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异甘草素通过PPARγ依赖途径减轻氧化应激和线粒体损伤诱导的椎间盘退变。

Isoliquiritigenin mitigates intervertebral disc degeneration induced by oxidative stress and mitochondrial impairment through a PPARγ-dependent pathway.

作者信息

Huang Yeheng, Sun Jing, Li Sunlong, Shi Yifeng, Yu Lianggao, Wu Aimin, Wang Xiangyang

机构信息

Cixi Biomedical Research Institute, Wenzhou Medical University, Zhejiang, China; Key Laboratory of Orthopaedics of Zhejiang Province, Wenzhou, Zhejiang Province, China.

Key Laboratory of Orthopaedics of Zhejiang Province, Wenzhou, Zhejiang Province, China; Department of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province, China.

出版信息

Free Radic Biol Med. 2024 Nov 20;225:98-111. doi: 10.1016/j.freeradbiomed.2024.10.001. Epub 2024 Oct 2.

Abstract

OBJECTIVES

Oxidative stress, mitochondrial dysfunction, and apoptosis play significant roles in the degradation of extracellular matrix (ECM) in nucleus pulposus cells (NPCs), ultimately contributing to intervertebral disc degeneration (IVDD). This study investigates the potential of isoliquiritigenin (ISL), a natural extract known for its antioxidant, anti-inflammatory, and anti-atherosclerotic properties, to alleviate IVDD.

METHODS

The viability of NPCs treated with ISL and tert-butyl hydroperoxide (TBHP) was assessed using the CCK-8 assay. Various techniques, including Western blot, qRT-PCR, immunofluorescence (IF), and immunohistochemistry, were employed to measure the expression of ECM components, oxidative stress markers, and apoptosis-related proteins. Mitochondrial function was evaluated through Western blot and IF analyses. Network pharmacology predicted ISL targets, and the expression levels of PPARγ were assessed using the aforementioned methods. The role of PPARγ in the therapeutic effects of ISL on IVDD was examined through siRNA knockdown. The therapeutic impact of ISL on puncture-induced IVDD in rats was evaluated using X-ray, MRI, and histological staining techniques.

RESULTS

In vitro, ISL reduced oxidative stress in NPCs, restored mitochondrial function, inhibited apoptosis, and improved the ECM phenotype. In vivo, ISL slowed the progression of IVDD in a rat model. Further analysis revealed that ISL enhances PPARγ activity and promotes its expression by direct binding, contributing to the delay of IVDD progression.

CONCLUSION

This study demonstrates that ISL effectively treats puncture-induced IVDD in rats by inhibiting oxidative stress, restoring mitochondrial function, and reducing NPC apoptosis through a PPARγ-dependent mechanism. By balancing ECM synthesis and degradation, ISL presents a novel therapeutic approach for IVDD and identifies a promising target for treatment.

摘要

目的

氧化应激、线粒体功能障碍和细胞凋亡在髓核细胞(NPCs)的细胞外基质(ECM)降解中起重要作用,最终导致椎间盘退变(IVDD)。本研究探讨了异甘草素(ISL),一种以其抗氧化、抗炎和抗动脉粥样硬化特性而闻名的天然提取物,缓解IVDD的潜力。

方法

使用CCK-8法评估用ISL和叔丁基过氧化氢(TBHP)处理的NPCs的活力。采用多种技术,包括蛋白质免疫印迹法、qRT-PCR、免疫荧光(IF)和免疫组织化学,来测量ECM成分、氧化应激标志物和凋亡相关蛋白的表达。通过蛋白质免疫印迹法和IF分析评估线粒体功能。网络药理学预测ISL靶点,并使用上述方法评估PPARγ的表达水平。通过siRNA敲低研究PPARγ在ISL对IVDD治疗作用中的作用。使用X射线、MRI和组织学染色技术评估ISL对大鼠穿刺诱导的IVDD的治疗效果。

结果

在体外,ISL降低了NPCs中的氧化应激,恢复了线粒体功能,抑制了细胞凋亡,并改善了ECM表型。在体内,ISL减缓了大鼠模型中IVDD的进展。进一步分析表明,ISL通过直接结合增强PPARγ活性并促进其表达,有助于延缓IVDD进展。

结论

本研究表明,ISL通过抑制氧化应激、恢复线粒体功能并通过PPARγ依赖性机制减少NPC凋亡,有效治疗大鼠穿刺诱导的IVDD。通过平衡ECM的合成和降解,ISL为IVDD提供了一种新的治疗方法,并确定了一个有前景的治疗靶点。

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