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再生神经的靶受体:神经瘤形成及当前治疗选择

Target Receptors of Regenerating Nerves: Neuroma Formation and Current Treatment Options.

作者信息

Shamoun Feras, Shamoun Valentina, Akhavan Arya, Tuffaha Sami H

机构信息

Peripheral Nerve Lab, Department of Plastic and Reconstructive Surgery, Johns Hopkins Hospital, Johns Hopkins University, Baltimore, MD, United States.

Department of Biological Sciences, University of Toronto at Scarborough, Scarborough, ON, Canada.

出版信息

Front Mol Neurosci. 2022 Jul 5;15:859221. doi: 10.3389/fnmol.2022.859221. eCollection 2022.

Abstract

Neuromas form as a result of disorganized sensory axonal regeneration following nerve injury. Painful neuromas lead to poor quality of life for patients and place a burden on healthcare systems. Modern surgical interventions for neuromas entail guided regeneration of sensory nerve fibers into muscle tissue leading to muscle innervation and neuroma treatment or prevention. However, it is unclear how innervating denervated muscle targets prevents painful neuroma formation, as little is known about the fate of sensory fibers, and more specifically pain fiber, as they regenerate into muscle. Golgi tendon organs and muscle spindles have been proposed as possible receptor targets for the regenerating sensory fibers; however, these receptors are not typically innervated by pain fibers, as these free nerve endings do not synapse on receptors. The mechanisms by which pain fibers are signaled to cease regeneration therefore remain unknown. In this article, we review the physiology underlying nerve regeneration, the guiding molecular signals, and the target receptor specificity of regenerating sensory axons as it pertains to the development and prevention of painful neuroma formation while highlighting gaps in literature. We discuss management options for painful neuromas and the current supporting evidence for the various interventions.

摘要

神经瘤是神经损伤后感觉轴突再生紊乱的结果。疼痛性神经瘤会导致患者生活质量下降,并给医疗系统带来负担。现代针对神经瘤的外科干预措施包括引导感觉神经纤维向肌肉组织再生,从而实现肌肉神经支配以及神经瘤的治疗或预防。然而,目前尚不清楚支配失神经肌肉靶点如何预防疼痛性神经瘤的形成,因为对于感觉纤维,尤其是疼痛纤维在向肌肉再生时的命运了解甚少。高尔基腱器官和肌梭被认为是再生感觉纤维可能的受体靶点;然而,这些受体通常不由疼痛纤维支配,因为这些游离神经末梢不会与受体形成突触。因此,疼痛纤维被信号通知停止再生的机制仍然未知。在本文中,我们回顾了神经再生的生理学基础、引导分子信号以及再生感觉轴突的靶受体特异性,这些与疼痛性神经瘤形成的发展和预防相关,同时突出文献中的空白。我们讨论了疼痛性神经瘤的管理选项以及各种干预措施目前的支持证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a3/9295905/d1bf9c58e672/fnmol-15-859221-g001.jpg

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