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

被引:31
作者
Jocken, J. W. E.
Blaak, E. E.
Schiffelers, S.
Arner, P.
van Baak, M. A.
Saris, W. H. M.
机构
[1] Maastricht Univ, Dept Human Biol, Nutr & Toxicol Res Inst, NL-6200 MD Maastricht, Netherlands
[2] Huddinge Univ Hosp, Karolinska Inst, Dept Med, Stockholm, Sweden
关键词
lipolysis; fat oxidation; single-nucleotide polymorphism; ADRB2; gene; GNB3;
D O I
10.1038/sj.ijo.0803499
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:813 / 819
页数:7
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