阿卡汀
过剩4
葡萄糖摄取
化学
内科学
内分泌学
染色体易位
生物化学
生物
胰岛素
医学
类黄酮
基因
抗氧化剂
芹菜素
作者
Eun-Bin Kwon,Myung-Ji Kang,Hyung Won Ryu,Seoghyen Lee,Jae‐Won Lee,Mi Kyeong Lee,Hyun-Sun Lee,Su Ui Lee,Sei‐Ryang Oh,Mun-Ock Kim
出处
期刊:Phytomedicine
[Elsevier]
日期:2020-02-08
卷期号:68: 153178-153178
被引量:31
标识
DOI:10.1016/j.phymed.2020.153178
摘要
Lowering blood glucose levels by increasing glucose uptake in insulin target tissues, such as skeletal muscle and adipose tissue, is one strategy to discover and develop antidiabetic drugs from natural products used as traditional medicines.Our goal was to reveal the mechanism and activity of acacetin (5,7-dihydroxy-4'-methoxyflavone), one of the major compounds in Agastache rugose, in stimulating glucose uptake in muscle cells.To determine whether acacetin promotes GLUT4-dependent glucose uptake in cultured L6 skeletal muscle cells, we performed a [14C] 2-deoxy-D-glucose (2-DG) uptake assay after treating differentiated L6-GLUT4myc cells with acacetin.Acacetin dose-dependently increased 2-DG uptake by enhancing GLUT4 translocation to the plasma membrane. Our results revealed that acacetin activated the CaMKII-AMPK pathway by increasing intracellular calcium concentrations. We also found that aPKCλ/ζ phosphorylation and intracellular reactive oxygen species (ROS) production were involved in acacetin-induced GLUT4 translocation. Moreover, acacetin-activated AMPK inhibited intracellular lipid accumulation and increased 2-DG uptake in HepG2 cells.Taken together, these results suggest that acacetin might be useful as an antidiabetic functional ingredient. Subsequent experiments using disease model animals are needed to verify our results.
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