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伊鲁坎吉水母(Carukia barnesi)刺丝囊毒液和触手提取物对大鼠的体内心血管影响。

The in vivo cardiovascular effects of the Irukandji jellyfish (Carukia barnesi) nematocyst venom and a tentacle extract in rats.

作者信息

Ramasamy Sharmaine, Isbister Geoffrey K, Seymour Jamie E, Hodgson Wayne C

机构信息

Department of Pharmacology, Monash University, Vic. 3800, Australia.

出版信息

Toxicol Lett. 2005 Jan 15;155(1):135-41. doi: 10.1016/j.toxlet.2004.09.004.

Abstract

Envenoming by Carukia barnesi may produce life-threatening Irukandji syndrome. There is little published on the activity of C. barnesi venom. This is the first study to investigate the in vivo cardiovascular effects of C. barnesi venom and a tentacle extract (devoid of nematocysts). Venom (50 microg/kg or 100 microg/kg, i.v.) produced a pressor response (42+/-3 and 44+/-6 mmHg, respectively; n=4) and increase in heart rate (31+/-5 and 13+/-2 bpm, respectively; n = 4) in anaesthetised rats. These changes were not dose-dependent and were followed by cardiovascular collapse in one of four rats receiving 50 microg/kg and three of four animals receiving 100 microg/kg. Prazosin (50 microg/kg, i.v.) significantly attenuated the venom (50 microg/kg, i.v.)-induced pressor response (-8+/-3 mmHg; P < 0.05; n = 4) and tachycardia (-9+/-4 bpm; P < 0.05; n = 4). Tentacle extract (100 microg/kg; i.v.) produced a pressor response (51+/-12 mmHg; n = 3) and an increase in heart rate (35+/-1 bpm; n = 3) in anaesthetised rats, with no subsequent cardiovascular collapse. The results of this study are consistent with the effects shown by humans envenomed by C. barnesi which are postulated to be a result of catecholamine release. We show, for the first time, that C. barnesi tentacle extract, free of nematocyst material, produces cardiovascular effects which are distinct from those caused by venom derived from isolated nematocysts.

摘要

被卡里库亚水母(Carukia barnesi)蜇伤可能会引发危及生命的伊鲁坎吉综合征。关于卡里库亚水母毒液的活性,发表的相关内容较少。这是第一项研究卡里库亚水母毒液及触手提取物(不含刺丝囊)对心血管的体内效应的研究。毒液(静脉注射,剂量为50微克/千克或100微克/千克)在麻醉大鼠中产生了升压反应(分别为42±3毫米汞柱和44±6毫米汞柱;n = 4)以及心率增加(分别为31±5次/分钟和13±2次/分钟;n = 4)。这些变化并非剂量依赖性,在接受50微克/千克毒液的四只大鼠中有一只、接受100微克/千克毒液的四只动物中有三只随后出现了心血管衰竭。哌唑嗪(静脉注射,剂量为50微克/千克)显著减弱了毒液(静脉注射,剂量为50微克/千克)诱导的升压反应(-8±3毫米汞柱;P < 0.05;n = 4)和心动过速(-9±4次/分钟;P < 0.05;n = 4)。触手提取物(静脉注射,剂量为100微克/千克)在麻醉大鼠中产生了升压反应(51±12毫米汞柱;n = 3)和心率增加(35±1次/分钟;n = 3),随后未出现心血管衰竭。本研究结果与被卡里库亚水母蜇伤的人类所表现出的效应一致,据推测这是儿茶酚胺释放的结果。我们首次表明,不含刺丝囊物质的卡里库亚水母触手提取物产生的心血管效应与分离出的刺丝囊毒液所引起的效应不同。

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