Becker K E, Ho I K
Res Commun Chem Pathol Pharmacol. 1977 Sep;18(1):23-8.
Uptake and distribution of pentobarbital in tolerant and nontolerant mice were studied. Mice were implanted with pentobarbital or placebo pellets s.c. 3 days prior to the injection of 60 mg/kg sodium pentobarbital i.p. One group of animals was sacrificed when they first awakened. Whole brain, five discrete brain areas, and plasma were assayed for pentobarbital by gas chromatography. In a second group, time studies were performed on brain sections and plasma. In tolerant vs nontolerant animals, sleeping time was markedly decreased (10-20 vs 50-70 min); whole brain, brain sections, and plasma levels on awakening were not significantly different; linear and exponential curves of pentobarbital levels vs time showed an increase in slope (-1.05 vs-0.40) and a decrease in T 1/2 (10.2 VS 35.7 min). These findings suggest that the tolerance development to pentobarbital in the central nervous system is due to functional mechanism rather than brain dispositional mechanism.
研究了戊巴比妥在耐受和非耐受小鼠体内的摄取和分布情况。在腹腔注射60mg/kg戊巴比妥钠前3天,给小鼠皮下植入戊巴比妥或安慰剂药丸。一组动物在首次苏醒时被处死。通过气相色谱法测定全脑、五个离散脑区和血浆中的戊巴比妥含量。在第二组中,对脑切片和血浆进行了时间研究。在耐受与非耐受动物中,睡眠时间显著缩短(10 - 20分钟对50 - 70分钟);苏醒时全脑、脑切片和血浆水平无显著差异;戊巴比妥水平与时间的线性和指数曲线显示斜率增加(-1.05对-0.40)和半衰期缩短(10.2分钟对35.7分钟)。这些发现表明,中枢神经系统对戊巴比妥的耐受性发展是由于功能机制而非脑处置机制。