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海马-下丘脑前区回路调节应激诱导的内分泌和行为反应。

Hippocampus-Anterior Hypothalamic Circuit Modulates Stress-Induced Endocrine and Behavioral Response.

机构信息

Department of Cell & Systems Biology, University of Toronto, Toronto, ON, Canada.

Department of Psychology, University of Toronto, Toronto, ON, Canada.

出版信息

Front Neural Circuits. 2022 Jun 20;16:894722. doi: 10.3389/fncir.2022.894722. eCollection 2022.

Abstract

Hippocampal input to the hypothalamus is known to be critically involved in mediating the negative feedback inhibition of stress response. However, the underlying neural circuitry has not been fully elucidated. Using a combination of rabies tracing, pathway-specific optogenetic inhibition, and cell-type specific synaptic silencing, the present study examined the role of hippocampal input to the hypothalamus in modulating neuroendocrine and behavioral responses to stress in mice. Transsynaptic rabies tracing revealed that the ventral hippocampus (vHPC) is monosynaptically connected to inhibitory cells in the anterior hypothalamic nucleus (AHN-GABA cells). Optogenetic inhibition of the vHPC→AHN pathway during a restraint stress resulted in a prolonged and exaggerated release of corticosterone, accompanied by an increase in stress-induced anxiety behaviors. Consistently, tetanus toxin-mediated synaptic inhibition in AHN-GABA cells produced a remarkably similar effect on the corticosterone release profile, corroborating the role of HPC→AHN pathway in mediating the hippocampal control of stress responses. Lastly, we found that chronic inhibition of AHN-GABA cells leads to cognitive impairments in both object and social recognition memory. Together, our data present a novel hypothalamic circuit for the modulation of adaptive stress responses, the dysfunction of which has been implicated in various affective disorders.

摘要

海马体向下丘脑的输入被认为在介导应激反应的负反馈抑制中起着至关重要的作用。然而,其潜在的神经回路尚未完全阐明。本研究采用狂犬病毒追踪、特定通路的光遗传学抑制和细胞类型特异性突触沉默相结合的方法,研究了海马体向下丘脑的输入在调节小鼠应激的神经内分泌和行为反应中的作用。逆行狂犬病毒追踪显示,腹侧海马体(vHPC)与下丘脑前核(AHN-GABA 细胞)中的抑制性细胞单突触连接。在束缚应激期间,对 vHPC→AHN 通路进行光遗传学抑制导致皮质酮释放延长和过度释放,并伴有应激诱导的焦虑行为增加。一致地,肉毒杆菌毒素介导的 AHN-GABA 细胞中的突触抑制对皮质酮释放谱产生了非常相似的影响,证实了 HPC→AHN 通路在介导海马体对应激反应的控制中的作用。最后,我们发现慢性抑制 AHN-GABA 细胞会导致物体和社交识别记忆的认知障碍。总之,我们的数据提出了一个新的下丘脑回路,用于调节适应性应激反应,其功能障碍与各种情感障碍有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61e6/9251012/409082aab843/fncir-16-894722-g0001.jpg

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