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小鼠肝微粒体(MLM)可保护红细胞免受三氟拉嗪(TFP)诱导的和机械性溶血,这是由于TFP的微粒体转化以及一种未知的水溶性微粒体因子(UF)的作用所致。

Mouse liver microsomes (MLM) protect erythrocytes against trifluoperazine (TFP) induced and mechanical hemolysis which are due to TFP microsomal transformation and to the action of an unidentified water-soluble microsomal factor (UF).

作者信息

Meirelles N C, Malheiros S V, Ruggiero A C, Degterev I A

机构信息

Department of Biochemistry, UNICAMP, São-Paulo, Brazil.

出版信息

Eur J Drug Metab Pharmacokinet. 1994 Oct-Dec;19(4):349-57. doi: 10.1007/BF03188862.

Abstract

Trifluoperazine (TFP), a phenothiazine derivative, produces either hemolysis or protection of erythrocytes under isosmotic conditions in a dose-dependent manner. The hemolytic effect of TFP is abolished in the presence of mouse liver microsomes (MLM) which is due, in part, to drug incorporation, transformation and a MLM enzyme driven metabolism. An unidentified water-soluble factor (or factors) derived from MLM has been found to protect erythrocytes against both mechanical and TFP-induced isosmotic hemolysis.

摘要

三氟拉嗪(TFP)是一种吩噻嗪衍生物,在等渗条件下,它以剂量依赖的方式对红细胞产生溶血或保护作用。在存在小鼠肝微粒体(MLM)的情况下,TFP的溶血作用会被消除,这部分归因于药物的掺入、转化以及由MLM酶驱动的代谢。已发现一种源自MLM的未鉴定的水溶性因子可保护红细胞免受机械性和TFP诱导的等渗溶血作用。

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