Repeated Superovulation Accelerates Primordial Follicle Activation and Atresia.
Qian WangShu-Xian ZhaoJian-Ning HeHua ZhaoBao-Xia GuJuan-Ke XieYi-Jun ZhaoCui-Lian ZhangZhao-Jia GePublished in: Cells (2022)
For humans, ARTs (assisted reproductive technologies) have become the most effective method to treat subfertility/infertility in clinic. To obtain enough oocytes during ART, ovarian stimulation is performed by exogenous hormones, and some patients undergo several ovarian stimulation cycles. Although some adverse effects of ARTs on women and offspring are reported, few studies are focused on the effects of multiple superovulation on ovarian reserve. In the present study, we found that repeated superovulation significantly reduced primordial follicle number and the serum AMH. Compared to the decreased antral follicle number, the expression of genes related to primordial follicle activation, such as Foxo3 , Akt , and Rptor, and the atretic follicle number in ovaries were increased by superovulation times. We further found that repeated superovulation reduced the plasma level of FSH, LH, and estradiol, and increased the expression of genes related to apoptosis ( Bax , Casp3 ( caspase-3 ), Casp8 , and Casp9 ) in granulosa cells, providing evidence that repeated superovulation disrupted the balance between survival and death in granulosa cells. In summary, our results suggest that repeated superovulation has adverse effects on folliculogenesis.
Keyphrases
- induced apoptosis
- cell cycle arrest
- polycystic ovary syndrome
- endoplasmic reticulum stress
- signaling pathway
- cell death
- poor prognosis
- oxidative stress
- pi k akt
- newly diagnosed
- germ cell
- end stage renal disease
- ejection fraction
- primary care
- genome wide
- cell proliferation
- high fat diet
- type diabetes
- metabolic syndrome
- prognostic factors
- dna methylation
- binding protein
- long non coding rna
- antiretroviral therapy
- skeletal muscle
- adipose tissue
- drug induced
- genome wide identification
- breast cancer risk