Stress and medial prefrontal cortex: Sex-dependent effects in rodent models.

International review of neurobiology Pub Date : 2026-01-01 Epub Date: 2026-09-14 DOI:10.1016/bs.irn.2026.08.013
Hailey Storsved, Cara L Wellman
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Abstract

Chronic stress significantly alters rodent medial prefrontal cortical (mPFC) structure and function, contributing to cognitive and affective dysfunction associated with stress-related psychiatric disorders. Although the effects of stress on the male mPFC have been extensively characterized, growing evidence demonstrates that females exhibit distinct behavioral, structural, and molecular responses to chronic stress. This review synthesizes current findings regarding sex differences in stress-induced plasticity within the adult mPFC, discussing the behavioral outcomes, activation, and neural plasticity of the region in response to stress exposure. Across stress paradigms, males generally exhibit earlier dendritic retraction, spine loss, and impairments in cognitive flexibility, whereas females often demonstrate delayed mPFC effects despite persistent affective behavioral deficits. Emerging evidence suggests that females may recruit compensatory inhibitory mechanisms, particularly through parvalbumin neuron activation, that transiently buffer pyramidal cells from stress-induced remodeling. In contrast, stress in males may influence mPFC structure and function via somatostatin interneuron signaling, glucocorticoid receptor-mediated pathways, and microglial-dependent synaptic remodeling. However, sex differences are strongly influenced by stress modality, duration, and intensity, which contributes to variability across studies. Despite this variability, patterns in the literature suggest that males and females recruit distinct mPFC mechanisms in response to stress. Improved understanding of sex-specific stress adaptations may inform the development of targeted interventions for stress-related psychiatric disorders.

应激和内侧前额皮质:啮齿动物模型的性别依赖效应。
慢性应激显著改变啮齿动物内侧前额叶皮质(mPFC)的结构和功能,导致应激相关精神疾病的认知和情感功能障碍。尽管压力对雄性mPFC的影响已经被广泛表征,但越来越多的证据表明,雌性对慢性压力表现出不同的行为、结构和分子反应。这篇综述综合了目前关于成人mPFC中应激诱导可塑性的性别差异的研究结果,讨论了应激暴露下该区域的行为结果、激活和神经可塑性。在各种应激模式下,男性通常表现出较早的树突回缩、脊柱丢失和认知灵活性受损,而女性尽管存在持续的情感行为缺陷,但通常表现出较晚的mPFC效应。新出现的证据表明,雌性可能会利用代偿性抑制机制,特别是通过小白蛋白神经元激活,暂时缓冲锥体细胞应激诱导的重塑。相反,雄性应激可能通过生长抑素神经元间信号传导、糖皮质激素受体介导的途径和小胶质依赖的突触重塑影响mPFC的结构和功能。然而,性别差异受到应激模式、持续时间和强度的强烈影响,这导致了研究中的差异。尽管存在这种可变性,但文献中的模式表明,男性和女性在应对压力时采用不同的mPFC机制。提高对性别特异性压力适应的理解,可以为针对性干预压力相关精神疾病的发展提供信息。
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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