Suppr超能文献

氯丙嗪在体内和体外的蛋白质结合:氯丙嗪代谢物对大鼠体内氯丙嗪蛋白质结合的影响。

Protein binding of chlorpromazine in vivo and in vitro: effect of chlorpromazine metabolite on chlorpromazine protein binding in rat.

作者信息

Sato S, Koshiro A

机构信息

Department of Pharmaceutics, Niigata College of Pharmacy, Japan.

出版信息

Biol Pharm Bull. 1995 Apr;18(4):586-92. doi: 10.1248/bpb.18.586.

Abstract

The serum protein binding curve of chlorpromazine (CPZ) on the Scatchard plot in vitro was a two-phase downward curve. However, after i.v. administration of CPZ the curve was altered to an upward curve. To clarify the reasons for these in vivo changes, the influence of chlorpromazine S-oxide (CPZSO), chlorpromazine N-oxide (CPZNO), desmethylchlorpromazine (nor1-CPZ), chlorpromazine sulfone (sul-CPZ) and 7-hydroxychlorpromazine (7-OH-CPZ) on CPZ protein binding were studied in vitro. The results indicated that the characteristics of the CPZ protein binding are altered by the combination of CPZSO or CPZNO or by either of them. Since it was very difficult to explain the relationship between serum total and free concentrations of CPZ in vivo using mass-balance equations like Hill's equation or a competitive inhibition equation on the multiple binding sites for drug, the correlation between the ratio ot total concentration of CPZ metabolites and CPZ (CPZSO/CPZ or CPZNO/CPZ) and the free fraction of CPZ was examined using the in vitro and in vivo data. The correlation between the ratio of CPZSO/CPZ and the free fraction of CPZ was good in both the in vivo and the in vitro studies. There was no statistically significant difference between the population regression coefficient of the two studies. The values of the slope and the intercept became almost the same as those obtained using the in vivo studies when combined with CPZNO.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

氯丙嗪(CPZ)在体外Scatchard图上的血清蛋白结合曲线为两相下降曲线。然而,静脉注射CPZ后,曲线变为上升曲线。为阐明这些体内变化的原因,在体外研究了氯丙嗪S-氧化物(CPZSO)、氯丙嗪N-氧化物(CPZNO)、去甲氯丙嗪(nor1-CPZ)、氯丙嗪砜(sul-CPZ)和7-羟基氯丙嗪(7-OH-CPZ)对CPZ蛋白结合的影响。结果表明,CPZSO或CPZNO或两者结合会改变CPZ蛋白结合的特性。由于使用诸如希尔方程或药物多结合位点的竞争性抑制方程等质量平衡方程来解释体内CPZ血清总浓度与游离浓度之间的关系非常困难,因此利用体外和体内数据研究了CPZ代谢物与CPZ总浓度之比(CPZSO/CPZ或CPZNO/CPZ)与CPZ游离分数之间的相关性。在体内和体外研究中,CPZSO/CPZ与CPZ游离分数之间的相关性均良好。两项研究的总体回归系数之间无统计学显著差异。当与CPZNO结合时,斜率和截距值几乎与体内研究得到的值相同。(摘要截短至250字)

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