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Effects of Prunus cerasifera Ehrh. polyphenol extract on glucose metabolism in insulin-resistant HepG2 cells based on AMPK signaling pathway.
- Source :
- Chinese Journal of Pathophysiology; Dec2023, Vol. 39 Issue 12, p2234-2241, 8p
- Publication Year :
- 2023
-
Abstract
- AIM: To investigate the effects of Prunus cerasifera Ehrh. polyphenol extract (PCE) on glucose metabolism in insulin-resistant HepG2 (lR-HepG2) cells. METHODS: An IR-HepG2 cells model was established using high sugar and high insulin induction; a control group, an insulin resistance (IR) model group, a PCE treatment group with different concentrations, and a metformin treatment group were set up. Cells were treated with 50, 100, 200, and 400 mg/L of polyphenol extract for 24 hours, respectively, to detect their effects on cellular glucose consumption. At the same time, use thiazole blue (MTT) colorimetry to evaluate cell viability. Real-time PCR and Western blot were used to detect expression of glucose metabolism-related mRNA and proteins. RESULTS: Prunus cerasifera Ehrh. polyphenol extract can significantly increase glucose consumption in IR-HepG2 cells, and cell activity tends to increase and then decline as its concentration increases; At mRNA and protein levels, in addition to significantly increasing the expression of phosphorylated adenosine monophosphate activated protein kinase (p-AMPK) protein in IR-HepG2 cells, it also decrease glycogen synthase kinase 3β (GSK3p) in glycogen synthesis and gluconeogenesis pathways, forked protein O1 (FoxOl), peroxisome proliferator activates gamma co-receptor activation 1-alpha (PGC-la), glucose-6-phosphatase (G6Pase) and phosphoenol pyruvate carboxykinase (PEPCK) expression. CONCLUSION: Prunus cerasifera Ehrh. polyphenol extract can activate the AMPK signaling pathway in IR-HepG2 cells, to further inhibit gluconeogenesis and glycogen synthesis pathways, thereby improving the insulin resistance state of HepG2 cells. [ABSTRACT FROM AUTHOR]
Details
- Language :
- Chinese
- ISSN :
- 10004718
- Volume :
- 39
- Issue :
- 12
- Database :
- Complementary Index
- Journal :
- Chinese Journal of Pathophysiology
- Publication Type :
- Academic Journal
- Accession number :
- 174757726
- Full Text :
- https://doi.org/10.3969/j.issn.1000-4718.2023.12.014