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首页> 外文期刊>Toxicology Letters: An International Journal Providing a Forum for Original and Pertinent Contributions in Toxicology Research >Lemnitoxin, the major component of Micrurus lemniscatus coral snake venom, is a myotoxic and pro-inflammatory phospholipase A(2)
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Lemnitoxin, the major component of Micrurus lemniscatus coral snake venom, is a myotoxic and pro-inflammatory phospholipase A(2)

机译:LemeNitoxin,Micrurus Lememistatus珊瑚蛇毒液的主要成分,是一种肌毒性和促炎磷脂酶A(2)

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摘要

The venom of Micrurus lemniscatus, a coral snake of wide geographical distribution in South America, was fractionated by reverse-phase HPLC and the fractions screened for phospholipase A(2) (PLA(2)) activity. The major component of the venom, a PLA(2), here referred to as `Lemnitoxin', was isolated and characterized biochemically and toxicologically. It induces myotoxicity upon intramuscular or intravenous injection into mice. The amino acid residues Arg15, Ala100, Asn108, and a hydrophobic residue at position 109, which are characteristic of myotoxic class I phospholipases A(2), are present in Lemnitoxin. This PLA(2) is antigenically related to M. nigrocinctus nigroxin, Notechis scutatus notexin, Pseudechis australis mulgotoxin, and Pseudonaja textilis textilotoxin, as demonstrated with monoclonal and polyclonal antibodies. Lemnitoxin is highly selective in its targeting of cells, being cytotoxic for differentiated myotubes in vitro and muscle fibers in vivo, but not for undifferentiated myoblasts or endothelial cells. Lemnitoxin is not lethal after intravenous injection at doses up to 2 mu g/g in mice, evidencing its lack of significant neurotoxicity. Lemnitoxin displays anticoagulant effect on human plasma and proinflammatory activity also, as it induces paw edema and mast cell degranulation. Thus, the results of this work demonstrate that Lemnitoxin is a potent myotoxic and proinflammatory class I PLA(2). (C) 2016 Elsevier Ireland Ltd. All rights reserved.
机译:Micrurus Lemonistatus的毒液是南美洲广大地理分布的珊瑚蛇,通过反相HPLC分馏和筛选磷脂酶A(2)(PLA(2))活性的级分。毒液的主要成分,PLA(2),这里被称为“LemeNitoxin”,被分离出,并在生物化学上表征和毒理学。它在肌内或静脉注射到小鼠时诱导肌毒性。氨基酸残基Arc15,Ala100,Asn108和疏水残留物在第109位,其是肌毒性类I磷脂酶A(2)的特征,存在于LemeNitoxin中。该PLA(2)抗原与M. nigrocinctus nigroxin,Notechis Scutatus Notexin,PseudeChis澳大利多毒素和Pseudonaja Textilis Textiloxin有关,如单克隆和多克隆抗体所证明的那样。 LemeNitoxin在其对细胞的靶向中具有高度选择性,对于体外体外和肌肉纤维的细胞毒性是细胞毒性,但不是针对未分化的肌细胞或内皮细胞。在小鼠中静脉注射后静脉注射后,延伸毒素并不致死,证明其缺乏显着的神经毒性。 LemeNitoxin也显示对人血浆和促炎活动的抗凝血作用,因为它诱导爪子水肿和肥大细胞脱粒。因此,这项工作的结果表明,LemeNitoxin是一种有效的肌毒性和促炎级别的I PLA(2)。 (c)2016 Elsevier Ireland Ltd.保留所有权利。

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