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水母蜇伤机制与治疗策略的进展

Advances in Jellyfish Sting Mechanisms and Treatment Strategies.

作者信息

Li Bingbing, Li Yueyue, Qiu Zhiwen, Zhang Chuantao, Li Yue, Li Wei, Yang Jishun

机构信息

Naval Medical Center of PLA, Naval Medical University, Shanghai 200052, China.

Shanghai Key Laboratory of Nautical Medicine and Translation of Drugs and Medical Devices, Shanghai 200433, China.

出版信息

Mar Drugs. 2025 May 28;23(6):231. doi: 10.3390/md23060231.

DOI:10.3390/md23060231
PMID:40559640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12194369/
Abstract

Jellyfish stings, as one of the most prevalent forms of marine injury, have increasingly become a subject of concern. Despite their simple morphology and structure, jellyfish possess a complex venom composition that can inflict varying degrees of damage on multiple human physiological systems. Consequently, the clinical symptoms associated with jellyfish stings are highly intricate. Although antivenoms have been developed for certain jellyfish species (e.g., ), specific antivenoms targeting the mechanisms of most jellyfish venoms remain understudied. To effectively prevent, treat, and cure jellyfish stings, we adhere to the principle of knowing their nature and their reasons. It is essential to investigate the emission mechanism of jellyfish nematocysts and the composition of their venom. Understanding these factors is crucial for the development of targeted treatment strategies. This review delves into the venom emission mechanism of jellyfish stinging cells, the symptoms resulting from jellyfish stings, and the comprehensive treatment strategies post-sting. It offers a scientific reference for comprehending jellyfish stings and establishes a theoretical foundation for subsequent research endeavors.

摘要

水母蜇伤作为海洋伤害最常见的形式之一,日益受到关注。尽管水母形态结构简单,但其毒液成分复杂,可对人体多个生理系统造成不同程度损伤。因此,水母蜇伤相关的临床症状非常复杂。虽然已针对某些水母种类研发出抗蛇毒血清(例如),但针对大多数水母毒液作用机制的特效抗蛇毒血清仍研究不足。为有效预防、治疗和治愈水母蜇伤,我们秉持知其然并知其所以然的原则。研究水母刺丝囊的发射机制及其毒液成分至关重要。了解这些因素对于制定针对性治疗策略至关重要。本综述深入探讨了水母刺细胞的毒液发射机制、水母蜇伤导致的症状以及蜇伤后的综合治疗策略。它为理解水母蜇伤提供了科学参考,并为后续研究奠定了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cce/12194369/30c9dbf8da76/marinedrugs-23-00231-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cce/12194369/21d52e240b4a/marinedrugs-23-00231-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cce/12194369/a933dff71c61/marinedrugs-23-00231-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cce/12194369/76f3b4b59a94/marinedrugs-23-00231-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cce/12194369/30c9dbf8da76/marinedrugs-23-00231-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cce/12194369/21d52e240b4a/marinedrugs-23-00231-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cce/12194369/a933dff71c61/marinedrugs-23-00231-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cce/12194369/76f3b4b59a94/marinedrugs-23-00231-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cce/12194369/30c9dbf8da76/marinedrugs-23-00231-g003.jpg

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Jellyfish Venom Peptides Targeting Human Potassium Channels Identified through Ligand Screening: Morphometric and Molecular Identification of the Species and Antibiotic Potential.通过配体筛选鉴定的靶向人钾通道的水母毒液肽:物种的形态计量学和分子鉴定及抗生素潜力。
Mar Drugs. 2024 Jul 24;22(8):333. doi: 10.3390/md22080333.
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Exploring the Efficacy of Hydroxybenzoic Acid Derivatives in Mitigating Jellyfish Toxin-Induced Skin Damage: Insights into Protective and Reparative Mechanisms.
探讨羟基苯甲酸衍生物在减轻水母毒素引起的皮肤损伤中的功效:对保护和修复机制的深入了解。
Mar Drugs. 2024 Apr 29;22(5):205. doi: 10.3390/md22050205.
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Troxerutin suppress inflammation response and oxidative stress in jellyfish dermatitis by activating Nrf2/HO-1 signaling pathway.曲克芦丁通过激活 Nrf2/HO-1 信号通路抑制海蜇皮炎的炎症反应和氧化应激。
Front Immunol. 2024 May 8;15:1369849. doi: 10.3389/fimmu.2024.1369849. eCollection 2024.
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Insights into the discovery and intervention of metalloproteinase in marine hazardous jellyfish.海洋有毒水母中金属蛋白酶的发现与干预研究进展。
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Toxin metalloproteinases exert a dominant influence on pro-inflammatory response and anti-inflammatory regulation in jellyfish sting dermatitis.毒素金属蛋白酶在水母蜇伤性皮炎的促炎反应和抗炎调节中发挥主导作用。
J Proteomics. 2024 Feb 10;292:105048. doi: 10.1016/j.jprot.2023.105048. Epub 2023 Nov 21.
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RMD Open. 2023 Nov;9(4). doi: 10.1136/rmdopen-2023-003569.
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