Peptide derived from RAGE efficiently improves oocyte development through attenuating oxidative stress in oocytes of mice with polycystic ovary syndrome.
Xiaojing HouZhonghui LingYaping GuoYan SuHanbin WangHang LiYuxia LuXiaojiao ChenXianwei CuiRong ShenPublished in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology (2024)
Polycystic ovary syndrome (PCOS) is a common and complex endocrine disorder in reproductive-aged women that frequently leads to infertility due to poor oocyte quality. In this study, we identified a new active peptide (advanced glycation end products receptors RAGE 344-355 ) from PCOS follicular fluid using mass spectrometry. We found that supplementing PCOS-like mouse oocytes with RAGE 344-355 attenuated both meiotic defects and oxidative stress levels, ultimately preventing developmental defects. Additionally, our results suggest that RAGE 344-355 may interact with eEF1a1 to mitigate oxidative meiotic defects in PCOS-like mouse oocytes. These findings highlight the potential for further clinical development of RAGE 344-355 as a potent supplement and therapeutic option for women with PCOS. This research addresses an important clinical problem and offers promising opportunities for improving oocyte quality in PCOS patients.
Keyphrases
- polycystic ovary syndrome
- insulin resistance
- oxidative stress
- mass spectrometry
- end stage renal disease
- chronic kidney disease
- ejection fraction
- dna damage
- newly diagnosed
- adipose tissue
- metabolic syndrome
- type diabetes
- ischemia reperfusion injury
- prognostic factors
- liquid chromatography
- skeletal muscle
- diabetic rats
- pregnant women
- signaling pathway
- high performance liquid chromatography
- patient reported outcomes