Neurotoxin Research Group, Department of Medical and Molecular Biosciences, University of Technology, Sydney, PO Box 123, Broadway, NSW, 2007, Australia.
Biochem Pharmacol. 2012 Sep 15;84(6):851-63. doi: 10.1016/j.bcp.2012.06.024. Epub 2012 Jul 4.
Despite the in vivo lethality of venom, neurotoxicity has not previously been considered a significant complication of envenoming by the Australian pygmy copperhead (Austrelaps labialis). However, recent evidence has emerged demonstrating that this venom contains potent presynaptic and postsynaptic neurotoxicity. The present study describes the isolation and pharmacological characterization of the first postsynaptic neurotoxin, α-EPTX-Al2a, from the venom of A. labialis. α-EPTX-Al2a (8072.77 Da) caused a concentration-dependent block of twitch contractions and a complete block of responses to cholinergic agonists in the chick biventer cervicis nerve-muscle preparation. This action is consistent with postjunctional neurotoxicity. Monovalent tiger snake antivenom prevented the onset of neurotoxicity if applied prior to toxin administration, but was only able to partially reverse neurotoxicity once muscle paralysis had developed. α-EPTX-Al2a produced a potent pseudo-irreversible antagonism of chick muscle nicotinic acetylcholine receptors (nAChRs), with an estimated pA(2) value of 7.902 (K(B) = 12.5 nM). Interestingly, the toxin only produced a modest block of neuronal α7 nAChRs, with an IC(50) of 1.2 μM, and failed to inhibit ganglionic α3β2/α3β4 nAChRs in a fluorescence-based FLIPR assay using SH-SY5Y cells. α-EPTX-Al2a contained 75 amino acid residues with five disulfide bonds that had significant homology to classical long-chain α-neurotoxins. While α-EPTX-Al2a retains most pharmacophore residues critical for binding to muscle-type (α1)(2)βγδ nAChRs it lacks the key Ala(28) and Arg(36) residues important for α7 nAChR affinity. Given that A. labialis venom contains both irreversible presynaptic and postsynaptic neurotoxins, clinicians need to be aware of potential neurotoxic complications associated with pygmy copperhead envenomation.
尽管毒液在体内具有致死性,但神经毒性以前并未被认为是澳大利亚小铜头蛇(Austrelaps labialis)咬伤的一个重要并发症。然而,最近的证据表明,这种毒液含有有效的突触前和突触后神经毒性。本研究描述了从 A. labialis 毒液中分离出的第一种突触后神经毒素α-EPTX-Al2a,并对其进行了药理学特征分析。α-EPTX-Al2a(8072.77 Da)可引起小鸡双颈椎神经-肌肉标本中抽搐收缩的浓度依赖性阻滞,并完全阻断对胆碱能激动剂的反应。这种作用与突触后神经毒性一致。单价虎蛇抗蛇毒血清如果在毒素给药前使用,可防止神经毒性的发生,但一旦肌肉麻痹发生,只能部分逆转神经毒性。α-EPTX-Al2a 对小鸡肌肉烟碱型乙酰胆碱受体(nAChRs)产生强烈的拟不可逆拮抗作用,估计 pA2 值为 7.902(Kb = 12.5 nM)。有趣的是,该毒素仅对神经元α7 nAChRs 产生中度阻滞,IC50 为 1.2 μM,并且在使用 SH-SY5Y 细胞的基于荧光的 FLIPR 测定中,未能抑制神经节α3β2/α3β4 nAChRs。α-EPTX-Al2a 含有 75 个氨基酸残基,有 5 个二硫键,与经典的长链α-神经毒素具有显著的同源性。虽然α-EPTX-Al2a 保留了与肌肉型(α1)(2)βγδ nAChRs 结合至关重要的大多数药效基团残基,但它缺乏对α7 nAChR 亲和力至关重要的关键 Ala(28)和 Arg(36)残基。鉴于 A. labialis 毒液同时含有不可逆的突触前和突触后神经毒素,临床医生需要意识到与小铜头蛇咬伤相关的潜在神经毒性并发症。