CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China; Laboratory for Marine Drugs and Bioproducts, Pilot National Laboratory for Marine Science and Technology (Qingdao), No. 1 Wenhai Road, Qingdao 266237, China; University of Chinese Academy of Sciences, Beijing 100049, China.
CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China; Laboratory for Marine Drugs and Bioproducts, Pilot National Laboratory for Marine Science and Technology (Qingdao), No. 1 Wenhai Road, Qingdao 266237, China.
Biomed Pharmacother. 2022 Jul;151:113192. doi: 10.1016/j.biopha.2022.113192. Epub 2022 May 26.
Jellyfish envenomation is a common medical problem in many countries. However, the myotoxicity and effector molecules of scyphozoan venoms remain uninvestigated. Here, we present the myotoxicity of nematocyst venom from Nemopilema nomurai (NnNV), a giant venomous scyphozoan from China, for the first time, using in vivo models with inhibitors. NnNV was able to induce remarkable myotoxicity including significant muscle swelling, increasing the content of CK and LDH in serum, stimulating inflammation of muscle tissue, and destroying the structure of muscle tissue. In addition, the metalloproteinase inhibitors BMT and EDTA significantly reduced the myotoxicity induced by NnNV. Moreover, BMT and EDTA could decrease the inflammatory stimulation and necrosis of muscle tissue caused by the venom. These observations suggest that the metalloproteinase components of NnNV make a considerable contribution to myotoxicity. This study contributes to understanding the effector molecules of muscle injury caused by jellyfish stings and suggests a new idea for the treatment of scyphozoan envenomation.
水母蜇伤是许多国家常见的医学问题。然而,目前仍未研究过曳手水母目毒液的肌毒性和效应分子。在这里,我们首次使用抑制剂在体内模型中展示了来自中国巨型有毒曳手水母 Nemopilema nomurai(NnNV)的刺丝囊毒液的肌毒性。NnNV 能够引起显著的肌毒性,包括显著的肌肉肿胀、血清中 CK 和 LDH 含量增加、刺激肌肉组织炎症以及破坏肌肉组织结构。此外,金属蛋白酶抑制剂 BMT 和 EDTA 显著降低了 NnNV 诱导的肌毒性。此外,BMT 和 EDTA 可以减少毒液引起的肌肉组织炎症刺激和坏死。这些观察结果表明,NnNV 的金属蛋白酶成分对肌毒性有很大的贡献。本研究有助于了解水母蜇伤引起的肌肉损伤的效应分子,并为治疗曳手水母目蜇伤提供了新的思路。