Combination of chlorogenic acid and salvianolic acid B protects against polychlorinated biphenyls-induced oxidative stress through Nrf2

Combination of chlorogenic acid and salvianolic acid B protects against polychlorinated biphenyls-induced oxidative stress through Nrf2
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绿原酸和丹酚酸 B 的组合可通过 Nrf2 防止多氯联苯诱导的氧化应激。

DOI:
10.1016/j.etap.2016.08.004
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发表时间:
2016-09-01
影响因子:
4.3
通讯作者:
Li, Lei
Li, Lei
中科院分区:
环境科学与生态学3区
文献类型:
--
作者:
Chen, Lijun;Li, Yuan;Li, Lei

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咖啡酸衍生物(CADs)是一类具有多种生理和药理活性的植物化学物质。本研究旨在探讨CADs对PCB 126诱导的小鼠肝损伤和氧化应激的联合保护作用。本研究采用化学发光法,筛选出绿原酸(CGA)、丹参素B(Sal B)作为抗氧化剂。然后,小鼠灌胃给予60 mg/kg/d的CGA、Sal B和CGA + Sal B(1:1)3周,然后暴露于0.05 mg/kg/d的PCB 126 2周。结果表明,CGA、Sal B、CGA + Sal B预处理均能有效减轻PCB 126所致的肝损伤和细胞毒作用,提高超氧化物歧化酶(SOD)、还原型谷胱甘肽(GSH)、血红素加氧酶-1(HO-1)和核因子E2相关因子2(Nrf 2)的表达,其中以CGA + Sal B的效果最好,具有协同保护作用。综上所述,由于Nrf 2通过上调抗氧化基因的表达来调节细胞保护反应,我们认为CGA和Sal B对PCB 126诱导的组织损伤具有联合保护作用,Nrf 2信号通路可能参与其中。(C)© 2016 Elsevier B. V.版权所有。
Caffeic acid derivatives (CADs) are well-known phytochemicals with multiple physiological and pharmacological activities. This study aimed to investigate the combined protective effects of CADs on PCB126-induced liver damages and oxidative stress in mice. Here, we used chemiluminescence and chose chlorogenic acid (CGA), salvianolic acid B (Sal B) as the best antioxidants. Then, mice were intra-gastrically administered with 60 mg/kg/d CGA, Sal B, and CGA plus Sal B (1:1) for 3 weeks before exposing to 0.05 mg/kg/d PCB126 for 2 weeks. We found that pretreatment with CGA, Sal B, and CGA plus Sal B effectively attenuated liver injury and cytotoxicity caused by PCB126, but improved the expressions of superoxide dismutase (SOD), glutathione reduced (GSH), heme oxygenase-1 (HO-1) and nuclear factor E2-related factor 2 (Nrf2), CGA plus Sal B especially, was found to have the best effects that indicated a synergetic protective effect. Taken together, as the Nrf2 regulates the cyto-protective response by up-regulating the expression of antioxidant genes, we suggested that CGA plus Sal B had a combined protection on PCB126-induced tissue damages and that the Nrf2 signaling might be involved. (C) 2016 Elsevier B.V. All rights reserved.