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齐墩果酸体外抗氧化活性:Nrf2 和 MAP 激酶的可能作用。

Antioxidant activities of oleanolic acid in vitro: possible role of Nrf2 and MAP kinases.

机构信息

Department of Toxicology, Faculty of Preventive Medicine, Fourth Military Medical University, Xi'an, 710032 Shaanxi, China.

出版信息

Chem Biol Interact. 2010 Mar 30;184(3):328-37. doi: 10.1016/j.cbi.2010.01.034. Epub 2010 Jan 25.

Abstract

Oleanolic acid (OA) is a natural triterpenoid, which has been used in Chinese medicine for the treatment of liver disorders for many years. Its pharmacological activities have been the focus of intense research in recent years. However, there is little research on the antioxidant activities of OA. In the present study, we aim to investigate whether OA produces its protective effects mainly through antioxidant mechanisms and whether OA plays as an antioxidant through quenching reactive oxygen species (ROS), inhibiting lipid peroxidation or stimulating cellular antioxidant defenses. In the in vitro antioxidant activity-assessing models, OA acted as not only a free radical-scavenger through direct chemical reactions but also a biological molecule, which may enhance the antioxidant defenses. tert-Butyl hydroperoxide (tBHP) induced ROS generation, damaged plasma membrane and decreased cell viability and the expression of key antioxidant enzymes and MAP kinases in QZG cells. OA ameliorated the oxidative injury induced by tBHP through increasing the generation of antioxidant (glutathione) and the expression of key antioxidant enzymes mediated by nuclear factorerythroid 2 p45-related factor 2 (Nrf2), in which process, activation of JNK and ERK, but not p38, was involved. The present study, for the first time, investigated the antioxidant activities of OA systematically. OA probably functions mainly through indirect biological effect and protects QZG cells against cytotoxicity induced by tBHP through increasing the generation of antioxidant and the expression of oxidative stress sensitive transcription factor-Nrf2, and MAP kinases, mainly JNK and ERK. These findings may significantly better the understanding of OA and advance therapeutic approaches to the diseases which are associated with oxidative stress.

摘要

齐墩果酸(OA)是一种天然的三萜类化合物,多年来一直被用于中医治疗肝脏疾病。近年来,其药理活性一直是研究的热点。然而,关于 OA 的抗氧化活性研究甚少。本研究旨在探讨 OA 是否主要通过抗氧化机制产生其保护作用,以及 OA 是否通过淬灭活性氧(ROS)、抑制脂质过氧化或刺激细胞抗氧化防御来发挥抗氧化作用。在体外抗氧化活性评估模型中,OA 不仅通过直接化学反应作为自由基清除剂,而且作为一种生物分子,可能增强抗氧化防御。叔丁基过氧化物(tBHP)诱导 ROS 的产生,破坏质膜,降低细胞活力以及 QZG 细胞中关键抗氧化酶和 MAP 激酶的表达。OA 通过增加抗氧化剂(谷胱甘肽)的产生和核因子红细胞 2 p45 相关因子 2(Nrf2)介导的关键抗氧化酶的表达,改善 tBHP 诱导的氧化损伤,在这个过程中,涉及 JNK 和 ERK 的激活,但不涉及 p38。本研究首次系统地研究了 OA 的抗氧化活性。OA 可能主要通过间接的生物学作用发挥作用,通过增加抗氧化剂的产生和氧化应激敏感转录因子 Nrf2 的表达以及 MAP 激酶(主要是 JNK 和 ERK)来保护 QZG 细胞免受 tBHP 诱导的细胞毒性。这些发现可能会显著加深对 OA 的理解,并推进与氧化应激相关疾病的治疗方法。

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