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Review of Pharmacology - 9E (2015)

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<strong>Review</strong> <strong>of</strong> <strong>Pharmacology</strong><br />

198. Ans. (a) Amiodarone (Ref: KDT 6/e p511)<br />

199. Ans. (a) Adenosine (Ref: KDT 6/e p519)<br />

200. Ans. (a) Verapamil (Ref: KDT 6/e p519)<br />

201. Ans. (c) Xylocaine (Ref: KDT 6/e p519, CMDT 2014/362)<br />

• DOC for ventricular arrhythmias after MI is lignocaine (lidocaine; xylocaine).<br />

• DOC for supraventricular arrhythmias after MI is beta blockers if cardiac function is adequate.<br />

202. Ans. (a) Diphenylhydantoin (Ref: KDT 6/e p498)<br />

Phenytoin is an alternative to lignocaine for digitalis induced ventricular arrhythmia.<br />

203. Ans. (c) Amiodarone (Ref: Katzung 11/e p241)<br />

204. Ans. (b) Na + channel blockade (Ref: Katzung. 11/e p237)<br />

205. Ans. (b) Decreased absorption <strong>of</strong> cholesterol (Ref: Katzung 10/e p571; KDT 6/e p618-619)<br />

Ezetimibe is an intestinal cholesterol absorption inhibitor and is combined with statins.<br />

206. Ans. (c) Absorbed good on empty stomach and absorption is delayed by fatty meals (Ref: KDT 6/e p616-617; Katzung 11/e<br />

p615)<br />

Cardiovascular System<br />

• Absorption <strong>of</strong> fibrates improve when they are taken with food.<br />

• Fibric acid derivatives acts by stimulating LPL by activating a nuclear receptor PPARa (peroxisome proliferators<br />

activated receptor alpha). Major effect <strong>of</strong> fibrates is to reduce TG (contained in VLDL) and to increase<br />

HDL.<br />

• Fibrates are the drugs <strong>of</strong> choice in hypertriglyceridemia (type III and IV) and can be used with other drugs in<br />

type IIb Zfen<strong>of</strong>ibrate, as it has maximum LDL reducing action).<br />

• GI distress and elevation <strong>of</strong> aminotransferases are important adverse effect <strong>of</strong> fibric acid derivatives. Risk <strong>of</strong><br />

myopathy is increased if these are used with statins except bezafibrate.<br />

207. Ans. (d) Fibrinogen levels are increased by pravastatin (Ref: Goodman & Gilman 11/e p950, 951, 952)<br />

Pravastatin has the least chances <strong>of</strong> drug interactions because it is metabolized by non-microsomal enzymes. It also has<br />

minimum chances <strong>of</strong> myopathy among statins. Bioavailability <strong>of</strong> pravastatin is least affected with food intake. It has little<br />

CNS penetration. Most studies indicate that pravastatin decreases serum fibrinogen levels.<br />

208. Ans. (c) Indirect increase <strong>of</strong> LDL receptor synthesis (Ref: KDT 6/e p614, 615)<br />

For explanation, see text<br />

209. Ans. (c) Niacin (Ref: KDT 6/e p618)<br />

210. Ans. (c) Statins (Ref: KDT 6/e p614)<br />

211. Ans. (d) Nicotinic acid (Ref: Katzung 11/e p613)<br />

212. Ans. (d) Activating lipoprotein lipase, resulting in VLDL degradation (Ref: KDT 6/e p616, 617)<br />

Fibrates activate PPAR-a that results in the increased transcription <strong>of</strong> genes for lipoprotein lipase.<br />

213. Ans. (b) Nicotinic acid (Ref: KDT 6/e p618)<br />

214. Ans. (b) Niacin (Ref: KDT 6/e p618)<br />

215. Ans. (d) Statins (Ref: KDT 6/e p614, 615)<br />

216. Ans (a) R<strong>of</strong>ecoxib (Ref: KDT 6/e p534, 197)<br />

• Angiotensin receptor blockers (like losartan) and beta blockers (like metoprolol) are cardioprotective in congestive<br />

heart failure. These decrease the mortality.<br />

• Nicorandil is a potassium channel opener used in angina. It is cardioprotective by causing ischemic preconditioning.<br />

• R<strong>of</strong>ecoxib is a selective COX-2 inhibitor that was withdrawn due to increased risk <strong>of</strong> myocardial infarction.<br />

208<br />

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