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小鼠中镇静催眠药物的24小时毒性节律

Twenty-four hour toxicity rhythms of sedative-hypnotic drugs in mice.

作者信息

Sermons A L, Ross F H, Walker C A

出版信息

Arch Toxicol. 1980 May;45(1):9-14. doi: 10.1007/BF00303289.

Abstract

Twenty-four hour LD50 values of secobarbital, pentobarbital, phenobarbital, in male Swiss-Webster mice weighing approximately 30 g each. The animals were adapted for three weeks in an environmental room equipped with an automatically-timed photoperiod lasting from 0800 to 2000 h daily. Each mouse was injected intraperitoneally at 6 h time intervals with either phenobarbital or chloral hydrate for toxicity analysis. Secobarbital, pentobarbital and hexobarbital were injected at 3 h time intervals. Peak toxicity was reached at D-0600 with all drugs screened except chloral hydrate which was 180 degrees out of phase. The drugs were least toxic at 1200 h with the exception of chloral hydrate which was least toxic at D-0600 h. These results suggest circadian periodicity in the toxicity of sedative hypnotics. Factors that could be responsible for these variations are discussed.

摘要

分别对体重约30克的雄性瑞士韦伯斯特小鼠测定速可巴比妥、戊巴比妥、苯巴比妥的24小时半数致死量(LD50)。将动物置于环境控制室内适应三周,该环境配备自动定时的光照周期,每天从08:00持续至20:00。每隔6小时对每只小鼠腹腔注射苯巴比妥或水合氯醛进行毒性分析。速可巴比妥、戊巴比妥和己巴比妥每隔3小时注射一次。除水合氯醛的毒性峰值出现时间与其他药物相差180度外,所有筛查的药物在D-06:00时达到毒性峰值。除水合氯醛在D-06:00时毒性最低外,所有药物在12:00时毒性最低。这些结果表明镇静催眠药的毒性存在昼夜周期性。文中讨论了可能导致这些差异的因素。

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