

A

beta-1 selective beta blocker, decreases cardiac contractions = reduces BP, minimal side effects

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7
Q

carvedilol

A

non selective beta blocker which inhibits both beta and alpha receptors, has an additional effect on peripheral resistance due to alpha receptors

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8
Q

amlodipine

A

blocks voltage gated Ca++ channels and prevents smooth muscle contraction

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9
Q

captopril

A

ACE inhibitor: prevents the cleavage of ATI and reduces generation of ATII and aldosterone

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10
Q

what are the side effects of using captopril?

A

dry cough due to bradykinin-mediated bronchoconstriction

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11
Q

losartan

A

AT1 blocker (ARBs): have a vasodilatory effect, inhibiting the vasoconstrictive effects of ATII

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12
Q

which is better tolerated: ACE inhibitors or ARBs?

A

ARBs

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13
Q

spironolactone

A

a competitive antagonist of the aldosterone receptor, has diuretic actions by inhibiting aldosterone effects

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14
Q

the primary treatment for atherosclerosis (reduction of thrombotic clots and LDL-C)

A

statins

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15
Q

which enzyme do statins target?

A

HMG-CoA reductase

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16
Q

competitive inhibitors of HMG-CoA reductase

A

statins

17
Q

atorvastatin (commercial name lipitor)

A

a prodrug which must be processes by first-pass metabolism in the liver, converted form is a competitive inhibitor of HMG-CoA reductase

18
Q

lovastatin

A

a prodrug and a statin, converted form is a competitive inhibitor of HMG-CoA reductase

19
Q

a class of drugs used to treat dislipidemias

A

fibrates

20
Q

fenofibrates

A

a type of fibrate which targets the peroxisome proliferator-activated receptors (PPARs)

21
Q

are fibrates agonists or antagonists of PPARs

A

agonists

22
Q

what are the important outcomes of using fibrates?

A
  • increased expression of lipoprotein lipase
  • increased breakdown of triglycerides in VLDLs
  • increased uptake of fatty acids as fuel in peripheral tissues
  • increased LDL uptake in the liver
  • reduced VLDL production in the liver
23
Q

which is more effective: statins or fibrates?

A

statins

24
Q

inhibits both COX1 and COX2

A

aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs)

25
Q

daily NSAID use can prevent ____ in those at risk of a stroke or heart attack

A

platlet aggregation

26
Q

which site on the COX enzymes do NSAIDs inhibit?

A

the catalytic site (where arachadonic acid binds)

27
Q

acetylsalicylic acid (Aspirin)

A

a non-competitive, irreversible inhibitor, covalently binds to the catalytic site of COX1 and COX2

28
Q

what is a negative side effect of NSAID use?

A

gastric toxicity (due to inhibition of COX1 enzymes in gastric mucosa), extreme cases can lead to: ulceration, upper GI bleeding, and renal failure

29
Q

ketoralac (toradol)

A

a highly effacious non-selective NSAID recommended for short term use (ex: post-surgical) to avoid gastric toxicity

30
Q

the three most widely used topical anesthetics

A

procain, lidocaine, bupivicaine

30
Q

acetaminophen

A

an analgesic and antipyretic that inhibits COX3, lacks anti-inflammatory effects

31
Q

capsaicin

A

an agonist for the TRPV1 receptor. initial application causes burning pain, but over time causes pain relief

32
Q

is capsaicin treatment reversible?

A

yes!

33
Q

codeine

A

a mu opioid receptor agonist, acts as an antitussive

34
Q

dextromethorphan

A

a centrally active NMDA receptor antagonist which inhibits neurons in the nucleus tractus solitarus

35
Q

diphenhydramine

A

an antihistamine (H1 inverse agonist), inhibits histamine action at the H1 receptors, crosses the blood brain barrier to suppress neurons in the nucleus tractus solitarus (nTS)

36
Q
A