Adiponectin resistance exacerbates insulin resistance in insulin receptor transgenic/knockout mice

Diabetes. 2007 Aug;56(8):1969-76. doi: 10.2337/db07-0127. Epub 2007 May 2.

Abstract

Objective: Adiponectin increases insulin sensitivity and contributes to insulin's indirect effects on hepatic glucose production.

Research design and methods: To examine adiponectin's contribution to insulin action, we analyzed adiponectin levels and activation of AMP-activated protein kinase (AMPK) in insulin receptor transgenic/knockout mice (L1), a genetic model of resistance to insulin's indirect effects on hepatic glucose production.

Results: In euglycemic, insulin-resistant L1 mice, we detected hyperadiponectinemia with normal levels of adiponectin receptor-1 and -2. Moreover, adiponectin administration is unable to lower glucose levels or induce activation of AMPK, consistent with a state of adiponectin resistance. In a subset of hyperglycemic L1 mice, we observed decreased mRNA expression of AdipoR2 in liver and muscle, as well as decreased peroxisome proliferator-activated receptor (PPAR)alpha target gene expression in liver, raising the possibility that deterioration of adiponectin/AdipoR2 signaling via PPARalpha activation contributes to the progression from compensated insulin resistance to diabetes. In contrast, we failed to detect changes in other markers of the systemic or local inflammatory response.

Conclusions: These data provide evidence for a mechanism of adiponectin resistance and corroborate the notion that adiponectin potentiates hepatic insulin sensitivity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • AMP-Activated Protein Kinases
  • Adiponectin / blood*
  • Adiponectin / pharmacology*
  • Animals
  • Biomarkers
  • Blood Glucose / metabolism
  • Disease Susceptibility
  • Gene Expression Regulation
  • Glucose Metabolism Disorders / metabolism
  • Glucose Metabolism Disorders / pathology
  • Humans
  • Insulin / blood
  • Insulin Resistance*
  • Liver / drug effects
  • Liver / metabolism
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Male
  • Mice
  • Mice, Transgenic
  • Multienzyme Complexes / metabolism
  • PPAR alpha / metabolism
  • Phosphorylation / drug effects
  • Protein Serine-Threonine Kinases / metabolism
  • Receptor, Insulin / deficiency*
  • Receptor, Insulin / genetics
  • Receptor, Insulin / metabolism*
  • Receptors, Adiponectin
  • Receptors, Cell Surface / genetics
  • Systemic Inflammatory Response Syndrome / blood
  • Time Factors

Substances

  • Adiponectin
  • Biomarkers
  • Blood Glucose
  • Insulin
  • Multienzyme Complexes
  • PPAR alpha
  • Receptors, Adiponectin
  • Receptors, Cell Surface
  • adiponectin receptor 2, mouse
  • Receptor, Insulin
  • Protein Serine-Threonine Kinases
  • AMP-Activated Protein Kinases