Histaminergic Innervation of the Ventral Anterior Thalamic Nucleus Alleviates Motor Deficits in a 6-OHDA-Induced Rat Model of Parkinson's Disease.

IF 5.9 2区 医学 Q1 NEUROSCIENCES
Han-Ting Xu, Xiao-Ya Xi, Shuang Zhou, Yun-Yong Xie, Zhi-San Cui, Bei-Bei Zhang, Shu-Tao Xie, Hong-Zhao Li, Qi-Peng Zhang, Yang Pan, Xiao-Yang Zhang, Jing-Ning Zhu
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Abstract

The ventral anterior (VA) nucleus of the thalamus is a major target of the basal ganglia and is closely associated with the pathogenesis of Parkinson's disease (PD). Notably, the VA receives direct innervation from the hypothalamic histaminergic system. However, its role in PD remains unknown. Here, we assessed the contribution of histamine to VA neuronal activity and PD motor deficits. Functional magnetic resonance imaging showed reduced VA activity in PD patients. Optogenetic activation of VA neurons or histaminergic afferents significantly alleviated motor deficits in 6-OHDA-induced PD rats. Furthermore, histamine excited VA neurons via H1 and H2 receptors and their coupled hyperpolarization-activated cyclic nucleotide-gated channels, inward-rectifier K+ channels, or Ca2+-activated K+ channels. These results demonstrate that histaminergic afferents actively compensate for Parkinsonian motor deficits by biasing VA activity. These findings suggest that targeting VA histamine receptors and downstream ion channels may be a potential therapeutic strategy for PD motor dysfunction.

丘脑腹侧前核的组胺能神经支配减轻6-羟多巴胺诱导的帕金森病大鼠模型的运动缺陷。
丘脑腹前核(VA)是基底神经节的主要靶点,与帕金森病(PD)的发病密切相关。值得注意的是,VA接受来自下丘脑组胺能系统的直接神经支配。然而,其在帕金森病中的作用尚不清楚。在这里,我们评估了组胺对VA神经元活动和PD运动缺陷的贡献。功能性磁共振成像显示PD患者的VA活性降低。光遗传学激活VA神经元或组胺能事件可显著减轻6-羟多巴胺诱导的PD大鼠的运动缺陷。此外,组胺通过H1和H2受体及其偶联的超极化激活的环核苷酸门控通道、内向整流K+通道或Ca2+激活的K+通道激活VA神经元。这些结果表明,组胺能事件通过偏倚VA活动积极补偿帕金森运动缺陷。这些发现提示,靶向VA组胺受体和下游离子通道可能是PD运动功能障碍的潜在治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuroscience bulletin
Neuroscience bulletin NEUROSCIENCES-
CiteScore
7.20
自引率
16.10%
发文量
163
审稿时长
6-12 weeks
期刊介绍: Neuroscience Bulletin (NB), the official journal of the Chinese Neuroscience Society, is published monthly by Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS) and Springer. NB aims to publish research advances in the field of neuroscience and promote exchange of scientific ideas within the community. The journal publishes original papers on various topics in neuroscience and focuses on potential disease implications on the nervous system. NB welcomes research contributions on molecular, cellular, or developmental neuroscience using multidisciplinary approaches and functional strategies. We feature full-length original articles, reviews, methods, letters to the editor, insights, and research highlights. As the official journal of the Chinese Neuroscience Society, which currently has more than 12,000 members in China, NB is devoted to facilitating communications between Chinese neuroscientists and their international colleagues. The journal is recognized as the most influential publication in neuroscience research in China.
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