Yaqiu Tang, Xin Gong, Mengyu Dai, Zhen Wang, Dongdong Shi
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引用次数: 0
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.
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.