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Review of Pharmacology - 9E (2015)

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

• It is active at µ receptors and side effects are similar to those <strong>of</strong> morphine.<br />

• Dezocine doesn’t increase plasma histamine and produces less hypotension than morphine or pentazocine.<br />

• Dezocine is effective for moderate to severe pain but can cause myocardial depression.<br />

314. Ans. (d) Subarachnoid (Ref: KDT 6/e p458, 437; Lee 12th/76-77)<br />

• Respiratory depression occurs due to depression <strong>of</strong> respiratory centre by morphine travelling through the subarachnoid<br />

space (intrathecal route)<br />

Routes <strong>of</strong> administration <strong>of</strong> morphine are:<br />

––<br />

Oral<br />

––<br />

Rectal<br />

––<br />

Intramuscular<br />

––<br />

Intravenous<br />

––<br />

Transdermal<br />

––<br />

Extradural/Epidural<br />

––<br />

Subcutaneous<br />

Central Nervous System<br />

315. Ans. (b) Rectal; (c) SC: (d) IV; (e) IM (Ref: KDT 6/e p458; Lee 12th/76)<br />

316. Ans. (a) It is an opioid antagonist; (c) It is used in alcohol dependence; (d) It is used to treat opioid dependence (Ref:<br />

KDT 6/e p467)<br />

317. Ans. (a) Acetaldehyde (Ref: KDT 6/e p386)<br />

• Disulfiram is an aldehyde dehydrogenase inhibitor that can be used for de-addiction <strong>of</strong> chronic alcoholics.<br />

Alcohol<br />

Aldehyde<br />

Ethyl alcohol Acetaldehyde Acetic acid<br />

dehydrogenase<br />

dehydrogenase<br />

Due to inhibition <strong>of</strong> aldehyde dehydrogenase, there is accumulation <strong>of</strong> acetaldehyde that leads to several distressing<br />

symptoms (which strengthens the resolution <strong>of</strong> a person to quit alcohol).<br />

318. Ans. (d) Antagonist <strong>of</strong> opioid receptors (Ref: KDT 6/e p467)<br />

• Naltrexone is used to decrease the craving for alcohol after de-addiction.<br />

319. Ans. (d) Pethidine (Ref: KD Tripathi 6/e p440)<br />

Most <strong>of</strong> pethidine is metabolized by MAO-A and is inactivated. Small amount is converted to nor-pethidine, which has<br />

CNS stimulant properties. Therefore, if combined with MAO inhibitors, most <strong>of</strong> pethidine will form nor-pethidine and the<br />

risk <strong>of</strong> seizures will increase.<br />

320. Ans. (c) Alcoholics psychologically but not physically dependent on alcohol (Ref: KDT 6/e p387)<br />

• If a patient is physically dependent on alcohol, disulfiram can precipitate severe withdrawl symptoms. It is therefore,<br />

not indicated for physically dependent alcoholics.<br />

321. Ans. (c) Inhibits the metabolism <strong>of</strong> methanol and generation <strong>of</strong> toxic metabolite (Ref: KDT 6/e p387)<br />

• Methanol produces toxic metabolites (formaldehyde and formic acid) that are responsible for blindness. This metabolism<br />

takes place with the help <strong>of</strong> alcohol and aldehyde dehydrogenase.<br />

Alcohol<br />

Aldehyde<br />

Methanol Formaldehyde Formic acid<br />

dehydrogenase<br />

dehydrogenase<br />

• Ehtanol is also metabolized by the same enzymes to produce acetaldehyde and acetic acid. It competes with methanol<br />

for above enzymes and inhibits the generation <strong>of</strong> toxic formaldehyde and formic acid.<br />

322. Ans. (d) Fomepizole (Ref: KDT 6/e p387)<br />

323. Ans. (a) Ischemic heart disease patients (Ref: KDT 6/e p457)<br />

• Morphine is used for the treatment <strong>of</strong> myocardial infarction (ischemic heart disease) and LVF.<br />

• Morphine is contra-indicated in extremes <strong>of</strong> age i.e., very young and elderly persons.<br />

• It is also contra-indicated in bronchial asthma because it can cause respiratory depression and worsen the condition.<br />

• By increasing intrabiliary pressure, morphine can worsen the pain <strong>of</strong> biliary colic.<br />

324. Ans. (a) Tramadol (Ref: KDT 6/e p460)<br />

325. Ans. (a) Pentazocine (Ref: KDT 6/e p464, 465)<br />

Pentazocine can cause dysphoric reactions (hallucinations) by stimulating the k receptors.<br />

390<br />

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