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Updated: Feb 2, 2026

A Method to Study the Impact of Chemically-induced Ovarian Failure on Exercise Capacity and Cardiac Adaptation in Mice
Published on: April 7, 2014
Tri-ortho-cresyl phosphate (TOCP) induced ovarian failure in mice is related to the Hippo signaling pathway
Liaoliao Hu1, Tingting Peng1, Jian Huang1
1Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi 330031, China; Jiangxi Key Laboratory of Reproductive Physiology and Pathology, Nanchang University, Nanchang, Jiangxi 330031, China.
Abstract:
As a plasticizer widely used in society, tri-ortho-cresyl phosphate (TOCP) is reported to inhibit spermatogenesis and growth of spermatogonial stem cells. However, its effects on female reproductive system are virtually unknown. The present study investigated the effects of TOCP on ovarian follicle development by using mouse model of chronic TOCP exposure, and examined the expression of the core components of the Hippo pathway, which had been proven to be crucial for ovarian follicle development. Furthermore, through up-regulation of Hippo-yes-associated protein 1 (Yap1) in ovaries, the potential protective effects of Yap1 over-expression on TOCP-induced ovarian dysfunction were observed. The results showed that TOCP impaired ovarian function in a dose-dependent manner, and the expression of the Hippo pathway changed significantly in TOCP-exposed ovaries. Further, YAP1 over-expression partially reversed the TOCP-induced ovarian impairment. Collectively, these data indicate that the Hippo pathway is involved in the mechanism by which TOCP elicits ovarian function impairment.
Insights
Tri-ortho-cresyl phosphate (TOCP) impairs ovarian function and alters the Hippo pathway in mice. Overexpressing YAP1 partially protected against TOCP-induced ovarian damage, suggesting pathway involvement.
Area of Science:
- Reproductive Toxicology
- Cell Signaling
- Developmental Biology
Background:
- Tri-ortho-cresyl phosphate (TOCP) is a widely used plasticizer with known adverse effects on male reproduction.
- The impact of TOCP on the female reproductive system, particularly ovarian follicle development, remains largely unexplored.
- The Hippo pathway is a critical regulator of organ size and cellular processes, including ovarian follicle development.
Purpose of the Study:
- To investigate the effects of chronic TOCP exposure on ovarian follicle development in a mouse model.
- To examine the role of the Hippo pathway in TOCP-induced ovarian dysfunction.
- To evaluate the potential protective effects of YAP1 (Yes-associated protein 1) overexpression against TOCP toxicity in the ovary.
Main Methods:
- Chronic exposure of mice to varying doses of TOCP.
- Assessment of ovarian function and follicle development.
- Analysis of Hippo pathway component expression in ovarian tissues.
- Overexpression of YAP1 in the ovaries to assess protective effects.
Main Results:
- TOCP exposure led to a dose-dependent impairment of ovarian function.
- Significant alterations in the expression of Hippo pathway components were observed in TOCP-exposed ovaries.
- Overexpression of YAP1 partially ameliorated the ovarian dysfunction induced by TOCP.
Conclusions:
- The Hippo pathway is implicated in the mechanism underlying TOCP-induced ovarian impairment.
- TOCP poses a risk to female reproductive health, affecting ovarian follicle development.
- YAP1 may play a protective role in mitigating TOCP's adverse effects on the ovary.
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