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首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Cardiovascular effects and lethality of venom from nematocysts of the box-jellyfish Chiropsalmus quadrigatus (Habu-kurage) in anaesthetized rats
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Cardiovascular effects and lethality of venom from nematocysts of the box-jellyfish Chiropsalmus quadrigatus (Habu-kurage) in anaesthetized rats

机译:箱形水母四肢蛇(Habu-kurage)的线虫囊的毒性作用及其对麻醉大鼠的杀伤力

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Haemodynamic effects of saline-extracted venom from nematocysts isolated from Chiropsalmus quadrigatus (Habu-kurage) were studied in anaesthetized rats. Intravenous administration of venom (0.2-5 Vg protein/kg) produced immediately dose-dependent hypertension and bradycardia. Femoral blood flow transiently increased but calculated femoral vascular conductance decreased. Changes caused by I mu g/kg of venom were reproducible, and were not affected by prazosin, atropine or BQ123 (ETA receptor antagonist) but were significantly attenuated by nicardipine. At doses over 2 mu g/kg, hypotension and a decrease in pulse pressure were observed subsequent to transient hypertension. In 5 of 8 rats received 5 mu g/kg venom and 6 of 6 rats at 10 mu g/kg, death due to irreversible cardiac arrest occurred within 30 min after intravenous injection. However, during nicardipine infusion, venom (10 mu g/kg) exerted only modest effects and the rats survived. Heating venom (50 degrees C for 10 min) before injection practically abolished the haemodynamic effects of 10 mu g/kg venom, indicating its thermolability. Data show that C. quadrigatus venom has both vasoconstrictor and cardiodepressive effects in rats, and suggest that a calcium channel blocker can protect against the cardiovascular and lethal effects of the venom. (c) 2005 Elsevier Ltd. All rights reserved.
机译:在麻醉的大鼠中研究了盐提取的毒液的血流动力学效应,该毒液是从四肢手足蛇(Habu-kurage)分离的线虫囊中提取的。静脉注射毒液(0.2-5 Vg蛋白/ kg)可立即产生剂量依赖性高血压和心动过缓。股动脉血流短暂增加,但计算得出的股血管电导降低。由1μg/ kg毒液引起的变化是可重现的,不受哌唑嗪,阿托品或BQ123(ETA受体拮抗剂)的影响,但被尼卡地平大大减轻。在超过2μg / kg的剂量下,短暂性高血压后出现低血压和脉压降低。 8只大鼠中有5只接受5μg/ kg毒液,6只大鼠中有6只以10μg/ kg毒液,由于静脉注射后30分钟内发生了不可逆的心脏骤停死亡。然而,在尼卡地平输注过程中,毒液(10μg / kg)仅发挥了中度作用,大鼠存活。注射前加热毒液(50摄氏度,持续10分钟)实际上消除了10 µg / kg毒液的血液动力学效应,表明其可热性。数据显示,C.quadrigatus毒液在大鼠中同时具有血管收缩作用和心脏降压作用,并且表明钙通道阻滞剂可以预防毒液的心血管和致命作用。 (c)2005 Elsevier Ltd.保留所有权利。

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