Actions of zopiclone and carbamazepine, alone and in combination, on human skilled performance in laboratory and clinical tests

1. Possible interactions of zopiclone and carbamazepine on human skilled performance were studied in a randomized, double‐blind, crossover trial with 12 healthy young subjects. 2. Psychomotor performance (coordination, reactions, attention, cognition) and subjective effects (VAS) were measured and v...

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Veröffentlicht in:British journal of clinical pharmacology 1990-09, Vol.30 (3), p.453-461
Hauptverfasser: Kuitunen, T, Mattila, MJ, Seppala, T, Aranko, K, Mattila, ME
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creator Kuitunen, T
Mattila, MJ
Seppala, T
Aranko, K
Mattila, ME
description 1. Possible interactions of zopiclone and carbamazepine on human skilled performance were studied in a randomized, double‐blind, crossover trial with 12 healthy young subjects. 2. Psychomotor performance (coordination, reactions, attention, cognition) and subjective effects (VAS) were measured and venous blood sampled before and 1.5, 3, 4.5 and 6 h after single oral doses of placebo, 7.5 mg of zopiclone and 600 mg of carbamazepine, which were given alone or combined. Clinical test for drunkenness (CTD) was done 2 and 5 h after drug intake. 3. Both zopiclone and carbamazepine, when administered alone, impaired performance on laboratory tests, the decrements being recorded 1.5 to 6 h after intake. In line with the plasma concentrations, the zopiclone effects peaked earlier (at 1.5 h) and lasted for a shorter time than those of carbamazepine. Zopiclone had a more pronounced effect on perceptual and cognitive functions (digit substitution) and it affected extraocular muscle tone (Maddox wing), whereas carbamazepine had stronger effects on attention. Additive pharmacodynamic actions were found in most tests after the combined treatment with zopiclone and carbamazepine. 4. CTD proved to be less sensitive than the laboratory tests in revealing drug‐induced decrement of performance after administration of one agent alone. However, it revealed the combined decremental effects of zopiclone and carbamazepine. 5. When the drugs were given together, the absorption of drugs was retarded. Carbamazepine‐10,11‐epoxide levels were lower after intake of the drug combination than those measured after intake of carbamazepine alone. 6. The results suggest that the clinical tests developed to detect alcohol effects do not necessarily reveal drug‐ induced impairment of performance.
doi_str_mv 10.1111/j.1365-2125.1990.tb03797.x
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Possible interactions of zopiclone and carbamazepine on human skilled performance were studied in a randomized, double‐blind, crossover trial with 12 healthy young subjects. 2. Psychomotor performance (coordination, reactions, attention, cognition) and subjective effects (VAS) were measured and venous blood sampled before and 1.5, 3, 4.5 and 6 h after single oral doses of placebo, 7.5 mg of zopiclone and 600 mg of carbamazepine, which were given alone or combined. Clinical test for drunkenness (CTD) was done 2 and 5 h after drug intake. 3. Both zopiclone and carbamazepine, when administered alone, impaired performance on laboratory tests, the decrements being recorded 1.5 to 6 h after intake. In line with the plasma concentrations, the zopiclone effects peaked earlier (at 1.5 h) and lasted for a shorter time than those of carbamazepine. Zopiclone had a more pronounced effect on perceptual and cognitive functions (digit substitution) and it affected extraocular muscle tone (Maddox wing), whereas carbamazepine had stronger effects on attention. Additive pharmacodynamic actions were found in most tests after the combined treatment with zopiclone and carbamazepine. 4. CTD proved to be less sensitive than the laboratory tests in revealing drug‐induced decrement of performance after administration of one agent alone. However, it revealed the combined decremental effects of zopiclone and carbamazepine. 5. When the drugs were given together, the absorption of drugs was retarded. Carbamazepine‐10,11‐epoxide levels were lower after intake of the drug combination than those measured after intake of carbamazepine alone. 6. 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Possible interactions of zopiclone and carbamazepine on human skilled performance were studied in a randomized, double‐blind, crossover trial with 12 healthy young subjects. 2. Psychomotor performance (coordination, reactions, attention, cognition) and subjective effects (VAS) were measured and venous blood sampled before and 1.5, 3, 4.5 and 6 h after single oral doses of placebo, 7.5 mg of zopiclone and 600 mg of carbamazepine, which were given alone or combined. Clinical test for drunkenness (CTD) was done 2 and 5 h after drug intake. 3. Both zopiclone and carbamazepine, when administered alone, impaired performance on laboratory tests, the decrements being recorded 1.5 to 6 h after intake. In line with the plasma concentrations, the zopiclone effects peaked earlier (at 1.5 h) and lasted for a shorter time than those of carbamazepine. 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The results suggest that the clinical tests developed to detect alcohol effects do not necessarily reveal drug‐ induced impairment of performance.