Jie Yang , Zhenwei Zhou , Xiaolei Ding , Rong He , Ailin Li , Yuchi Wei , Mingyue Wang , Zeyu Peng , Zhanliang Jiang , Daqing Zhao , Xiangyan Li , Xiangyang Leng , Haisi Dong
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It was estimated by Micro-CT, Gait Analysis, Histological Stain. RNA-seq technology was performed with OA Rats' cartilage, and primary chondrocytes induced by IL-1β (mimics OA chondrocytes) were utilized to evaluated and investigated the mechanism of how GBZTF protected OA cartilage from being damaged with some functional experiments.</p></div><div><h3>Results</h3><p>A total of 1006 compounds were identified under positive and negative ion modes by LC-MS. Then, we assessed the function of GBZTF through <em>in vitro</em> and <em>vivo</em>. It was found GBZTF could significantly up-regulate OA rats’ limb coordination and weight-bearing capacity, and reduce the surface and sub-chondral bone erosions of OA joints, and protect cartilage from being destroyed by inflammatory factors (iNOS, IL-6, IL-1β, TNF- α, MMP13, ADAMTS5), and promote OA chondrocytes proliferation and increase the S phage of cell cycle. In terms of mechanism, RNA-seq analysis of cartilage tissues revealed 1,778 and 3,824 differentially expressed genes (DEGs) in model vs control group and GBZTF vs model group, respectively. The mitophagy pathway was most significantly enriched in these DEGs. Further results of subunits of OA chondrocytes confirmed that GBZTF could alleviate OA-associated inflammation and cartilage damage through modulation BCL2 interacting protein 3-like (BNIP3L)-mediated mitophagy.</p></div><div><h3>Conclusion</h3><p>The therapeutic effectiveness of GBZTF on OA were first time verified <em>in vivo</em> and <em>vitro</em> through functional experiments and RNA-seq, which provides convincing evidence to support the molecular mechanisms of GBZTF as a promising therapeutic decoction for OA.</p></div>","PeriodicalId":20212,"journal":{"name":"Phytomedicine","volume":"128 ","pages":"Article 155279"},"PeriodicalIF":6.7000,"publicationDate":"2024-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Gubi Zhitong formula alleviates osteoarthritis in vitro and in vivo via regulating BNIP3L-mediated mitophagy\",\"authors\":\"Jie Yang , Zhenwei Zhou , Xiaolei Ding , Rong He , Ailin Li , Yuchi Wei , Mingyue Wang , Zeyu Peng , Zhanliang Jiang , Daqing Zhao , Xiangyan Li , Xiangyang Leng , Haisi Dong\",\"doi\":\"10.1016/j.phymed.2023.155279\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Osteoarthritis (OA) is characterized by degeneration of articular cartilage, leading to joint pain and dysfunction. Gubi Zhitong formula (GBZTF), a traditional Chinese medicine formula, has been used in the clinical treatment of OA for decades, demonstrating definite efficacy. However, its mechanism of action remains unclear, hindering its further application.</p></div><div><h3>Methods</h3><p>The ingredients of GBZTF were analyzed and performed with liquid chromatography-mass spectrometry (LC-MS). 6 weeks old SD rats were underwent running exercise (25 m/min, 80 min, 0°) to construct OA model with cartilage wear and tear. It was estimated by Micro-CT, Gait Analysis, Histological Stain. RNA-seq technology was performed with OA Rats' cartilage, and primary chondrocytes induced by IL-1β (mimics OA chondrocytes) were utilized to evaluated and investigated the mechanism of how GBZTF protected OA cartilage from being damaged with some functional experiments.