Flunitrazepam and triazolam: a comparison of behavioral effects and abuse liability
The performance, observer-rated, and participant-rated effects of orally administered placebo, and two benzodiazepines, flunitrazepam (2, 4 and 8 mg/70 kg) and triazolam (0.25, 0.5 and 1 mg/70 kg), were compared in 14 sedative drug abusers using a double-blind crossover design. Both flunitrazepam an...
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Veröffentlicht in: | Drug and alcohol dependence 1998-12, Vol.53 (1), p.49-66 |
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description | The performance, observer-rated, and participant-rated effects of orally administered placebo, and two benzodiazepines, flunitrazepam (2, 4 and 8 mg/70 kg) and triazolam (0.25, 0.5 and 1 mg/70 kg), were compared in 14 sedative drug abusers using a double-blind crossover design. Both flunitrazepam and triazolam produced dose-related decrements in memory and psychomotor/cognitive performance, and increases in many participant- and observer-rated measures. Effects of flunitrazepam had an earlier onset and a longer duration than those of triazolam. Although there was evidence that the flunitrazepam doses selected for study were somewhat higher overall relative to the selected triazolam doses, analysis of the participant-rated measures collected 24 h after drug administration (next-day) suggests that flunitrazepam may have a greater abuse liability than triazolam when abuse liability is assessed 24 h after drug administration. The highest flunitrazepam dose produced effects that were significantly greater than those of the highest triazolam dose on next-day ratings of good effects, take again, and worth; all tested flunitrazepam doses produced effects greater than any triazolam dose on next-day ratings of liking and take again. The highest flunitrazepam dose, but no triazolam dose, significantly increased the maximum dollar value at which participants chose drug over money in a Drug versus Money Choice Procedure. |
doi_str_mv | 10.1016/S0376-8716(98)00110-0 |
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Both flunitrazepam and triazolam produced dose-related decrements in memory and psychomotor/cognitive performance, and increases in many participant- and observer-rated measures. Effects of flunitrazepam had an earlier onset and a longer duration than those of triazolam. Although there was evidence that the flunitrazepam doses selected for study were somewhat higher overall relative to the selected triazolam doses, analysis of the participant-rated measures collected 24 h after drug administration (next-day) suggests that flunitrazepam may have a greater abuse liability than triazolam when abuse liability is assessed 24 h after drug administration. The highest flunitrazepam dose produced effects that were significantly greater than those of the highest triazolam dose on next-day ratings of good effects, take again, and worth; all tested flunitrazepam doses produced effects greater than any triazolam dose on next-day ratings of liking and take again. 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Both flunitrazepam and triazolam produced dose-related decrements in memory and psychomotor/cognitive performance, and increases in many participant- and observer-rated measures. Effects of flunitrazepam had an earlier onset and a longer duration than those of triazolam. Although there was evidence that the flunitrazepam doses selected for study were somewhat higher overall relative to the selected triazolam doses, analysis of the participant-rated measures collected 24 h after drug administration (next-day) suggests that flunitrazepam may have a greater abuse liability than triazolam when abuse liability is assessed 24 h after drug administration. The highest flunitrazepam dose produced effects that were significantly greater than those of the highest triazolam dose on next-day ratings of good effects, take again, and worth; all tested flunitrazepam doses produced effects greater than any triazolam dose on next-day ratings of liking and take again. The highest flunitrazepam dose, but no triazolam dose, significantly increased the maximum dollar value at which participants chose drug over money in a Drug versus Money Choice Procedure.