Alterations in apoptotic caspases and antioxidant enzymes in arsenic exposed rat brain regions: Reversal effect of essential metals and a chelating agent

被引:28
作者
Kadeyala, Praveen Kumar [1 ]
Sannadi, Saritha [1 ]
Gottipolu, Rajarami Reddy [2 ]
机构
[1] Sri Venkateswara Univ, Dept Biotechnol, Tirupati 517502, Andhra Pradesh, India
[2] Sri Venkateswara Univ, Dept Zool, Tirupati 517502, Andhra Pradesh, India
关键词
Arsenic toxicity; Apoptosis; Chelation therapy; Calcium and zinc supplementation; Brain regions; INDUCED OXIDATIVE STRESS; MONOISOAMYL DMSA; RENAL ALTERATIONS; ARJUNOLIC ACID; HUMAN HEALTH; LIPOIC ACID; TOXICITY; LEAD; GLUTATHIONE; MITOCHONDRIA;
D O I
10.1016/j.etap.2013.09.021
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Arsenic (As) widely studied for its effects as a neurotoxicant. The present study was designed to evaluate the protective effect of calcium, zinc or monoisoamyl dimercaptosuccinic acid (MiADMSA), either individually or in combination on As induced oxidative stress and apoptosis in brain regions (cerebral cortex, hippocampus and cerebellum) of postnatal day (PND) 21, 28 and 3 months old rats. Arsenic exposure significantly decreased the activities of superoxide dismutase (SOD) isoforms, catalase (CAT), glutathione peroxidase (GPx) and glutathione reductase (GR) with increase in glutathione s transferase (GST) while lipid peroxidation (LPx), arsenic levels, mRNA expression of caspase 3 and 9 were significantly increased in different brain regions. Arsenic induced alterations in these parameters were greater in PND 28 and more pronounced in cerebral cortex. From the results it is evident that combined supplementation of calcium and zinc along with MiADMSA would be most effective compared to individual administration in reducing arsenic induced neurotoxicity. (C) 2013 Published by Elsevier B.V.
引用
收藏
页码:1150 / 1166
页数:17
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