安普克
芦丁
非酒精性脂肪肝
脂质代谢
化学
医学
氧化应激
药理学
脂肪肝
内科学
内分泌学
生物化学
抗氧化剂
蛋白激酶A
激酶
疾病
作者
Yadi Liu,Zhongyan Sun,Ruixue Dong,Peiyu Liu,Xi Zhang,Yiran Li,Xiaoshan Lai,Hio-Fai Cheong,Yuwei Wu,Yilin Wang,Hua Zhou,Dingkun Gui,Youhua Xu
出处
期刊:Phytomedicine
[Elsevier]
日期:2024-02-09
卷期号:126: 155437-155437
被引量:33
标识
DOI:10.1016/j.phymed.2024.155437
摘要
In diabetic liver injury, nonalcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disease. Rutin is a bioflavonoid produced by the hydrolysis of glucosidases to quercetin. Its biological activities include lowering blood glucose, regulating insulin secretion, regulating dyslipidemia, and exerting anti-inflammatory effects have been demonstrated. However, its effect on diabetic NAFLD is rarely reported. Our study aimed to investigate the protective effects of Rutin on diabetic NAFLD and potential pharmacological mechanism. We used db/db mice as the animal model to investigate diabetic NAFLD. Oleic acid-treated (OA) HeLa cells were examined whether Rutin had the ability to ameliorate lipid accumulation. HepG2 cells treated with 30 mM/l d-glucose and palmitic acid (PA) were used as diabetic NAFLD in vitro models. Total cholesterol (TC) and Triglycerides (TG) levels were determined. Oil red O staining and BODIPY 493/503 were used to detect lipid deposition within cells. The indicators of inflammation and oxidative stress were detected. The mechanism of Rutin in diabetic liver injury with NAFLD was analyzed using RNA-sequence and 16S rRNA, and the expression of fat-synthesizing proteins in the 5′ adenosine monophosphate-activated protein kinase (AMPK) pathway was investigated. Compound C inhibitors were used to further verify the relationship between AMPK and Rutin in diabetic NAFLD. Rutin ameliorated lipid accumulation in OA-treated HeLa. In in vitro and in vivo models of diabetic NAFLD, Rutin alleviated lipid accumulation, inflammation, and oxidative stress. 16S analysis showed that Rutin could reduce gut microbiota dysregulation, such as the ratio of Firmicutes to Bacteroidetes. RNA-seq showed that the significantly differentially genes were mainly related to liver lipid metabolism. And the ameliorating effect of Rutin on diabetic NAFLD was through AMPK/SREBP1 pathway and the related lipid synthesis proteins was involved in this process. Rutin ameliorated diabetic NAFLD by activating the AMPK pathway and Rutin might be a potential new drug ingredient for diabetic NAFLD.
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