Activity of VMS-projecting mPFC neurons encodes individual vulnerability to chronic restraint stress in male mice

IF 4.2 2区 医学 Q1 NEUROSCIENCES
Yaqiu Tang, Xin Gong, Mengyu Dai, Zhen Wang, Dongdong Shi
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Abstract

The medial prefrontal cortex (mPFC) is critically involved in stress-related behaviors, specifically via the subpopulation of neurons that project to the ventromedial striatum (VMS). However, whether VMS-projecting mPFC neurons contribute to individual differences in behavioral responses to chronic stress remains unclear. Here, using a chronic restraint stress (CRS) model, we observed heterogeneous CRS-induced behavioral responses and stratified mice into relatively susceptible (SUS) and resilient (RES) subgroups based on a composite stress-related behavioral profile. To investigate the underlying neural basis, we performed in vivo fiber photometry to monitor calcium dynamics of VMS-projecting mPFC excitatory neurons before (baseline), during, and after CRS. We found that SUS mice exhibited significantly higher peak ΔF/F signals compared to RES mice even prior to stress exposure, and displayed persistently elevated activity during and after CRS. To further assess cellular mechanisms, we performed ex vivo whole-cell recordings from projection-defined neurons and found that VMS-projecting mPFC neurons in SUS mice exhibit increased intrinsic excitability, characterized by enhanced firing responses to depolarizing current injection. Chemogenetic activation of these neurons increased stress-related behaviors, whereas their inhibition attenuated CRS-associated behavioral abnormalities in susceptible mice. What's more, future studies are needed to determine whether these mPFC–VMS circuit features generalize to females. Together, these findings support the VMS-projecting mPFC neurons as a candidate neural substrate associated with individual differences in stress-related behavioral vulnerability.
雄性小鼠vm -投射mPFC神经元的活动编码个体对慢性约束应激的脆弱性。
内侧前额叶皮层(mPFC)在压力相关行为中起着至关重要的作用,特别是通过投射到腹内侧纹状体(VMS)的神经元亚群。然而,vms -突起的mPFC神经元是否有助于慢性应激行为反应的个体差异仍不清楚。本研究采用慢性约束应激(CRS)模型,观察了异质性CRS诱导的行为反应,并根据复合应激相关行为特征将小鼠分为相对易感(SUS)和弹性(RES)亚组。为了研究潜在的神经基础,我们在体内进行了纤维光度测定,以监测vms -投射mPFC兴奋性神经元在CRS之前(基线)、期间和之后的钙动力学。我们发现,即使在应激暴露之前,SUS小鼠也比RES小鼠表现出更高的峰值ΔF/F信号,并且在应激暴露期间和之后表现出持续升高的活性。为了进一步评估细胞机制,我们对投射定义的神经元进行了离体全细胞记录,发现SUS小鼠vms -投射的mPFC神经元表现出增强的内在兴奋性,其特征是对去极化电流注射的放电反应增强。这些神经元的化学发生激活增加了应激相关的行为,而在易感小鼠中,它们的抑制减弱了crs相关的行为异常。更重要的是,未来的研究需要确定这些mPFC-VMS电路特征是否适用于女性。总之,这些发现支持vms -突起的mPFC神经元作为与压力相关行为易感性个体差异相关的候选神经基质。
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
Neurobiology of Stress
Neurobiology of Stress Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
9.40
自引率
4.00%
发文量
74
审稿时长
48 days
期刊介绍: Neurobiology of Stress is a multidisciplinary journal for the publication of original research and review articles on basic, translational and clinical research into stress and related disorders. It will focus on the impact of stress on the brain from cellular to behavioral functions and stress-related neuropsychiatric disorders (such as depression, trauma and anxiety). The translation of basic research findings into real-world applications will be a key aim of the journal. Basic, translational and clinical research on the following topics as they relate to stress will be covered: Molecular substrates and cell signaling, Genetics and epigenetics, Stress circuitry, Structural and physiological plasticity, Developmental Aspects, Laboratory models of stress, Neuroinflammation and pathology, Memory and Cognition, Motivational Processes, Fear and Anxiety, Stress-related neuropsychiatric disorders (including depression, PTSD, substance abuse), Neuropsychopharmacology.
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