Gonadectomy differentially regulates steroid receptor coactivator-1 and synaptic proteins in the hippocampus of adult female and male C57BL/6 mice.

Synapse (New York, N.y.) Pub Date : 2012-10-01 Epub Date: 2012-06-13 DOI:10.1002/syn.21574
Chen Bian, Kongjiang Zhu, Li Yang, Sen Lin, Shurong Li, Bingyin Su, Jiqiang Zhang
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引用次数: 20

Abstract

Hippocampus is one of the most important structures that mediates learning and memory, cognition, and mental behaviors and profoundly regulated by sex hormones in a sex-specific manner, but the mechanism of underlying sex differences regulation is still unclear. We have previously reported that in the male and female mice, steroid receptor coactivator-1 (SRC-1) and some key synaptic proteins share similar developmental profile in the hippocampus, but how circulating sex hormones affect hippocampal SRC-1 as well as these synaptic proteins remain unclear. In this study, we examined how gonad sex hormones regulate hippocampal SRC-1, synaptophysin, PSD-95, and AMPA receptor subtype GluR1 by using immunohistochemistry and Western blot. The results showed that in the female mice, ovariectomy affected hippocampal SRC-1 and GluR1 were only detected at 2 weeks post operation, then it recovered to sham level; synaptophysin was unaffected at any timepoint examined; significant decrease of PSD-95 was only detected at 4 weeks post operation. However, in the male hippocampus, SRC-1 and PSD-95 were decreased from one week and lasted to 4 weeks after orchidectomy, GluR1 decreased from 2 weeks after orchidectomy, but synaptophysin remained unchanged as in the females. Correlation analysis showed the profiles of SRC-1 were positively correlated with GluR1 of the females, PSD-95 and GluR1 of the males, respectively. The above results suggested a distinct regulatory mode between female and male gonad hormones in the regulation of hippocampal SRC-1 and synaptic proteins, which may be one of the mechanisms contributing to the dimorphism of hippocampus during development and ageing.

性腺切除术对成年雌性和雄性C57BL/6小鼠海马皮质激素受体共激活因子-1和突触蛋白的调节存在差异。
海马体是调节学习记忆、认知和心理行为的重要结构之一,受性激素的深刻调节,具有性别特异性,但其潜在的性别差异调节机制尚不清楚。我们之前报道过,在雄性和雌性小鼠中,类固醇受体共激活因子-1 (SRC-1)和一些关键的突触蛋白在海马体中具有相似的发育特征,但循环性激素如何影响海马体SRC-1以及这些突触蛋白尚不清楚。在本研究中,我们采用免疫组织化学和Western blot检测了性腺性激素对海马SRC-1、突触素、PSD-95和AMPA受体亚型GluR1的调节作用。结果表明,雌性小鼠卵巢切除术后仅在术后2周检测到海马SRC-1和GluR1,随后恢复到假手术水平;Synaptophysin在检测的任何时间点均未受影响;PSD-95仅在术后4周出现明显下降。然而,在雄性海马中,睾丸切除术后1周至4周,SRC-1和PSD-95下降,GluR1从睾丸切除术后2周开始下降,但突触素与雌性保持不变。相关分析显示,SRC-1基因谱分别与雌性、雄性PSD-95和GluR1基因谱呈正相关。上述结果提示雌雄性腺激素对海马SRC-1和突触蛋白的调控模式不同,这可能是海马在发育和衰老过程中出现二态性的机制之一。
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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