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首页> 外文期刊>Biochemical Pharmacology >Pharmacological characterization of α-elapitoxin-Al2a from the venom of the Australian pygmy copperhead (Austrelaps labialis): An atypical long-chain α-neurotoxin with only weak affinity for α7 nicotinic receptors
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Pharmacological characterization of α-elapitoxin-Al2a from the venom of the Australian pygmy copperhead (Austrelaps labialis): An atypical long-chain α-neurotoxin with only weak affinity for α7 nicotinic receptors

机译:来自澳大利亚侏儒铜头蛇(Austrelaps labialis)毒液中α-elapitoxin-Al2a的药理学表征:一种非典型的长链α-神经毒素,仅对α7烟碱受体具有弱亲和力

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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) 2βγδ 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.
机译:尽管毒液具有体内杀伤力,但澳大利亚侏儒铜头((Austrelaps labialis)以前尚未将神经毒性视为毒液的重大并发症。但是,最近的证据表明这种毒液含有强的突触前和突触后神经毒性。本研究描述了第一个突触后神经毒素α-EPTX-Al2a的分离和药理学特性。 α-EPTX-Al2a(8072.77 Da)引起了浓度依赖性的抽搐收缩阻滞,并完全阻滞了雏鸡颈静脉神经肌肉制剂对胆碱能激动剂的反应。该作用与结后神经毒性一致。如果在施用毒素之前应用单价虎蛇抗蛇毒,可以预防神经毒性的发作,但是一旦肌肉麻痹发生,它只能部分逆转神经毒性。 α-EPTX-Al2a对鸡的肌肉烟碱乙酰胆碱受体(nAChRs)产生了强烈的拟不可逆拮抗作用,估计pA 2值为7.902(K B = 12.5 nM)。有趣的是,在使用SH-SY5Y细胞的基于荧光的FLIPR分析中,该毒素仅产生了适度的神经元α7nAChRs阻滞,IC 50为1.2μM,未能抑制神经节α3β2/α3β4nAChRs。 α-EPTX-Al2a包含75个具有5个二硫键的氨基酸残基,这些残基与经典的长链α-神经毒素具有显着的同源性。尽管α-EPTX-Al2a保留了对结合肌肉型(α1)2βγδnAChRs至关重要的大多数药效团残基,但它缺少对α7nAChR亲和力重要的关键Ala 28和Arg 36残基。鉴于阴唇曲霉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侏儒铜头蛇毒相关的潜在神经毒性并发症。

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