Ascorbic acid protects against cadmium-induced endoplasmic reticulum stress and germ cell apoptosis in testes

被引:51
作者
Ji, Yan-Li [1 ]
Wang, Zhen [1 ]
Wang, Hua [1 ]
Zhang, Cheng [1 ]
Zhang, Ying [1 ]
Zhao, Mei [1 ]
Chen, Yuan-Hua [1 ]
Meng, Xiu-Hong [1 ]
Xu, De-Xiang [1 ]
机构
[1] Anhui Med Univ, Sch Publ Hlth, Dept Toxicol, Hefei 230032, Peoples R China
基金
中国国家自然科学基金;
关键词
Cadmium; Ascorbic acid; Testis; Apoptosis; Endoplasmic reticulum stress; INDUCED TESTICULAR DAMAGE; SEMINAL PLASMA; RAT TESTES; SPERM QUALITY; SEMEN QUALITY; VITAMIN-C; DEATH; MICE; CHOP; LEAD;
D O I
10.1016/j.reprotox.2012.04.011
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cadmium (Cd) is a testicular toxicant which induces endoplasmic reticulum (ER) stress and germ cell apoptosis in testes. This study investigated the effects of ascorbic acid on Cd-evoked ER stress and germ cell apoptosis in testes. Male mice were intraperitoneally injected with CdCl2 (2.0 mg/kg). As expected, a single dose of Cd induced testicular germ cell apoptosis. Interestingly, Cd-triggered testicular germ cell apoptosis was almost completely inhibited in mice treated with ascorbic acid. Interestingly, ascorbic acid significantly attenuated Cd-induced upregulation of GRP78 in testes. In addition, ascorbic acid significantly attenuated Cd-triggered testicular IRE1 alpha and eIF2 alpha phosphorylation and XBP-1 activation, indicating that this antioxidant counteracts Cd-induced unfolded protein response (UPR) in testes. Finally, ascorbic acid significantly attenuated Cd-evoked upregulation of CHOP and JNK phosphorylation, two components in ER stress-mediated apoptotic pathway. In conclusion, ascorbic acid protects mice from Cd-triggered germ cell apoptosis via inhibiting ER stress and UPR in testes. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:357 / 363
页数:7
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