Therapeutic Potential of Scolopendra subspinipes: A Comprehensive Scoping Review of Its Bioactive Compounds, Preclinical Pharmacology, and Clinical Applications.

IF 3.9 3区 医学 Q2 FOOD SCIENCE & TECHNOLOGY
Toxins Pub Date : 2025-05-05 DOI:10.3390/toxins17050229
Ye-Seul Lee, Yoon Jae Lee, In-Hyuk Ha
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引用次数: 0

Abstract

Scolopendra subspinipes, commonly known as the Chinese red-headed centipede, has been utilized in traditional East Asian medicine for centuries to treat conditions such as chronic pain, inflammation, convulsions, and infections. Recent pharmacological investigations have uncovered a wide array of bioactive molecules-including peptides, alkaloids, and polysaccharide-protein complexes-from both venom and whole-body extracts. This review synthesizes findings from 45 in vitro, in vivo, and clinical studies investigating the pharmacological effects of venom-derived and whole-body-derived compounds from S. subspinipes across multiple domains, including analgesic, anti-inflammatory, antimicrobial, antifungal, antioxidant, antitumor, antithrombotic, anti-fibrotic, and neuroprotective activities, along with a brief scoping review of clinical practice guidelines. Key venom-derived compounds such as the peptide SsmTX-I, immunomodulatory antimicrobial peptide scolopendrasin IX, and antitumor peptide scolopentide exhibit strong mechanistic rationale and preclinical efficacy, positioning them as lead candidates for clinical development. Compounds derived from whole-body extracts, including alkaloids and polysaccharide-protein complexes, also demonstrate promising therapeutic potential. Mechanistic studies suggest these compounds operate via distinct pathways-such as ion-channel inhibition, NF-κB suppression, and apoptosis induction-offering potential advantages over existing therapies. However, current evidence remains primarily preclinical, and challenges such as extract variability, immunogenicity, and lack of standardized dosing must be addressed. Future research should prioritize isolation and structural optimization of key peptides, standardized formulation development, toxicological profiling, and early-phase human trials. The integration of traditional knowledge and modern pharmacological insights underscores the potential of venom- and whole-body-derived S. subspinipes agents to enrich the drug discovery, particularly for conditions with unmet therapeutic needs.

亚棘蜈蚣的治疗潜力:其生物活性化合物,临床前药理学和临床应用的综合范围综述。
亚棘蜈蚣,俗称中国红头蜈蚣,几个世纪以来一直在东亚传统医学中用于治疗慢性疼痛、炎症、抽搐和感染等疾病。最近的药理学研究已经从毒液和全身提取物中发现了一系列广泛的生物活性分子,包括多肽、生物碱和多糖-蛋白质复合物。本综述综合了45项体外、体内和临床研究的发现,这些研究调查了刺棘蛇毒液衍生和全身衍生化合物在多个领域的药理作用,包括镇痛、抗炎、抗菌、抗真菌、抗氧化、抗肿瘤、抗血栓形成、抗纤维化和神经保护活性,并简要回顾了临床实践指南的范围。关键的毒液衍生化合物,如肽SsmTX-I、免疫调节抗菌肽scolopdrasin IX和抗肿瘤肽scolopentide,表现出强大的机制基础和临床前疗效,使其成为临床开发的主要候选物质。从全身提取物中提取的化合物,包括生物碱和多糖-蛋白质复合物,也显示出有希望的治疗潜力。机制研究表明,这些化合物通过不同的途径起作用,如离子通道抑制、NF-κB抑制和细胞凋亡诱导,比现有的治疗方法具有潜在的优势。然而,目前的证据仍然主要是临床前的,并且必须解决诸如提取物可变性、免疫原性和缺乏标准化剂量等挑战。未来的研究应优先考虑关键肽的分离和结构优化、标准化配方开发、毒理学分析和早期人体试验。传统知识和现代药理学见解的整合强调了蛇毒和全身衍生的刺棘蛇制剂丰富药物发现的潜力,特别是对于未满足治疗需求的条件。
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
Toxins
Toxins TOXICOLOGY-
CiteScore
7.50
自引率
16.70%
发文量
765
审稿时长
16.24 days
期刊介绍: Toxins (ISSN 2072-6651) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to toxins and toxinology. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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