α -Ketoglutarate Improves Meiotic Maturation of Porcine Oocytes and Promotes the Development of PA Embryos, Potentially by Reducing Oxidative Stress through the Nrf2 Pathway.
Qiang ChenLeilei GaoJiannan LiYitian YuanRuibin WangYiqi TianAnmin LeiPublished in: Oxidative medicine and cellular longevity (2022)
α -Ketoglutarate ( α -KG) is a metabolite in the tricarboxylic acid cycle. It has a strong antioxidant function and can effectively prevent oxidative damage. Previous studies have shown that α -KG exists in porcine follicles, and its content gradually increases as the follicles grow and mature. However, the potential mechanism of supplementation of α -KG on porcine oocytes during in vitro maturation (IVM) has not yet been reported. The purpose of this study was to explore the effect of α -KG on the early embryonic development of pigs and the mechanisms underlying these effects. We found that α -KG can enhance the development of early pig embryos. Adding 20 μ M α -KG to the in vitro culture medium significantly increased the rate of blastocyst formation and the total cell number. Compared with to that of the control group, apoptosis in blastocysts of the supplement group was significantly reduced. α -KG reduced the production of reactive oxygen species and glutathione levels in cells. α -KG not only improved the activity of mitochondria but also inhibited the occurrence of apoptosis. After supplementation with α -KG, pig embryo pluripotency-related genes (OCT4, NANOG, and SOX2) and antiapoptotic genes (Bcl2) were upregulated. In terms of mechanism, α -KG activates the Nrf2/ARE signaling pathway to regulate the expression of antioxidant-related targets, thus combating oxidative stress during the in vitro culture of oocytes. Activated Nrf2 promotes the transcription of Bcl2 genes and inhibits cell apoptosis. These results indicate that α -KG supplements have a beneficial effect on IVM by regulating oxidative stress during the IVM of porcine oocytes and can be used as a potential antioxidant for IVM of porcine oocytes.
Keyphrases
- oxidative stress
- induced apoptosis
- dna damage
- ischemia reperfusion injury
- diabetic rats
- cell cycle arrest
- signaling pathway
- reactive oxygen species
- cell death
- endoplasmic reticulum stress
- stem cells
- transcription factor
- anti inflammatory
- single cell
- long non coding rna
- optical coherence tomography
- gene expression
- pi k akt