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首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >A Novel Bibenzyl Compound (20C) Protects Mice from 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine/Probenecid Toxicity by Regulating the alpha-Synuclein-Related Inflammatory Response
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A Novel Bibenzyl Compound (20C) Protects Mice from 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine/Probenecid Toxicity by Regulating the alpha-Synuclein-Related Inflammatory Response

机译:一种新的苄基化合物(20c)通过调节与α-突触核蛋白相关的炎症反应来保护1-甲基-4-苯基-1,2,3,6-四氢吡啶/丙烯酸毒性的小鼠

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摘要

The novel bibenzyl compound 2-[4-hydroxy-3-(4-hydroxyphenyl) benzyl]-4-(4-hydroxyphenyl) phenol (20C) plays a neuroprotective role in vitro, but its effects in vivo have not yet been elucidated. In this study, we estimated the efficacy of 20C in vivo using a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine/probenecid (MPTP/p) mouse model from behavior, dopamine, and neuron and then the possible mechanisms for these effects were further investigated. The experimental results showed that 20C improved behavioral deficits, attenuated dopamine depletion, reduced dopaminergic neuron loss, protected the blood-brain barrier (BBB) structure, ameliorated alpha-synuclein dysfunction, suppressed glial activation, and regulated both nuclear factor-kappa B (NF-kappa B) signaling and the NOD-like receptor protein (NLRP) 3 inflamma-some pathway. Our results indicated that 20C may prevent neurodegeneration in the MPTP/p mouse model by targeting alpha-synuclein and regulating alpha-synuclein-related inflammatory responses, including BBB damage, glial activation, NF-kappa B signaling, and the NLRP3 inflammasome pathway.
机译:新颖的联苄化合物2- [4-羟基-3-(4-羟基苯基)苄基] -4-(4-羟基苯基)苯酚(20℃)起的体外神经保护作用,但其在体内的作用尚未阐明。在这项研究中,我们使用1-甲基-4-苯基-1,2,3,6-四氢吡啶/丙磺舒(MPTP / P)从行为,多巴胺和神经元和小鼠模型然后估计在体内20C的功效这些效应可能的机制进行了进一步调查。实验结果表明,20℃改善行为缺陷的,减毒的多巴胺耗竭,降低的多巴胺能神经元的损失,保护的血 - 脑屏障(BBB)的结构,改良后的α-突触核蛋白功能障碍,抑制神经胶质活化,并且调节的两个核因子-κB(NF -κB)信令和NOD样受体蛋白质(NLRP)3 inflamma-一些途径。我们的结果表明,20C可以防止神经变性在MPTP / P小鼠模型通过靶向α-突触核蛋白和调节α-突触核蛋白相关炎性反应,包括BBB损伤,神经胶质激活,NF-κB信号,并且NLRP3炎性途径。

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