Independent and combined effects of calorie restriction and AICAR on glucose uptake and insulin signaling in skeletal muscles from 24-month-old female and male rats

Appl Physiol Nutr Metab. 2024 May 1;49(5):614-625. doi: 10.1139/apnm-2023-0522. Epub 2024 Jan 5.

Abstract

We assessed the effects of two levels of calorie restriction (CR; eating either 15% or 35% less than ad libitum, AL, food intake for 8 weeks) by 24-month-old female and male rats on glucose uptake (GU) and phosphorylation of key signaling proteins (Akt; AMP-activated protein kinase, AMPK; Akt substrate of 160 kDa, AS160) measured in isolated skeletal muscles that underwent four incubation conditions (without either insulin or AICAR, an AMPK activator; with AICAR alone; with insulin alone; or with insulin and AICAR). Regardless of sex: (1) neither CR group versus the AL group had greater GU by insulin-stimulated muscles; (2) phosphorylation of Akt in insulin-stimulated muscles was increased in 35% CR versus AL rats; (3) prior AICAR treatment of muscle resulted in greater GU by insulin-stimulated muscles, regardless of diet; and (4) AICAR caused elevated phosphorylation of acetyl CoA carboxylase, an indicator of AMPK activation, in all diet groups. There was a sexually dimorphic diet effect on AS160 phosphorylation, with 35% CR exceeding AL for insulin-stimulated muscles in male rats, but not in female rats. Our working hypothesis is that the lack of a CR-effect on GU by insulin-stimulated muscles was related to the extended duration of the ex vivo incubation period (290 min compared to 40-50 min that was previously reported to be effective). The observed efficacy of prior treatment of muscles with AICAR to improve glucose uptake in insulin-stimulated muscles supports the strategy of targeting AMPK with the goal of improving insulin sensitivity in older females and males.

Keywords: aging; diet; glucose transport; insulin resistance; insulin sensitivity.

MeSH terms

  • AMP-Activated Protein Kinases* / metabolism
  • Acetyl-CoA Carboxylase / metabolism
  • Aminoimidazole Carboxamide* / analogs & derivatives
  • Aminoimidazole Carboxamide* / pharmacology
  • Animals
  • Caloric Restriction*
  • Female
  • GTPase-Activating Proteins / metabolism
  • Glucose* / metabolism
  • Hypoglycemic Agents / pharmacology
  • Insulin*
  • Male
  • Muscle, Skeletal* / drug effects
  • Muscle, Skeletal* / metabolism
  • Phosphoribosylaminoimidazolecarboxamide Formyltransferase / metabolism
  • Phosphorylation
  • Proteins*
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Rats
  • Ribonucleotides* / pharmacology
  • Sex Factors
  • Signal Transduction* / drug effects

Substances

  • Acetyl-CoA Carboxylase
  • AICA ribonucleotide
  • Aminoimidazole Carboxamide
  • AMP-Activated Protein Kinases
  • Glucose
  • GTPase-Activating Proteins
  • Hypoglycemic Agents
  • Insulin
  • Proteins
  • Proto-Oncogene Proteins c-akt
  • Ribonucleotides
  • TBC1D1 protein, rat
  • TBC1D4 protein, rat
  • Phosphoribosylaminoimidazolecarboxamide Formyltransferase