A-769662 inhibits adipocyte glucose uptake in an AMPK-independent manner

Biochem J. 2021 Feb 12;478(3):633-646. doi: 10.1042/BCJ20200659.

Abstract

Activation of AMP-activated protein kinase (AMPK) is considered a valid strategy for the treatment of type 2 diabetes. However, despite the importance of adipose tissue for whole-body energy homeostasis, the effect of AMPK activation in adipocytes has only been studied to a limited extent and mainly with the AMP-mimetic 5-aminoimidazole-4-carboxamide-1-β-d-ribofuranoside (AICAR), which has limited specificity. The aim of this study was to evaluate the effect of the allosteric AMPK activators A-769662 and 991 on glucose uptake in adipocytes. For this purpose, primary rat or human adipocytes, and cultured 3T3-L1 adipocytes, were treated with either of the allosteric activators, or AICAR, and basal and insulin-stimulated glucose uptake was assessed. Additionally, the effect of AMPK activators on insulin-stimulated phosphorylation of Akt and Akt substrate of 160 kDa was assessed. Furthermore, primary adipocytes from ADaM site binding drug-resistant AMPKβ1 S108A knock-in mice were employed to investigate the specificity of the drugs for the observed effects. Our results show that insulin-stimulated adipocyte glucose uptake was significantly reduced by A-769662 but not 991, yet neither activator had any clear effects on basal or insulin-stimulated Akt/AS160 signaling. The use of AMPKβ1 S108A mutant-expressing adipocytes revealed that the observed inhibition of glucose uptake by A-769662 is most likely AMPK-independent, a finding which is supported by the rapid inhibitory effect A-769662 exerts on glucose uptake in 3T3-L1 adipocytes. These data suggest that AMPK activation per se does not inhibit glucose uptake in adipocytes and that the effects of AICAR and A-769662 are AMPK-independent.

Keywords: A-769662; AMPK; AMPKβ1 S108A; adipocytes; glucose uptake; insulin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism
  • Adenylate Kinase / physiology*
  • Adipocytes / drug effects*
  • Adipocytes / metabolism
  • Allosteric Site
  • Amino Acid Substitution
  • Aminoimidazole Carboxamide / analogs & derivatives
  • Aminoimidazole Carboxamide / pharmacology
  • Animals
  • Benzimidazoles / pharmacology
  • Benzoates / pharmacology
  • Biphenyl Compounds / pharmacology*
  • Cells, Cultured
  • Enzyme Activation / drug effects
  • Female
  • Gene Knock-In Techniques
  • Glucose / metabolism*
  • Humans
  • Insulin / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mutation, Missense
  • Phosphorylation
  • Protein Processing, Post-Translational
  • Pyrones / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Ribonucleotides / pharmacology
  • Thiophenes / pharmacology*

Substances

  • 5-((6-chloro-5-(1-methylindol-5-yl)-1H-benzimidazol-2-yl)oxy)-2-methylbenzoic acid
  • Benzimidazoles
  • Benzoates
  • Biphenyl Compounds
  • Insulin
  • Pyrones
  • Ribonucleotides
  • Thiophenes
  • Aminoimidazole Carboxamide
  • Prkab1 protein, mouse
  • AMP-Activated Protein Kinases
  • Adenylate Kinase
  • AICA ribonucleotide
  • Glucose
  • 4-hydroxy-3-(4-(2-hydroxyphenyl)phenyl)-6-oxo-7H-thieno(2,3-b)pyridine-5-carbonitrile