NGF induced differentiated PC12 cells as in vitro tool to study 4-hydroxynonenal induced cellular damage

被引:8
|
作者
Siddiqui, M. A.
Kashyap, M. P.
Khanna, V. K.
Yadav, S.
Pant, A. B. [1 ]
机构
[1] Indian Inst Toxicol Res, In Vitro Toxicol Lab, Lucknow 226001, Uttar Pradesh, India
关键词
PC12; cells; 4-HNE; DA-D-2; receptor; Glutathione; GSTP1-1; Intracellular Ca++; LIPID-PEROXIDATION PRODUCT; S-TRANSFERASE P1-1; OXIDATIVE STRESS; ALDOSE REDUCTASE; GLUTATHIONE; EXPRESSION; ACTIVATION; NEURONS; NEUROTOXICITY; INVOLVEMENT;
D O I
10.1016/j.tiv.2010.05.019
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Investigations were carried out to examine the suitability of PC12 cells as an in vitro tool to examine 4-hydroxynonenal (4-HNE)-induced toxicity in nervous tissue. On days of differentiation, markers of neural effects and oxidative stress were measured following exposure of PC12 cells to 1-50 mu M 4-HNE for 1-8 h. Endpoints included dopamine DA-D-2 receptor and glutathione S-transferase (GSTP1-1) protein levels, 4-HNE-protein binding, glutathione (GSH) concentrations and intracellular calcium levels. GSH levels were maximally depleted after 4 h. 4-HNE also induced depletion of GSTP1-1 and increased intracellular Ca++, with the latter seen as early as 1 h after exposure. Responses at 8 h were not greater than responses at earlier times. The experiments suggest that PC12 cells could be an in vitro tool for understanding toxicant-cell interactions, especially those that result in oxidative stress. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1681 / 1688
页数:8
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