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大鼠对巴比妥酸盐的急性耐受性

Acute tolerance to barbiturate in the rat.

作者信息

Turnbull M J, Watkins J W

出版信息

Eur J Pharmacol. 1976 Mar;36(1):15-20. doi: 10.1016/0014-2999(76)90251-x.

Abstract

3 experimental approaches to the quantitation of acute barbiturate tolerance have been compared in the rat. There was no difference between the brain hexobarbitone or barbitone concentration found at the time of loss of righting reflex compared with the concentration found on return of the righting reflex following the period of anaesthesia produced by a single i.p. injection of the drug. However, tolerance was induced by a 7 hr infusion of pentobarbitone which kept rats anaesthetized for approximately 8 hr. Such rats awakened with a significantly higher brain pentobarbitone concentration compared with rats awakening after a single i.p. injection. Repeated i.p. injections of pentobarbitone, sufficient to keep animals anaesthetized for 12 hr, also induced a tolerance to pentobarbitone, as indicated by a reduced sleeping time and higher brain barbiturate concentration on awakening following intracerebroventricularly administered pentobarbitone injected 12 hr after the last i.p. injection. The possible relationship between acute cellular tolerance and physical dependence is discussed.

摘要

已在大鼠中比较了三种定量急性巴比妥类药物耐受性的实验方法。与单次腹腔注射药物产生麻醉期后恢复翻正反射时所测得的浓度相比,翻正反射消失时所测得的脑内己巴比妥或巴比妥浓度并无差异。然而,通过静脉输注戊巴比妥7小时诱导出了耐受性,这使得大鼠麻醉约8小时。与单次腹腔注射后苏醒的大鼠相比,此类大鼠苏醒时脑内戊巴比妥浓度显著更高。重复腹腔注射戊巴比妥足以使动物麻醉12小时,这也诱导出了对戊巴比妥的耐受性,末次腹腔注射12小时后脑室内注射戊巴比妥,随后苏醒时睡眠时间缩短以及脑内巴比妥浓度升高即表明了这一点。文中讨论了急性细胞耐受性与身体依赖性之间的可能关系。

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