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褪黑素通过PGC-1α信号通路恢复线粒体稳态来减轻椎间盘退变。

Melatonin attenuates intervertebral disc degeneration by restoring mitochondrial homeostasis through PGC-1α signaling pathway.

作者信息

Lan Tao, Yang Wenhan, Yan Bin, Guo Weizhuang, Zhang Yuantao

机构信息

Department of Spine Surgery, Shenzhen Second People's Hospital, the First Affiliated Hospital of Shenzhen University, Shenzhen, China.

Department of Orthopaedics, the First Affiliated Hospital of Shantou University Medical College, Shantou, China.

出版信息

Cell Mol Life Sci. 2025 Aug 31;82(1):330. doi: 10.1007/s00018-025-05877-5.

Abstract

Intervertebral disc degeneration (IVDD) is a major cause of low back pain (LBP) and poses a substantial economic burden worldwide. Mitochondrial dysfunction, associated with oxidative stress and apoptosis, is linked to various degenerative diseases. Melatonin has emerged as a potential therapeutic agent for preventing IVDD because of its capacity to regulate cellular rhythms. The impact of melatonin on mitochondrial dysfunction and its underlying mechanisms is not yet fully understood. Firstly, Cell Counting Kit-8 (CCK-8) assay was used to evaluate nucleus pulposus (NP) cell viability treated with melatonin and advanced oxidation protein products (AOPP). Then, Western blotting, immunofluorescence and tunnel staining were employed to explore the underlying mechanisms in vitro. Next, a needle-punctured rat model followed by radiographic analysis and immunohistochemical staining was used to evaluate the potential effect of melatonin in vivo. This study demonstrated that AOPP triggered oxidative stress, exacerbated mitochondrial injury, and increased NP cell apoptosis. Additionally, melatonin enhanced mitochondrial function and protected NP cells from oxidative injury. Further studies demonstrated that melatonin enhanced mitochondrial biogenesis and modulated mitochondrial dynamics and mitophagy via the Peroxisome proliferator-activated receptorγcoactivator 1α (PGC-1α) signaling pathway, maintaining mitochondrial homeostasis and thereby decreasing excessive apoptosis and extracellular matrix (ECM) degradation. A PGC-1α inhibitor lessened melatonin's effect on the mitochondrial quality system, weakening its protective function in NP cells against oxidative stress. Furthermore, in vivo experiments confirmed that melatonin slowed the progression of IVDD. These findings provide a theoretical basis for treating IVDD by targeting mitochondrial dysfunction and modulating the mitochondrial quality control system. Melatonin could be an effective treatment for IVDD.

摘要

椎间盘退变(IVDD)是腰痛(LBP)的主要原因,在全球范围内造成了巨大的经济负担。线粒体功能障碍与氧化应激和细胞凋亡相关,与多种退行性疾病有关。褪黑素因其调节细胞节律的能力,已成为预防IVDD的潜在治疗药物。褪黑素对线粒体功能障碍的影响及其潜在机制尚未完全明确。首先,使用细胞计数试剂盒-8(CCK-8)检测法评估褪黑素和晚期氧化蛋白产物(AOPP)处理后的髓核(NP)细胞活力。然后,采用蛋白质免疫印迹法、免疫荧光法和隧道染色法在体外探索其潜在机制。接下来,使用针刺大鼠模型并进行影像学分析和免疫组织化学染色,以评估褪黑素在体内的潜在作用。本研究表明,AOPP引发氧化应激,加剧线粒体损伤,并增加NP细胞凋亡。此外,褪黑素增强线粒体功能,保护NP细胞免受氧化损伤。进一步研究表明,褪黑素通过过氧化物酶体增殖物激活受体γ辅激活因子1α(PGC-1α)信号通路增强线粒体生物合成,调节线粒体动力学和线粒体自噬,维持线粒体稳态,从而减少过度凋亡和细胞外基质(ECM)降解。PGC-1α抑制剂减弱了褪黑素对线粒体质量系统的作用,削弱了其对NP细胞抗氧化应激的保护功能。此外,体内实验证实褪黑素减缓了IVDD的进展。这些发现为通过靶向线粒体功能障碍和调节线粒体质量控制系统治疗IVDD提供了理论依据。褪黑素可能是治疗IVDD的有效药物。

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