Deck 7: Sedative-Hypnotic and Anxiolytic Medications
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Deck 7: Sedative-Hypnotic and Anxiolytic Medications
1
The elimination half-life of all the various barbiturates is:
A)a few minutes.
B)up to 48 hours.
C)longer than 48 hours.
D)All of the answers are correct.
A)a few minutes.
B)up to 48 hours.
C)longer than 48 hours.
D)All of the answers are correct.
D
2
The most common symptom(s)of withdrawal from excessively high doses of barbiturates is:
A)hallucinations.
B)convulsions.
C)disorientation.
D)All of the answers are correct.
A)hallucinations.
B)convulsions.
C)disorientation.
D)All of the answers are correct.
D
3
The sedative-hypnotic properties of sedatives most likely results from effects on:
A)acetylcholine.
B)glutamate.
C)GABA.
D)AMPA.
A)acetylcholine.
B)glutamate.
C)GABA.
D)AMPA.
C
4
Gamma hydroxybutyric acid (GHB)acts to:
A)enhance bodybuilding much like the anabolic steroids.
B)enhance sexual performance.
C)potentiate sedation and depress central nervous system function.
D)All of the answers are correct.
A)enhance bodybuilding much like the anabolic steroids.
B)enhance sexual performance.
C)potentiate sedation and depress central nervous system function.
D)All of the answers are correct.
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5
Quaaludes can be classified as:
A)barbiturates sedatives.
B)nonbarbiturates sedatives.
C)aphrodisiacs.
D)narcotics.
A)barbiturates sedatives.
B)nonbarbiturates sedatives.
C)aphrodisiacs.
D)narcotics.
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6
The sedative-hypnotic properties of sedatives most likely results from:
A)impairment of GABA-induced neurotransmission.
B)facilitation of GABA-induced neurotransmission.
C)impairment of glutamate-induced neurotransmission.
D)stimulation of glutamate-induced neurotransmission.
A)impairment of GABA-induced neurotransmission.
B)facilitation of GABA-induced neurotransmission.
C)impairment of glutamate-induced neurotransmission.
D)stimulation of glutamate-induced neurotransmission.
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7
The most common symptom of withdrawal from normal clinical doses of barbiturates is:
A)hallucinations.
B)convulsions.
C)disorientation.
D)sleeplessness.
A)hallucinations.
B)convulsions.
C)disorientation.
D)sleeplessness.
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8
Generally speaking,the long-acting benzodiazepines are biotransformed into ________; the short-acting benzodiazepines are biotransformed into ________.
A)inactive products; inactive products
B)active products; active products
C)inactive products; active products
D)active products; inactive products
A)inactive products; inactive products
B)active products; active products
C)inactive products; active products
D)active products; inactive products
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9
The hypnotic action of the ultrashort-acting barbiturates is terminated by:
A)absorption.
B)redistribution.
C)degradation.
D)elimination.
A)absorption.
B)redistribution.
C)degradation.
D)elimination.
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10
The ultrashort-acting barbiturates are ________; the longer-acting barbiturates are ________.
A)highly water soluble; highly fat soluble
B)highly fat soluble; highly fat soluble
C)highly water soluble; highly water soluble
D)highly fat soluble; moderately fat soluble
A)highly water soluble; highly fat soluble
B)highly fat soluble; highly fat soluble
C)highly water soluble; highly water soluble
D)highly fat soluble; moderately fat soluble
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11
Compared with young adults,the elderly:
A)are less sensitive to the benzodiazepines.
B)are more tolerant to the benzodiazepines.
C)more readily metabolize benzodiazepines.
D)less readily metabolize benzodiazepines.
A)are less sensitive to the benzodiazepines.
B)are more tolerant to the benzodiazepines.
C)more readily metabolize benzodiazepines.
D)less readily metabolize benzodiazepines.
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12
The "nonbarbiturate" sedatives:
A)neither structurally resemble nor act like barbiturates.
B)structurally resemble,but do not act like,barbiturates.
C)act like,but do not structurally resemble,the barbiturates.
D)both structurally resemble and act like the barbiturates.
A)neither structurally resemble nor act like barbiturates.
B)structurally resemble,but do not act like,barbiturates.
C)act like,but do not structurally resemble,the barbiturates.
D)both structurally resemble and act like the barbiturates.
