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桦木酸通过抑制 p38/ERK MAPK 和激活 Nrf2 介导的抗氧化防御作用改善玉米赤霉烯酮暴露引起的小鼠睾丸功能障碍和氧化应激。

Ameliorative effect of betulinic acid against zearalenone exposure triggers testicular dysfunction and oxidative stress in mice via p38/ERK MAPK inhibition and Nrf2-mediated antioxidant defense activation.

机构信息

Hunan Engineering Research Center of Livestock and Poultry Health Care, College of Veterinary Medicine, Hunan Agricultural University, Changsha 410128, China.

Hunan Engineering Research Center of Livestock and Poultry Health Care, College of Veterinary Medicine, Hunan Agricultural University, Changsha 410128, China.

出版信息

Ecotoxicol Environ Saf. 2022 Jun 15;238:113561. doi: 10.1016/j.ecoenv.2022.113561. Epub 2022 Apr 27.

Abstract

Zearalenone (ZEA) is a nonsteroidal estrogenic mycotoxin, which mainly contaminates grains and has estrogen-like effects on the reproductive system. Betulinic acid (BA), a natural lupane-type pentacyclic triterpene, has anti-oxidative and anti-inflammatory properties. This study aimed to investigate whether BA alleviates ZEA-induced testicular damage and explore the possible mechanism. Here, BA ameliorated testicular damage by mitigating the disordered arrangement of seminiferous tubules, the exfoliation of lumen cells, and the increase of cell apoptosis caused by ZEA. Meanwhile, BA alleviated ZEA-triggered testicular damage by restoring hormone levels and sperm motility, and reconstructing the blood-testis-barrier. Moreover, BA alleviated ZEA-exposed testicular oxidative stress by activating Nrf2 pathway. Furthermore, BA moderated ZEA-evoked testicular inflammation by inhibiting p38/ERK MAPK pathway. Overall, our results revealed that BA has a therapeutic protective effect on ZEA-induced testicular injury and oxidative stress via p38/ERK MAPK inhibition and Nrf2-mediated antioxidant defense activation, which provides a viable alternative to alleviate ZEA-induced male reproductive toxicology.

摘要

玉米赤霉烯酮(ZEA)是一种非甾体类雌激素真菌毒素,主要污染谷物,对生殖系统具有类雌激素作用。白桦脂酸(BA)是一种天然的羽扇豆烷型五环三萜,具有抗氧化和抗炎特性。本研究旨在探讨 BA 是否能缓解 ZEA 诱导的睾丸损伤,并探讨其可能的机制。结果表明,BA 通过减轻曲细精管排列紊乱、管腔细胞脱落以及细胞凋亡增加,改善了 ZEA 引起的睾丸损伤。此外,BA 通过恢复激素水平和精子活力以及重建血睾屏障,缓解了 ZEA 触发的睾丸损伤。此外,BA 通过激活 Nrf2 通路缓解了 ZEA 暴露引起的睾丸氧化应激。此外,BA 通过抑制 p38/ERK MAPK 通路调节 ZEA 诱导的睾丸炎症。综上所述,BA 通过抑制 p38/ERK MAPK 通路和激活 Nrf2 介导的抗氧化防御,对 ZEA 诱导的睾丸损伤和氧化应激具有治疗保护作用,为缓解 ZEA 诱导的男性生殖毒性提供了可行的替代方法。

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