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基于微小RNA的背根神经节慢性神经性疼痛治疗递送系统

MicroRNA-Based Delivery Systems for Chronic Neuropathic Pain Treatment in Dorsal Root Ganglion.

作者信息

Jackson Stefan, Gigliobianco Maria Rosa, Casadidio Cristina, Di Martino Piera, Censi Roberta

机构信息

ChIP Chemistry Interdisciplinary Project Research Centre, School of Pharmacy, University of Camerino, Via Madonna delle Carceri, 62032 Camerino, MC, Italy.

Department of Pharmacy, "G. D'Annunzio" of Chieti and Pescara University, Via dei Vestini 1, 66100 Chieti, CH, Italy.

出版信息

Pharmaceutics. 2025 Jul 18;17(7):930. doi: 10.3390/pharmaceutics17070930.

Abstract

Neuropathic pain is a significant global clinical issue that poses substantial challenges to both public health and the economy due to its complex underlying mechanisms. It has emerged as a serious health concern worldwide. Recent studies involving dorsal root ganglion (DRG) stimulation have provided strong evidence supporting its effectiveness in alleviating chronic pain and its potential for sustaining long-term pain relief. In addition to that, there has been ongoing research with clinical evidence relating to the role of small non-coding ribonucleic acids known as microRNAs in regulating gene expressions affecting pain signals. The signal pathway involves alterations in neuronal excitation, synaptic transmission, dysregulated signaling, and subsequent pro-inflammatory response activation and pain development. When microRNAs are dysregulated in the dorsal root ganglia neurons, they polarize macrophages from anti-inflammatory M2 to inflammatory M1 macrophages causing pain signal generation. By reversing this polarization, a therapeutic activity can be induced. However, the direct delivery of these nucleotides has been challenging due to limitations such as rapid clearance, degradation, and reduction in half-life. Therefore, safe and efficient carrier vehicles are fundamental for microRNA delivery. Here, we present a comprehensive analysis of miRNA-based nano-systems for chronic neuropathic pain, focusing on their impact in dorsal root ganglia. This review provides a critical evaluation of various delivery platforms, including viral, polymeric, lipid-based, and inorganic nanocarriers, emphasizing their therapeutic potential as well as their limitations in the treatment of chronic neuropathic pain. Innovative strategies such as hybrid nanocarriers and stimulus-responsive systems are also proposed to enhance the prospects for clinical translation. Serving as a roadmap for future research, this review aims to guide the development and optimization of miRNA-based therapies for effective and sustained neuropathic pain management.

摘要

神经性疼痛是一个重大的全球性临床问题,由于其复杂的潜在机制,对公共卫生和经济都构成了重大挑战。它已成为全球范围内严重的健康问题。最近涉及背根神经节(DRG)刺激的研究提供了强有力的证据,支持其在缓解慢性疼痛方面的有效性以及维持长期疼痛缓解的潜力。除此之外,关于被称为微小RNA的小非编码核糖核酸在调节影响疼痛信号的基因表达中的作用,也有持续的临床证据研究。信号通路涉及神经元兴奋性改变、突触传递、信号失调,以及随后的促炎反应激活和疼痛发展。当背根神经节神经元中的微小RNA失调时,它们会将巨噬细胞从抗炎的M2型极化到促炎的M1型巨噬细胞,从而导致疼痛信号产生。通过逆转这种极化,可以诱导治疗活性。然而,由于快速清除、降解和半衰期缩短等限制,这些核苷酸的直接递送一直具有挑战性。因此,安全有效的载体对于微小RNA的递送至关重要。在这里,我们对用于慢性神经性疼痛的基于微小RNA的纳米系统进行了全面分析,重点关注它们在背根神经节中的影响。本综述对各种递送平台进行了批判性评估,包括病毒、聚合物、脂质基和无机纳米载体,强调了它们在治疗慢性神经性疼痛方面的治疗潜力以及局限性。还提出了诸如混合纳米载体和刺激响应系统等创新策略,以提高临床转化的前景。作为未来研究的路线图,本综述旨在指导基于微小RNA的疗法的开发和优化,以实现有效和持续的神经性疼痛管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8f5/12299933/0299ab32ec0f/pharmaceutics-17-00930-g001.jpg

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