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13
Benzodiazepines differ from one another in:
A)their basic structure.
B)their plasma half-lives.
C)their binding sites.
D)their site of action.
A)their basic structure.
B)their plasma half-lives.
C)their binding sites.
D)their site of action.
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14
The barbiturates:
A)suppress memory and increase REM sleep.
B)suppress memory and decrease REM sleep.
C)decrease REM sleep but do not affect memory.
D)increase REM sleep but do not affect memory.
A)suppress memory and increase REM sleep.
B)suppress memory and decrease REM sleep.
C)decrease REM sleep but do not affect memory.
D)increase REM sleep but do not affect memory.
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15
At nontoxic doses,barbiturates significantly affect:
A)the cardiovascular system.
B)the kidneys.
C)the gastrointestinal tract.
D)None of the answers are correct.
A)the cardiovascular system.
B)the kidneys.
C)the gastrointestinal tract.
D)None of the answers are correct.
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16
Benzodiazepines differ from one another mainly in:
A)pharmacodynamics.
B)pharmacokinetics.
C)both pharmacodynamics and pharmacokinetics.
D)neither pharmacodynamics nor pharmacokinetics.
A)pharmacodynamics.
B)pharmacokinetics.
C)both pharmacodynamics and pharmacokinetics.
D)neither pharmacodynamics nor pharmacokinetics.
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17
The so-called "Mickey Finn" is comprised of:
A)Soma and ethanol.
B)Quaaludes and ethanol.
C)paraldehyde and ethanol.
D)chloral hydrate and ethanol.
A)Soma and ethanol.
B)Quaaludes and ethanol.
C)paraldehyde and ethanol.
D)chloral hydrate and ethanol.
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18
The most common cause of death when combining benzodiazepines with another CNS depressant or alcohol is:
A)hypotension.
B)bradychardia.
C)seizures.
D)respiratory depression.
A)hypotension.
B)bradychardia.
C)seizures.
D)respiratory depression.
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19
The reason that the use of barbiturates has declined rapidly over the years is that:
A)barbiturates are usually lethal in overdose.
B)the dosage range for the effectiveness of barbiturates is very close to its toxic range.
C)barbiturates interact dangerously with a wide range of drugs.
D)All of the answers are correct.
A)barbiturates are usually lethal in overdose.
B)the dosage range for the effectiveness of barbiturates is very close to its toxic range.
C)barbiturates interact dangerously with a wide range of drugs.
D)All of the answers are correct.
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20
The treatment for overdose of barbiturates is:
A)administration of the specific antidote for barbiturates.
B)respiratory support.
C)cardiovascular support.
D)both respiratory and cardiovascular support.
A)administration of the specific antidote for barbiturates.
B)respiratory support.
C)cardiovascular support.
D)both respiratory and cardiovascular support.
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21
Zaleplon (Sonata)is a:
A)long-acting anxiolytic.
B)long-acting hypnotic.
C)short-acting anxiolytic.
D)short-acting hypnotic.
A)long-acting anxiolytic.
B)long-acting hypnotic.
C)short-acting anxiolytic.
D)short-acting hypnotic.
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22
The aim of research into "partial GABA agonists" is to manufacture a drug that produces:
A)sedation without anxiolysis.
B)anxiolysis without sedation.
C)sedation without ataxia.
D)ataxia without sedation.
A)sedation without anxiolysis.
B)anxiolysis without sedation.
C)sedation without ataxia.
D)ataxia without sedation.
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23
Higher doses of benzodiazepines produce:
A)anxiolysis.
B)depression.
C)amnesia.
D)both anxiolysis and amnesia.
A)anxiolysis.
B)depression.
C)amnesia.
D)both anxiolysis and amnesia.
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24
Effects of the benzodiazepines include:
A)sedation.
B)anxiolysis.
C)muscle relaxation.
D)All of the answers are correct.
A)sedation.
B)anxiolysis.
C)muscle relaxation.
D)All of the answers are correct.
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25
Benzodiazepines ________ binding at the ________ receptor.
A)facilitate; GABA
B)facilitate; 5-HT
C)inhibit; GABA
D)inhibit; 5-HT
A)facilitate; GABA
B)facilitate; 5-HT
C)inhibit; GABA
D)inhibit; 5-HT
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26
Benzodiazepines may be useful for treating all of the following EXCEPT:
A)anxiety.
