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蓝斑核-CA1 投射参与慢性抑郁应激诱导的海马对短暂全脑缺血的易损性。

Locus coeruleus-CA1 projections are involved in chronic depressive stress-induced hippocampal vulnerability to transient global ischaemia.

机构信息

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

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

出版信息

Nat Commun. 2019 Jul 3;10(1):2942. doi: 10.1038/s41467-019-10795-9.

Abstract

Depression and transient ischaemic attack represent the common psychological and neurological diseases, respectively, and are tightly associated. However, studies of depression-affected ischaemic attack have been limited to epidemiological evidences, and the neural circuits underlying depression-modulated ischaemic injury remain unknown. Here, we find that chronic social defeat stress (CSDS) and chronic footshock stress (CFS) exacerbate CA1 neuron loss and spatial learning/memory impairment after a short transient global ischaemia (TGI) attack in mice. Whole-brain mapping of direct outputs of locus coeruleus (LC)-tyrosine hydroxylase (TH, Th:) positive neurons reveals that LC-CA1 projections are decreased in CSDS or CFS mice. Furthermore, using designer receptors exclusively activated by designer drugs (DREADDs)-based chemogenetic tools, we determine that Th:LC-CA1 circuit is necessary and sufficient for depression-induced aggravated outcomes of TGI. Collectively, we suggest that Th:LC-CA1 pathway plays a crucial role in depression-induced TGI vulnerability and offers a potential intervention for preventing depression-related transient ischaemic attack.

摘要

抑郁和短暂性脑缺血发作分别代表常见的心理和神经疾病,且两者紧密相关。然而,关于抑郁影响脑缺血损伤的研究仅限于流行病学证据,抑郁调节的脑缺血损伤的神经回路仍不清楚。在这里,我们发现慢性社会挫败应激(CSDS)和慢性足底电击应激(CFS)会加重短暂性全脑缺血(TGI)攻击后小鼠 CA1 神经元丢失和空间学习/记忆损伤。蓝斑核(LC)-酪氨酸羟化酶(TH,Th:)阳性神经元直接输出的全脑映射显示,CSDS 或 CFS 小鼠的 LC-CA1 投射减少。此外,我们使用受特定药物激活的设计受体(DREADDs)为基础的化学遗传学工具确定,Th:LC-CA1 回路对于抑郁引起的 TGI 加重结果是必需且充分的。总的来说,我们认为 Th:LC-CA1 通路在抑郁引起的 TGI 易感性中起着关键作用,并为预防与抑郁相关的短暂性脑缺血发作提供了一种潜在的干预方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e3/6610150/65e98ced4eb3/41467_2019_10795_Fig1_HTML.jpg

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