Phytochemical-based therapeutics from traditional eastern medicine: analgesic effects and ion channel modulation.

IF 2.5 Q2 CLINICAL NEUROLOGY
Frontiers in pain research (Lausanne, Switzerland) Pub Date : 2025-01-31 eCollection Date: 2025-01-01 DOI:10.3389/fpain.2025.1537154
Sung Eun Kim, Geehoon Chung, Sun Kwang Kim
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引用次数: 0

Abstract

Pain management remains a major challenge in the healthcare system. While synthetic analgesics are widely used for pain management, their effectiveness in managing chronic pain is often limited due to low efficacy or side effects. Thus, there is growing interest in exploring alternative pain relief methods, particularly using medicinal plants from traditional Eastern medicine and their phytochemicals. Previous studies have demonstrated the modulatory effects of various phytochemicals derived from herbal medicine on pain-related ion channels, such as voltage-gated sodium channels (Nav), calcium channels (Ca2+), and transient receptor potential (TRP) channels. Since these ion channels are integral to the transmission and modulation of pain signals, the ability of specific phytochemicals to activate or inhibit these channels presents a promising avenue for the development of novel analgesics. The goal of this review is to merge herbal insights with ion channel research to highlight the potential of natural compounds for safe and effective pain management. In this regard, we summarize the discovery and characterization of pain-relieving phytochemicals from herbal medicine, and we discuss their mechanisms of action and their potential to mimic or enhance the effects of conventional analgesics through ion channel modulation.

传统东方医学植物化学疗法:镇痛作用和离子通道调节。
疼痛管理仍然是医疗保健系统的一个主要挑战。虽然合成镇痛药广泛用于疼痛管理,但由于低疗效或副作用,其在慢性疼痛管理中的有效性往往受到限制。因此,人们对探索替代疼痛缓解方法的兴趣日益浓厚,特别是利用传统东方医学中的药用植物及其植物化学物质。先前的研究已经证明了草药衍生的各种植物化学物质对疼痛相关离子通道的调节作用,如电压门控钠通道(Nav)、钙通道(Ca2+)和瞬态受体电位(TRP)通道。由于这些离子通道对疼痛信号的传递和调节是不可或缺的,特定植物化学物质激活或抑制这些通道的能力为开发新型镇痛药提供了一个有希望的途径。本综述的目的是将草药见解与离子通道研究相结合,以突出天然化合物在安全有效的疼痛管理方面的潜力。在这方面,我们总结了从草药中发现的缓解疼痛的植物化学物质的特征,并讨论了它们的作用机制以及它们通过离子通道调节模仿或增强传统镇痛药作用的潜力。
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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来源期刊
CiteScore
2.10
自引率
0.00%
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0
审稿时长
13 weeks
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