Vasodilators in Angina Flashcards
Angina pathophys
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Major types of angina + characteristics
- stable = narrowed lumen by plaque. inappropriate vasoconstrict 2. unstable = plaque rupture, thrombus form, unopposed vasoconstrict 2. variant = no plaque, intense vasospasm
Stable angina: major precipitating cause
-fixed stenotic endothelialized atheromatous plaque -imbalance occurs when O2 demand increases and supply (coronary blood flow) is unable to increase in response
Variant angina: major precipitating cause
-coronary vasospasm with or without atheromatous plaque -imbalance occurs as oxygen supply decreases due to reversible coronary vasospasm (associated with atheromas) -commonly occurs at rest
Unstable angina: major precipitating cause
-ruptured atheromatous plague with subocclusive thrombus -myocardial infarction from occlusive thrombus -angina at rest, signaled by change in frequency, character, duration, and precipitating factors in patients with stable angina
Summary of anti-anginal drug efficacy (table)
Nitrates: MOA
-Nitrates –> nitric oxide (NO) @ plasma membrane of vascular smooth muscle cells -NO activates guanylate cyclase –> GTP to cGMP –> relaxation of smooth muscle -vasodilation –> decreased venous return & systemic vascular resistance –> decreased wall tension –> decreases myocardial O2 requirement (primary effect) -also improves perfusion of ischemic myocardium (secondary effect).
Nitrates: Pharmacokinetics
-Low oral bioavailabilty; administered orally (sustained-release), sublingually, transdermally, parenterally. -Best route=sublingual -Half-lives of 2-8 min (rapid denitration in liver). Sublingual administration. Rapid pain relief (45 sec-5 min) lasting < 30 min. May repeat x 3 every 5 min; if no relief seek assistance (strongly indicative of impending MI).
Nitrates: Adverse rxns
-Throbbing headache (30-60%), -orthostatic hypotension -reflex tachycardia -facial flushing -tachyphylaxis (tolerance) can occur with continuous exposure –>nitrate free interval of 6-14 hours each day is recommended.
Ca2+ channel blockers: MOA
-block of L-type Ca++ channels in cardiac and smooth muscle (vascular smooth muscle is most sensitive, arterioles > veins). -Prevents calcium entry into cell leading to smooth muscle relaxation and vasodilation -Agents differ in selectivity for vascular vs heart calcium channels.
Ca2+ channel blockers: Major drugs
-Verapamil -Diltiazem -Nifedipine
Ca2+ channel blockers: various drug selectivities
- Dihydropyridines (nifedipine) have a greater ratio of vascular (relaxation) to cardiac (contractility, SA node impulse generation, AV nodal conduction) effects
- Verapamil and diltiazem, each at a distinct site, have prominent effects at cardiac nodal tissue (phase 0 at SA and AV node) and on cardiac muscle (phase 2)
Ranolazine: MOA
-no effect on HR or BP -failure of late Na+ current to inactivate in heart disease –> intracellular Na+ overload –> reversal of the Na+-Ca++ exchanger –> intracellular Ca++ overload Ca++ overload can result in both mechanical dysfunction (increased diastolic tension) and further imbalance between O2 demand and supply Ranolazine inhibits this late Na+ current
Beta-blockers: MOA
Useful in stable angina due to hemodynamic effects that result in decreased heart rate, blood pressure, and contractility with a subsequent decrease in O2 requirements (during rest and exercise) Can block the reflex tachycardia associated with use of nitrate vasodilators in chronic stable angina NOT vasodilators, thus no role in variant (vasospastic angina)
Beta-blockers: Site of Action
Target is block of beta-1 adrenergic receptors in the heart, reducing rate and contractility, leading to a reduction in myocardial oxygen demand