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首页> 外文期刊>Natural product communications >Asiatic acid derivatives protect primary cultures of rat hepatocytes against carbon tetrachloride-induced injury via the cellular antioxidant system
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Asiatic acid derivatives protect primary cultures of rat hepatocytes against carbon tetrachloride-induced injury via the cellular antioxidant system

机译:亚洲酸衍生物通过细胞抗氧化剂系统保护大鼠肝细胞的原代培养物免受四氯化碳诱导的损伤

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摘要

We attempted to elucidate the hepatoprotective mechanism of two asiatic acid (AS) derivatives, 3β,23-dihydroxyurs-2-oxo-12-ene-28-oic acid (AS-10) and 3β,23-dihydroxyurs-12-ene-28-oic acid (AS-14), which exhibited significant protective activity against carbon tetrachloride (CCl _4)-induced hepatotoxicity in primary cultures of rat hepatocytes. Our findings showed that AS-10 and AS-14 preserved the level of glutathione and the activities of antioxidant enzymes such as glutathione reductase, glutathione peroxidase, superoxide dismutase and catalase. In addition, these compounds ameliorated lipid peroxidation, as demonstrated by a reduction in the production of malondialdehyde. Furthermore, AS-10 and AS-14 did not restore the reduced total GSH level by BSO, indicating that the hepatoprotective activities of these compounds may be involved, in part, by regulating GSH synthesis. From these results, we suggest that both AS-10 and AS-14 exerted their hepatoprotective activities against CCl4-induced injury by preserving the cellular antioxidative defense system.
机译:我们试图阐明两种积雪草酸(AS)衍生物3β,23-dihydroxyurs-2-oxo-12-ene-28-oic acid(AS-10)和3β,23-dihydroxyurs-12-ene-的肝保护机制。 28-oic acid(AS-14)在大鼠肝细胞的原代培养物中表现出显着的抗四氯化碳(CCl _4)诱导的肝毒性的保护活性。我们的发现表明,AS-10和AS-14保留了谷胱甘肽的水平以及抗氧化酶的活性,如谷胱甘肽还原酶,谷胱甘肽过氧化物酶,超氧化物歧化酶和过氧化氢酶。此外,这些化合物改善了脂质过氧化作用,如丙二醛产量减少所证明。此外,AS-10和AS-14不能通过BSO恢复降低的总GSH水平,表明这些化合物的保肝活性可能部分地通过调节GSH合成而发挥作用。从这些结果,我们建议AS-10和AS-14都通过保留细胞抗氧化防御系统发挥其对CCl4诱导的损伤的肝保护活性。

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