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Review of Pharmacology - 9E (2015)

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Autonomic Nervous System<br />

9. Ans. (a) Timolol (Ref KDT 6/e p139)<br />

Timolol is a non-selective beta blocker and can precipitate acute attacks <strong>of</strong> asthma in a susceptible individual via blockade<br />

<strong>of</strong> b 2<br />

receptors. Betaxolol is a cardioselective beta blocker and is less likely to cause this adverse effect.<br />

10. Ans. (b) Clozapine (Ref: Katzung 10/e p461; KDT 6/e p426)<br />

Friends, this seems to be another blunder from paper-setter. According to us, the question should contain ‘EXCEPT’ in the<br />

stem.<br />

Three drugs given in the options i.e. clozapine, fluphenazine and paroxetine have anti-cholinergic properties and should<br />

be avoided in angle closure glaucoma. Therefore, if the question was correctly framed as ‘all should be avoided in glaucoma<br />

except’, the answer would have been pilocarpine.<br />

But, if we have to choose the answer for the question as such, we will go with clozapine, as it has maximum anti-cholinergic<br />

properties.<br />

11. Ans. (c) Cholinergic (Ref: Katzung 10/e p76; KDT 6/e p93)<br />

• Autonomic ganglia (both sympathetic as well as parasympathetic) release ACh that stimulates the N N<br />

nicotinic<br />

receptors on the post-ganglionic fibres.<br />

12. Ans. (b) VI (Ref: Katzung 10/e p75; KDT 6/e p89)<br />

• Parasympathetic system is craniosacral in outflow. Cranial part involves III (oculomotor), VII (facial), IX (glossopharyngeal)<br />

and X (vagus) nerves whereas sacral portion includes S2 to S4.<br />

13. Ans. (b) Nor-adrenaline (Ref: Katzung 10/e p76; KDT 6/e p116)<br />

• Neurotransmitter secreted at end organ effectors <strong>of</strong> sympathetic system is mostly nor-adrenaline (except in sweat<br />

glands and hair follicle, where it is acetylcholine) whereas it is acetyl-choline at parasympathetic system.<br />

14. Ans. (d) Metoprolol (Ref: Katzung 10/e p103, 152; KDT 6/e p144-147)<br />

• Metoprolol is a beta blocker with local anaesthetic activity. Such beta blockers are not indicated in glaucoma.<br />

• Apraclonidine (alpha 2 agonist), timolol (beta blocker without local anaesthetic activity) and pilocarpine (directly<br />

acting miotic) are used in glaucoma.<br />

15. Ans. (b) Brimonidine (Ref: Goodman & Gilman 12/e p1788; KDT 6/e p146-147)<br />

• Apraclonidine and brimonidine can cross blood brain barrier and may result in CNS depression and apnea in<br />

neonates. These are therefore contra-indicated in children less than 2 years.<br />

16. Ans. (d) Reactivation <strong>of</strong> AChE enzyme (Ref: Katzung 10/e p116; KDT 6/e p105)<br />

• Pralidoxime and diacetylmonoxime are cholinesterase regenerator compounds used for organophosphate poisoning.<br />

17. Ans. (a) Edrophonium (Ref: KDT 6/e p104)<br />

Myasthenia gravis can be differentiated from cholinergic crisis with the help <strong>of</strong> a short acting anticholinesterase agent,<br />

edrophonium. It improves the symptoms in myasthenia gravis whereas worsens the condition in cases <strong>of</strong> cholinergic crisis.<br />

Neostigmine is used for the treatment <strong>of</strong> myasthenia.<br />

18. Ans. (a) Hemicholinium prevents the release <strong>of</strong> acetylcholine from the storage vesicles; (b) Botulinum toxin increase<br />

the ACh release; (d) Vesamicol inhibit the uptake <strong>of</strong> choline (Ref: KDT 6/e p94)<br />

Autonomic General <strong>Pharmacology</strong><br />

Nervous System<br />

• Hemicholinium blocks choline uptake (the rate limiting step in ACh synthesis).<br />

• Vesamicol block the transport <strong>of</strong> ACh into the synaptic vesicles.<br />

• Botulinum toxin inhibits the release <strong>of</strong> acetylcholine.<br />

• Acetylcholine esterase is inhibited by organophosphates and carbamates.<br />

• Pralidoxime reactives ACh.<br />

19. Ans. (a) It is a quarternary ammonium compound; (e) It possess agonistic action on N M<br />

receptors (Ref: KDT 6/e p101-102;<br />

Lee 12/e p217)<br />

• Neostigmine is a reversible cholinesterase inhibitor. It is a quarternary ammonium compound. (lipid insoluble agent),<br />

so it does not cross blood-brain-barrier.<br />

• It is partly hydrolyzed by serum cholinesterase and partly excreted unchanged by the kidneys.<br />

• It possesses some agonistic action on N M<br />

receptors.<br />

20. Ans. (b) Rise in blood pressure (Ref: KDT 6/e p97)<br />

Stimulation <strong>of</strong> muscarinic (M 3<br />

) receptors decreases BP whereas parasympathetic system stimulation has no effect on BP<br />

because blood vessels contain M 3<br />

receptors but no parasympathetic supply.<br />

21. Ans. (d) Cycloplegia (Ref: KDT 6/e p97)<br />

Pilocarpine is a directly acting cholinergic drug. It causes miosis and cyclospasm (not cycloplegia). It can increase all secretions<br />

<strong>of</strong> the body.<br />

95<br />

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