MCQs-Autacoids and Related Drugs part 2 I Pharmacology KD Tripathi mcqs part 11




11.1 The following biogenic amine is not actively taken up into its storage site by an active amine pump:
A. Histamine
B. 5-Hydroxy tryptamine
C. Dopamine
D. Noradrenaline

11.2 The following action of 5 Hydroxy tryptamine is mediated by the 5-HT3 receptor:
A. Vasoconstriction
B. Bradycardia
C. EDRF release
D. Platelet aggregation

11.3 The typical response to intravenous injection of 5-HT in an anaesthetised animal is:
A. Rise in BP
B. Fall in BP
C. Rise followed by brief fall in BP
D. Transient fall, followed by brief rise, followed by prolonged fall in BP

11.4 The following 5-HT receptor is not a G protein coupled receptor:
A. 5-HT1
B. 5-HT2
C. 5-HT3
D. 5-HT4

11.5 Tachyphylaxis to many actions on repeated injection is a feature of the following autacoid:
A. Histamine
B. 5-Hydroxytryptamine
C. Bradykinin
D. Prostaglandin E2

11.6 The following is a selective 5-HT1D receptor agonist:
A. Buspirone
B. Ondansetron
C. Sumatriptan
D. α-methyl 5-HT

11.7 Actions of 5-HT2 receptor activation are primarily mediated by:
A. Increased membrane permeability to Na+ ions
B. Increased formation of cAMP
C. Activation of guanylyl cyclase
D. Generation of inositol trisphosphate and diacyl glycerols

11.8 The following serotonergic receptor functions primarily as an autoreceptor on neurones:
A. 5-HT1A
B. 5-HT2A
C. 5-HT3
D. 5-HT4

11.9 The smooth muscle stimulating action of 5-HT is most marked in the:
A. Bronchi
B. Intestines
C. Ureter
D. Biliary tract

11.10 5-HT appears to play a role in the following except:
A. Regulation of normal BP
B. Regulation of intestinal peristalsis
C. Haemostasis
D. Causation of migraine

11.11 The most important receptor involved in cytotoxic drug induced vomiting is:
A. Histamine H1 receptor
B. Serotonin 5-HT3 receptor
C. Dopamine D2 receptor
D. Opioid μ receptor

11.12 The following is a selective 5-HT4 agonist:
A. Buspirone
B. Sumatriptan
C. Cisapride
D. Clozapine

11.13 Methysergide has lost popularity as a prophylactic drug for migraine because of its:
A. Poor efficacy
B. Potential to cause visceral fibrosis
C. Oxytocic action
D. Potential to aggravate ischaemic heart disease

11.14 Blockade of both dopamine D2 and serotonin 5-HT2A/2C receptors is a distinctive feature of:
A. Pimozide
B. Haloperidol
C. Ketanserin
D. Clozapine

11.15 Dihydroergotamine (DHE) differs from ergotamine in the following respect:
A. It is a more potent oxytocic
B. It has antiemetic property
C. It has high oral bioavailability
D. It is a more potent α adrenergic blocker and less potent vasoconstrictor

11.16 Choose the ergot alkaloid that is well absorbed orally, has weak vascular but prominent uterine stimulant action:
A. Ergometrine
B. Ergotamine
C. Dihydroergotamine
D. Dihydroergotoxine

11.17 Select the ergot compound which is primarily used for dementia:
A. Bromocriptine
B. Ergotamine
C. Codergocrine
D. Methysergide

11.18 The ‘amine’ ergot alkaloid differs from ‘amino acid’ ergot alkaloid in that it has:
A. High oral bioavailability
B. Better CNS penetrability
C. Weaker oxytocic action
D. Strong anti-5-HT action

11.19 Select the correct statement in relation to drug therapy of migraine:
A. Simple analgesics like paracetamol are ineffective in migraine
B. Ergot alkaloids are used for prophylaxis as well as treatment of migraine attacks
C. Use of ergot alkaloids is restricted to severe or resistant cases
D. Ergot alkaloids should be given till 24 hours after an attack has subsided

11.20 The nonsteroidal anti inflammatory drugs are more effective in migraine:
A. Without aura
B. With aura
C. Than ergotamine
D. When combined with propranolol

11.21 Ergotamine relieves migraine by:
A. Blocking vascular α adrenergic receptors
B. Blocking vascular 5-HT2 receptors
C. Dilating cranial arterio-venous shunt channels
D. Constricting cranial vessels and reducing perivascular neurogenic inflammation

11.22 The most important risk in the use of sumatriptan for treatment of migraine is:
A. Precipitation of seizures
B. Precipitation of psychosis
C. Development of hypertension
D. Coronary vasospasm

11.23 Choose the correct statement about sumatriptan:
A. It activates serotonergic neurones in raphe nuclei
B. It tends to suppress both pain and vomiting in migraine
C. It does not carry risk of precipitating coronary vasospasm
D. It is combined with ergotamine for treatment of severe migraine

11.24 Which of the following drugs is most commonly used for prophylaxis of migraine:
A. Ergotamine
B. Propranolol
C. Methysergide
D. Sumatriptan

11.25 Select the β blocker which does not afford prophylaxis in migraine:
A. Propranolol
B. Timolol
C. Atenolol
D. Pindolol

11.26 Prophylactic therapy of migraine:
A. Is recommended in all cases
B. Benefits upto 70% patients of moderate to severe migraine
C. Needs to be continued lifelong without interruption
D. Reduces the severity but increases the frequency of migraine attacks

11 .1 A 11.2 B 11.3 D 11.4 C 11.5 B 11.6 C 11.7 D 11.8 A 11.9 B 11.10 A 11.11 B 11.12 C 11.13 B 11.14 D 11.15 D 11.16 A 11.17 C 11.18 A 11.19 C 11.20 A 11.21 D 11.22 D 11.23 B 11.24 B 11.25 D 11.26 B
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