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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.
Abstract:
4-Vinylcyclohexene diepoxide (VCD), an industrial occupational health hazard chemical associated with premature ovarian insufficiency (POI) and reproductive failure. Recently, investigators have paid an increasing attention on VCD model of menopause recapitulates the natural, physiological transition through perimenopause to menopause. The current study sought to examining the mechanisms of follicular loss and exploring the effect of the model on systems outside of the ovaries. In this study, 28 days female SD rats were injected with VCD (160 mg/kg) vehicle for 15 consecutive days, euthanized in the diestrus phase approximately 100 days after the onset of treatment. Reproductive system injury, Neuroendocrine, sex hormone levels and receptor were observed, the levels of N6-methyladenosine (m6A) RNA modification and the expression of modulator genes were first measured. The VCD treated rats showing irregular estrous cycles, significantly reduced in the number of primordial follicles, the preantral and antral follicles also decreased significantly, accompanied by the plasma level of FSH increased and anti-Mullerian hormone (AMH) were decreased. The total m6A level was significantly decreased after exposure to VCD. Moreover, ALKBH5-mediated YAP m6A modification changed in VCD - induced premature ovarian insufficiency. These present work provides a new perspective on m6A modification in the VCD-induced POI rat model, which could provide valuable insights into the mechanisms underlying follicle development and finding new therapeutic targets for follicle prematurely exhausted. Also provide novel methodological guidance and endocrine basis to guide research and extend the applications in premature ovarian insufficiency model.
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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