Title : Endogenous Ligand for GPR120, Docosahexaenoic Acid, Exerts Benign Metabolic Effects on the Skeletal Muscles via AMP-activated Protein Kinase Pathway.

Pub. Date : 2015 Aug 14

PMID : 26134561






8 Functional Relationships(s)
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1 Endogenous Ligand for GPR120, Docosahexaenoic Acid, Exerts Benign Metabolic Effects on the Skeletal Muscles via AMP-activated Protein Kinase Pathway. Docosahexaenoic Acids protein kinase AMP-activated catalytic subunit alpha 2 Homo sapiens
2 In this study, DHA stimulated glucose uptake in the skeletal muscles in an AMP-activated protein kinase (AMPK)-dependent manner. Docosahexaenoic Acids protein kinase AMP-activated catalytic subunit alpha 2 Homo sapiens
3 In this study, DHA stimulated glucose uptake in the skeletal muscles in an AMP-activated protein kinase (AMPK)-dependent manner. Docosahexaenoic Acids protein kinase AMP-activated catalytic subunit alpha 2 Homo sapiens
4 GPR120-mediated increase in intracellular Ca(2+) was critical for DHA-mediated AMPK phosphorylation and glucose uptake. Docosahexaenoic Acids protein kinase AMP-activated catalytic subunit alpha 2 Homo sapiens
5 In addition, DHA stimulated GLUT4 translocation AMPK-dependently. Docosahexaenoic Acids protein kinase AMP-activated catalytic subunit alpha 2 Homo sapiens
6 Inhibition of AMPK and Ca(2+)/calmodulin-dependent protein kinase kinase blocked DHA-induced glucose uptake. Docosahexaenoic Acids protein kinase AMP-activated catalytic subunit alpha 2 Homo sapiens
7 DHA increased AMPK phosphorylation, glucose uptake, and intracellular Ca(2+) concentration in primary cultured myoblasts. Docosahexaenoic Acids protein kinase AMP-activated catalytic subunit alpha 2 Homo sapiens
8 Taken together, these results indicated that the beneficial metabolic role of DHA was attributed to its ability to regulate glucose via the GPR120-mediated AMPK pathway in the skeletal muscles. Docosahexaenoic Acids protein kinase AMP-activated catalytic subunit alpha 2 Homo sapiens