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背侧海马 CA3 到小蝙蝠核的回路介导慢性社会挫败应激引起的对社会新颖性偏好的缺陷。

A circuit from dorsal hippocampal CA3 to parvafox nucleus mediates chronic social defeat stress-induced deficits in preference for social novelty.

机构信息

Department of Pharmacology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

The Key Laboratory of Neurological Diseases (HUST), Ministry of Education of China, Wuhan 430030, China.

出版信息

Sci Adv. 2022 Feb 25;8(8):eabe8828. doi: 10.1126/sciadv.abe8828. Epub 2022 Feb 23.

Abstract

The preference for social novelty is crucial to the social life of humans and rodents. However, the neural mechanisms underlying social novelty preference are poorly understood. Here, we found that chronic social defeat stress (CSDS) reduced the preference for social novelty in mice by impairing the response of CaMKIIα neurons in the CA3 region of dorsal hippocampus (dCA3) during approach to an unfamiliar mouse. The deficits of social novelty preference in CSDS-treated mice were reversed by activating the output from dCA3 to the GABAergic neurons in the lateral septum (LS). The activation of GABAergic projection from LS recruited a circuit that inhibited the Foxb1 neurons in the parvafox nucleus (PFN), which drove social avoidance by projecting to the lateral periaqueductal gray (lPAG). These results suggest that a previously unidentified circuit of dCA3→LS→PFN→lPAG mediates the deficits of social novelty preference induced by CSDS.

摘要

社交新颖性偏好对于人类和啮齿动物的社交生活至关重要。然而,社交新颖性偏好的神经机制尚不清楚。在这里,我们发现慢性社交挫败应激(CSDS)通过损害背侧海马 CA3 区(dCA3)中 CaMKIIα 神经元对陌生小鼠接近时的反应,减少了小鼠对社交新颖性的偏好。通过激活 dCA3 到侧隔核(LS)中 GABA 能神经元的输出,CSDS 处理小鼠的社交新颖性偏好缺陷得到了逆转。LS 的 GABA 能投射的激活募集了一个抑制小泡核(PFN)中 Foxb1 神经元的回路,该神经元通过投射到外侧导水管周围灰质(lPAG)来驱动社交回避。这些结果表明,一个以前未被识别的 dCA3→LS→PFN→lPAG 回路介导了 CSDS 诱导的社交新颖性偏好缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d211/8865774/c7ae533b7956/sciadv.abe8828-f1.jpg

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