Altered m6A modification is involved YAP-mediated apoptosis response in 4-vinylcyclohexene diepoxide induced

Yang Li1, Meifang Li2, Jian Liu1

  • 1Department of Gynaecology, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510120, China.

Insights

4-Vinylcyclohexene diepoxide (VCD) exposure in rats induces premature ovarian insufficiency (POI) by reducing ovarian follicles and altering N6-methyladenosine (m6A) RNA modification. This study reveals m6A modification changes, offering insights into POI mechanisms and potential therapeutic targets.

Area of Science:

  • Reproductive Biology
  • Toxicology
  • Molecular Biology

Background:

  • 4-Vinylcyclohexene diepoxide (VCD) is an industrial chemical linked to premature ovarian insufficiency (POI) and reproductive failure.
  • The VCD-induced rat model mimics natural menopause, making it valuable for studying reproductive system changes.

Purpose of the Study:

  • To investigate the mechanisms of follicular loss in the VCD-induced POI rat model.
  • To explore the effects of VCD exposure on systems beyond the ovaries.
  • To examine the role of N6-methyladenosine (m6A) RNA modification in VCD-induced POI.

Main Methods:

  • Female Sprague-Dawley rats were administered VCD (160 mg/kg) for 15 days.
  • Reproductive parameters, neuroendocrine function, sex hormone levels, and m6A RNA modification levels were assessed.
  • Follicle counts and m6A levels in VCD-treated and control rats were compared.

Main Results:

  • VCD exposure led to irregular estrous cycles and significantly reduced primordial, preantral, and antral follicle numbers.
  • Follicle Stimulating Hormone (FSH) levels increased, while anti-Mullerian hormone (AMH) levels decreased in VCD-treated rats.
  • Total m6A levels significantly decreased, with notable changes in ALKBH5-mediated YAP m6A modification.

Conclusions:

  • VCD-induced POI in rats is associated with significant follicular depletion and altered sex hormone profiles.
  • N6-methyladenosine (m6A) RNA modification is significantly dysregulated in this POI model.
  • This study provides novel insights into m6A modification's role in follicle development and suggests potential therapeutic targets for POI.

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