MCQs-Drugs Acting on Central Nervous System part 3 I Pharmacology KD Tripathi mcqs part 27

 7.1 Barbiturates exert the following actions except:

A. Anticonvulsant

B. Analgesic

C. Antianxiety

D. Respiratory depressant 


27.2 The mechanism of action of barbiturates differs

from that of benzodiazepines in that they:

A. Do not affect the GABA-benzodiazepine receptor-chloride channel complex

B. Act as inverse agonists at the benzodiazepine receptor

C. Increase the frequency of chloride channel opening without affecting its life time

D. Have both GABA-facilitatory as well as

GABA-mimetic actions


27.3 Which of the following processes plays the major

role in terminating the action of phenobarbitone:

A. Biliary excretion

B. Renal excretion

C. Hepatic metabolism

D. Redistribution 


27.4 Currently barbiturates are primarily used as:

A. Hypnotic

B. Sedative

C. Antiepileptic

D. Preanaesthetic medicant 


27.5 Benzodiazepines differ from barbiturates in the

following aspects except:

A. They have a steeper dose response curve

B. They have higher therapeutic index

C. They have lower abuse liability

D. They do not induce microsomal drug metabolizing enzymes 


27.6 Hypnotic benzodiazepines increase the period of

time spent in the following stage of sleep:

A. Stage II

B. Stage III

C. Stage IV

D. REM stage 


27.7 Select the correct statement about benzodiazepines (BZDs):

A. All BZDs facilitate GABA mediated Cl¯ influx into neurones

B. Different BZDs exert the same degrees of hypnotic, anxiolytic and anticonvulsant

actions

C. The BZD receptor is homogeneous at all neuronal sites

D. The muscle relaxant action of BZDs is not blocked by flumazenil 


27.8 Hypnotic dose of diazepam produces the following action:

A. Tachycardia

B. Constipation

C. Hyperalgesia

D. Decreased nocturnal gastric secretion


27.9 The primary mechanism of action of benzodiazepines is:

A. Dopamine antagonism

B. Adenosine antagonism

C. Opening of neuronal chloride channels

D. Facilitation of GABA-mediated chloride influx


27.10 Select the drug that antagonises diazepam action noncompetitively:

A. Adenosine

B. Flumazenil

C. Bicuculline

D. Valproic acid 


27.11 The following drugs exert their action through the

GABAA-benzodiazepine–receptor Cl¯ channel complex except:

A. Baclofen

B. Zolpidem

C. Bicuculline

D. Phenobarbitone 


27.12 At a single hypnotic dose, the pharmacokinetics of

diazepam is characterised by:

A. Slow elimination and little redistribution

B. Slow elimination with marked redistribution

C. Rapid elimination and marked redistribution

D. Ultra rapid elimination 


27.13 The following is a very potent and short acting

benzodiazepine whose use as hypnotic has been

noted to cause psychiatric disturbances in some

cases:

A. Flurazepam

B. Nitrazepam

C. Temazepam

D. Triazolam


27.14 Which of the following statements is not true of zopiclone:

A. It is a nonbenzodiazepine hypnotic with efficacy and safety similar to benzodiazepines

B. It does not produce rebound sleep disturbances on discontinuation

C. It does not act by potentiating GABA

D. It is used to wean off insomniacs from regular benzodiazepine use 


27.15 Choose the drug that has been found to be more

selective for the ω1 subtype of BZD receptor, and

produces hypnotic action but little antianxiety,

muscle relaxant or anticonvulsant actions:

A. Zopiclone

B. Zolpidem

C. Flumazenil

D. Melatonin 


27.16 Zolpidem differs from diazepam in that:

A. It is safer in overdose than diazepam

B. Its hypnotic action shows little fading on repeated nightly use

C. It causes more marked suppression of REM sleep

D. It has more potent muscle relaxant action


27.17 Diazepam is indicated in the following conditions except:

A. Generalized tonic-clonic (grand mal) epilepsy

B. Tetanus

C. Febrile convulsions

D. Cardiac catheterization 


27.18 The following drug is used to reverse the CNS depression produced by diazepam:

A. Dexamphetamine

B. Doxapram

C. Physostigmine

D. Flumazenil 


27.19 Select the correct statement about flumazenil:

A. It is a CNS stimulant used as an antidote for benzodiazepine poisoning

B. It is a CNS depressant but blocks the action of diazepam

C. It has no CNS effect of its own but blocks the

depressant effects of benzodiazepines as well

as barbiturates

D. It has no CNS effect of its own but blocks the

depressant effect of diazepam as well as stimulant

effect of beta carbolines


27.20 The general principles in the use of hypnotics include the following except:

A. A hypnotic may be used intermittently for

upto 2-3 weeks in short-term insomnia due

to emotional stress

B. In patients with chronic insomnia a hypnotic should be used regularly

C. All hypnotics aggravate sleep apnoea

D. A hypnotic with slow elimination is preferred

in patients with early morning awakening


27.21 Which of the following is not a CNS depressant but

increases the tendency to fall asleep at night:

A. Pyridoxine

B. Diphenhydramine

C. Melatonin

D. Ethanol


Ans:

27.1 B 27.2D 27.3 B 27.4 C 27.5 A 27.6 A 27.7 A 27.8D 27.9D 27.10 C 27.11 A 27.12 B 27.13D 27.14 C 27.15 B 27.16 B 27.17 A 27.18D 27.19D 27.20 B 27.21 C

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