Autophagy and apoptosis mediated nano-copper-induced testicular damage

被引:30
作者
Chen, Helin [1 ]
Wang, Yanyan [1 ]
Luo, Jie [1 ,2 ]
Kang, Min [1 ]
Hou, Jin [1 ]
Tang, Ruoping [1 ]
Zhao, Ling [1 ]
Shi, Fei [1 ]
Ye, Gang [1 ]
He, Xiaoli [3 ]
Cui, Hengmin [1 ]
Guo, Hongrui [1 ]
Li, Yinglun [1 ]
Tang, Huaqiao [1 ]
机构
[1] Sichuan Agr Univ, Coll Vet Med, 211 Huimin Rd, Chengdu 611130, Sichuan, Peoples R China
[2] Tongren Polytech Coll, Natl Ethn Affairs Commiss, Key Open Lab Tradit Chinese Vet Med, Tongren 554300, Guizhou, Peoples R China
[3] Sichuan Agr Univ, Coll Sci, 211 Huimin Rd, Chengdu 611130, Sichuan, Peoples R China
关键词
Apoptosis; Akt; mTOR; Autophagy; Nano-copper; Oxidative stress; Rat testicular; OXIDATIVE STRESS; SERTOLI-CELLS; DNA-DAMAGE; TOXICITY; MTOR; NANOPARTICLES; EXPOSURE; RATS; ACTIVATION; PARTICLES;
D O I
10.1016/j.ecoenv.2021.113039
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nano-copper has been increasingly employed in various products. In previous studies, we showed that nano-copper caused damage in the rat testis, but it remains unclear whether the toxic reaction can affect the repro-ductive function. In this study, following 28 d of exposure to nano-copper at a dose of 44, 88, and 175 mg/kg/ day, there was a decrease in sperm quality, fructose content, and the secretion of sex hormones. Nano-copper also increased the level of oxidative stress, sperm malformation rate, and induced abnormal structural changes in testicular tissue. Moreover, Nano-copper upregulated the expression of apoptosis-related protein Bax and autophagy-related protein Beclin, and downregulated the expression of Bcl2 and p62. Furthermore, nano-copper (175 mg/kg) downregulated the protein expression of AMPK, p-AKT, mTOR, p-mTOR, p-4E-BP1, p70S6K, and p-p70S6K, and upregulated the protein expression of p-AMPK. Therefore, nano-copper induced damage in testicular tissues and spermatogenesis is highly related to cell apoptosis and autophagy by regulating the Akt/ mTOR signaling pathway. In summary, excess exposure to nano-copper may induce testicular apoptosis and autophagy through AKT/mTOR signaling pathways, and damage the reproductive system in adult males, which is associated with oxidative stress in the testes.
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页数:11
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