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  • 屈啸声,钟桃珍,樊兰兰,夏祥华,李刚,陈莹.北部湾金黄水母Chrysaora helvola Brandt刺细胞毒液溶血活性[J].广西科学,2016,23(1):79-85.    [点击复制]
  • QU Xiaosheng,ZHONG Taozhen,FAN Lanlan,XIA Xianghua,LI Gang,CHEN Ying.An in vitro Study on the Erythrocytes Hemolytic Activity of the Nematocysts Venom from Chrysaora helvola Brandt[J].Guangxi Sciences,2016,23(1):79-85.   [点击复制]
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北部湾金黄水母Chrysaora helvola Brandt刺细胞毒液溶血活性
屈啸声1, 钟桃珍1, 樊兰兰1, 夏祥华1, 李刚1, 陈莹2
0
(1.广西药用植物园, 西南濒危药材资源开发国家工程实验室, 广西南宁 530023;2.百洋水产集团股份有限公司, 广西南宁 530004)
摘要:
[目的]探讨金黄水母Chrysaora helvola Brandt刺细胞毒液(nematocysts venom,NV)的红细胞溶血活性特征及可能机制。[方法]通过分光光度法测定红细胞溶解释放血红蛋白的量来确认不同条件和药物对NV诱导红细胞溶血行为的影响。[结果]NV诱导的红细胞溶血与其总蛋白浓度存在依赖关系。溶液pH值、大分子非电解质渗透压保护剂PEGs均能显著影响其溶血活性;非电解质小分子糖类渗透压保护剂D-甘油和D-半乳糖对溶血活性影响很小,但D-葡萄糖能显著延缓溶血。NV同时具有Ca2+依赖的弱磷酸酯酶A2(PLA2)活性,且受组氨酸烷基化试剂p-BPB抑制。这一PLA2活性可能对其红细胞溶血活性也有贡献。[结论]NV的红细胞溶血活性可能由膜穿孔机制和所含PLA2酶成分造成,并受到含葡萄糖单元结构的糖受体调节。
关键词:  红细胞  溶血  刺细胞毒液  磷酸酯酶A2  金黄水母
DOI:10.13656/j.cnki.gxkx.20160315.007
投稿时间:2015-10-16
基金项目:广西科技攻关计划项目(桂科攻11107011-3,1222015-3A)资助。
An in vitro Study on the Erythrocytes Hemolytic Activity of the Nematocysts Venom from Chrysaora helvola Brandt
QU Xiaosheng1, ZHONG Taozhen1, FAN Lanlan1, XIA Xianghua1, LI Gang1, CHEN Ying2
(1.National Engineering Institute for the Research and Development of Endangered Medicinal Resources in Southwest China, Guangxi Medicinal Plant Garden, Nanning, Guangxi, 530023, China;2.Baiyang Aquatic Products Group Limited Company, Nanning, Guangxi, 530004, China)
Abstract:
[Objective] The characterization and possible mechanisms of the erythrocytes hemolysis induced by nematocysts venom from the Chrysaora helvola Brandt jellyfish were discussed.[Methods] The hemoglobin content released from hemolysis was calorimetrically determined in the presence of NV only or NV and other reagents.[Results] A concentration-dependent hemolytic effect of the NV was revealed.The solution pH as well as non-electrolytic osmotic protectants with high molecular weight, such as PEGs, can significantly affect the hemolysis induced by the NV.Non-electrolytic osmotic protectants, D-glycerol and D-galactose, have no sig-nificant effect on the hemolysis, while D-glucose can effectively retard it.Weak enzymatic activity of phospholipase A2 was also detected in the NV.This PLA2 activity is Ca2+-needed and can be inhibited by the alkylating reagent p-BPB.Inhibition of the PLA2 enzymatic activity can partially inhibit the hemolysis induced by the NV.[Conclusion] The hemolysis induced by NV from C.helvolais possibly caused by the membrane pore-forming mechanism and its PLA2 ingredient, and mediated by glucose-containing receptors.
Key words:  erythrocyte  hemolysis  nematocysts venom  PLA2  Chrysaora helvola Brandt

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