The neuromuscular activity of Micrurus pyrrhocryptus venom and its neutralization by commercial and specific coral snake antivenoms.

Journal of Venom Research Pub Date : 2011-01-01 Epub Date: 2011-06-24
Thiago Magalhães Camargo, Adolfo Rafael de Roodt, Maria Alice da Cruz-Höfling, Léa Rodrigues-Simioni
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Abstract

The neuromuscular activity ofMicrurus pyrrochryptus venom was studied in chick biventer cervicis (BC) and mouse phrenic nerve-diaphragm (PND) preparations. The venom (0.5-50μg/ml) caused irreversible, time- and concentration-dependent blockade, with BC being more sensitive than PND (50% blockade with 10μg/ml in 22±;3min and 62±4min, respectively; mean±SEM, n=6; p<0.05). In BC preparations, venom (0.5μg/ml) progressively abolished ACh-induced contractures, whereas contractures to exogenous KCl and muscle twitches in curarized preparations were unaffected. The venom neither altered creatine kinase release (venom: 25.8±1.75IU/l vs control: 24.3±2.2IU/l, n=6, after 120min), nor it caused significant muscle damage (50μg of venom/ml vs control: 3.5±0.8% vs 1.1±0.7% for PND; 4.3±1.5% vs 1.2±0.5% for BC, n=5). The venom had low PLA(2) activity. Neurotoxicity was effectively neutralized by commercial Micrurus antivenom and specific antivenom. These findings indicate that M. pyrrhocryptus venom acts postsynaptically on nicotinic receptors, with no significant myotoxicity.

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红嘴蛇毒液的神经肌肉活性及其在商用和专用珊瑚蛇毒血清中的中和作用。
研究了毒毒在鸡颈(BC)和小鼠膈神经膈(PND)制剂中的神经肌肉活性。毒液(0.5 ~ 50μg/ml)引起不可逆的、时间依赖性和浓度依赖性的阻断作用,BC比PND更敏感(10μg/ml 50%阻断作用分别在22±3min和62±4min;意味着±SEM, n = 6;p
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