Chronic stress causes ovarian fibrosis to impair female fertility in mice

IF 4.4 2区 生物学 Q2 CELL BIOLOGY Cellular signalling Pub Date : 2024-08-03 DOI:10.1016/j.cellsig.2024.111334
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引用次数: 0

Abstract

Objective

Chronic psychological stress is associated with impaired follicular development and ovarian dysfunction. Many aspects of this dysfunction and the underlying mechanisms remain unclear. Using a chronic unpredictable mild stress (CUMS) mouse model, we investigate the influence of chronic stress on ovarian function and explore potential mechanisms.

Methods

A CUMS mouse model was constructed over eight months, covering the period from sexual maturity to the onset of declining fertility in mice. At the end of the 2nd, 4th, 6th, and 8th months of exposure to CUMS, behavioral and physiological assays, including the sucrose preference test, tail suspension test, and serum corticosterone levels, were conducted to validate the effectiveness of the stress model. Fertility and ovarian function were assessed by analyzing the estrous cycle, number of offspring, sex hormone levels, follicle counts, granulosa cell proliferation and apoptosis, and the expression levels of fibrosis markers. Furthermore, proteomic analyses were performed on the ovaries to investigate the molecular mechanisms of ovarian fibrosis induced by CUMS.

Results

With continued CUMS exposure, there was a gradual decline in both the ovary-to-body weight ratio and the number of offspring. Moreover, the percentage of atretic follicles was notably higher in the CUMS-exposed groups compared to the control groups. It is noticeable that CUMS triggered granulosa cell apoptosis and halted proliferation. Additionally, increased expression of α-SMA and Collagen I in the ovaries of CUMS-exposed mice indicated that CUMS could induce ovarian fibrosis. Proteomic analysis provided insights into the activation of specific biological processes and molecules associated with fibrosis induced by chronic stress.

Conclusions

Our results strongly suggest that exposure to CUMS induces ovarian fibrosis, which influences follicular development and ultimately contributes to fertility decline. These findings offer novel perspectives on the impact of chronic stress on ovarian dysfunction.

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慢性压力导致卵巢纤维化,从而损害小鼠的雌性生育能力。
目的:慢性心理压力与卵泡发育受损和卵巢功能障碍有关。这种功能障碍的许多方面及其内在机制仍不清楚。我们利用慢性不可预测轻度应激(CUMS)小鼠模型,研究慢性应激对卵巢功能的影响,并探索其潜在机制:方法:我们构建了一个为期八个月的CUMS小鼠模型,涵盖了小鼠从性成熟到生育能力开始下降的时期。在暴露于 CUMS 的第 2、4、6 和 8 个月结束时,进行行为和生理检测,包括蔗糖偏好试验、尾悬试验和血清皮质酮水平,以验证应激模型的有效性。通过分析发情周期、后代数量、性激素水平、卵泡数量、颗粒细胞增殖和凋亡以及纤维化标志物的表达水平,对生育能力和卵巢功能进行了评估。此外,还对卵巢进行了蛋白质组分析,以研究 CUMS 诱导卵巢纤维化的分子机制:结果:随着CUMS的持续暴露,卵巢与体重的比率和后代数量都逐渐下降。此外,与对照组相比,CUMS 暴露组闭锁卵泡的比例明显更高。值得注意的是,CUMS 引发了颗粒细胞凋亡并阻止了增殖。此外,CUMS暴露小鼠卵巢中α-SMA和胶原蛋白I的表达增加,表明CUMS可诱导卵巢纤维化。蛋白质组分析有助于深入了解与慢性应激诱导的纤维化相关的特定生物过程和分子的激活情况:我们的研究结果有力地表明,暴露于 CUMS 会诱导卵巢纤维化,从而影响卵泡发育并最终导致生育能力下降。这些发现为慢性压力对卵巢功能障碍的影响提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cellular signalling
Cellular signalling 生物-细胞生物学
CiteScore
8.40
自引率
0.00%
发文量
250
审稿时长
27 days
期刊介绍: Cellular Signalling publishes original research describing fundamental and clinical findings on the mechanisms, actions and structural components of cellular signalling systems in vitro and in vivo. Cellular Signalling aims at full length research papers defining signalling systems ranging from microorganisms to cells, tissues and higher organisms.
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