Association of a beta-2 adrenoceptor (ADRB2) gene variant with a blunted in vivo lipolysis and fat oxidation

Int J Obes (Lond). 2007 May;31(5):813-9. doi: 10.1038/sj.ijo.0803499. Epub 2006 Nov 28.

Abstract

Background and aims: Obesity is associated with a blunted beta-adrenoceptor-mediated lipolysis and fat oxidation. We investigated whether polymorphisms in codon 16, 27 and 164 of the beta (2)-adrenoceptor gene (ADRB2) and exon 10 of the G protein beta (3)-subunit gene (GNB3) are associated with alterations in in vivo lipolysis and fat oxidation.

Design and methods: Sixty-five male and 43 female overweight and obese subjects (body mass index (BMI) range: 26.1-48.4 kg/m(2)) were included. Energy expenditure (EE), respiratory quotient (RQ), circulating free fatty acid (FFA) and glycerol levels were determined after stepwise infusion of increasing doses of the non-selective beta-agonist isoprenaline (ISO).

Results: In women, the Arg16 allele of the ADRB2 gene was associated with a blunted increase in circulating FFA, glycerol and a decreased fat oxidation during ISO stimulation. In men, the Arg16 allele was significantly associated with a blunted increase in FFA but not in glycerol or fat oxidation.

Conclusion: These results suggest that genetic variation in the ADRB2 gene is associated with disturbances in in vivo beta-adrenoceptor-mediated lipolysis and fat oxidation during beta-adrenergic stimulation in overweight and obese subjects; these effects are influenced by gene-gender interactions.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / metabolism*
  • Adrenergic beta-Agonists / pharmacology
  • Adult
  • Anthropometry
  • Energy Metabolism
  • Female
  • Genetic Variation
  • Heterotrimeric GTP-Binding Proteins / genetics*
  • Humans
  • Isoproterenol / pharmacology
  • Lipolysis / genetics*
  • Male
  • Obesity / genetics*
  • Obesity / metabolism
  • Oxidation-Reduction / drug effects
  • Polymorphism, Single Nucleotide / genetics
  • Receptors, Adrenergic, beta-2 / drug effects
  • Receptors, Adrenergic, beta-2 / genetics*

Substances

  • Adrenergic beta-Agonists
  • G-protein beta3 subunit
  • Receptors, Adrenergic, beta-2
  • Heterotrimeric GTP-Binding Proteins
  • Isoproterenol