Prenatal androgen induced lean PCOS impairs mitochondria and mRNA profiles in oocytes. Issue 3 (March 2020)

• Record Type: Journal Article
• Authors: Chappell, Neil R; Zhou, Beth; Schutt, Amy K; Gibbons, William E; Blesson, Chellakkan S
• Is Part Of: Endocrine connections. Volume 9:Issue 3(2020)
• Page Start: 261
• Page End: 270
• Publication Date: 2020-03
• Subjects: PCOS -- mitochondria -- oocytes -- glucose intolerance; Endocrinology -- Periodicals; 616.4005
• DOI: 10.1530/EC-19-0553
• Languages: English
• ISSNs: 2049-3614

Abstract

Abstract : Polycystic ovary syndrome (PCOS) is the most common ovulatory defect in women. Although most PCOS patients are obese, a subset of PCOS women are lean but show similar risks for adverse fertility outcomes. A lean PCOS mouse model was created using prenatal androgen administration. This developmentally programmed mouse model was used for this study. Our objective was to investigate if mitochondrial structure and functions were compromised in oocytes obtained from lean PCOS mouse. The lean PCOS mouse model was validated by performing glucose tolerance test, HbA1c levels, body weight and estrous cycle analyses. Oocytes were isolated and were used to investigate inner mitochondrial membrane potential, oxidative stress, lipid peroxidation, ATP production, mtDNA copy number, transcript abundance and electron microscopy. Our results demonstrate that lean PCOS mice have similar weight to that of the controls but exhibit glucose intolerance and hyperinsulinemia along with dysregulated estrus cycle. Analysis of their oocytes show impaired inner mitochondrial membrane function, elevated reactive oxygen species (ROS) and increased RNA transcript abundance. Electron microscopy of the oocytes showed impaired mitochondrial ultrastructure. In conclusion, the lean PCOS mouse model shows a decreased oocyte quality related to impaired mitochondrial ultrastructure and function.