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牛磺熊去氧胆酸通过自噬保护人神经母细胞瘤细胞免受线粒体功能障碍和细胞死亡。

Tauroursodeoxycholic Acid Protects Against Mitochondrial Dysfunction and Cell Death via Mitophagy in Human Neuroblastoma Cells.

机构信息

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003, Lisbon, Portugal.

Department of Biochemistry and Human Biology, Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003, Lisbon, Portugal.

出版信息

Mol Neurobiol. 2017 Oct;54(8):6107-6119. doi: 10.1007/s12035-016-0145-3. Epub 2016 Oct 3.

Abstract

Mitochondrial dysfunction has been deeply implicated in the pathogenesis of several neurodegenerative diseases. Thus, to keep a healthy mitochondrial population, a balanced mitochondrial turnover must be achieved. Tauroursodeoxycholic acid (TUDCA) is neuroprotective in various neurodegenerative disease models; however, the mechanisms involved are still incompletely characterized. In this study, we investigated the neuroprotective role of TUDCA against mitochondrial damage triggered by the mitochondrial uncoupler carbonyl cyanide m-chlorophelyhydrazone (CCCP). Herein, we show that TUDCA significantly prevents CCCP-induced cell death, ROS generation, and mitochondrial damage. Our results indicate that the neuroprotective role of TUDCA in this cell model is mediated by parkin and depends on mitophagy. The demonstration that pharmacological up-regulation of mitophagy by TUDCA prevents neurodegeneration provides new insights for the use of TUDCA as a modulator of mitochondrial activity and turnover, with implications in neurodegenerative diseases.

摘要

线粒体功能障碍与多种神经退行性疾病的发病机制密切相关。因此,为了保持健康的线粒体群体,必须实现平衡的线粒体周转。牛磺熊脱氧胆酸(TUDCA)在多种神经退行性疾病模型中具有神经保护作用;然而,相关的机制仍不完全清楚。在这项研究中,我们研究了 TUDCA 对线粒体解偶联剂羰基氰化物 m-氯代苯腙(CCCP)引发的线粒体损伤的神经保护作用。在此,我们表明 TUDCA 可显著预防 CCCP 诱导的细胞死亡、ROS 生成和线粒体损伤。我们的结果表明,TUDCA 在该细胞模型中的神经保护作用是通过 parkin 介导的,并且依赖于线粒体自噬。证明 TUDCA 通过药理学上调线粒体自噬可预防神经退行性变,为 TUDCA 作为线粒体活性和周转调节剂的使用提供了新的见解,这与神经退行性疾病有关。

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