A synthetic peptide AWRK6 ameliorates metabolic associated fatty liver disease: involvement of lipid and glucose homeostasis

• Published in: Peptides (New York, N.Y. : 1980) N.Y. : 1980), 2021-09, Vol.143, p.170597-170597, Article 170597
• Main Authors: Jin, Lili, Sun, Yuxin, Li, Yuying, Zhang, Hanyu, Yu, Wenxue, Li, Yiling, Xin, Yi, Alsareii, Saeed Ali, Wang, Qiuyu, Zhang, Dianbao
• Format: Article
• Language: English
• Subjects: Animals; AWRK6; Diet, High-Fat; Glucose homeostasis; Hep G2 Cells; Humans; Insulin Resistance; Lipid Metabolism; MAFLD; Male; Mice; Mice, Obese; NAFLD; Non-alcoholic Fatty Liver Disease - drug therapy; Non-alcoholic Fatty Liver Disease - metabolism; Peptide; Peptides - pharmacology; Peptides - therapeutic use; Phosphatidylinositol 3-Kinases - metabolism; Signal Transduction
• ISSN: 0196-9781; 1873-5169
• DOI: 10.1016/j.peptides.2021.170597

•AWRK6 alleviates obesity and hepatic steatosis in high energy diet fed mice.•Abnormal lipid metabolism is relieved by AWRK6.•AWRK6 treatment improves glucose metabolism. Metabolic associated fatty liver disease (MAFLD) is the leading common chronic liver disease affecting more than one-quarter of the population worldwide, but no pharmacological therapy was approved specifically. A synthetic peptide AWRK6 developed in our group based on the antimicrobial peptide Dybowskin-2CDYa was found to attenuated diabetes as a novel GLP-1 receptor agonist candidate. The effects of AWRK6 on MAFLD and its underlying mechanisms were investigated in this paper. In high energy diet (HED)-induced MAFLD mice, obesity and hepatic steatosis were alleviated by AWRK6 via intraperitoneal injection. The biochemistry measurements data indicated that the abnormal lipid metabolism was relieved and the glucose metabolism was improved significantly. Further, the phosphorylation of liver PI3K/AKT/AMPK/ACC was elevated significantly by AWRK6 treatment. Moreover, the effects of AWRK6 on lipid accumulation and insulin sensitivity in human cells were verified using oleic acid-induced HepG2 fatty liver cell model and insulin-induced HepG2 cells, respectively. These in vitro and in vivo results demonstrated that the peptide AWRK6 ameliorates MAFLD by improving lipid and glucose metabolism homeostasis, and it is mediated by the PI3K/AKT/AMPK/ACC signaling pathway. Thus, AWRK6 has a potential in preventing MAFLD.