B)insomnia.
C)alcohol withdrawal.
D)intoxication.
A)anxiety.
B)insomnia.
C)alcohol withdrawal.
D)intoxication.
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27
The main effect of the benzodiazepine antagonist flumazenil is:
A)anxiolysis.
B)anxiety.
C)sedation.
D)None of the answers is correct.
A)anxiolysis.
B)anxiety.
C)sedation.
D)None of the answers is correct.
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28
The benzodiazepines are best prescribed for:
A)directly relaxing muscles.
B)alleviating depression.
C)treating chronic anxiety.
D)treating short-term anxiety.
A)directly relaxing muscles.
B)alleviating depression.
C)treating chronic anxiety.
D)treating short-term anxiety.
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29
Ambien (zolpidem)differs from BZRAs in that:
A)its effects are qualitatively similar but greater than BZRAs.
B)its effects are qualitatively similar but weaker than BZRAs.
C)it produces anxiolysis without sedation.
D)it produces sedation without anxiolysis.
A)its effects are qualitatively similar but greater than BZRAs.
B)its effects are qualitatively similar but weaker than BZRAs.
C)it produces anxiolysis without sedation.
D)it produces sedation without anxiolysis.
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30
Perhaps the best use of benzodiazepines is in:
A)treating epilepsy.
B)treating chronic anxiety.
C)treating panic disorder.
D)intentionally producing anterograde amnesia.
A)treating epilepsy.
B)treating chronic anxiety.
C)treating panic disorder.
D)intentionally producing anterograde amnesia.
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31
Ambien (zolpidem)differs from diazepam (Valium):
A)even though it binds to the same receptor subtypes.
B)in that it binds to GABAA receptors.
C)in that it binds to receptors other than GABAA receptors.
D)in that it binds to a subset of GABAA receptors.
A)even though it binds to the same receptor subtypes.
B)in that it binds to GABAA receptors.
C)in that it binds to receptors other than GABAA receptors.
D)in that it binds to a subset of GABAA receptors.
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32
Zolpidem is a:
A)benzodiazepine receptor agonist.
B)benzodiazepine receptor antagonist.
C)nonbenzodiazepine BZRA.
D)nonbenzodiazepine receptor antagonist.
A)benzodiazepine receptor agonist.
B)benzodiazepine receptor antagonist.
C)nonbenzodiazepine BZRA.
D)nonbenzodiazepine receptor antagonist.
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33
Benzodiazepines facilitate the action of the neurotransmitter:
A)GABA.
B)ACh.
C)NE.
D)5-HT.
A)GABA.
B)ACh.
C)NE.
D)5-HT.
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34
Early withdrawal signs following cessation of long-term benzodiazepine use include:
A)agitation.
B)insomnia.
C)restlessness.
D)All of the answers are correct.
A)agitation.
B)insomnia.
C)restlessness.
D)All of the answers are correct.
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35
The drug Ambien (zolpidem)is prescribed for treating:
A)anxiety.
B)depression.
C)insomnia.
D)agitation.
A)anxiety.
B)depression.
C)insomnia.
D)agitation.
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36
The brain site(s)mediating anxiety and/or panic is(are)the:
A)amygdala.
B)orbitofrontal cortex.
C)insula.
D)All of the answers are correct.
A)amygdala.
B)orbitofrontal cortex.
C)insula.
D)All of the answers are correct.
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37
The preferred pharmacological treatment for benzodiazepine overdose is:
A)stimulants.
B)coffee.
C)GABAA receptor antagonists.
D)benzodiazepine receptor antagonists.
A)stimulants.
B)coffee.
C)GABAA receptor antagonists.
D)benzodiazepine receptor antagonists.
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38
The drug of choice for the treatment of panic attacks is:
A)benzodiazepines.
B)depressants.
C)sedatives.
D)antidepressants.
A)benzodiazepines.
B)depressants.
C)sedatives.
D)antidepressants.
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39
Presently,the drug of choice for the treatment of chronic anxiety is:
A)benzodiazepines.
B)depressants.
C)sedatives.
D)antidepressants and atypical antipsychotics.
A)benzodiazepines.
B)depressants.
C)sedatives.
D)antidepressants and atypical antipsychotics.
