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Review of Pharmacology - 9E (2015)

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

Explanations<br />

1. Ans (b) Cyclizine (Ref: Goodman and Gilman 12/e p921,922)<br />

Antihistaminics may be classified into first generation and second generation compounds on the basis <strong>of</strong> CNS penetration<br />

and anticholinergic properties. First Generation Anti-histaminics can penetrate blood brain barrier and possess additional<br />

anticholinergic properties which are lacking in second generation drugs. Cyclizine is a first generation whereas cetririzine,<br />

loratidine and fex<strong>of</strong>enadine are second generation drugs.<br />

2. Ans. (c) Bradykinin (Ref: KDT 6/e p490, 491)<br />

Although both histamine as well as bradykinin can cause edema and increase in permeability, histamine is an amine<br />

whereas bradykinin is a peptide.<br />

3. Ans. (a) Post partum hemorrhage (Ref: KDT 6/e p322)<br />

Obstetric indications <strong>of</strong> ergometrine (Ergonovine):<br />

• To control and prevent Post partum hemorrhage. It is given at the time <strong>of</strong> delivery <strong>of</strong> anterior shoulder.<br />

• After Caesarean Section/instrumental delivery – to prevent uterine atony.<br />

• To ensure normal involution in multipara.<br />

Autacoids<br />

4. Ans. (d) Cetirizine (Ref: KDT 6/e p157)<br />

It is a non-sedating second generation antihistaminic agent and is preferred for the patients requiring constant attention.<br />

It does not cause sedation or impairment <strong>of</strong> psychomotor function. Other drugs listed in the question are first generation<br />

antihistaminics.<br />

5. Ans. (a) Cyclizine (Ref: KDT 6/e p156)<br />

6. Ans. (b) Increase in H 1<br />

mediated gastrin release (Ref: KDT 6/e p153)<br />

H 3<br />

receptors act as pre-synaptic receptors and decrease the release <strong>of</strong> histamine and other neurotransmitters. These antagonize<br />

H 1<br />

mediated wakefulness and bronchoconstriction. These also decrease gastrin release and produce negative<br />

chronotropic effect. Inverse agonist <strong>of</strong> H 3<br />

receptor (tiprolisant) is approved for Narcolepsy.<br />

7. Ans. (a) Azelastine; (b) Fex<strong>of</strong>enadine; (d) Desloratidine (Ref: KDT 6/e p158-159)<br />

Chlorpheniramine and promethazine are first generation anti-histaminics.<br />

8. Ans. (b) Direct action on vascular smooth muscle causing vasodilation (Ref: KDT 6/e p153)<br />

Both H 1<br />

and H 2<br />

receptors cause vasodilation. H 1<br />

receptors are present in the endothelium and cause vasodilation by<br />

releasing NO. However, H 2<br />

receptors are present on the smooth muscles and cause direct vasodilation.<br />

9. Ans. (c) Morphine (Ref: KDT 6/e p155)<br />

Basic drugs like morphine, d-TC and amphotericin B etc. act as histamine liberators and can cause acute reaction leading<br />

to itching and hypotension.<br />

10. Ans. (a) Promethazine (Ref: KDT 6/e p158)<br />

All the drugs listed in the question are second generation anti-histaminic agents except promethazine.<br />

11. Ans. (c) Cyproheptadine (Ref: KDT 6/e p166)<br />

12. Ans. (a) Driving motor vehicles (Ref: KDT 6/e p157)<br />

First generation antihistaminic agents cause sedation and impairment <strong>of</strong> psychomotor function.<br />

13. Ans. (b) These possess high anti-motion sickness activity (Ref: KDT 6/e p157)<br />

Anti-motion sickness activity is related to anticholinergic property. This property is exhibited by first generation compounds<br />

whereas second generation antihistaminics lack this potential.<br />

14. Ans. (c) Astemizole (Ref: KDT 6/e p158)<br />

15. Ans. (b) Cinnarizine (Ref: KDT 6/e p160)<br />

138<br />

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