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Metabolic Profiling of Buddleia indica Leaves using LC/MS and Evidence of their Antioxidant and Hepatoprotective Activity Using Different In Vitro and In Vivo Experimental Models

机译:LC / MS对醉鱼d叶片的代谢谱分析以及不同体内和体外实验模型的抗氧化和保肝活性的证据

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摘要

LC-ESI-MS (Liquid Chromatography coupled with Electrospray Ionization Mass Spectrometry profiling of a methanol extract from Buddleia indica (BIM) leaves revealed 12 main peaks in which verbascoside and buddlenoid B represent the major compounds. The antioxidant and hepatoprotective activities of BIM were investigated using different in vitro and in vivo experimental models. BIM exhibited substantial in vitro antioxidant properties in DPPH· and HepG2 assays. Regarding CCl4 (carbon tetrachloride) induced hepatotoxicity in a rat model, oxidative stress markers became significantly ameliorated after oral administration of BIM. Lipid peroxide levels showed a 51.85% decline relative to CCl4-treated rats. Super oxide dismutase (SOD), total antioxidant status (TAS), and catalase (CAT) revealed a marked increase by 132.48%, 187.18%, and 114.94% relative to the CCl4 group. In a tamoxifen-induced hepatotoxicity model, BIM showed a considerable alleviation in liver stress markers manifested by a 46.06% and 40% decline in ALT (Alanine Transaminase) and AST (Aspartate Transaminase) respectively. Thiobarbituric acid reactive substances (TBARS) were reduced by 28.57% and the tumor necrosis factor alpha (TNF-α) level by 50%. A virtual screening of major secondary metabolites of BIM to TNF-alpha employing the C-docker protocol showed that gmelinoside H caused the most potent TNF- α inhibition as indicated from their high fitting scores. Thus, BIM exhibited a potent hepatoprotective activity owing to its richness in antioxidant metabolites.
机译:LC-ESI-MS(液相色谱-电喷雾电离质谱联用技术对印度醉鱼草(BIM)叶片中甲醇提取物的分析显示了12个主要峰,其中马齿ver甙和芽孢杆菌B代表主要化合物,并研究了BIM的抗氧化和保肝活性使用不同的体外和体内实验模型,BIM在DPPH·和HepG2分析中显示出显着的体外抗氧化特性;关于CCl4(四氯化碳)在大鼠模型中引起的肝毒性,口服BIM后氧化应激标志物明显改善。相对于CCl4处理的大鼠,过氧化物水平降低了51.85%,超氧化物歧化酶(SOD),总抗氧化剂状态(TAS)和过氧化氢酶(CAT)则相对于CCl4处理的大鼠显着增加了132.48%,187.18%和114.94%。 CCl4组:在他莫昔芬诱导的肝毒性模型中,BIM显着减轻了肝应激标志物,其表现为ALT(丙氨酸转氨酶)和AST(天冬氨酸转氨酶)分别下降46.06%和40%。硫代巴比妥酸反应性物质(TBARS)降低了28.57%,肿瘤坏死因子α(TNF-α)水平降低了50%。使用C-docker协议对BIM对TNF-α的BIM主要次要代谢产物进行虚拟筛选显示,从其高拟合度得分来看,g子苷H引起最强的TNF-α抑制作用。因此,由于BIM富含抗氧化剂代谢物,因此具有强大的保肝活性。

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