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首页> 外文期刊>International Journal of Molecular Sciences >3-O-Acyl-epicatechins Increase Glucose Uptake Activity and GLUT4 Translocation through Activation of PI3K Signaling in Skeletal Muscle Cells
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3-O-Acyl-epicatechins Increase Glucose Uptake Activity and GLUT4 Translocation through Activation of PI3K Signaling in Skeletal Muscle Cells

机译:3-O-酰基-表观微素通过激活骨骼肌细胞中的PI3K信号传导增加葡萄糖摄取活性和GLUT4易位。

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摘要

Tea catechins promote glucose uptake in skeletal muscle cells. In this study, we investigated whether the addition of an acyl group to the C-3 position of catechins to generate 3-O-acyl-catechins promoted glucose uptake in L6 myotubes. 3-O-Myristoyl-(−)-epicatechin (EC-C14) and 3-O-palmitoyl-(−)-epicatechin (EC-C16) promoted glucose uptake and translocation of glucose transporter (GLUT) 4 in the cells. The effect of 3-O-acyl-(−)-epicatechins was stronger than that of (−)-epicatechin (EC), whereas neither 3-O-myristoyl-(+)-catechin (C-C14) nor 3-O-palmitoyl-(+)catechin (C-C16) promoted glucose uptake or GLUT4 translocation as well as (+)-catechin (C). We further investigated an affinity of catechins and 3-O-acyl-catechins to the lipid bilayer membrane by using surface plasma resonance analysis. Maximum binding amounts of EC-C16 and C-C16 to the lipid bilayer clearly increased compared with that of (−)-EC and (+)-C, respectively. We also examined the mechanism of GLUT4 translocation and found EC-C14 and EC-C16 induced the phosphorylation of PI3K, but did not affect phosphorylation of Akt or IR. In conclusion, the addition of an acyl group to the C-3 position of (−)-EC increases its affinity for the lipid bilayer membrane and promotes GLUT4 translocation through PI3K-dependent pathways in L6 myotubes.
机译:茶儿茶素可促进骨骼肌细胞摄取葡萄糖。在这项研究中,我们调查了在儿茶素的C-3位置添加酰基以生成3-O-酰基儿茶素是否促进L6肌管中的葡萄糖摄取。 3-O-肉豆蔻酰-(-)-表儿茶素(EC-C14)和3-O-棕榈酰-(-)-表儿茶素(EC-C16)促进了葡萄糖的吸收和细胞中葡萄糖转运蛋白(GLUT)4的转运。 3-O-酰基-(-)-表儿茶素的作用比(-)-表儿茶素(EC)的作用更强,而3-O-肉豆蔻酰基-(+)-儿茶素(C-C14)和3-O都没有-棕榈酰-(+)儿茶素(C-C16)促进葡萄糖摄取或GLUT4易位以及(+)-儿茶素(C)。我们通过使用表面等离子体共振分析进一步研究了儿茶素和3-O-酰基儿茶素对脂质双层膜的亲和力。与(-)-EC和(+)-C相比,EC-C16和C-C16与脂质双层的最大结合量明显增加。我们还检查了GLUT4易位的机制,发现EC-C14和EC-C16诱导了PI3K的磷酸化,但不影响Akt或IR的磷酸化。总之,在(-)-EC的C-3位置添加酰基会增加其对脂质双层膜的亲和力,并通过L6肌管中的PI3K依赖性途径促进GLUT4易位。

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