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从致死性澳大利亚普通铜头蛇(Austrelaps superbus)毒液中分离鉴定单体和多聚体蛇神经毒素及其他生物活性蛋白。

Characterization of monomeric and multimeric snake neurotoxins and other bioactive proteins from the venom of the lethal Australian common copperhead (Austrelaps superbus).

机构信息

Neurotoxin Research Group, School of Medical and Molecular Biosciences, University of Technology, Sydney, P.O. Box 123, Broadway, NSW 2007, Australia.

出版信息

Biochem Pharmacol. 2013 May 15;85(10):1555-73. doi: 10.1016/j.bcp.2013.02.034. Epub 2013 Mar 13.

Abstract

Envenomation by Australian copperheads results mainly in muscle paralysis largely attributed to the presence of postsynaptic α-neurotoxins. However, poorly reversible neurotoxic effects suggest that these venoms may contain snake presynaptic phospholipase A2 neurotoxins (SPANs) that irreversibly inhibit neurotransmitter release. Using size-exclusion liquid chromatography, the present study isolated the first multimeric SPAN complex from the venom of the Australian common copperhead, Austrelaps superbus. The multimeric SPAN P-elapitoxin-As1a (P-EPTX-As1a) along with two novel monomeric SPANs and a new postsynaptic α-neurotoxin were then pharmacologically characterized using the chick biventer cervicis nerve-muscle preparation. All SPANs inhibited nerve-evoked twitch contractions at the neuromuscular junction without inhibiting contractile responses to cholinergic agonists or KCl. These actions are consistent with a prejunctional action to inhibit neurotransmitter release, without direct myotoxicity. Furthermore, the multimeric P-EPTX-As1a caused tetanic 'fade' in muscle tension under high frequency nerve stimulation, and produced a triphasic alteration to neurotransmitter release. These actions have been previously noted with other multimeric SPAN complexes such as taipoxin. Moreover, the neurotoxic α-subunit of P-EPTX-As1a shows high homology to taipoxin α-chain. Several other coagulopathic and myotoxic high mass proteins including a class PIII snake venom metalloproteinase, C-type lectin, l-amino acid oxidase, acetylcholinesterase and phospholipase B were also identified that may contribute to the overall toxicity of A. superbus venom. In conclusion, clinicians should be aware that early antivenom intervention might be necessary to prevent the onset of irreversible presynaptic neurotoxicity caused by multimeric and monomeric SPANs and that A. superbus venom is potentially capable of producing coagulopathic and myotoxic effects.

摘要

被澳大利亚铜斑蛇咬伤主要会导致肌肉瘫痪,这主要归因于存在突触后α-神经毒素。然而,神经毒性作用难以逆转表明这些毒液可能含有蛇突触前磷脂酶 A2 神经毒素(SPAN),它们不可逆地抑制神经递质释放。本研究使用排阻液相色谱法从澳大利亚普通铜斑蛇 Austrelaps superbus 的毒液中分离出第一个多聚体 SPAN 复合物。然后,使用鸡双颈神经根-肌肉标本对多聚体 SPAN P-埃拉皮托辛-As1a(P-EPTX-As1a)以及两种新型单体 SPAN 和一种新的突触后α-神经毒素进行了药理学表征。所有的 SPAN 都抑制了神经-肌肉接头处的神经诱发的抽搐收缩,而不抑制对胆碱能激动剂或 KCl 的收缩反应。这些作用与在节前抑制神经递质释放的作用一致,而没有直接的肌毒性。此外,多聚体 P-EPTX-As1a 在高频神经刺激下引起肌肉张力的强直性“衰退”,并导致神经递质释放发生三相改变。以前已经注意到其他多聚体 SPAN 复合物,如 taipoxin 具有这种作用。此外,P-EPTX-As1a 的神经毒性α-亚基与 taipoxin α-链具有高度同源性。还鉴定了其他几种促凝和肌毒性的高分子量蛋白,包括 III 类蛇毒金属蛋白酶、C 型凝集素、L-氨基酸氧化酶、乙酰胆碱酯酶和磷脂酶 B,它们可能有助于 A. superbus 毒液的整体毒性。总之,临床医生应该意识到,早期使用抗蛇毒血清干预可能是必要的,以防止多聚体和单体 SPAN 引起的不可逆的节前神经毒性的发生,并且 A. superbus 毒液有可能产生促凝和肌毒性作用。

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