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白藜芦醇诱导的自噬可预防人朊病毒蛋白介导的神经毒性。

Autophagy induced by resveratrol prevents human prion protein-mediated neurotoxicity.

机构信息

Korea Zoonoses Research Institute, Bio-Safety Research Institute, Center for Healthcare Technology Development, College of Veterinary Medicine, Chonbuk National University, Jeonju 561-756, South Korea.

出版信息

Neurosci Res. 2012 Jun;73(2):99-105. doi: 10.1016/j.neures.2012.03.005. Epub 2012 Mar 23.

Abstract

Our previous study revealed that resveratrol blocks prion protein peptide PrP(106-126)-induced neurotoxicity. However, the mechanism of resveratrol-mediated neuroprotection in prion diseases is not clear. Resveratrol initiates neuroprotective effects via the activation of autophagy, which protects organelles, cells, and organisms against misfolded protein-disorders, including Alzheimer's disease and Parkinson's disease via regulation of mitochondrial homeostasis. Thus, we focused on elucidating the mechanisms responsible for resveratrol-mediated neuroprotection related to mitochondrial homeostasis as a result of autophagy activation. Resveratrol prevented PrP(106-126)-induced neuronal cell death by activating autophagy. Moreover, resveratrol-induced autophagy prevented the PrP(106-126)-induced reduction in mitochondrial potential and translocation of Bax to the mitochondria and cytochrome c release. Our results indicate that treatment with resveratrol appears to protect against neurotoxicity caused by prion protein peptides and the neuroprotection is induced by resveratrol-mediated autophagy signals.

摘要

我们之前的研究表明白藜芦醇可阻断朊病毒蛋白肽 PrP(106-126)诱导的神经毒性。然而,白藜芦醇在朊病毒病中介导神经保护的机制尚不清楚。白藜芦醇通过激活自噬来启动神经保护作用,自噬通过调节线粒体稳态来保护细胞器、细胞和生物体免受包括阿尔茨海默病和帕金森病在内的错误折叠蛋白紊乱的影响。因此,我们专注于阐明与线粒体稳态相关的白藜芦醇介导的神经保护机制,作为自噬激活的结果。白藜芦醇通过激活自噬来防止 PrP(106-126)诱导的神经元细胞死亡。此外,白藜芦醇诱导的自噬可防止 PrP(106-126)诱导的线粒体电位降低、Bax 向线粒体易位和细胞色素 c 释放。我们的结果表明,白藜芦醇的治疗似乎可以预防朊病毒蛋白肽引起的神经毒性,并且白藜芦醇介导的自噬信号诱导了神经保护作用。

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