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岩藻依聚糖对响尾蛇毒肌毒性磷脂酶A(2)活性的抑制作用。

Inhibitory effect of fucoidan on the activities of crotaline snake venom myotoxic phospholipases A(2).

作者信息

Angulo Yamileth, Lomonte Bruno

机构信息

Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica, San José, Costa Rica.

出版信息

Biochem Pharmacol. 2003 Nov 15;66(10):1993-2000. doi: 10.1016/s0006-2952(03)00579-3.

Abstract

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.

摘要

肌毒性磷脂酶A(2)是导致响尾蛇科蛇咬伤中毒后肌肉坏死的主要原因。在本研究中,我们调查了岩藻依聚糖(一种从褐藻墨角藻中提取的天然硫酸化多糖)对一组来自响尾蛇科蛇毒的磷脂酶A(2)肌毒素的细胞毒性和肌毒性活性的保护作用:矛头蝮蛇肌毒素I、II、III和IV,哥德曼氏犀咝蝰肌毒素I和II,纳氏矛头蝮肌毒素I和II,以及施氏竹叶青肌毒素I。所有测试的毒素在细胞毒性和肌毒性作用方面均被岩藻依聚糖有效抑制。通过比浊分析证明,这种抑制作用的基础似乎是岩藻依聚糖与肌毒素之间迅速形成复合物。使用代表其中三种毒素膜损伤区域(第115 - 129位氨基酸残基)的短合成肽研究了岩藻依聚糖在肌毒素上可能的结合位点。岩藻依聚糖明显抑制了这些肽的细胞溶解活性,表明其能够与这些磷脂酶A(2)的C末端肌毒性区域相互作用。在用矛头蝮粗毒进行实验性中毒后立即局部给予岩藻依聚糖时,它能显著抑制小鼠的肌肉损伤。这些结果鼓励进一步研究硫酸化岩藻聚糖作为潜在用于改善响尾蛇科蛇咬伤中毒治疗的化合物。

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