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腹侧海马CA1区锥体神经元编码伤害性信息。

Ventral Hippocampal CA1 Pyramidal Neurons Encode Nociceptive Information.

作者信息

Wang Yue, Liu Naizheng, Ma Longyu, Yue Lupeng, Cui Shuang, Liu Feng-Yu, Yi Ming, Wan You

机构信息

Neuroscience Research Institute and Department of Neurobiology, School of Basic Medical Sciences, Peking University, Beijing, 100083, China.

CAS Key Laboratory of Mental Health, Institute of Psychology, Chinese Academy of Sciences, Beijing, 100101, China.

出版信息

Neurosci Bull. 2024 Feb;40(2):201-217. doi: 10.1007/s12264-023-01086-x. Epub 2023 Jul 13.

DOI:10.1007/s12264-023-01086-x
PMID:37440103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10838882/
Abstract

As a main structure of the limbic system, the hippocampus plays a critical role in pain perception and chronicity. The ventral hippocampal CA1 (vCA1) is closely associated with negative emotions such as anxiety, stress, and fear, yet how vCA1 neurons encode nociceptive information remains unclear. Using in vivo electrophysiological recording, we characterized vCA1 pyramidal neuron subpopulations that exhibited inhibitory or excitatory responses to plantar stimuli and were implicated in encoding stimuli modalities in naïve rats. Functional heterogeneity of the vCA1 pyramidal neurons was further identified in neuropathic pain conditions: the proportion and magnitude of the inhibitory response neurons paralleled mechanical allodynia and contributed to the confounded encoding of innocuous and noxious stimuli, whereas the excitatory response neurons were still instrumental in the discrimination of stimulus properties. Increased theta power and theta-spike coupling in vCA1 correlated with nociceptive behaviors. Optogenetic inhibition of vCA1 pyramidal neurons induced mechanical allodynia in naïve rats, whereas chemogenetic reversal of the overall suppressed vCA1 activity had analgesic effects in rats with neuropathic pain. These results provide direct evidence for the representations of nociceptive information in vCA1.

摘要

作为边缘系统的主要结构,海马体在疼痛感知和慢性疼痛中起着关键作用。腹侧海马CA1区(vCA1)与焦虑、压力和恐惧等负面情绪密切相关,但vCA1神经元如何编码伤害性信息仍不清楚。利用体内电生理记录,我们对vCA1锥体神经元亚群进行了表征,这些亚群对足底刺激表现出抑制或兴奋反应,并参与了对未处理大鼠刺激模式的编码。在神经性疼痛条件下,进一步确定了vCA1锥体神经元的功能异质性:抑制反应神经元的比例和幅度与机械性异常性疼痛平行,并导致对无害和有害刺激的混淆编码,而兴奋反应神经元在刺激属性的辨别中仍起作用。vCA1区θ波功率和θ波-棘波耦合增加与伤害性行为相关。对vCA1锥体神经元进行光遗传学抑制可在未处理大鼠中诱发机械性异常性疼痛,而对整体受抑制的vCA1活动进行化学遗传学逆转则对神经性疼痛大鼠具有镇痛作用。这些结果为vCA1中伤害性信息的表征提供了直接证据。

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