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Antioxidant activities of anastatin A & B derivatives and compound 38c's protective effect in a mouse model of CCl4-induced acute liver injury

机译:Anastatin A&B衍生物和化合物38C在CCL4诱导的急性肝损伤小鼠模型中的保护作用的抗氧化活性

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Anastatins A and B, two flavonoid compounds isolated from desert plant Anastatica hierochuntica , have protective activities for primary rat hepatocytes. Anastatins A and B, and their derivatives, were synthesized by our group previously. In this study, the antioxidant activity and cytotoxicity of these compounds were studied using chemical assessment methods, cell proliferation inhibition experiments, and cell oxidative damage models. The best compound, 38c , was used to study the hepatoprotection activity and mechanism by using a CCl _(4) -induced liver injury model in mice. The results show that most of these flavonoid compounds have good antioxidant activity and low cytotoxicity in vitro . Among them, the most potent compound was 38c , which exhibited a protective effect on CCl _(4) -induced hepatic injury by suppressing the amount of CYP2E1. These findings indicate that anastatin flavonoid derivatives have potential therapeutic utility against oxidative hepatic injury.
机译:Anastatins A和B,两种从沙漠植物Anastatica Hierochuntica分离的类黄酮化合物,对原代大鼠肝细胞具有保护性。 anastatins a和b及其衍生物由我们之前的组合成。在本研究中,使用化学评估方法,细胞增殖抑制实验和细胞氧化损伤模型研究了这些化合物的抗氧化活性和细胞毒性。通过使用小鼠中的CCl _(4)诱导的肝损伤模型,使用最佳化合物38℃来研究肝脏应戊接受活性和机制。结果表明,大多数这些类黄酮化合物具有良好的抗氧化活性和体外低细胞毒性。其中,最有效的化合物是38℃,这通过抑制CPO 2E1的量,对CCL _(4)诱导肝损伤的保护作用。这些发现表明,脂素黄酮衍生物具有抵抗氧化肝损伤的潜在治疗效用。

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