电针调节小鼠和人胃功能的神经解剖学组织。

IF 15 1区 医学 Q1 NEUROSCIENCES
Shun Dong, Lijuan Zhao, Jing Liu, Xuan Sha, Yi Wu, Weili Liu, Junlong Sun, Yangshuai Su, Zhidi Zhuang, Jian Chen, Ying Dong, Beijing Xie, Anqi Zhou, Hongyan Ji, Yuchun Wang, Xiaoman Deng, Xianghong Jing, Qiufu Ma, Nianhong Wang, Shenbin Liu
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引用次数: 0

摘要

电针诱发的体感-迷走神经反射可以调节内脏功能。然而,潜在的原理和神经机制仍然知之甚少,阻碍了进一步的优化。在这里,我们确定了EA在地形上驱动小鼠体感-迷走-胃反射所必需的关键神经成分。EA通过激活瞬时受体电位香草素-1 (TRPV1)+伤害感受器亚群来驱动这种反射,该亚群以Adra2a的表达为标志,仅位于深筋膜组织。通过TRPV1+纤维,EA激活了源自迷走神经背侧运动核(DMV)的胃投射Oxtr+纤维亚型。基因消融TRPV1+纤维或Oxtr+ DMV神经元可减弱ea诱导的胃反射。相反,这些神经元的光遗传激活足以驱动小鼠的胃运动。使用类似的刺激参数,我们证明了EA成功地改善了运动障碍样功能性消化不良患者的胃功能。因此,我们的发现为EA在地形上促进和治疗胃运动障碍提供了神经解剖学基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuroanatomical organization of electroacupuncture in modulating gastric function in mice and humans.

Somatosensory-vagal reflexes evoked by electroacupuncture (EA) can modulate visceral functions. However, the underlying principles and neural mechanisms remain poorly understood, hindering further optimization. Here, we identified key neural components essential for EA topographically driving the somatosensory-vagal-gastric reflex in mice. EA drove this reflex via activation of a subset of transient receptor potential vanilloid-1 (TRPV1)+ nociceptors marked by the expression of Adra2a and located exclusively in deep fascial tissues. Through TRPV1+ fibers, EA activated a subtype of gastro-projecting Oxtr+ fibers originating from the dorsal motor nucleus of the vagus (DMV). Genetic ablation of TRPV1+ fibers or Oxtr+ DMV neurons attenuated EA-induced gastric reflexes. Conversely, optogenetic activation of these neurons was sufficient to drive gastric motility in mice. Using similar stimulation parameters, we demonstrated that EA successfully improved gastric functions in patients with dysmotility-like functional dyspepsia (chictr.org.cn: ChiCTR2300072636). Our findings thus provide a neural anatomical basis for EA topographically to promote and treat gastric motility disorders.

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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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