Sedative & Hypnotic Drugs Flashcards
T.t 27. one of the following is a mechanism of action of sedative and hypnotic drug
except
a. GABA a agonist
b. Histamine antagonist
c.Orexin Agonist
d. sympatholytic action
c.Orexin Agonist
T.t 28. zaleplone does not cause muscle relaxation because
a. it block BZ1 receptors
b.it block BZ2 receptors
c. it activate BZ1 receptors
d. it does not bind to BZ2 receptors
- hypnosis is mediated by…. in q28
28 d. it does not bind to BZ2 receptors
29 c. it activate BZ1 receptors
T.t 24. one of the following orexin antagonist
a.Suvorexant
b.Spironolactone
c.Celecoxib
d.Tolvaptan
a.Suvorexant
T.t 23. all are benzodiazepine: of choice In elderly Except
a.diazepam
b. temazepam
c. lorazepam
d.oxazepam
a.diazepam
T.t 25. the hormone of sleep is produced by
a. suprachiasmatic nucleus
b.pineal gland
c.mammillary body
d. posterior hypothalamus
b.pineal gland
T.t 21 the following is true regarding BDZ
a.It alters sleep pattern
b. B.All have pharmacologically active
metabolites
c. Induce liver enzyme
d. If taken in higher doses it is less toxic than
other sedatives
d. If taken in higher doses it is less toxic than
other sedatives
T.t which important enzyme play role in BDZ metabolizm
a.Cyp 3A4
b. CYp 2e3
c.Cyp 2c9
d. Cyp 2c19
a.Cyp 3A4
T.t 19. barbiturate preferred in induction of
general anesthesia is
a. pentobarbital
b.phenobarbital
c.thiopentone
d. phenobarbitone
c.thiopentone
T.t 17. all are non BDZ hypnotics except
a. Zolpidem
b.Ziprasidone
c. Zaleplone
d. Zopiclone
- the shortest acting non BDZ drug among Q17 is……….
- b.Ziprasidone
- c. Zaleplone
16 . the mechanism of action of barbiturate differ
from that of BDZ in that they
a.do not affect GABA-benzodiazepine chloride channel complex receptor
b. act as inverse agonist at BDZ receptors
c.increse the frequency of chloride channel opening
d.have both GABA facilitatory action as well as GABA mimetic action
d.have both GABA facilitatory action as well as GABA mimetic action
T.t 6- Which one of the following statements is correct?
A. Phenobarbital shows analgesic properties.
B. Diazepam and phenobarbital induce the P450 enzyme system.
C. Phenobarbital is useful in the treatment of acute intermittent porphyria.
D.Phenobarbital induces respiratory depression, which is enhanced
by the consumption of ethanol.
E. Buspirone has actions similar to those of the benzodiazepines
D.Phenobarbital induces respiratory depression, which is enhanced
by the consumption of ethanol.
T.t 10-Which of the following activity of hepatic hypnotics increase the drug-metabolizing enzyme systems?
A.Phenobarbital.
B. Flurazepam.
C. Zaleplon.
D. Triazolam.
A.Phenobarbital
T.t 7 .Which of the following is not related to effects of sedative hypnotic agents
a) Zolpidem is structurally related to
benzodiazepines used in insomnia
b) Triazolam is good benzodiazepine for sleep induction
but poor for maintaining it
c) Barbiturates have multiplicity of sites of action
d) Flumazenil is a BZD analogue which has no intrinsic
activity
a) Zolpidem is structurally related to
benzodiazepines used in insomnia
T.t 30. which among treatment of insomnia (Difficult
falling a sleep) does not caue day time sedation
a. Temazepam
b.Flurazepam
c.zaleplone
d. Buspirone
c.zaleplone
d. Buspirone
T.t 11- Inverse agonist of benzodiazepine receptor is
a. phenobarbital
b. flumazenil
c. beta carboline
d. Gabapentine
c. beta carboline