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牛磺酸通过激活 PINK1/Parkin 通路介导的自噬来拯救椎间盘退变。

Taurine rescues intervertebral disc degeneration by activating mitophagy through the PINK1/Parkin pathway.

机构信息

Department of Orthopaedics, Changsha Hospital of Traditional Chinese Medicine (Changsha Eighth Hospital), Changsha, 410199, China.

Department of Orthopaedics, Changsha Hospital of Traditional Chinese Medicine (Changsha Eighth Hospital), Changsha, 410199, China.

出版信息

Biochem Biophys Res Commun. 2024 Dec 20;739:150587. doi: 10.1016/j.bbrc.2024.150587. Epub 2024 Aug 22.

Abstract

Intervertebral disc degeneration (IDD) is a common cause of low back pain and disability. Recent studies have highlighted the critical role of mitochondrial dysfunction in the progression of IDD. In this study, we investigated the therapeutic potential of taurine in delaying IDD through the activation of mitophagy via the PINK1/Parkin pathway. Our in vitro and in vivo experiments demonstrate that taurine treatment significantly enhances mitophagy, reduces oxidative stress, delays cell senescence, and promotes the removal of damaged mitochondria in nucleus pulposus cells (NPC). Additionally, taurine-mediated activation of the PINK1/Parkin pathway leads to improved mitochondrial homeostasis and slows the progression of disc degeneration. These findings provide new insights into the protective effects of taurine and highlight its potential as a therapeutic agent for IDD.

摘要

椎间盘退变(IDD)是导致腰痛和残疾的常见原因。最近的研究强调了线粒体功能障碍在 IDD 进展中的关键作用。在这项研究中,我们通过 PINK1/Parkin 通路激活自噬来研究牛磺酸通过延迟 IDD 的治疗潜力。我们的体外和体内实验表明,牛磺酸治疗可显著增强自噬作用,减轻氧化应激,延缓细胞衰老,并促进核髓核细胞(NPC)中受损线粒体的清除。此外,牛磺酸介导的 PINK1/Parkin 通路的激活导致线粒体稳态的改善,并减缓椎间盘退变的进展。这些发现为牛磺酸的保护作用提供了新的见解,并强调了其作为 IDD 治疗剂的潜力。

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