Resveratrol improves estrus disorder induced by bisphenol A through attenuating oxidative stress, autophagy, and apoptosis.
Jun-Heng JiaoLei GaoWen-Long YongZhong-Yun KouZhi-Qiang RenRui CaiGui-Yan ChuWei-Jun PangPublished in: Journal of biochemical and molecular toxicology (2022)
Bisphenol A (BPA), as a widely used plasticizer, is easily absorbed by animals and humans. It has certain toxic effects on various tissues, including liver, heart, kidney, testis, and ovary. The toxic effects of BPA on animal reproduction have aroused widespread concern, but its regulatory mechanism and antidote in female animals estrus cycle remain unclear. In this study, the results displayed that BPA destroyed the normal estrus cycle of mice through decreasing the levels of progesterone and estradiol. Furthermore, BPA significantly increased the levels of oxidative stress, autophagy, and apoptosis in ovaries and granulosa cells. Interestingly, we found that the natural antioxidant resveratrol rescued estrus disorder and impaired estradiol secretion, reduced the abnormal reactive oxygen species accumulation, autophagy, and apoptosis in BPA exposed ovarian tissues. Moreover, transmission electron microscopy showed that resveratrol reduced BPA-induced autophagic vesicles formation and flow cytometry showed that resveratrol inhibited the increase of apoptotic cells induced by BPA on granulosa cells. Therefore, the supplement of resveratrol could restore BPA-induced estrus disorder by protecting ovarian granulosa cells. Overall, resveratrol is a potential drug to alleviate BPA-induced estrous cycle disorders and ovarian damage.
Keyphrases
- oxidative stress
- induced apoptosis
- cell cycle arrest
- cell death
- endoplasmic reticulum stress
- diabetic rats
- signaling pathway
- ischemia reperfusion injury
- flow cytometry
- heart failure
- adipose tissue
- gene expression
- emergency department
- metabolic syndrome
- estrogen receptor
- endothelial cells
- skeletal muscle
- heat shock protein