Xu Lu, Li Wei, Chen Shu-Yi, Deng Xi-Wen, Deng Wei-Feng, Liu Guo, Chen Yun-Jiao, Cao Yong
Guangdong Provincial Key Laboratory of Nutraceuticals and Functional Foods, Guangdong Research Center for Engineering Technology in Bioactive Natural Products, College of Food Science, South China Agricultural University, Guangzhou, China.
Institute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Shenzhen, China.
Front Nutr. 2022 Dec 12;9:1053718. doi: 10.3389/fnut.2022.1053718. eCollection 2022.
Alcoholic liver disease (ALD) is a global health problem for which there is no current food and drug administration (FDA)-approved therapy. Oenothein B (OEB) is a macrocyclic dimer ellagic tannin that possesses abundant biological activities including antioxidant, anti-inflammation, antitumor, immunomodulatory, and antimicrobial properties.
In this study, the hepatoprotective effect of OEB against ALD was investigated and .
We found that OEB treatment dramatically reduced alcohol-induced hepatic injury, as evidenced by decreased levels of aminotransferases and inflammatory biomarkers and increased antioxidant capacity in OEB-treated groups.
OEB treatment alleviated oxidative stress by upregulating the Keap1/Nrf2 signaling pathway and inhibited inflammation by downregulating the TLR4/NF-κB signaling pathway. Additionally, OEB treatment positively improved alcohol-induced intestinal microbial dysbiosis by modulating the structure and composition of gut microbiota. Interestingly, we observed the increasement of short-chain fatty acid (SCFA) producers () and the decreasement of Gram-negative bacteria () in the OEB treatment groups, which may contribute to the inhibition of hepatic oxidative stress and inflammation via the gut-liver axis. In summary, our findings indicate that OEB is a promising therapeutic strategy for preventing and treating ALD.
酒精性肝病(ALD)是一个全球性的健康问题,目前尚无美国食品药品监督管理局(FDA)批准的治疗方法。oenothein B(OEB)是一种大环二聚体鞣花单宁,具有丰富的生物活性,包括抗氧化、抗炎、抗肿瘤、免疫调节和抗菌特性。
在本研究中,研究了OEB对ALD的肝脏保护作用。
我们发现,OEB治疗显著减轻了酒精诱导的肝损伤,OEB治疗组中氨基转移酶和炎症生物标志物水平降低以及抗氧化能力增强证明了这一点。
OEB治疗通过上调Keap1/Nrf2信号通路减轻氧化应激,并通过下调TLR4/NF-κB信号通路抑制炎症。此外,OEB治疗通过调节肠道微生物群的结构和组成,积极改善了酒精诱导的肠道微生物失调。有趣的是,我们观察到OEB治疗组中短链脂肪酸(SCFA)产生菌增加,革兰氏阴性菌减少,这可能通过肠-肝轴有助于抑制肝脏氧化应激和炎症。总之,我们的研究结果表明,OEB是预防和治疗ALD的一种有前景的治疗策略。