大鼠海马 DG 中的 RAGE/AP-1/OTR 信号通路参与了 CUS 诱导的抑郁样行为。

IF 2.9 3区 心理学 Q2 BEHAVIORAL SCIENCES Behavioural Brain Research Pub Date : 2025-05-08 Epub Date: 2025-03-14 DOI:10.1016/j.bbr.2025.115540
Xuemei Li , Xin Wang , Lifen Xue, Lan Luo, Lingxiao Hu, Wengao Jiang
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引用次数: 0

摘要

近年来,越来越多的证据表明,催产素(OT)系统在慢性应激相关情绪障碍的神经生理学中起着重要作用。然而,对慢性应激反应的确切改变及其潜在机制尚不清楚。本研究表明,慢性不可预测应激(CUS)导致RAGE和OTR表达降低,并抑制AP-1磷酸化。RAGE在海马DG中下调可诱导抑郁样行为,下调OTR蛋白和mRNA水平,降低AP-1磷酸化水平。经鼻给药可逆转RAGE下调引起的抑郁样行为,增加BDNF表达水平和AP-1磷酸化水平。另一方面,RAGE在海马DG中的过表达抑制了CUS对抑郁样行为、AP-1磷酸化和OTR表达的影响。这些发现表明RAGE信号通路至少部分通过调节OTR的表达参与了CUS诱导的抑郁样行为。
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RAGE/AP-1/OTR signaling pathway in rat hippocampus DG involved in CUS induced depressive-like behaviors
There has been a growing body of evidence indicating that the oxytocin (OT) system plays a significant role in the neurophysiology of chronic stress-related mood disorders in recent years. However, the precise alterations for the OT system in response to chronic stress and the underlying mechanism remains unclear. The present study demonstrated that chronic unpredictable stress (CUS) resulted in a reduction in the expression of RAGE and OTR, as well as an inhibition of AP-1 phosphorylation. RAGE knockdown in hippocampus DG induced depressive-like behaviors, down-regulated the OTR protein and mRNA levels, and reduced the AP-1 phosphorylation. The administration of OT via the nasal route reversed the depressive-like behaviors induced by RAGE knockdown, increased the levels of BDNF expression and AP-1 phosphorylation. On the other hand, RAGE over-expression in the hippocampus DG resisted the effects of CUS on depression-like behaviors, AP-1 phosphorylation, and OTR expression. These finding suggested that RAGE signaling pathway is involved in CUS induced depressive-like behaviors at least partially by regulating OTR expression.
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来源期刊
Behavioural Brain Research
Behavioural Brain Research 医学-行为科学
CiteScore
5.60
自引率
0.00%
发文量
383
审稿时长
61 days
期刊介绍: Behavioural Brain Research is an international, interdisciplinary journal dedicated to the publication of articles in the field of behavioural neuroscience, broadly defined. Contributions from the entire range of disciplines that comprise the neurosciences, behavioural sciences or cognitive sciences are appropriate, as long as the goal is to delineate the neural mechanisms underlying behaviour. Thus, studies may range from neurophysiological, neuroanatomical, neurochemical or neuropharmacological analysis of brain-behaviour relations, including the use of molecular genetic or behavioural genetic approaches, to studies that involve the use of brain imaging techniques, to neuroethological studies. Reports of original research, of major methodological advances, or of novel conceptual approaches are all encouraged. The journal will also consider critical reviews on selected topics.
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