microRNA-17-5p modulates ventral hippocampal transcriptome and synaptic proteome: Implications for emotional regulation in adult male rats.

海马体 神经科学 生物 海马结构 转录组 长时程增强 加巴能 突触可塑性 前额叶皮质 慢性应激 神经可塑性 小RNA 树突棘 心理学 习惯化 高架加迷宫 蛋白质组 开阔地 抑制性突触后电位 环境富集 帕尔瓦布明 边缘系统 神经传递 扣带回前部 基因表达
作者
Felipe A. Olave,Wladimir A. Corrales,Tiziana Guarnieri,Juan Pablo Silva,Francisco Aguayo,Marcelo Alarcón,Luciano Román-Albasini,Julia Catalán,Pablo I. González,Natalia Palacios,V Mora-González,Carlos Alvarez-Navarro,Esteban Aliaga,John A. Cidlowski,Pedro Zamorano,Jenny L. Fiedler
出处
期刊:Neurobiology of Disease [Elsevier BV]
卷期号:218: 107198-107198 被引量:2
标识
DOI:10.1016/j.nbd.2025.107198
摘要

The hippocampus plays a crucial role in memory and emotional regulation, with its dorsal pole supporting cognitive functions and the ventral hippocampus modulating anxiety and affective processing via limbic interactions. Chronic restraint stress induces anxious- and depressive-like behaviors in rodents, alongside transcriptomic changes in the ventral hippocampus. Emerging evidence highlights microRNAs as modulators of synaptic architecture and gene expression. Notably, miR-17-5p-part of the miR-17-92 cluster- shows increased cortical expression in individuals with mood disorders, and its levels in neural extracellular vesicles correlate directly with depressive symptom severity in male patients, suggesting translational relevance. In rodent models, chronic stress exposure produces divergent hippocampal expression patterns of miR-17-5p. Whether miR-17-5p acts as a passive biomarker of mood disorder or actively contributes to stress adaptation remains unclear. In the present study, chronic stress exposure increased miR-17-5p expression specifically in the ventral hippocampus of male rats, with no changes detected in females. To assess its functional relevance, we reproduced this alteration in the ventral hippocampus of naïve male to evaluate behavioral outcomes and characterize both global and synaptic transcriptomic and proteomic profiles. Behaviorally, miR-17-5p mimic administration increased the sucrose preference, revealing an antidepressant-like effect. On the other hand, the open field test did not reveal anxiety-related differences, whereas the novelty-suppressed feeding test indicated a decrease in anxious-like behavior following miR-17-5p administration. Molecular analyses in ventral hippocampus homogenates and synaptic-enriched fractions revealed modulation of ribosomal protein composition and translational regulation-likely through mTOR pathway activation-favoring GABAergic adaptation and synaptic remodeling. These findings suggest a region-specific role of miR-17-5p in the ventral hippocampus that may contribute to its anxiolytic and antidepressant-like effects. These results provide novel insights into miR-17-5p-mediated mood regulation, highlighting its potential as a therapeutic target for anxiety and depressive disorders.
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