释放 RNA 干扰:小干扰 RNA (siRNA) 疗法治疗神经病理性疼痛的当前前景。

IF 4.9 Q1 CHEMISTRY, MEDICINAL ACS Pharmacology and Translational Science Pub Date : 2024-09-23 eCollection Date: 2024-10-11 DOI:10.1021/acsptsci.4c00329
Priya Saha, Shyam S Sharma
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引用次数: 0

摘要

神经性疼痛(NP)是一种使人衰弱的疼痛表型,会导致中枢和周围神经系统逐渐退化。神经病理性疼痛通常伴有痛觉减退、异痛症、麻痹、刺痛和灼烧感,导致患者残疾、运动功能障碍和心理状态受损。由于疗效有限、副作用大、病理生理学复杂,大多数传统药物都无法改善疼痛的破坏性状况。随着新发 NP 病例的迅速增加,有必要开展进一步研究,以确定治疗 NP 的潜在新型疗法。最近,小干扰 RNA(siRNA)方法在包括 NP 在内的许多疾病中显示出了治疗潜力。siRNAs 的递送可潜在地、选择性地下调目标 mRNA,并消除疼痛相关行为/病理生理疼痛反应。考虑到 siRNA 疗法可控制与 NP 相关的所有通路,人们讨论了 siRNA 在治疗 NP 中的关键作用。然而,siRNA 的治疗应用受到一些障碍的限制,如由于其负电荷和膜不渗透性导致其在全身循环中的不稳定性、脱靶效应、免疫原性以及无法到达预期的作用位点等。本综述还强调了克服这些障碍的几种策略和技术,以便将这些治疗性 siRNA 从实验室转化为临床应用,为获得治疗 NP 的潜在治疗方法开辟一条新途径。
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RNA Interference Unleashed: Current Perspective of Small Interfering RNA (siRNA) Therapeutics in the Treatment of Neuropathic Pain.

Neuropathic pain (NP) is one of the debilitating pain phenotypes that leads to the progressive degeneration of the central as well as peripheral nervous system. NP is often associated with hyperalgesia, allodynia, paresthesia, tingling, and burning sensations leading to disability, motor dysfunction, and compromised psychological state of the patients. Most of the conventional pharmacological agents are unable to improve the devastating conditions of pain because of their limited efficacy, undesirable side effects, and multifaceted pathophysiology of the diseased condition. A rapid rise in new cases of NP warrants further research for identifying the potential novel therapeutic modalities for treating NP. Recently, small interfering RNA (siRNA) approach has shown therapeutic potential in many disease conditions including NP. Delivery of siRNAs led to potential and selective downregulation of target mRNA and abolished the pain-related behaviors/pathophysiological pain response. The crucial role of siRNA in the treatment of NP by considering all of the pathways associated with NP that could be managed by siRNA therapeutics has been discussed. However, their therapeutic use is limited by several hurdles such as instability in systemic circulation due to their negative charge and membrane impermeability, off-target effects, immunogenicity, and inability to reach the intended site of action. This review also emphasizes several strategies and techniques to overcome these hurdles for translating these therapeutic siRNAs from bench to bedside by opening a new avenue for obtaining a potential therapeutic approach for treating NP.

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ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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