</description><subject>Adult</subject><subject>Alcoholic Intoxication - diagnosis</subject><subject>Azabicyclo Compounds</subject><subject>Carbamazepine - blood</subject><subject>Carbamazepine - pharmacokinetics</subject><subject>Carbamazepine - pharmacology</subject><subject>Double-Blind Method</subject><subject>Drug Combinations</subject><subject>Female</subject><subject>Humans</subject><subject>Hypnotics and Sedatives - blood</subject><subject>Hypnotics and Sedatives - pharmacokinetics</subject><subject>Hypnotics and Sedatives - pharmacology</subject><subject>Male</subject><subject>Piperazines - blood</subject><subject>Piperazines - pharmacokinetics</subject><subject>Piperazines - pharmacology</subject><subject>Psychomotor Performance</subject><issn>0306-5251</issn><issn>1365-2125</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkU9v1DAQxS1UVJbCR0CyODfBf-I46YGqXdGCVKk9wNmynQn11rEjO4VuL_3qJNrVCo74Ys-8eT9L8xD6SElJ5_NpU1Jei4JRJkratqScDOGyleXTK7Q6SEdoRTipC8EEfYPe5rwhhHJai2N0zBjjFatW6OXCTi6GjGOPn-PorI8BsA4dtjoZPehnGF2AU6wPggvYxsG4oBfnKY4B3z8OOuD84LyHDo-Q-pjmjoVl2GsTk55i2u643gVntccT5Cm_Q6977TO8398n6MfVl-_rr8XN7fW39cVNYSspZcGZbKxtmGwFBdPOhWGm6UGKGkjb6VbWmtKqMV0_dyrOiOg1QF03TU256PkJ-rzjjo9mgM5CmJL2akxu0GmronbqXyW4e_Uz_lLzOhtatTPgbAewKeacoD94KVFLKmqzzAq1rF4tqah9KuppNn_4-_eDdR_DrJ_v9N_Ow_Y_yOpyfbe8-B9mGqCj</recordid><startdate>199009</startdate><enddate>199009</enddate><creator>Kuitunen, T</creator><creator>Mattila, MJ</creator><creator>Seppala, T</creator><creator>Aranko, K</creator><creator>Mattila, ME</creator><general>Blackwell Publishing Ltd</general><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>5PM</scope></search><sort><creationdate>199009</creationdate><title>Actions of zopiclone and carbamazepine, alone and in combination, on human skilled performance in laboratory and clinical tests</title><author>Kuitunen, T ; Mattila, MJ ; Seppala, T ; Aranko, K ; Mattila, ME</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4777-3278cc827951eb978cb2b8fe756e09da976a1148bdf56e43205faee66886135f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Adult</topic><topic>Alcoholic Intoxication - diagnosis</topic><topic>Azabicyclo Compounds</topic><topic>Carbamazepine - blood</topic><topic>Carbamazepine - pharmacokinetics</topic><topic>Carbamazepine - pharmacology</topic><topic>Double-Blind Method</topic><topic>Drug Combinations</topic><topic>Female</topic><topic>Humans</topic><topic>Hypnotics and Sedatives - blood</topic><topic>Hypnotics and Sedatives - pharmacokinetics</topic><topic>Hypnotics and Sedatives - pharmacology</topic><topic>Male</topic><topic>Piperazines - blood</topic><topic>Piperazines - pharmacokinetics</topic><topic>Piperazines - pharmacology</topic><topic>Psychomotor Performance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuitunen, T</creatorcontrib><creatorcontrib>Mattila, MJ</creatorcontrib><creatorcontrib>Seppala, T</creatorcontrib><creatorcontrib>Aranko, K</creatorcontrib><creatorcontrib>Mattila, ME</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuitunen, T</au><au>Mattila, MJ</au><au>Seppala, T</au><au>Aranko, K</au><au>Mattila, ME</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Actions of zopiclone and carbamazepine, alone and in combination, on human skilled performance in laboratory and clinical tests</atitle><jtitle>British journal of clinical pharmacology</jtitle><addtitle>Br J Clin Pharmacol</addtitle><date>1990-09</date><risdate>1990</risdate><volume>30</volume><issue>3</issue><spage>453</spage><epage>461</epage><pages>453-461</pages><issn>0306-5251</issn><eissn>1365-2125</eissn><abstract>1. Possible interactions of zopiclone and carbamazepine on human skilled performance were studied in a randomized, double‐blind, crossover trial with 12 healthy young subjects. 2. Psychomotor performance (coordination, reactions, attention, cognition) and subjective effects (VAS) were measured and venous blood sampled before and 1.5, 3, 4.5 and 6 h after single oral doses of placebo, 7.5 mg of zopiclone and 600 mg of carbamazepine, which were given alone or combined. Clinical test for drunkenness (CTD) was done 2 and 5 h after drug intake. 3. Both zopiclone and carbamazepine, when administered alone, impaired performance on laboratory tests, the decrements being recorded 1.5 to 6 h after intake. In line with the plasma concentrations, the zopiclone effects peaked earlier (at 1.5 h) and lasted for a shorter time than those of carbamazepine. Zopiclone had a more pronounced effect on perceptual and cognitive functions (digit substitution) and it affected extraocular muscle tone (Maddox wing), whereas carbamazepine had stronger effects on attention. Additive pharmacodynamic actions were found in most tests after the combined treatment with zopiclone and carbamazepine. 4. CTD proved to be less sensitive than the laboratory tests in revealing drug‐induced decrement of performance after administration of one agent alone. However, it revealed the combined decremental effects of zopiclone and carbamazepine. 5. When the drugs were given together, the absorption of drugs was retarded. Carbamazepine‐10,11‐epoxide levels were lower after intake of the drug combination than those measured after intake of carbamazepine alone. 6. 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source MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adult
Alcoholic Intoxication - diagnosis
Azabicyclo Compounds
Carbamazepine - blood
Carbamazepine - pharmacokinetics
Carbamazepine - pharmacology
Double-Blind Method
Drug Combinations
Female
Humans
Hypnotics and Sedatives - blood
Hypnotics and Sedatives - pharmacokinetics
Hypnotics and Sedatives - pharmacology
Male
Piperazines - blood
Piperazines - pharmacokinetics
Piperazines - pharmacology
Psychomotor Performance
title Actions of zopiclone and carbamazepine, alone and in combination, on human skilled performance in laboratory and clinical tests
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