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牛樟芝提取物调控Nrf2/HO-1通路对酒精性肝损伤的保护作用
引用本文:冯彩玲,杨彬君,吴岩斌,易骏,吴锦忠,吴建国.牛樟芝提取物调控Nrf2/HO-1通路对酒精性肝损伤的保护作用[J].菌物学报,2021,40(9):2433-2444.
作者姓名:冯彩玲  杨彬君  吴岩斌  易骏  吴锦忠  吴建国
作者单位:1.福建中医药大学药学院 福建 福州 3501222.福建教育学院理科部 福建 福州 350001
基金项目:国家自然科学基金(81700524);福建省自然科学基金(2019J01341)
摘    要:研究不同剂量(100、200和400mg/kg)的牛樟芝水提物(WE)、醇提后水提取物(WEE)和醇提物(EE)对酒精诱导的ICR小鼠急性肝损伤的保护作用和对Nrf2/HO-1抗氧化信号通路的影响。研究结果表明:与模型组比较,400mg/kg的WE和WEE均能显著抑制血清ALT和AST水平的升高,200mg/kg的WE和WEE分别显著降低血清ALT和AST含量。各剂量的WE、WEE和EE均能显著降低肝脏MDA含量,200和400mg/kg的WE和不同剂量的WEE均可明显提高肝脏的SOD和CAT活力。H&E染色结果表明WE、WEE和EE对酒精诱导的肝损伤均有一定的改善作用,EE处理组的效果相对较差。免疫组化染色结果表明各剂量的WE、WEE和EE均能促进Nrf2的核转位,诱导HO-1的表达,提高肝脏的抗氧化能力,对酒精诱导的急性肝损伤具有明显的保护作用。提示牛樟芝能通过调节Nrf2/HO-1抗氧化信号通路发挥解酒保肝功效。

关 键 词:牛樟芝  提取物  酒精性肝损伤  Nrf2/HO-1抗氧化信号通路  保护作用  
收稿时间:2021-03-30

Hepatoprotective effects of extracts of Taiwanofungus camphoratus on liver with alcohol-induced injury through regulation of Nrf2/HO-1 signaling pathway
Authors:FENG Cai-Ling  YANG Bin-Jun  WU Yan-Bin  YI Jun  WU Jin-Zhong  WU Jian-Guo
Institution:1. School of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, Fujian 350122, China2. Department of Science, Fujian Institute of Education, Fuzhou, Fujian 350001, China
Abstract:Protective effects of different doses (100, 200 and 400mg/kg) of water extract (WE), water extract after extraction by ethanol (WEE) and ethanol extract (EE) of Taiwanofungus camphoratu on alcohol-induced acute liver injury in ICR mice, as well as Nrf2/HO-1 antioxidant signaling pathway were investigated. Compared with the model group, 400mg/kg dosage of both WE and WEE could inhibit the increase of serum ALT and AST levels significantly, and 200mg/kg of WE and WEE could obviously decrease the serum ALT and AST content, respectively. Different doses of WE, WEE and EE could significantly reduce the content of hepatic MDA; 200 and 400mg/kg of WE and different doses of WEE could markedly increase hepatic SOD and CAT activities. H&E staining observation indicated that WE, WEE and EE could mitigate alcoholic liver injury to a certain degree, but a relative lower effect was observed in EE-treated groups. The immunohistochemical staining results indicated that different dose of WE, WEE and EE could enhance the nuclear translocation of Nrf2 and promote the expression of HO-1 to improve the hepatic antioxidant capacity, thus presenting a significant protective effect on alcohol-induced acute liver injury. It was suggested that Taiwanofungus camphoratus exhibited drunkenness-alleviating and liver-protecting effects via regulating the Nrf2 antioxidant signaling pathway.
Keywords:Taiwanofungus camphoratus  extracts  alcoholic liver injury  Nrf2/HO-1 antioxidant signaling pathway  protective effect  
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