The Fat-Derived Hormone Adiponectin Reverses Insulin Resistance Associated With Both Lipoatrophy and Obesity

Nat Med. 2001 Aug;7(8):941-6. doi: 10.1038/90984.

Abstract

Adiponectin is an adipocyte-derived hormone. Recent genome-wide scans have mapped a susceptibility locus for type 2 diabetes and metabolic syndrome to chromosome 3q27, where the gene encoding adiponectin is located. Here we show that decreased expression of adiponectin correlates with insulin resistance in mouse models of altered insulin sensitivity. Adiponectin decreases insulin resistance by decreasing triglyceride content in muscle and liver in obese mice. This effect results from increased expression of molecules involved in both fatty-acid combustion and energy dissipation in muscle. Moreover, insulin resistance in lipoatrophic mice was completely reversed by the combination of physiological doses of adiponectin and leptin, but only partially by either adiponectin or leptin alone. We conclude that decreased adiponectin is implicated in the development of insulin resistance in mouse models of both obesity and lipoatrophy. These data also indicate that the replenishment of adiponectin might provide a novel treatment modality for insulin resistance and type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin
  • Adipose Tissue / metabolism
  • Adipose Tissue / physiopathology*
  • Amino Acid Sequence
  • Animals
  • Insulin Resistance*
  • Intercellular Signaling Peptides and Proteins*
  • Leptin / metabolism
  • Mice
  • Molecular Sequence Data
  • Obesity / physiopathology*
  • Oxidation-Reduction
  • Proteins / physiology*
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / physiology
  • Signal Transduction
  • Transcription Factors / genetics
  • Transcription Factors / physiology
  • Triglycerides / metabolism

Substances

  • Adiponectin
  • Intercellular Signaling Peptides and Proteins
  • Leptin
  • Proteins
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Triglycerides