Metabolomics and molecular docking-directed antiarthritic study of the ethyl acetate extract from Celastrus orbiculatus Thunb.

IF 4.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Journal of ethnopharmacology Pub Date : 2022-08-10 DOI:10.1016/j.jep.2022.115369
Mengying Lv , Qiaoling Liang , Xiayun Wan , Zheng Wang , Yayun Qian , Jie Xiang , Zhaoyong Luo , Tengyang Ni , Wei Jiang , Weimin Wang , Haibo Wang , Yanqing Liu
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引用次数: 4

Abstract

Ethnopharmacological relevance

Celastrus orbiculatus Thunb., an important folk medicine, has long been used for the treatment of rheumatoid arthritis and its ethyl acetate extract (COE) has been reported to possess anticancer, antiinflammation and antiarthritic effects. However, the therapeutic effect and mechanism of COE treatment in rheumatoid arthritis has been rarely studied especially from the perspective of metabolomics.

Aim of study

To reveal the therapeutic effects of COE on adjuvant–induced arthritis (AIA) rats through histopathological analysis, non-targeted metabolomics, and molecular docking study.

Materials and methods

Forty-three Wistar rats were randomly divided into normal group, AIA model group, methotrexate group, and COE groups (80 mg/kg, 160 mg/kg and 320 mg/kg of ethyl acetate extract). Paw swelling and arthritis score were monitored through the experiment. Serum levels of tumor necrosis factor α (TNF-α) and nitric oxide were determined and histopathological evaluation was performed. Furthermore, Ultra-high performance liquid chromatography-linear trap quadrupole-Orbitrap-based metabolomics was employed to characterize metabolic changes of AIA rats after COE treatment and molecular docking was performed to predict the potential phytochemicals of COE against TNF-α.

Results

COE at three dosages could significantly relieve paw swelling and reduce arthritis scores of AIA rat. Histopathological analysis revealed remarkable decrease in synovial inflammation and bone erosion after COE treatment, especially at middle and high dosage. Additionally, COE down-regulated serum levels of TNF-α and nitric oxide. Serum metabolomics showed that 22 potential biomarkers for the COE treatment of AIA rats were identified, which were closely related to fatty acid metabolism, glycerophospholipid catabolism, and tryptophan metabolism. The molecular docking models predicted that olean-type triterpenes in COE may contribute most to therapeutic effects of rheumatoid arthritis through targeting TNF-α.

Conclusions

COE could significantly relieve the arthritic symptoms in AIA rats and the ultra-high performance liquid chromatography-mass spectrometry based metabolomics proved to be an efficient method to characterize subtle metabolic changes of AIA rats after COE treatment.

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环芹乙酸乙酯提取物的代谢组学及分子对接抗关节炎研究。
民族药理学相关性:黄鳝。黄芪是一种重要的民间药物,长期以来被用于治疗类风湿性关节炎,其乙酸乙酯提取物(COE)具有抗癌、抗炎和抗关节炎的作用。然而,COE治疗类风湿关节炎的疗效和机制研究很少,特别是从代谢组学的角度研究。研究目的通过组织病理学分析、非靶向代谢组学和分子对接研究,揭示COE对佐剂性关节炎(AIA)大鼠的治疗作用。材料与方法43只Wistar大鼠随机分为正常组、AIA模型组、甲氨蝶呤组和COE组(乙酸乙酯提取物80 mg/kg、160 mg/kg和320 mg/kg)。通过实验监测足跖肿胀和关节炎评分。测定血清肿瘤坏死因子α (TNF-α)和一氧化氮水平,并进行组织病理学评价。此外,采用超高高效液相色谱-线性陷阱-四极轨道代谢组学方法表征COE处理后AIA大鼠的代谢变化,并进行分子对接预测COE对TNF-α的潜在植物化学物质。结果三剂量scoe均能显著缓解AIA大鼠足跖肿胀,降低关节炎评分。组织病理学分析显示,COE治疗后滑膜炎症和骨侵蚀明显减少,特别是中、高剂量组。此外,COE降低血清TNF-α和一氧化氮水平。血清代谢组学结果显示,鉴定出22个COE治疗AIA大鼠的潜在生物标志物,它们与脂肪酸代谢、甘油磷脂分解代谢和色氨酸代谢密切相关。分子对接模型预测,COE中的齐墩型三萜可能通过靶向TNF-α对类风湿关节炎的治疗作用贡献最大。结论COE能显著缓解AIA大鼠的关节炎症状,基于超高效液相色谱-质谱的代谢组学方法是表征COE治疗后AIA大鼠细微代谢变化的有效方法。
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来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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