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齐美利定对非抑郁型重度饮酒者酒精摄入量的影响。

Zimelidine-induced variations in alcohol intake by nondepressed heavy drinkers.

作者信息

Naranjo C A, Sellers E M, Roach C A, Woodley D V, Sanchez-Craig M, Sykora K

出版信息

Clin Pharmacol Ther. 1984 Mar;35(3):374-81. doi: 10.1038/clpt.1984.46.

Abstract

The effect of zimelidine, a specific serotonin-reuptake inhibitor, on alcohol intake was tested in 13 healthy male, nondepressed heavy drinkers who were randomly allocated to receive zimelidine or placebo in a double-blind, crossover experiment. There were five 2-wk experimental periods (baseline, placebo 1 and 2, and zimelidine 1 and 2). Treatment was discontinued in three subjects due to a suspected adverse reaction and three other subjects dropped out. Thus, 13 subjects participated in at least two experimental drug periods and only 10 participated in all the periods. In the 13 subjects zimelidine increased the days of abstinence and decreased the daily number of drinks consumed, whereas in the 10 subjects only the number of days of abstinence increased. Subjects did not report aversive alcohol-sensitizing reactions. Spielberger state-anxiety test scores and depression scores (Montgomery/Asberg and Hamilton) were low at the beginning and throughout the study. Our data suggest that zimelidine modifies alcohol intake by a different mechanism than previously tested drugs, possibly by modulating the central neural mechanism that controls drinking of alcohol.

摘要

在一项双盲交叉实验中,对13名健康、非抑郁的男性重度饮酒者进行了试验,以测试特异性5-羟色胺再摄取抑制剂齐美利定对酒精摄入量的影响。这些受试者被随机分配接受齐美利定或安慰剂。实验共有五个为期2周的阶段(基线期、安慰剂1期、安慰剂2期、齐美利定1期和齐美利定2期)。由于怀疑出现不良反应,有3名受试者停止了治疗,另外3名受试者退出。因此,13名受试者至少参与了两个实验药物阶段,只有10名受试者参与了所有阶段。在这13名受试者中,齐美利定增加了戒酒天数,并减少了每日饮酒量,而在10名受试者中,只有戒酒天数增加。受试者未报告酒精致敏的不良反应。斯皮尔伯格状态焦虑测试得分以及抑郁得分(蒙哥马利/阿斯伯格和汉密尔顿量表)在研究开始时及整个研究过程中均较低。我们的数据表明,齐美利定改变酒精摄入量的机制与之前测试的药物不同,可能是通过调节控制饮酒的中枢神经机制来实现的。

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