Biflavanone-kolaviron protects human dopaminergic SH-SY5Y cells against atrazine induced toxic insult

被引:29
|
作者
Abarikwu, S. O. [2 ]
Farombi, E. O. [3 ]
Pant, A. B. [1 ]
机构
[1] CSIR, Indian Inst Toxicol Res Lucknow, Vitro Toxicol Lab, Lucknow 226001, Uttar Pradesh, India
[2] Redeemers Univ, Dept Chem Sci, Coll Nat Sci, Redemption City, Ogun State, Nigeria
[3] Univ Ibadan, Drug Metab & Toxicol Res Labs, Dept Biochem, Ibadan, Oyo State, Nigeria
关键词
Atrazine; Kolaviron; Apoptosis; Oxidative damage; SH-SY5Y; HERBICIDE ATRAZINE; INDUCED APOPTOSIS; OXIDATIVE STRESS; NEUROBLASTOMA-CELLS; PARKINSONS-DISEASE; LIPID-PEROXIDATION; PC12; CELLS; EXPOSURE; DAMAGE; MECHANISMS;
D O I
10.1016/j.tiv.2011.02.005
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Atrazine (ATR) is a widespread agrochemical contaminant frequently detected in water systems and kolaviron (KV) is a seed-derived biflavonoid which is reported to modulate the effects of many mutagens and carcinogens. We investigated the protective effects of KV on ATR-induced cell death in the human neuroblastoma cell line (SHY-SY5Y). KV prevents ATR-induced generation of reactive oxygen species (ROS), cell death and inhibited cell proliferation by reduction of cell proliferation. Further, ATR-induced levels malondialdehyde (MDA), catalase (CAT), glutathione peroxidase (GSH-Px), glutathione reductase (GR) activities, increased leakage of lactate dehydrogenase (LDH), inhibited cellular LDH activity and depleted glutathione (GSH) levels in SHY-SY5Y cells were blocked by KV. Comparable to the control, KV increased GR but not GSH-Px activities. ATR mediated nuclear changes associated with apoptosis; including nuclear fragmentation, condensation, DNA laddering, and increased caspase-3 activity were blocked on addition of KV. ATR-induced changes in the expressions of p53, Bax, Bcl-2, p21, and mRNA levels of caspase-3 and caspase-9 were prevented by KV. Based on these results, we propose a model for the protective effect of KV on ATR-induced cell injury in neuronal cell. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:848 / 858
页数:11
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