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首页> 外文期刊>Biochemical Pharmacology >Inhibitory effect of fucoidan on the activities of crotaline snake venom myotoxic phospholipases A(2).
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Inhibitory effect of fucoidan on the activities of crotaline snake venom myotoxic phospholipases A(2).

机译:岩藻依聚糖对角鲨碱蛇毒肌毒性磷脂酶A(2)的抑制作用。

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摘要

Myotoxic phospholipases A(2) account for most of the muscle necrosis that results from envenenomation by crotaline snakes. In this study, we investigated the protective effect of fucoidan, a natural sulfated polysaccharide obtained from the brown seaweed Fucus vesiculosus, against the cytotoxic and myotoxic activities of a group of phospholipase A(2) myotoxins from crotaline snake venoms: Bothrops asper myotoxins I, II, III, and IV, Cerrophidion godmani myotoxins I and II, Atropoides nummifer myotoxins I and II, and Bothriechis schlegelii myotoxin I. All of the toxins tested were efficiently inhibited by fucoidan, in both their cytotoxic and myotoxic effects. The basis for this inhibition appears to be the rapid formation of complexes between fucoidan and myotoxins, as evidenced by turbidimetric analysis. The possible binding site of fucoidan on the myotoxins was investigated using short synthetic peptides that represent the membrane-damaging region (residues 115-129) for three of these toxins. Fucoidan clearly inhibited the cytolytic activity of the peptides, indicating its ability to interact with the C-terminal myotoxic region of these phospholipases A(2). Fucoidan significantly inhibited muscle damage in mice, when administered locally, immediately after experimental envenomation with crude venom from B. asper. These results encourage further studies of sulfated fucans as compounds of potential use to improve the treatment of envenomations by crotaline snakes.
机译:肌毒性磷脂酶A(2)造成了大部分的肌肉坏死,而肌坏死是由角鲨烷蛇引起的。在这项研究中,我们调查了岩藻依聚糖(一种从褐藻海藻Fucus vesiculosus中获得的天然硫酸化多糖)对一群从草甘膦蛇毒中产生的磷脂酶A(2)肌毒素的细胞毒性和肌毒性的保护作用: II,III和IV,Cerrophidion godmani肌毒素I和II,Atropoides nummifer肌毒素I和II和Bothriechis schlegelii肌毒素I。岩藻依聚糖有效地抑制了所有测试的毒素的细胞毒性和肌毒性作用。浊度分析表明,这种抑制作用的基础似乎是岩藻依聚糖和肌毒素之间复合物的快速形成。使用短合成肽研究了岩藻依聚糖在肌毒素上的可能结合位点,这些肽代表了其中三种毒素的膜破坏区域(残基115-129)。岩藻依聚糖明显抑制了肽的溶细胞活性,表明其与这些磷脂酶A(2)的C端肌毒性区域相互作用的能力。在用鼠疫双歧杆菌的粗毒液进行实验毒化后,当局部给药时,岩藻糖聚糖可显着抑制小鼠的肌肉损伤。这些结果鼓励了对硫酸化岩藻糖酯作为潜在化合物来改善草甘膦蛇毒化毒的进一步研究。

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