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Review of Pharmacology - 9E (2015)

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Autonomic Nervous System<br />

39. Ans. (b) Inhibition <strong>of</strong> nor-epinephrine release from adrenergic nerve endings (Ref: Goodman & Gilman 11/e p184-185;<br />

KDT 6/e p96)<br />

• Most <strong>of</strong> the blood vessels contain cholinergic M 3<br />

receptors but no parasympathetic nerve supply.<br />

• Exogenously administered ACh can stimulate M 3<br />

receptors and result in vasodilation.<br />

• Stimulation <strong>of</strong> M 3<br />

receptors increases the production <strong>of</strong> NO (endothelium derived relaxing factor; EDRF) that<br />

causes smooth muscle relaxation resulting in vasodilation.<br />

• Vasodilation also may arise indirectly due to inhibition <strong>of</strong> NA release from nerve endings by ACh.<br />

• If endothelium is damaged, ACh can stimulate receptors on vascular smooth muscle cells resulting in<br />

vasoconstriction.<br />

40. Ans. (d) Therapy with pralidoxime should ideally be monitored by measuring blood cholinesterase levels. (Ref: KDT<br />

6/e p105, Drug facts and comparisons 2010/599)<br />

• Pralidoxime is ACh esterase reactivator used for organophosphate poisoning.<br />

• Blood cholinesterase levels can be used to monitor therapy, however RBC cholinesterase levels better reflect ACh<br />

esterase activity than serum or plasma levels because with chronic exposure to organophosphates, serum levels may<br />

return to normal but RBC levels remain depressed.<br />

• Chlorinated pesticides like DDT are CNS stimulants and their overdose is treated by diazepam like drugs. Pralidoxime<br />

has no role in their treatment.<br />

• Nerve gases used in warfare act by inhibiting acetyl cholinesterase. Atropine and oximes are used for their treatment.<br />

• When atropine and pralidoxime are used together, the signs <strong>of</strong> atropinization may occur earlier than might be expected<br />

when atropine is used alone.<br />

41. Ans. (a) Tacrine (Ref: KDT 6/e p104, 472, 473)<br />

Because <strong>of</strong> hepatotoxicity, and requirement <strong>of</strong> frequent dosing, tacrine is less <strong>of</strong>ten used than other agents.<br />

42. Ans. (b) Esteratic site <strong>of</strong> AChEs (Ref: KDT 6/e p99-100)<br />

• The active region <strong>of</strong> Acetylcholinesterase (AChE) has two sites i.e. an anionic site and an esteratic site. Anticholinesterase<br />

poisoning like Organophosphate compounds binds to esteratic site <strong>of</strong> AChE.<br />

43. Ans. (b) Edrophonium (Ref: KDT 6/e p104)<br />

• Drug used in ameliorative test (tensilon test) for myasthenia gravis is edrophonium. It is a cholinergic drug and can be<br />

used for diagnosis <strong>of</strong> myasthenia gravis because <strong>of</strong> its short duration <strong>of</strong> action (10 – 30 min.)<br />

44. Ans. (d) Is a competitive antagonist <strong>of</strong> acetylcholine (Ref: KDT 6/e p106)<br />

Atropine acts as an antagonist at muscarinic receptors. It has no activity on nicotinic receptors and do not interfere with<br />

the release <strong>of</strong> ACh.<br />

45. Ans. (c) Malathion Poisoning (Ref: KDT 6/e p105)<br />

• Pralidoxime is cholinesterase reactivator useful for organophosphate (malathion, parathion) poisoning.<br />

46. Ans. (b) Opiates (Ref: KDT 6/e p102, 456)<br />

Causes <strong>of</strong> Pin-Point Pupil<br />

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

Nervous System<br />

• Opioids Poisoning<br />

• Organophosphate Poisoning<br />

• Carbamate Poisoning<br />

• Carbolic acid Poisoning<br />

• Pontine Hemorrhage<br />

47. Ans. (c) Neostigmine (Ref: KDT 6/e p103)<br />

48. Ans. (a) Pralidoxime (Ref: Katzung 11/e p121)<br />

49. Ans. (b) Carbamate poisoning (Ref: Katzung 11/e p106-107)<br />

50. Ans. (c) Rapidly destroyed in the body (Ref: Katzung 11/e p97)<br />

51. Ans. (c) Acetylcholine (Ref: KDT 6/e p91)<br />

52. Ans. (a) Edrophonium (Ref: KDT 6/e p101)<br />

53. Ans. (c) Physostigmine (Ref: KDT 6/e p101)<br />

54. Ans. (a) Physostigmine (Ref: KDT 6/e p102)<br />

97<br />

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