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Chemical Profiling of Polyphenolics in Eucalyptus globulus and Evaluation of Its Hepato–Renal Protective Potential Against Cyclophosphamide Induced Toxicity in Mice

机译:桉树茶中多酚类化合物的化学谱分析及其对环磷酰胺诱导的小鼠肝毒性的肾脏保护作用

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摘要

Cyclophosphamide (CP) is a potent anti-neoplastic and immunosuppressive agent; however, it causes multi-organ toxicity. We elucidated the protective activities of Eucalyptus globulus (EG) leaf extract against CP-induced hepato–renal toxicity. Mice were treated with EG for 15 days plus CP on day 12 and 13 of the experiment. Using HPLC-DAD-ESI-MS/MS, 26 secondary metabolites were identified in EG leaf extract. Out of them, 4 polyphenolic compounds were isolated: (1) 4-(O-β-d-xylopyranosyloxy)-3,5-di-hydroxy-benzoic acid, (2) 4-(O-α-l-rhamnopyranosyloxy)-3,5-di-hydroxy-benzoic acid, (3) gallic acid, and (4) methyl gallate. Effects of EG extract on biochemical parameters, gene expression, and immune-histopathological changes were assessed in comparison to mesna positive control. Results showed that EG improved CP-increased serum ALT, AST, creatinine, and blood urea nitrogen levels. The hepatic and renal tissue levels of MDA, nitric oxide, protein carbonyl, TNF-α, IL-6, and immunohistochemical expression of nuclear factor kappa-B (NF-kB) and caspase-3 were reduced. Also, hepatic and renal GSH contents, and nuclear factor E2-related factor 2 (NRf2)/ hemoxygenase-1 (HO-1) signaling levels were increased. Histopathological findings supported our findings where hepatic and renal architecture were almost restored. Results revealed the protective effects of EG against CP-induced hepato–renal toxicity. These effects may be related to EG antioxidant, anti-inflammatory, and anti-apoptotic properties coupled with activation of Nrf2/HO-1 signaling.
机译:环磷酰胺(CP)是一种有效的抗肿瘤和免疫抑制剂;但是,它会引起多器官毒性。我们阐明了桉树叶提取物对CP诱导的肝肾毒性的保护作用。在实验的第12天和第13天,用EG对小鼠进行15天加CP的治疗。使用HPLC-DAD-ESI-MS / MS,在EG叶提取物中鉴定出26种次级代谢产物。从其中分离出4种多酚化合物:(1)4-(O-β-d-吡喃并吡喃糖基氧基)-3,5-二羟基苯甲酸,(2)4-(O-α-l-鼠李糖基吡喃糖基氧基) -3,5-二羟基苯甲酸,(3)没食子酸和(4)没食子酸甲酯。与mesna阳性对照相比,评估了EG提取物对生化参数,基因表达和免疫组织病理学变化的影响。结果显示,EG改善了CP增加的血清ALT,AST,肌酐和血液尿素氮水平。肝和肾组织中的MDA,一氧化氮,蛋白质羰基,TNF-α,IL-6以及核因子κB(NF-kB)和caspase-3的免疫组织化学表达均降低。此外,肝和肾中GSH的含量以及核因子E2相关因子2(NRf2)/ hemoxygenase-1(HO-1)信号水平均升高。组织病理学发现支持了我们的肝和肾结构几乎得以恢复的发现。结果显示了EG对CP诱导的肝肾毒性的保护作用。这些作用可能与EG抗氧化剂,抗炎和抗凋亡特性以及Nrf2 / HO-1信号的激活有关。

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