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40
As shown in the figure below,compared with the dose-response curve for young adults (curve A),the dose-response curve for the elderly will be shifted in the direction of:
A)A.
B)B.
C)C.
D)The point cannot be predicted.
A)A.
B)B.
C)C.
D)The point cannot be predicted.
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41
The most common cause of death with nitrous oxide is:
A)convulsions.
B)hypotension.
C)stroke.
D)hypoxia.
A)convulsions.
B)hypotension.
C)stroke.
D)hypoxia.
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42
The major mechanism of action of the antiepileptics is:
A)blockade of voltage-dependent sodium channels.
B)enhanced GABA-mediated inhibition of neural activity.
C)blockade of GABA receptors.
D)enhanced glutamate-mediated neurotransmission.
A)blockade of voltage-dependent sodium channels.
B)enhanced GABA-mediated inhibition of neural activity.
C)blockade of GABA receptors.
D)enhanced glutamate-mediated neurotransmission.
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43
Benzodiazepines are a form of barbiturates.
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44
The inhaled anesthetics include:
A)morphine.
B)ketamine.
C)phenobarbital.
D)nitrous oxide.
A)morphine.
B)ketamine.
C)phenobarbital.
D)nitrous oxide.
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45
A number of benzodiazepines are biotransformed into active metabolites.
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46
Buspirone is also useful for treating:
A)alcohol withdrawal.
B)benzodiazepine withdrawal.
C)insomnia.
D)depression.
A)alcohol withdrawal.
B)benzodiazepine withdrawal.
C)insomnia.
D)depression.
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47
Benzodiazepines have a higher overdose toxicity than barbiturates.
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48
The nonbarbiturate sedatives act like,but do not structurally resemble,the barbiturates.
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49
Buspirone reduces:
A)both anxiety and depression within hours of administration.
B)anxiety within hours of administration,but depression only after weeks of
C)depression within hours of administration,but anxiety only after weeks of
D)both anxiety and depression,but only after weeks of administration.
A)both anxiety and depression within hours of administration.
B)anxiety within hours of administration,but depression only after weeks of
C)depression within hours of administration,but anxiety only after weeks of
D)both anxiety and depression,but only after weeks of administration.
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50
At the receptor level,buspirone acts:
A)as an agonist at 5-HT3 (postsynaptic)receptors.
B)as an antagonist at 5-HT3 (postsynaptic)receptors.
C)as an agonist at 5-HT1A (postsynaptic)receptors.
D)as an antagonist at 5-HT1A (postsynaptic)receptors.
A)as an agonist at 5-HT3 (postsynaptic)receptors.
B)as an antagonist at 5-HT3 (postsynaptic)receptors.
C)as an agonist at 5-HT1A (postsynaptic)receptors.
D)as an antagonist at 5-HT1A (postsynaptic)receptors.
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51
At the cellular level,the novel antiepileptic agent Vimpat (lacosamide)affects:
A)K+ channel activation.
B)K+ channel inactivation.
C)Na+ channel activation.
D)Na+ channel inactivation.
A)K+ channel activation.
B)K+ channel inactivation.
C)Na+ channel activation.
D)Na+ channel inactivation.
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52
Barbiturates can,paradoxically,induce a state of aggression.
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53
Drowsiness is a common,but not inevitable,consequence of barbiturate usage.
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54
The major mechanism of action of the injectable anesthetics is probably:
A)perturbation of the cell membrane.
B)potentiation of GABAA-induced neurotransmission.
C)potentiation of glutamate-induced neurotransmission.
D)induction of analgesia.
A)perturbation of the cell membrane.
B)potentiation of GABAA-induced neurotransmission.
C)potentiation of glutamate-induced neurotransmission.
D)induction of analgesia.
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55
The therapeutic-to-toxic range for barbiturates is very narrow.
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56
REM sleep is unaffected by barbiturates.
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57
Barbiturates are anticonvulsants.
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58
Benzodiazepines act directly to stimulate the GABA receptor.
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59
Fortunately,there are specific antidotes to barbiturates overdose.
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60
Benzodiazepines are the treatment of choice for chronic anxiety.
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61
Partial GABAAantagonists like zolpidem reduce anxiety without producing sedation.
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62
The benzodiazepines reduce anxiety,and benzodiazepine blockers produce anxiety.
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63
A major side effect of the benzodiazepines is amnesia.
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