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FA cardiopharmmech
mechanisms of cardio drugs
Question | Answer |
---|---|
increases cGMP causing smooth muscle relaxation. | Hydralazine |
vasodilates arterioles>veins = decrease afterload | Hydralazine |
Blcok voltage dependent L type calcium channels of cardiac and smooth muscle | nifedipine, verapamil, diltiazem (CCBs) |
reduce contractility | nifedipine, verapamil, diltiazem (CCBs) |
vasodilate by release NO in smooth muscle. = increased cGMP and smooth muscle relaxation | Nitroglycerin, isosorbide dinitrate |
dilate veins>>arterioles = decrease preload | Nitroglycerin, isosorbide dinitrate |
increases cGMP via dirct release of NO. short acting. can cause cyanide tox | Nitroprusside |
dopamine D1 receptor agonist - relaxes renal vascular sm. muscle | Fenoldopam |
K+ channel opener - hyperpolarizes and relaxes vascular smooth muscle. Can cause hyperglycemia. | Diazoxide |
Malignant HTN tx | Nitroprusside, Fenoldopam, Diazoxide |
inhibits cholesterol precursor, mevalonate via HMG-COA reductase inhibition | statins |
inhibits lipolysis in adipose tissue; reduces hepatic VLDL secretion into circulation | niacin |
prevents intestinal reabsorption of bile acids; liver must use cholesterol to make more | cholestyramine, colestipol, colesevelam (bile acid resins) |
prevent cholesterol reabsorptionat small intestine brush border | ezetimibe (cholesterol absorption blockers) |
upregulate LPL --> increased triglyceride clearance | gemfibrozil, clofibrate, bezafibrate, fenofibrate (fibrates) |
direct inhibition of Na+/K+ ATPase leads to indirect inhibition of Na+/Ca2+ exchanger/antiport, increasing intracellular calcium | digoxin, digitoxin (cardiac glycosides) |
decreases resting heart rate, increases contractility | digoxin, digitoxin (cardiac glycosides) |
increase AP duration, increase ERP, increase QT interval | Quinidine, Procainamide, Disopyramide (Class IA) |
decrease AP duration, preferentially affect ischemic or depolarized purkinje and ventricular tissue | Lidocaine, Mexiletine, Tocainide (Class IB) |
No effect on AP duration. contraindicated post MI | Flecainide, Encainide, Propafenone (class IC) |
decrease cAMP, decrease Ca currents. supress abn pacemakers by decreasing slope of phase 4. | Propranolol, esmolol, metoprolol, atenolol, timolol (Class II (beta blockers)) |
increase AP duration, increase ERP, increase QT interval. Used when other antiarrhythmics fail. | Sotalol, amiodarone, ibutilide, bretylium, dofetilide (Class III (K+ blockers)) |
decrease conduction velocity, increase ERP, increase PR interval. used in prevention of nodal arrhythmias | Verapamil, Diltiazem (class IV (Na blockers) |
increase K+ out of cells cause hyperpolarization and decreased ICa. SVT dx/abolition. | Adenosine |