Zearalenone induces oxidative stress and autophagy in goat Sertoli cells

被引:24
作者
Liu, Xinyu [1 ]
Xi, Huaming [2 ,3 ]
Han, Shuaiqi [1 ]
Zhang, Hongyun [1 ]
Hu, Jianhong [1 ,4 ]
机构
[1] Northwest Agr & Forestry Univ, Coll Anim Sci & Technol, Key Lab Anim Genet Breeding & Reprod Shaanxi Prov, Yangling 712100, Shaanxi, Peoples R China
[2] Zhejiang A&F Univ, Zhejiang Prov Engn Lab Anim Hlth Inspect & Interne, Zhejiang Int Sci & Technol Cooperat Base Vet Med &, China Australia Joint Lab Anim Hlth Big Data Analy, Hangzhou 311300, Peoples R China
[3] Zhejiang A&F Univ, Coll Vet Med, Hangzhou 311300, Peoples R China
[4] Northwest Agr & Forestry Univ, Coll Anim Sci & Technol, 22 Xinong Rd, Yangling 712100, Shaanxi, Peoples R China
关键词
Zearalenone; Oxidative stress; Autophagy; Goat; Sertoli cell; APOPTOSIS; DEATH; ACTIVATION; ROS; PROLIFERATION; RECEPTOR;
D O I
10.1016/j.ecoenv.2023.114571
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Zearalenone (ZEA), one of the non-steroidal estrogen mycotoxin, can cause male reproductive damage and genotoxicity in mammals. Testicular oxidative injury is an important factor causing male sterility. Testicular Sertoli cells are essential for spermatogenesis and male fertility. At present, the mechanism of oxidative injury in dairy goat Sertoli cells after exposure to ZEA remains unclear. This study explored the effects of ZEA on oxidative stress and autophagy in dairy goat Sertoli cells. It was found that treatment of primary Sertoli cells with 25, 50 and 100 mu mol/L ZEA for 24 h can promote ROS production, decrease cell viability, antioxidant enzyme activity and mitochondrial membrane potential, induce caspase-dependent cell apoptosis and autophagy activity. ZEA-induced autophagy was confirmed by LC3-I/LC3-II transformation. More importantly, N-acetylcysteine (NAC) pretreatment can remarkably inhibit ZEA-induced oxidative stress, apoptosis and autophagy in Sertoli cells by eliminating ROS. In conclusion, this study indicates that ZEA induces oxidative stress and autophagy in dairy goat Sertoli cells by promoting ROS production.
引用
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页数:10
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