Lisboa Antonio, Melaré Rodolfo, Franco Junia R B, Bis Carolina V, Gracia Marta, Ponce-Soto Luis A, Marangoni Sérgio, Rodrigues-Simioni Léa, da Cruz-Höfling Maria Alice, Rocha Thalita
Multidisciplinary Research Laboratory, São Francisco University (USF), Avenida São Francisco de Assis 218, Jardim São José, 12916-350 Bragança Paulista, SP, Brazil.
Department of Biochemistry and Tissue Biology, Institute of Biology, State University of Campinas (UNICAMP), Rua Monteiro Lobato, 255, Cidade Universitária Zeferino Vaz, 13083-365 Campinas, SP, Brazil.
Biochem Res Int. 2016;2016:2053459. doi: 10.1155/2016/2053459. Epub 2016 Aug 18.
Neuromuscular preparations exposed to B. marajoensis venom show increases in the frequency of miniature end-plate potentials and twitch tension facilitation followed by presynaptic neuromuscular paralysis, without evidences of muscle damage. Considering that presynaptic toxins interfere into the machinery involved in neurotransmitter release (synaptophysin, synaptobrevin, and SNAP25 proteins), the main objective of this communication is to analyze, by immunofluorescence and western blotting, the expression of the synaptic proteins, synaptophysin, synaptobrevin, and SNAP25 and by myography, light, and transmission electron microscopy the pathology of motor nerve terminals and skeletal muscle fibres of chick biventer cervicis preparations (CBC) exposed in vitro to BmjeTX-I and BmjeTX-II toxins from B. marajoensis venom. CBC incubated with toxins showed irreversible twitch tension blockade and unaffected KCl- and ACh-evoked contractures, and the positive colabelling of acetylcholine receptors confirmed that their action was primarily at the motor nerve terminal. Hypercontraction and loose myofilaments and synaptic vesicle depletion and motor nerve damage indicated that the toxins displayed both myotoxic and neurotoxic effect. The blockade resulted from interference on synaptophysin, synaptobrevin, and SNAP25 proteins leading to the conclusion that BmjeTX-I and BmjeTX-II affected neurotransmitter release machinery by preventing the docking of synaptic vesicles to the axolemma of the nerve terminal.
暴露于马拉开波湖响尾蛇毒液中的神经肌肉制剂显示,微小终板电位频率增加,抽搐张力增强,随后出现突触前神经肌肉麻痹,且无肌肉损伤迹象。鉴于突触前毒素会干扰参与神经递质释放的机制(突触素、突触小泡蛋白和SNAP25蛋白),本通讯的主要目的是通过免疫荧光和蛋白质印迹法分析突触蛋白突触素、突触小泡蛋白和SNAP25的表达,并通过肌动描记法、光学显微镜和透射电子显微镜观察体外暴露于马拉开波湖响尾蛇毒液中的BmjeTX-I和BmjeTX-II毒素的鸡双头肌颈肌制剂(CBC)的运动神经末梢和骨骼肌纤维的病理学变化。用毒素孵育的CBC显示出不可逆的抽搐张力阻断,且氯化钾和乙酰胆碱诱发的挛缩未受影响,乙酰胆碱受体的阳性共标记证实其作用主要在运动神经末梢。过度收缩、肌丝松散、突触小泡耗竭和运动神经损伤表明毒素具有肌毒性和神经毒性作用。这种阻断是由于对突触素、突触小泡蛋白和SNAP25蛋白的干扰导致的,从而得出结论,BmjeTX-I和BmjeTX-II通过阻止突触小泡与神经末梢轴膜对接来影响神经递质释放机制。