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基底前脑胆碱能神经支配通过腹侧海马下区过度兴奋诱导抑郁样行为。

Basal Forebrain Cholinergic Innervation Induces Depression-Like Behaviors Through Ventral Subiculum Hyperactivation.

机构信息

Department of Physiology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.

Department of Pathophysiology, Key Laboratory of Ministry of Education for Neurological Disorders, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.

出版信息

Neurosci Bull. 2023 Apr;39(4):617-630. doi: 10.1007/s12264-022-00962-2. Epub 2022 Nov 7.

Abstract

Malfunction of the ventral subiculum (vSub), the main subregion controlling the output connections from the hippocampus, is associated with major depressive disorder (MDD). Although the vSub receives cholinergic innervation from the medial septum and diagonal band of Broca (MSDB), whether and how the MSDB-to-vSub cholinergic circuit is involved in MDD is elusive. Here, we found that chronic unpredictable mild stress (CUMS) induced depression-like behaviors with hyperactivation of vSub neurons, measured by c-fos staining and whole-cell patch-clamp recording. By retrograde and anterograde tracing, we confirmed the dense MSDB cholinergic innervation of the vSub. In addition, transient restraint stress in CUMS increased the level of ACh in the vSub. Furthermore, chemogenetic stimulation of this MSDB-vSub innervation in ChAT-Cre mice induced hyperactivation of vSub pyramidal neurons along with depression-like behaviors; and local infusion of atropine, a muscarinic receptor antagonist, into the vSub attenuated the depression-like behaviors induced by chemogenetic stimulation of this pathway and CUMS. Together, these findings suggest that activating the MSDB-vSub cholinergic pathway induces hyperactivation of vSub pyramidal neurons and depression-like behaviors, revealing a novel circuit underlying vSub pyramidal neuronal hyperactivation and its associated depression.

摘要

腹侧下托(vSub)的功能障碍与重度抑郁症(MDD)有关,vSub 是控制海马体输出连接的主要亚区。尽管 vSub 接收来自中隔和 Broca 斜角带(MSDB)的胆碱能神经支配,但 MSDB-vSub 胆碱能回路是否以及如何参与 MDD 尚不清楚。在这里,我们发现慢性不可预测轻度应激(CUMS)诱导了 vSub 神经元的过度激活,表现为 c-fos 染色和全细胞膜片钳记录。通过逆行和顺行示踪,我们证实了 vSub 中密集的 MSDB 胆碱能神经支配。此外,CUMS 中的短暂束缚应激增加了 vSub 中的 ACh 水平。此外,在 ChAT-Cre 小鼠中化学遗传刺激这条 MSDB-vSub 神经支配会诱导 vSub 锥体神经元的过度激活以及类似抑郁的行为;而将毒蕈碱受体拮抗剂阿托品局部注入 vSub 会减弱这条通路的化学遗传刺激和 CUMS 诱导的类似抑郁的行为。总之,这些发现表明激活 MSDB-vSub 胆碱能通路会诱导 vSub 锥体神经元的过度激活和类似抑郁的行为,揭示了 vSub 锥体神经元过度激活及其相关抑郁的新环路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dec/10073402/4b157f254486/12264_2022_962_Fig1_HTML.jpg

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