</description><subject>Abuse liability</subject><subject>Adult</subject><subject>Anti-Anxiety Agents</subject><subject>Arousal - drug effects</subject><subject>Behaviour</subject><subject>Benzodiazepine</subject><subject>Biological and medical sciences</subject><subject>Cross-Over Studies</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Drug abuse</subject><subject>Female</subject><subject>Flunitrazepam</subject><subject>Humans</subject><subject>Hypnotic</subject><subject>Hypnotics and Sedatives</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mental Recall - drug effects</subject><subject>Motivation</subject><subject>Neuropharmacology</subject><subject>Neuropsychological Tests</subject><subject>Pharmacology. Drug treatments</subject><subject>Psycholeptics: tranquillizer, neuroleptic</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychomotor Performance - drug effects</subject><subject>Psychopharmacology</subject><subject>Substance-Related Disorders - psychology</subject><subject>Triazolam</subject><issn>0376-8716</issn><issn>1879-0046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqFkE1r3DAQhkVJabZpf0KDD6G0B6ejla2PXEoJTRoI5JDkLMbaEVWRra1kB5JfH-8HTW-Zy8DwvDPDw9gnDqccuPx2C0LJWisuvxj9FYBzqOENW3CtTA3QyAO2-Iccsvel_IG5pIF37JCDEUI0sGC3F3EawpjxidbYVzisqjEHfEoR-7MKK5f6NeZQ0lAlX3X0Gx9Cyhgr8p7cWLYJ7KZCVQzYhRjGxw_srcdY6OO-H7H7i59357_q65vLq_Mf17VrpB5r2SpA3XEhdDcPGu7Q88Zp0y3V0mlSRkjghreeOvRNa8h4lIJIt0pruRRH7PNu7zqnvxOV0fahOIoRB0pTsa1SIJWGGWx3oMuplEzernPoMT9aDnZj025t2o0qa7Td2rSb3PH-wNT1tPovtdM3Ayd7AIvD6DMOLpQXThpuzAb7vsNotvEQKNviAg2OViHPEu0qhVc-eQZx4pCj</recordid><startdate>19981201</startdate><enddate>19981201</enddate><creator>Mintzer, Miriam Z</creator><creator>Griffiths, Roland R</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope></search><sort><creationdate>19981201</creationdate><title>Flunitrazepam and triazolam: a comparison of behavioral effects and abuse liability</title><author>Mintzer, Miriam Z ; Griffiths, Roland R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-6570a8b1338b46841caf14c89b272c8e793601915febaf459e9fa63ee85788623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Abuse liability</topic><topic>Adult</topic><topic>Anti-Anxiety Agents</topic><topic>Arousal - drug effects</topic><topic>Behaviour</topic><topic>Benzodiazepine</topic><topic>Biological and medical sciences</topic><topic>Cross-Over Studies</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>Drug abuse</topic><topic>Female</topic><topic>Flunitrazepam</topic><topic>Humans</topic><topic>Hypnotic</topic><topic>Hypnotics and Sedatives</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mental Recall - drug effects</topic><topic>Motivation</topic><topic>Neuropharmacology</topic><topic>Neuropsychological Tests</topic><topic>Pharmacology. Drug treatments</topic><topic>Psycholeptics: tranquillizer, neuroleptic</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychomotor Performance - drug effects</topic><topic>Psychopharmacology</topic><topic>Substance-Related Disorders - psychology</topic><topic>Triazolam</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mintzer, Miriam Z</creatorcontrib><creatorcontrib>Griffiths, Roland R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><jtitle>Drug and alcohol dependence</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mintzer, Miriam Z</au><au>Griffiths, Roland R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Flunitrazepam and triazolam: a comparison of behavioral effects and abuse liability</atitle><jtitle>Drug and alcohol dependence</jtitle><addtitle>Drug Alcohol Depend</addtitle><date>1998-12-01</date><risdate>1998</risdate><volume>53</volume><issue>1</issue><spage>49</spage><epage>66</epage><pages>49-66</pages><issn>0376-8716</issn><eissn>1879-0046</eissn><coden>DADEDV</coden><abstract>The performance, observer-rated, and participant-rated effects of orally administered placebo, and two benzodiazepines, flunitrazepam (2, 4 and 8 mg/70 kg) and triazolam (0.25, 0.5 and 1 mg/70 kg), were compared in 14 sedative drug abusers using a double-blind crossover design. 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subjects | Abuse liability Adult Anti-Anxiety Agents Arousal - drug effects Behaviour Benzodiazepine Biological and medical sciences Cross-Over Studies Dose-Response Relationship, Drug Double-Blind Method Drug abuse Female Flunitrazepam Humans Hypnotic Hypnotics and Sedatives Male Medical sciences Mental Recall - drug effects Motivation Neuropharmacology Neuropsychological Tests Pharmacology. Drug treatments Psycholeptics: tranquillizer, neuroleptic Psychology. Psychoanalysis. Psychiatry Psychomotor Performance - drug effects Psychopharmacology Substance-Related Disorders - psychology Triazolam |
title | Flunitrazepam and triazolam: a comparison of behavioral effects and abuse liability |
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