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慢性间歇性冷应激激活大鼠卵巢交感神经并改变其卵泡发育。

Chronic intermittent cold stress activates ovarian sympathetic nerves and modifies ovarian follicular development in the rat.

作者信息

Dorfman M, Arancibia S, Fiedler J L, Lara H E

机构信息

Laboratory of Neurobiochemistry, Faculty of Chemistry and Pharmaceutical Sciences, Universidad de Chile, Santiago, Chile.

出版信息

Biol Reprod. 2003 Jun;68(6):2038-43. doi: 10.1095/biolreprod.102.008318. Epub 2003 Jan 8.

Abstract

We studied the effects of a chronic intermittent cold stress regime on sympathetic nerve activation and ovarian physiology. This paradigm (4 degrees C for 3 h/day, Monday-Friday, for 3 or 4 wk) does not affect basal plasma levels of corticosterone. After 3 wk of stress, we detected a decrease in noradrenaline (NA) in the ovary, but after 4 wk, this ovarian neurotransmitter concentration increased over that of unstressed control rats. To analyze whether this effect on NA is preceded by an activation of the neurotrophic factor system responsible for growth and survival of sympathetic neurons, we measured both nerve growth factor (NGF) (by enzyme immunoassay) and the intraovarian levels of its low affinity receptor mRNA (by reverse transcription-polymerase chain reaction). The activation of sympathetic nerves was followed by an increase in NGF concentration without affecting the ovarian levels of either NGF or the mRNA of its receptor. Interestingly, follicular development changed during the stress procedure; after 3 or 4 wk of stress, we found a decrease in preantral healthy follicles without a compensatory increase in atresia. Concomitantly with the increase in NA and NGF in the ovary, we observed that a new population of follicles with hypertrophied thecal cell layers appeared after 4 wk of stress. These results suggest that chronic stress, through an intraovarian neurotrophin-mediated sympathetic activation, produces changes in follicular development that could lead to an impairment of reproductive function.

摘要

我们研究了慢性间歇性冷应激对交感神经激活和卵巢生理的影响。这种模式(周一至周五,每天3小时处于4摄氏度环境,持续3或4周)不会影响皮质酮的基础血浆水平。应激3周后,我们检测到卵巢中去甲肾上腺素(NA)减少,但4周后,该卵巢神经递质浓度比未应激的对照大鼠有所增加。为了分析这种对NA的影响是否先于负责交感神经元生长和存活的神经营养因子系统的激活,我们测量了神经生长因子(NGF)(通过酶免疫测定法)及其低亲和力受体mRNA的卵巢内水平(通过逆转录-聚合酶链反应)。交感神经激活后,NGF浓度增加,而卵巢中NGF及其受体的mRNA水平均未受影响。有趣的是,在应激过程中卵泡发育发生了变化;应激3或4周后,我们发现窦前健康卵泡减少,闭锁没有代偿性增加。随着卵巢中NA和NGF的增加,我们观察到应激4周后出现了一群新的卵泡,其卵泡膜细胞层肥大。这些结果表明,慢性应激通过卵巢内神经营养因子介导的交感神经激活,导致卵泡发育变化,进而可能损害生殖功能。

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