Cardio Medications Flashcards
ACE inhibitors and mechanism:
- the “-prils”: enalapril, lisinopril, captopril, etc.
- Mechanism: impede the production of angiotensin II.
What is the suffix of ACE inhibitors?
“-prils”: enalapril, lisinopril, captopril, etc
What is Angiotensin II?
- a vasoconstrictor that stimulates the secretion of aldosterone.
- production is inhibited by ACE inhibitors.
What drugs impede the production of angiotensin II?
- ACE inhibitors
- the “-prils”: enalapril, lisinopril, captopril, etc.
Angiotensin receptor blockers (ARBs) and mechanism:
- the “-sartans”: losartan, irbesartan, etc.
- Mechanism: same rationale as for ACE inhibitors, except these compounds selectively block the type AT1 angiotensin II receptor.
What is the suffix of Angiotensin receptor blockers (ARBs)?
the “-sartans”: losartan, irbesartan, etc.
What drugs selectively block the type AT1 angiotensin II receptor?
- Angiotensin receptor blockers (ARBs)
- the “-sartans”: losartan, irbesartan, etc.
What drug is a cholinergic muscarinic receptor antagonist?
atropine
Atropine mechanism:
- blocks the cholinergic-muscarinic receptor effects of ACh
- an antiparasympathetic.
β-blockers and mechanism:
- the “-olols”: metoprolol, atenolol, etc.
- Mechanism: impede the β1-mediated SNS effects; β blockers have varying degrees of specificity for β1 over β2.
In medical practice, the term “β blocker” implies blockade of what receptors?
type β1 receptors.
β-blockers suffix:
the “-olols”: metoprolol, atenolol, etc.
What drug is a Type L Ca2+ channel antagonist:
amlodipine
Amlodipine Mechanism:
- preferentially blocks type L Ca2+ channels expressed within VSM
- mediates VSM contraction.
What drugs are positive inotropics (increase contractile force)?
- epinephrine, norepinephrine, cardiac glycosides (i.e. digoxin)
- Mechanism: enhance cardiac contractility (all three) and/or rate (epi and norepi).
What drugs enhance cardiac contractility?
- epinephrine, norepinephrine, cardiac glycosides (i.e. digoxin)
What drugs inrease heart rate?
epinephrine and norepinephrine
What drug is a loop diuretic?
furosemide
Furosemide mechanism:
- loop diuretic
- impairs Na+, K+, and Cl- reabsorption by the kidneys. This holds H2O in forming urine and thus induces diuresis.
What drug is a thiazide diuretic?
hydrochlorothiazide (HCTZ)
Hydrochlorothiazide (HCTZ) mechanism:
- thiazide diuretic
- impairs Na+ reabsorption by the kidneys; other blood pressure lowering effects with poorly understood mechanism of action.
What drugs are calcium channel blockers?
verapamil and diltiazem
Verapamil and diltiazem mechanism:
- block cardiac type L Ca2+ channels
- delays AV nodal conduction, negative inotropy; little effect on non-cardiac type L channels.
What drugs delay AV nodal conduction and inotropy?
- verapamil and diltiazem
- block cardiac type L Ca2+ channels
β2 adrenoceptor agonists and mechanism:
- albuterol and salmeterol
- Mechanism: short-acting and long-acting β2 agonists, respectively. Promote bronchiolar smooth muscle relaxation.
What drug is a short-acting β2 adrenoreceptor agonist?
albuterol
What drug is a long-acting β2 adrenoreceptor agonist?
salmeterol
Albuterol and salmeterol mechanism:
- β2 adrenoceptor agonists
- Promote bronchiolar smooth muscle relaxation.
Fluticasone Mechanism:
- inhaled glucocorticoid receptor agonist
- anti-inflammatory.