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蝎毒耐热肽保护转基因秀丽隐杆线虫免受β-淀粉样蛋白毒性作用。

Scorpion Venom Heat-Resistant Peptide Protects Transgenic Caenorhabditis elegans from β-Amyloid Toxicity.

作者信息

Zhang Xiao-Gang, Wang Xi, Zhou Ting-Ting, Wu Xue-Fei, Peng Yan, Zhang Wan-Qin, Li Shao, Zhao Jie

机构信息

Department of Physiology, Dalian Medical University Dalian, China.

Department of Neurology, the First Affiliated Hospital of Dalian Medical University Dalian, China.

出版信息

Front Pharmacol. 2016 Jul 26;7:227. doi: 10.3389/fphar.2016.00227. eCollection 2016.

DOI:10.3389/fphar.2016.00227
PMID:27507947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4960250/
Abstract

Scorpion venom heat-resistant peptide (SVHRP) is a component purified from Buthus martensii Karsch scorpion venom. Our previous studies found SVHRP could enhance neurogenesis and inhibit microglia-mediated neuroinflammation in vivo. Here, we use the transgenic CL4176, CL2006, and CL2355 strains of Caenorhabditis elegans which express the human Aβ1-42 to investigate the effects and the possible mechanisms of SVHRP mediated protection against Aβ toxicity in vivo. The results showed that SVHRP-fed worms displayed remarkably decreased paralysis, less abundant toxic Aβ oligomers, reduced Aβ plaque deposition with respect to untreated animals. SVHRP also suppressed neuronal Aβ expression-induced defects in chemotaxis behavior and attenuated levels of ROS in the transgenic C. elegans. Taken together, these results suggest SVHRP could protect against Aβ-induced toxicity in C. elegans. Further studies need to be conducted in murine models and humans to analyze the effectiveness of the peptide.

摘要

蝎毒耐热肽(SVHRP)是从东亚钳蝎毒液中纯化得到的一种成分。我们之前的研究发现,SVHRP在体内可增强神经发生并抑制小胶质细胞介导的神经炎症。在此,我们使用表达人Aβ1-42的秀丽隐杆线虫转基因CL4176、CL2006和CL2355品系,来研究SVHRP在体内介导的对Aβ毒性的保护作用及其可能机制。结果显示,与未处理的动物相比,喂食SVHRP的线虫麻痹明显减轻,有毒Aβ寡聚体数量减少,Aβ斑块沉积减少。SVHRP还抑制了神经元Aβ表达诱导的趋化行为缺陷,并降低了转基因秀丽隐杆线虫中的活性氧水平。综上所述,这些结果表明SVHRP可保护秀丽隐杆线虫免受Aβ诱导的毒性。需要在小鼠模型和人类中进行进一步研究,以分析该肽的有效性。

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本文引用的文献

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Intracellular amyloid β oligomers impair organelle transport and induce dendritic spine loss in primary neurons.细胞内淀粉样β寡聚体损害细胞器运输并诱导原代神经元树突棘丢失。
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对羟基苯甲醛可抵御氧化应激和β-淀粉样蛋白毒性。
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Protein mimetic 2D FAST rescues alpha synuclein aggregation mediated early and post disease Parkinson's phenotypes.蛋白模拟 2D FAST 挽救了与帕金森病早发和发病后相关的α-突触核蛋白聚集。
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Insights into the Neuroprotective Potential of Epicatechin: Effects against Aβ-Induced Toxicity in .表儿茶素的神经保护潜力洞察:对β淀粉样蛋白诱导毒性的作用
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