SIRT1/PGC-1α is involved in arsenic-induced male reproductive damage through mitochondrial dysfunction, which is blocked by the antioxidative effect of zinc

被引:14
|
作者
Ye, Fuping [1 ]
Wu, Lu [1 ,2 ]
Li, Han [1 ]
Peng, Xiaoshan [1 ,3 ]
Xu, Yuan [1 ,3 ]
Li, Wenqi [1 ]
Wei, Yongyue [1 ,4 ]
Chen, Feng [1 ,4 ]
Zhang, Jingshu [1 ,3 ]
Liu, Qizhan [1 ,2 ]
机构
[1] Nanjing Med Univ, Sch Publ Hlth, China Int Cooperat Ctr Environm & Human Hlth, Ctr Global Hlth,Key Lab Modern Toxicol,Minist Educ, Nanjing 211166, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Gusu Sch, Suzhou Inst Adv Study Publ Hlth, Suzhou Ctr Dis Control & Prevent, Suzhou 215004, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Sch Publ Hlth, Jiangsu Safety Assessment & Res Ctr Drug Pesticide, Nanjing 211166, Jiangsu, Peoples R China
[4] Nanjing Med Univ, State Key Lab Reprod Med, Nanjing 211166, Jiangsu, Peoples R China
关键词
Arsenic; Zinc; Male reproductive damage; Oxidative stress; Mitochondrial dysfunction; OXIDATIVE STRESS; DEFICIENCY; APOPTOSIS;
D O I
10.1016/j.envpol.2023.121084
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Exposure to arsenic poses threats to male reproductive system, including impairing the testes and sperm quality. Although an association regarding arsenic exposure and male reproductive damage has been reported, the undergoing molecular mechanisms and interventions for prevention remain unclear. For the present work, male mice were exposed to 0, 2.5, 5, or 10 ppm sodium arsenite (NaAsO2) for 8 months. The results showed that arsenic-exposed mice had reduced fertility with abnormalities in the testes, epididymides, and sperm. Exposure of mice to arsenic caused a redox imbalance, decreased SIRT1 and PGC-1 alpha levels, and affected mitochondrial biogenesis and proteins related to mitochondrial dynamics. For immortalized spermatogenic (GC-2) cells, arsenic caused apoptosis and oxidative stress, reduced SIRT1/PGC-1 alpha levels and ATP production, inhibited mitochondrial respiration, and changed the mitochondrial membrane potential (MMP). Mitochondrial biogenesis and dynamics were also impaired. However, by reducing mitochondrial damage in GC-2 cells, upregulation of SIRT1 or zinc (Zn) supplementation reversed the apoptosis induced by arsenic. For mice, Zn supplementation blocked arsenic-induced oxidative stress, the decreases of SIRT1 and PGC-1 alpha levels, and the impairment of mitochondrial function, and it reversed the damage to testes, low sperm quality, and low litter size. Collectively, these results suggest that arsenic causes excessive production of ROS, inhibits the SIRT1/PGC-1 alpha pathway, and causing mitochondrial dysfunction by mediating impairment of mitochondrial biogenesis and dynamics, which results in germ cells apoptosis and male reproductive damage, processes that are blocked by Zn via an antioxidative effect. Our study contributes to understanding of the mechanisms for arsenic-induced male reproductive damage and points to the therapeutic significance of Zn.
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页数:13
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