Suppr超能文献

大鼠同时给予己巴比妥和庚巴比妥的药代动力学:代谢相关性研究的一种替代方法。

Pharmacokinetics of simultaneously administered hexobarbital and heptabarbital in rats: an alternative approach to metabolic correlation studies.

作者信息

van der Graaff M, Vermeulen N P, Langendijk P N, Breimer D D

出版信息

J Pharmacol Exp Ther. 1983 Jun;225(3):747-51.

PMID:6134816
Abstract

The pharmacokinetics of hexobarbital and heptabarbital were studied after simultaneous oral administration to rats in order to correlate their rates of metabolism. Hexobarbital and heptabarbital were chosen for this purpose as model substrates because of their structural, pharmacokinetic as well as metabolic similarity. Blood concentrations were measured for 2 hr after administration by a capillary gas chromatographic method. In control rats (n = 8) elimination half-lives and intrinsic clearance values ranged between 13 to 28 min and 96 to 435 ml/min X kg for hexobarbital and between 8 to 21 min and 84 to 371 ml/min X kg for heptabarbital, respectively. A short-term pretreatment of rats (n = 7) with phenobarbital resulted in small but significant increases in the rates of metabolism of both barbiturates, whereas treatment of rats with 3-methylcholanthrene (n = 5) resulted in a reversed effect. Correlation of the elimination half-lives of the two drugs in all experiments was only weak (r = 0.70). The intrinsic clearance values reflecting enzyme activity in vivo, however, were found to correlate very strongly (r = 0.97). The results of this study suggest that an experimental approach, in which intraindividual differences are eliminated, appropriate kinetic parameters are studied and similarity of metabolic profiles are taken into consideration are preferable to the previously applied longitudinally designed correlation studies.

摘要

为了关联己巴比妥和庚巴比妥的代谢速率,在给大鼠同时口服给药后对它们的药代动力学进行了研究。由于己巴比妥和庚巴比妥在结构、药代动力学以及代谢方面具有相似性,因此被选作模型底物用于此目的。给药后通过毛细管气相色谱法测量2小时内的血药浓度。在对照大鼠(n = 8)中,己巴比妥的消除半衰期和内在清除率值分别在13至28分钟和96至435 ml/min×kg之间,庚巴比妥的消除半衰期和内在清除率值分别在8至21分钟和84至371 ml/min×kg之间。用苯巴比妥对大鼠(n = 7)进行短期预处理导致两种巴比妥类药物的代谢速率均有小幅但显著的增加,而用3 - 甲基胆蒽处理大鼠(n = 5)则产生相反的效果。在所有实验中,两种药物的消除半衰期之间的相关性仅较弱(r = 0.70)。然而,发现反映体内酶活性的内在清除率值具有非常强的相关性(r = 0.97)。本研究结果表明,一种消除个体内差异、研究适当的动力学参数并考虑代谢谱相似性的实验方法比先前应用的纵向设计的相关性研究更可取。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验