Effects of obesity on insulin: insulin-like growth factor 1 hybrid receptor expression and Akt phosphorylation in conduit and resistance arteries

Diab Vasc Dis Res. 2019 Mar;16(2):160-170. doi: 10.1177/1479164118802550. Epub 2018 Oct 8.

Abstract

Insulin and insulin-like growth factor-1 stimulate specific responses in arteries, which may be disrupted by diet-induced obesity. We examined (1) temporal effects of high-fat diet compared to low-fat diet in mice on insulin receptor, insulin-like growth factor-1 receptor, insulin receptor/insulin-like growth factor-1 receptor hybrid receptor expression and insulin/insulin-like growth factor-1-mediated Akt phosphorylation in aorta; and (2) effects of high-fat diet on insulin and insulin-like growth factor-1-mediated Akt phosphorylation and vascular tone in resistance arteries. Medium-term high-fat diet (5 weeks) decreased insulin-like growth factor-1 receptor expression and increased hybrid expression (~30%) only. After long-term (16 weeks) high-fat diet, insulin receptor expression was reduced by ~30%, insulin-like growth factor-1 receptor expression decreased a further ~40% and hybrid expression increased a further ~60%. Independent correlates of hybrid receptor expression were high-fat diet, duration of high-fat diet and plasma insulin-like growth factor-1 (all p < 0.05). In aorta, insulin was a more potent activator of Akt than insulin-like growth factor-1, whereas in resistance arteries, insulin-like growth factor-1 was more potent than insulin. High-fat diet blunted insulin-mediated vasorelaxation ( p < 0.01) but had no effect on insulin-like growth factor-1-mediated vasorelaxation in resistance arteries. Our findings support the possibility that hybrid receptor level is influenced by nutritional and metabolic cues. Moreover, vessel-dependent effects of insulin and insulin-like growth factor-1 on vascular tone and Akt activation may have implications in treating obesity-related vascular disease.

Keywords: IGF-1 receptors; Obesity; hybrid receptors.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Aorta / drug effects*
  • Aorta / enzymology
  • Cells, Cultured
  • Diet, Fat-Restricted
  • Diet, High-Fat
  • Disease Models, Animal
  • Enzyme Activation
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Human Umbilical Vein Endothelial Cells / enzymology
  • Humans
  • Insulin / pharmacology*
  • Insulin-Like Growth Factor I / pharmacology
  • Male
  • Mesenteric Arteries / drug effects*
  • Mesenteric Arteries / enzymology
  • Mesenteric Arteries / physiopathology
  • Mice, Inbred C57BL
  • Obesity / blood
  • Obesity / enzymology*
  • Obesity / physiopathology
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Receptor, IGF Type 1 / genetics
  • Receptor, IGF Type 1 / metabolism*
  • Receptor, Insulin / metabolism
  • Receptors, Somatomedin / metabolism
  • Signal Transduction / drug effects
  • Vascular Resistance / drug effects*
  • Vasodilation / drug effects

Substances

  • Antigens, CD
  • IGF1 protein, human
  • IGF1R protein, human
  • Igf1r protein, mouse
  • Insulin
  • Receptors, Somatomedin
  • Insulin-Like Growth Factor I
  • INSR protein, human
  • Receptor, IGF Type 1
  • Receptor, Insulin
  • Proto-Oncogene Proteins c-akt