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光遗传学和化学生物学控制疼痛信号:分子标记。

Optogenetic and Chemogenic Control of Pain Signaling: Molecular Markers.

机构信息

Escuela de Ciencias Químicas Sede Ocozocoautla, Universidad Autónoma de Chiapas, Ocozocoautla de Espinosa 29140, Mexico.

Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City 14080, Mexico.

出版信息

Int J Mol Sci. 2023 Jun 16;24(12):10220. doi: 10.3390/ijms241210220.

DOI:10.3390/ijms241210220
PMID:37373365
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10299175/
Abstract

Pain is a complex experience that involves physical, emotional, and cognitive aspects. This review focuses specifically on the physiological processes underlying pain perception, with a particular emphasis on the various types of sensory neurons involved in transmitting pain signals to the central nervous system. Recent advances in techniques like optogenetics and chemogenetics have allowed researchers to selectively activate or inactivate specific neuronal circuits, offering a promising avenue for developing more effective pain management strategies. The article delves into the molecular targets of different types of sensory fibers such as channels, for example, TRPV1 in C-peptidergic fiber, TRPA1 in C-non-peptidergic receptors expressed differentially as MOR and DOR, and transcription factors, and their colocalization with the vesicular transporter of glutamate, which enable researchers to identify specific subtypes of neurons within the pain pathway and allows for selective transfection and expression of opsins to modulate their activity.

摘要

疼痛是一种复杂的体验,涉及身体、情感和认知方面。本篇综述特别关注疼痛感知的生理过程,特别强调了将疼痛信号传递到中枢神经系统的各种类型的感觉神经元。像光遗传学和化学遗传学这样的技术的最新进展使得研究人员能够选择性地激活或失活特定的神经元回路,为开发更有效的疼痛管理策略提供了有希望的途径。这篇文章深入探讨了不同类型的感觉纤维(例如,C 肽纤维中的 TRPV1、C-非肽能受体中的 TRPA1,它们在 MOR 和 DOR 中表达不同)的分子靶点,以及转录因子,及其与谷氨酸囊泡转运体的共定位,这使得研究人员能够在疼痛途径中识别特定的神经元亚型,并允许选择性地转染和表达光感受器来调节它们的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4399/10299175/2d1e08decea2/ijms-24-10220-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4399/10299175/7e7d94dae555/ijms-24-10220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4399/10299175/2d1e08decea2/ijms-24-10220-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4399/10299175/7e7d94dae555/ijms-24-10220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4399/10299175/2d1e08decea2/ijms-24-10220-g002.jpg

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Nat Biotechnol. 2021 Feb;39(2):179-185. doi: 10.1038/s41587-020-0673-2. Epub 2020 Sep 21.
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TRP Channels Role in Pain Associated With Neurodegenerative Diseases.瞬时受体电位通道在神经退行性疾病相关疼痛中的作用。
Front Neurosci. 2020 Aug 4;14:782. doi: 10.3389/fnins.2020.00782. eCollection 2020.
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The revised International Association for the Study of Pain definition of pain: concepts, challenges, and compromises.
修订后的国际疼痛研究协会疼痛定义:概念、挑战和妥协。
Pain. 2020 Sep 1;161(9):1976-1982. doi: 10.1097/j.pain.0000000000001939.
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Different neuronal populations mediate inflammatory pain analgesia by exogenous and endogenous opioids.不同的神经元群体通过外源性和内源性阿片类药物介导炎症性疼痛的镇痛作用。
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Functional Anatomy of the Sensory Nervous System: Updates From the Neuroscience Bench.感觉神经系统的功能解剖学:神经科学研究的最新进展。
Toxicol Pathol. 2020 Jan;48(1):174-189. doi: 10.1177/0192623319869011. Epub 2019 Sep 25.
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