Roadmap update: Sensory neurodegeneration in diabetes.

International review of neurobiology Pub Date : 2026-01-01 Epub Date: 2026-09-04 DOI:10.1016/bs.irn.2026.08.018
Douglas W Zochodne, Maskaki Kobayashi, Prashanth Komirishetty, Aparna Areti
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引用次数: 0

Abstract

Human diabetic polyneuropathy (DPN) is a pervasive disabling complication of both types 1 and 2 diabetes mellitus (DM). Here we build on our previous report in this journal, addressing the direct targeting of sensory neurons and the subsequent withdrawal of their distal axon terminals. Specific, albeit largely untested, translational therapeutic approaches are available to 'shore up' the sensory neuron and enable it to regrow its branches. This review provides updated information over several selected pathways our research team has been focused on. We review the evidence for sensory neuron targeting in DM including new human work, specific molecules within neuron perikarya (cell bodies) that foster sensory regeneration and newer ideas on how local nonsystemic targeting of growth cones might also promote regrowth. Our update presupposes important connections between the molecular machinery that supports intact neurons and the capacity of neurons to regrow, reversing DPN deficits. This review is limited in scope but may be a template to investigate the wide repertoire of proteins and noncoding RNAs that might be employed to eventually treat and reverse DPN.

路线图更新:糖尿病的感觉神经变性。
人类糖尿病多发神经病变(DPN)是1型和2型糖尿病(DM)的普遍致残并发症。在这里,我们建立在我们之前的报告在这个杂志上,解决直接靶向感觉神经元和随后撤回其远端轴突终端。具体的,尽管在很大程度上未经测试,转化治疗方法可以“支撑”感觉神经元并使其分支再生。这篇综述提供了我们研究小组所关注的几种途径的最新信息。我们回顾了糖尿病中感觉神经元靶向的证据,包括新的人类工作,神经元核周(细胞体)内促进感觉再生的特定分子,以及关于生长锥的局部非系统性靶向如何促进再生的新想法。我们的更新假设了支持完整神经元的分子机制与神经元再生能力之间的重要联系,从而逆转DPN缺陷。这篇综述的范围有限,但可能是研究广泛的蛋白质和非编码rna的模板,这些蛋白质和非编码rna可能最终用于治疗和逆转DPN。
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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