糖尿病周围神经病变:病理生理学和高浓度外用辣椒素作用机制的新见解。

Q2 Medicine
Journal of Experimental Pharmacology Pub Date : 2025-09-09 eCollection Date: 2025-01-01 DOI:10.2147/JEP.S526968
David G Armstrong, Keith Bley, David M Simpson, Peter Staats, Samuel Allen, Audrey Carnevale, Lizandra Marcondes
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引用次数: 0

摘要

糖尿病周围神经病变(DPN)是一种慢性进行性糖尿病并发症。DPN的疼痛是严重的,对患者的生活质量有害。在这篇综述中,我们提供了高浓度辣椒素局部系统(HCCTS)治疗疼痛性DPN的作用机制(MOA)的最新进展,重点是神经再生。在糖尿病中,高血糖和其他代谢失衡导致氧化应激和炎症,从而导致外周神经系统传入神经元轴突(特别是C和Aδ纤维)的变性。支持神经的微血管功能障碍进一步加剧了神经损伤。结果,表皮神经纤维密度(ENFD)减少,剩余的传入纤维发生物理和化学变化,使它们对疼痛刺激过敏,对正常刺激不敏感。由于最长的轴突通常首先受损,DPN通常从脚开始,然后是腿,最后是手。HCCTS采用基质技术,将高浓度辣椒素(一种TRPV1激动剂)强行扩散到真皮和表皮,靶向在DPN中上调并在疼痛产生中起关键作用的TRPV1受体。HCCTS激活神经元细胞膜和内质网上表达的TRPV1受体,导致细胞质钙离子过载,然后一系列细胞事件导致这些传入末端可逆的神经溶解。1-3个月后,末梢以“更健康”的表型再生,增加ENFD,导致血管舒张,这可能导致有利于改善神经再生的微环境。临床证据表明,与基线相比,重复HCCTS治疗在疼痛和足部感觉功能改善方面提供了累积益处,这一MOA得到了支持。如果对感觉功能的影响在大规模临床研究中得到证实,HCCTS可能有助于减缓DPN向更严重形式的糖尿病足综合征的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Diabetic Peripheral Neuropathy: Pathophysiology and New Insights into the Mechanism of Action of High-Concentration Topical Capsaicin.

Diabetic Peripheral Neuropathy: Pathophysiology and New Insights into the Mechanism of Action of High-Concentration Topical Capsaicin.

Diabetic Peripheral Neuropathy: Pathophysiology and New Insights into the Mechanism of Action of High-Concentration Topical Capsaicin.

Diabetic Peripheral Neuropathy: Pathophysiology and New Insights into the Mechanism of Action of High-Concentration Topical Capsaicin.

Diabetic peripheral neuropathy (DPN) is a chronic, progressive complication of diabetes. Pain in DPN can be severe and detrimental to the patient's quality of life. In this review, we provide an update on the mechanism of action (MOA) of high-concentration capsaicin topical system (HCCTS) for treatment of painful DPN, with an emphasis on neuroregeneration. In diabetes, hyperglycemia and other metabolic imbalances lead to oxidative stress and inflammation, which result in degeneration of the axons of afferent neurons (particularly C and Aδ fibers) within the peripheral nervous system. Dysfunction of the microvasculature supporting the nerves further exacerbates neural damage. As a result, epidermal nerve fiber density (ENFD) diminishes, and physical and chemical changes to the remaining afferent fibers render them hypersensitive to painful stimuli and hyposensitive to normal stimuli. As the longest axons are usually damaged first, DPN normally begins in the feet, then legs, and finally the hands. HCCTS incorporates a matrix technology that forcibly diffuses a high concentration of capsaicin (a TRPV1 agonist) to the dermis and epidermis, targeting TRPV1 receptors that are upregulated in DPN and play a key role in pain generation. HCCTS activates TRPV1 receptors expressed on the neuron cell membrane and endoplasmic reticulum, leading to cytoplasmic calcium ion overload, and then a cascade of cellular events resulting in reversible neurolysis of these afferent terminals. After 1-3 months, the terminals regenerate with a "healthier" phenotype, increasing ENFD, resulting in vasodilation, which may lead to a microenvironment conducive to improved neuroregeneration. This MOA is supported by clinical evidence demonstrating that repeated HCCTS treatment provides cumulative benefits in pain and improvements in sensory function of the feet compared with baseline. If effects on sensory function are confirmed in large-scale clinical studies, HCCTS could help slow the progression of DPN to more severe forms of diabetic foot syndrome.

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来源期刊
Journal of Experimental Pharmacology
Journal of Experimental Pharmacology Medicine-Pharmacology (medical)
CiteScore
7.40
自引率
0.00%
发文量
43
审稿时长
16 weeks
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