The Association between Trp64Arg Polymorphism of the β3-Adrenergic Receptor and Autonomic Nervous System Activity1
Author(s) -
Nobuyuki Shihara,
Koichiro Yasuda,
Toshio Moritani,
Hidetoshi Ue,
Tetsuya Adachi,
Hisako Tanaka,
Kinsuke Tsuda,
Yutaka Seino
Publication year - 1999
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jcem.84.5.5701
Subject(s) - endocrinology , medicine , autonomic nervous system , supine position , sympathetic nervous system , heterozygote advantage , thermogenesis , adrenergic , receptor , biology , obesity , allele , blood pressure , heart rate , gene , genetics
The beta3-adrenergic receptor plays a significant role in the control of lipolysis and thermogenesis in brown adipose tissue through autonomic nervous system (ANS) activity. As the Trp64Arg polymorphism of the beta3-adrenergic receptor gene might affect ANS activity, we investigated the association of the polymorphism with ANS activity. The prevalence of the polymorphism was determined in 204 subjects. Ten normal homozygous, 10 heterozygous, and 1 variant homozygous subjects were examined for ANS activity during supine rest and standing by electrocardiogram R-R interval power spectral analysis. Subjects with the variant did not differ from subjects without the variant in body mass index, plasma glucose, plasma insulin, or family history of diabetes or obesity. The total power of heterozygotes at supine rest was lower than that of normal subjects (1124.6 +/- 191.6 vs. 3029.8 +/- 758.8 ms2; mean +/- SE). With a postural change to standing, the parasympathetic and sympathetic nervous system activity indexes of heterozygotes showed a higher response than those of normal subjects (parasympathetic nervous system index, 0.10 +/- 0.02 vs. 0.17 +/- 0.02; sympathetic nervous system index, 10.55 +/- 1.47 vs. 6.26 +/- 1.09), and the difference in total power disappeared. These findings show that subjects with the variant, even the heterozygotes, had lower resting ANS activity than normal subjects.
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