首页> 美国卫生研究院文献>Toxins >Varespladib (LY315920) and Methyl Varespladib (LY333013) Abrogate or Delay Lethality Induced by Presynaptically Acting Neurotoxic Snake Venoms
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Varespladib (LY315920) and Methyl Varespladib (LY333013) Abrogate or Delay Lethality Induced by Presynaptically Acting Neurotoxic Snake Venoms

机译:Varespladib(LY315920)和甲基Varespladib(LY333013)通过突触前作用神经毒性蛇毒引起的废除或延迟致死率

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摘要

The phospholipase A (PLA ) inhibitor Varespladib ( ) and its orally bioavailable prodrug, methyl-Varespladib ( ) inhibit PLA activity of a wide variety of snake venoms. In this study, the ability of these two forms of Varespladib to halt or delay lethality of potent neurotoxic snake venoms was tested in a mouse model. The venoms of , , and , all of which have potent presynaptically acting neurotoxic PLA s of variable quaternary structure, were used to evaluate simple dosing regimens. A supralethal dose of each venom was injected subcutaneously in mice, followed by the bolus intravenous ( ) or oral ( ) administration of the inhibitors, immediately and at various time intervals after envenoming. Control mice receiving venom alone died within 3 h of envenoming. Mice injected with venom and treated with or survived the 24 h observation period, whereas those receiving and venoms survived at 3 h or 6 h with a single dose of either form of Varespladib, but not at 24 h. In contrast, mice receiving venom and then the inhibitors died within 3 h, similarly to the control animals injected with venom alone. was able to reverse the severe paralytic manifestations in mice injected with venoms of and Overall, results suggest that the two forms of Varespladib are effective in abrogating, or delaying, neurotoxic manifestations induced by some venoms whose neurotoxicity is mainly dependent on presynaptically acting PLA s. is able to reverse paralytic manifestations in severely envenomed mice, but further work is needed to understand the significance of species-specific differences in animal models as they compare to clinical syndromes in human and for potential use in veterinary medicine.
机译:磷脂酶A(PLA)抑制剂Varespladib()及其口服生物可利用的前药甲基-Varespladib()抑制多种蛇毒的PLA活性。在这项研究中,在小鼠模型中测试了这两种形式的Varespladib阻止或延迟强效神经毒性蛇毒致死性的能力。 ,和的毒液均具有有效的突触前作用的具有可变四级结构的神经毒性PLA,用于评估简单的给药方案。将超毒剂量的每种毒液经皮下注射到小鼠体内,然后在毒液形成后的各个时间间隔立即静脉推注()或口服()抑制剂。仅接受毒液的对照小鼠在毒液后3小时内死亡。注射了毒液并经24小时观察期治疗或存活的小鼠,而接受和毒液的小鼠在单剂两种形式的Varespladib的情况下在3 h或6 h存活,但在24 h却没有。相反,与单独注射毒液的对照动物相似,接受毒液然后抑制剂的小鼠在3小时内死亡。能够逆转注射有和毒液的小鼠的严重麻痹表现,结果表明两种形式的Varespladib可有效消除或延迟某些毒液诱导的神经毒性表现,这些毒液的神经毒性主要取决于突触前作用的PLA。能够逆转严重毒死小鼠的麻痹表现,但还需要做进一步的工作来了解动物模型中物种特异性差异与人的临床综合征以及在兽药中的潜在用途之间的关系。

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