</p></div><div><h3>Results</h3><p>A total of 1006 compounds were identified under positive and negative ion modes by LC-MS. Then, we assessed the function of GBZTF through <em>in vitro</em> and <em>vivo</em>. It was found GBZTF could significantly up-regulate OA rats’ limb coordination and weight-bearing capacity, and reduce the surface and sub-chondral bone erosions of OA joints, and protect cartilage from being destroyed by inflammatory factors (iNOS, IL-6, IL-1β, TNF- α, MMP13, ADAMTS5), and promote OA chondrocytes proliferation and increase the S phage of cell cycle. In terms of mechanism, RNA-seq analysis of cartilage tissues revealed 1,778 and 3,824 differentially expressed genes (DEGs) in model vs control group and GBZTF vs model group, respectively. The mitophagy pathway was most significantly enriched in these DEGs. 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引用次数: 0
摘要
背景骨关节炎(OA)的特点是关节软骨退化,导致关节疼痛和功能障碍。传统中药古方 "归脾汤"(GBZTF)用于临床治疗 OA 已有数十年历史,疗效确切,但其作用机制尚不明确,阻碍了其进一步应用。方法采用液相色谱-质谱法(LC-MS)分析 GBZTF 的成分。对 6 周龄 SD 大鼠进行跑步运动(25 米/分钟,80 分钟,0°),以建立软骨磨损的 OA 模型。通过显微 CT、步态分析和组织学染色进行评估。对OA大鼠软骨进行RNA-seq技术研究,并利用IL-1β诱导的原代软骨细胞(模拟OA软骨细胞)进行功能实验,评估和研究GBZTF保护OA软骨免受损伤的机制。然后,我们通过体外和体内实验评估了GBZTF的功能。结果发现,GBZTF能显著提高OA大鼠的肢体协调性和负重能力,减少OA关节表面和软骨下骨的侵蚀,保护软骨免受炎症因子(iNOS、IL-6、IL-1β、TNF- α、MMP13、ADAMTS5)的破坏,促进OA软骨细胞增殖和细胞周期S期的延长。在机制方面,软骨组织的RNA-seq分析显示,模型组与对照组、GBZTF组与模型组分别有1778个和3824个差异表达基因(DEGs)。在这些差异表达基因中,有丝分裂途径的表达最为丰富。结论 通过功能实验和RNA-seq,首次在体内和体外验证了GBZTF对OA的治疗效果,为GBZTF作为一种有前景的OA治疗煎剂的分子机制提供了令人信服的证据。
Gubi Zhitong formula alleviates osteoarthritis in vitro and in vivo via regulating BNIP3L-mediated mitophagy
Background
Osteoarthritis (OA) is characterized by degeneration of articular cartilage, leading to joint pain and dysfunction. Gubi Zhitong formula (GBZTF), a traditional Chinese medicine formula, has been used in the clinical treatment of OA for decades, demonstrating definite efficacy. However, its mechanism of action remains unclear, hindering its further application.
Methods
The ingredients of GBZTF were analyzed and performed with liquid chromatography-mass spectrometry (LC-MS). 6 weeks old SD rats were underwent running exercise (25 m/min, 80 min, 0°) to construct OA model with cartilage wear and tear. It was estimated by Micro-CT, Gait Analysis, Histological Stain. RNA-seq technology was performed with OA Rats' cartilage, and primary chondrocytes induced by IL-1β (mimics OA chondrocytes) were utilized to evaluated and investigated the mechanism of how GBZTF protected OA cartilage from being damaged with some functional experiments.
Results
A total of 1006 compounds were identified under positive and negative ion modes by LC-MS. Then, we assessed the function of GBZTF through in vitro and vivo. It was found GBZTF could significantly up-regulate OA rats’ limb coordination and weight-bearing capacity, and reduce the surface and sub-chondral bone erosions of OA joints, and protect cartilage from being destroyed by inflammatory factors (iNOS, IL-6, IL-1β, TNF- α, MMP13, ADAMTS5), and promote OA chondrocytes proliferation and increase the S phage of cell cycle. In terms of mechanism, RNA-seq analysis of cartilage tissues revealed 1,778 and 3,824 differentially expressed genes (DEGs) in model vs control group and GBZTF vs model group, respectively. The mitophagy pathway was most significantly enriched in these DEGs. Further results of subunits of OA chondrocytes confirmed that GBZTF could alleviate OA-associated inflammation and cartilage damage through modulation BCL2 interacting protein 3-like (BNIP3L)-mediated mitophagy.
Conclusion
The therapeutic effectiveness of GBZTF on OA were first time verified in vivo and vitro through functional experiments and RNA-seq, which provides convincing evidence to support the molecular mechanisms of GBZTF as a promising therapeutic decoction for OA.
期刊介绍:
Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.