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二甲双胍和木犀草素联合使用可协同保护四氯化碳诱导的肝毒性:其机制涉及抗氧化、抗炎、抗凋亡和 Nrf2/HO-1 信号通路。

Combination of metformin and luteolin synergistically protects carbon tetrachloride-induced hepatotoxicity: Mechanism involves antioxidant, anti-inflammatory, antiapoptotic, and Nrf2/HO-1 signaling pathway.

机构信息

Department of Digestive Medicine, Hefei Second People's Hospital, Hefei, China.

Department of Internal Medicine, CAS Cancer Hospital, Hefei, China.

出版信息

Biofactors. 2019 Jul;45(4):598-606. doi: 10.1002/biof.1521. Epub 2019 Jul 23.

Abstract

Liver diseases are one of the fatal disorders due to the vital role of the liver. Carbon tetrachloride (CCl ) is the most perceived chemical substance utilized in developing models of hepatic damage. Metformin (Met) is a potent antidiabetic and redox modulatory agent that has shown anticancer and protective effects on various organs. Therefore, addition of therapy with natural antioxidative agents or herbal extracts shows defensive impacts against different injuries inside the body. Luteolin (Lut) can be found in several customary Chinese remedies. It has been reported for various pharmacological actions such as antitumor, antioxidative, and anti-inflammatory impacts. Here, the liver injury rat model was established using CCl (1.00 mL/kg body weight) in vivo. The protective roles of Met and Lut separately or in combination were observed in hepatotoxicity induced by CCl . The result was shown that both Met and Lut, while individually used, were normally active in diminishing CCl -caused hepatotoxicity. The combination of two drugs performed synergistically to improve liver damage caused by CCl , as shown by the considerably improved liver dysfunction. Met and Lut showed highly antioxidative effects on CCl -treated rats moderately by increasing the activities and expression of the antioxidant enzymes. Along with this, a combination of Met and Lut significantly suppressed inflammatory responses, which is evidenced by the reduced level of inflammatory cytokines together with interleukin 1 beta (IL-1β), tumor necrosis factor alpha (TNF-α), and interleukin 6 (IL-6). Additionally, CCl -agitated apoptosis was intensely reduced by Met and Lut through reducing cleaved caspase-3 and Bax (pro-apoptotic factor) while increasing Bcl-2 (antiapoptotic factor) signaling pathways. Cotreatments of Met and Lut upregulated nuclear factor erythroid 2-related factor 2 (NRF2) and heme oxygenase-1 (HO-1) expression in the CCl -intoxicated rat's liver. The above result recommended that combination of Met and Lut may have a substantial potential and synergizing impact against CCl -induced hepatotoxicity.

摘要

肝脏疾病是一种致命的疾病,因为肝脏起着至关重要的作用。四氯化碳(CCl )是用于开发肝损伤模型的最常见的化学物质。二甲双胍(Met)是一种有效的抗糖尿病和氧化还原调节剂,对各种器官具有抗癌和保护作用。因此,添加天然抗氧化剂或草药提取物的治疗方法显示出对体内不同损伤的防御作用。木犀草素(Lut)可以在几种常用的中药中找到。据报道,它具有多种药理作用,如抗肿瘤、抗氧化和抗炎作用。在这里,使用 CCl (1.00 毫升/千克体重)在体内建立了肝损伤大鼠模型。观察了 Met 和 Lut 单独或联合使用时对 CCl 诱导的肝毒性的保护作用。结果表明,Met 和 Lut 单独使用时,均可有效减轻 CCl 引起的肝毒性。两种药物联合使用可协同改善 CCl 引起的肝损伤,表现为肝功能显著改善。Met 和 Lut 对 CCl 处理的大鼠具有很强的抗氧化作用,适度增加抗氧化酶的活性和表达。此外,Met 和 Lut 联合显著抑制了炎症反应,这表现在炎症细胞因子水平的降低,以及白细胞介素 1β(IL-1β)、肿瘤坏死因子α(TNF-α)和白细胞介素 6(IL-6)的减少。此外,Met 和 Lut 通过减少 cleaved caspase-3 和 Bax(促凋亡因子),同时增加 Bcl-2(抗凋亡因子)信号通路,强烈减少 CCl 引起的细胞凋亡。Met 和 Lut 的联合治疗上调了 CCl 中毒大鼠肝脏中核因子红细胞 2 相关因子 2(NRF2)和血红素加氧酶-1(HO-1)的表达。上述结果表明,Met 和 Lut 的联合治疗可能对 CCl 诱导的肝毒性具有显著的潜力和协同作用。

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