Comparative effects of drugs on P-glycoprotein expression and activity using rat and human trophoblast models

被引:13
作者
Beghin, D. [1 ,2 ,3 ]
Delongeas, J. -L. [2 ,3 ]
Claude, N. [2 ,3 ]
Farinotti, R. [1 ,4 ]
Forestier, F. [1 ]
Gil, S. [1 ]
机构
[1] Univ Paris 11, Fac Pharm, EA 2706, F-92296 Chatenay Malabry, France
[2] Servier Grp, Gidy, France
[3] Servier Grp, Paris, France
[4] Grp Hosp Pitie Salpetriere, AP HP, Serv Pharm, F-75634 Paris, France
关键词
Placenta; Rat trophoblasts; Human trophoblasts; Culture; P-glycoprotein; Therapeutic drugs; Drug safety; RESISTANCE PROTEIN; IN-VITRO; THALIDOMIDE; PLACENTA; THROMBOXANE; METHADONE; ASPIRIN; FETAL; CYTOTROPHOBLASTS; DIFFERENTIATION;
D O I
10.1016/j.tiv.2009.10.005
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The drug efflux transporter P-glycoprotein (P-gp) is an active component of the placental barrier which protects the fetus against maternal xenobiotics. The goal of the study was to compare species difference between human and rat in terms of susceptibility to drugs at the level of the placental barrier using in vitro models in order to improve translation from rat to human. Effects of selected drugs (Aspirin, Methadone, a Cardiovascular Proprietary Compound, Thalidomide) on cytotoxicity and P-gp expression and activity were compared using human and rat trophoblast cultures. No direct cytotoxicity of drugs on trophoblasts was noted in both in vitro models, but for Thalidomide a proliferative effect on human trophoblast primocultures was observed. All tested drugs induced changes towards P-gp: for each drug the same profile was noted in both human and rat trophoblast models except for Thalidomide. Observation of this similar response between these two in vitro trophoblast models is promising for assessment between P-gp expression and activity of drugs towards placental function. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:630 / 637
页数:8
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