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RESEARCH PAPER / 2024-07-26

PrG protects postovulatory oocytes aging in mice through the putrescine pathway.

Ronghua Ma, Xi Zhao, Jing Zhao, Yi Yi, Shengyan Jian, Xueman Ma, Zhanhai Su

Research Center for High Altitude Medicine, Key Laboratory for High Altitude Medicine, Ministry of Education, Qinghai University, Xining, 810016, China; Qinghai Provincial People's Hospital, Xining, 810000, China.Research Center for High Altitude Medicine, Key Laboratory for High Altitude Medicine, Ministry of Education, Qinghai University, Xining, 810016, China; Qinghai Provincial People's Hospital, Xining, 810000, China. · pubmed

Abstract

Postovulatory aging of oocytes involves a series of deleterious molecular and cellular changes, which adversely affect oocyte maturation, fertilization, and early embryonic development. Petunidin-3-O-(6-O-pcoumaroyl)-rutinoside-5-O-glucoside (PrG), the main active ingredient of anthocyanin, exerts antioxidant effects. This study investigated whether PrG supplementation could delay postovulatory oocyte aging by alleviating oxidative stress. Our results showed that PrG supplementation decreased the number of abnormal morphology oocytes and improved the oxidative stress of aged oocytes by facilitating the reduction of the reactive oxygen species, the increase in glutathione content, and the recovery of expression of antioxidant-related gene expression. In addition, PrG treatment recovered mitochondrial dysfunction, including mitochondrial distribution, mitochondrial membrane potential and adenosine triphosphate in aged oocytes. PrG-treated oocytes returned to normal levels of cytoplasmic and mitochondrial calcium. Notably, PrG inhibited early apoptosis in aged oocytes. RNA-seq and qRT-PCR results revealed that PrG ameliorated oxidative stress injury in postovulatory aging oocytes of mice via the putrescine pathway. In conclusion, in vitro PrG supplementation is a potential therapy for delaying postovulatory oocyte aging.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper investigates the effects of PrG on postovulatory oocyte aging, focusing on oxidative stress and mitochondrial dysfunction, which are relevant to the aging process. However, while it contributes to understanding mechanisms of oocyte aging, the findings are specific to reproductive biology and do not broadly address the root causes of aging or lifespan extension. Thus, the impact is solid but limited.

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