Acute effect of L-796568, a novel β3-adrenergic receptor agonist, on energy expenditure in obese men

被引:77
作者
van Baak, MA
Hul, GBJ
Toubro, S
Astrup, A
Gottesdiener, KM
DeSmet, M
Saris, WHM
机构
[1] Maastricht Univ, Dept Human Biol, Nutr & Toxicol Res Inst, NL-6200 MD Maastricht, Netherlands
[2] Royal Vet & Agr Univ, Res Dept Human Nutr, Copenhagen, Denmark
[3] Merck & Co Inc, Rahway, NJ 07065 USA
关键词
D O I
10.1067/mcp.2002.122527
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: Our objective was to investigate the thermogenic efficacy of single oral doses of the novel beta(3)-adrenergic receptor agonist L-796568 [(R)-N-[4-[2-[[2-hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4-[4-(trifluoromethyl)phenyl]thiazol-2-yl]-benzenesulfonamide, dihydrochloride] in humans. Methods: Twelve healthy overweight to obese men participated in this 2-center, 3-period, randomized, placebo-controlled, crossover trial. In each period subjects received 250 mg L-796568, 1000 mg L-796568, or placebo. Energy expenditure and respiratory quotient were determined by indirect calorimetry; blood samples were taken; and ear temperature, heart rate, and blood pressure were measured at baseline and during the 4-hour period after administration. Results: Energy expenditure increased significantly after the 1000-mg dose (about 8%) and this was accompanied by an increase in plasma glycerol and free fatty acid concentrations. Systolic blood pressure also increased significantly. No changes in heart rate, diastolic blood pressure, ear temperature, plasma catecholamine, potassium, or leptin were found. Conclusions: Single-dose administration of 1000 mg of the novel beta(3)-adrenergic receptor agonist L-796568 increased lipolysis and energy expenditure in overweight men. This is the first study to show such an effect of beta(3)-adrenergic receptor agonists in humans without significant evidence for beta(2)-adrenergic receptor involvement.
引用
收藏
页码:272 / 279
页数:8
相关论文
共 34 条
[1]  
Arch JRS, 1996, INT J OBESITY, V20, P191
[2]   In situ assessment of the role of the beta(1)-, beta(2)- and beta(3)-adrenoceptors in the control of lipolysis and nutritive blood flow in human subcutaneous adipose tissue [J].
Barbe, P ;
Millet, L ;
Galitzky, J ;
Lafontan, M ;
Berlan, M .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 117 (05) :907-913
[3]   DISTRIBUTION OF BETA(3)-ADRENOCEPTOR MESSENGER-RNA IN HUMAN TISSUES [J].
BERKOWITZ, DE ;
NARDONE, NA ;
SMILEY, RM ;
PRICE, DT ;
KREUTTER, DK ;
FREMEAU, RT ;
SCHWINN, DA .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1995, 289 (02) :223-228
[4]   ROLE OF ALPHA-ADRENOCEPTORS AND BETA-ADRENOCEPTORS IN SYMPATHETICALLY MEDIATED THERMOGENESIS [J].
BLAAK, EE ;
VANBAAK, MA ;
KEMPEN, KPG ;
SARIS, WHM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (01) :E11-E17
[5]  
BLAAK EE, 1993, INT J OBESITY, V17, pS78
[6]   BETA-ADRENERGIC STIMULATION OF ENERGY-EXPENDITURE AND FOREARM SKELETAL-MUSCLE METABOLISM IN LEAN AND OBESE MEN [J].
BLAAK, EE ;
VANBAAK, MA ;
KEMERINK, GJ ;
PAKBIERS, MTW ;
HEIDENDAL, GAK ;
SARIS, WHM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (02) :E306-E315
[7]   Effects of the two β3-agonists, ZD7114 and ZD2079 on 24 hour energy expenditure and respiratory quotient in obese subjects [J].
Buemann, B ;
Toubro, S ;
Astrup, A .
INTERNATIONAL JOURNAL OF OBESITY, 2000, 24 (12) :1553-1560
[8]   The tissue distribution of the human β3-adrenoceptor studied using a monoclonal antibody:: Direct evidence of the β3-adrenoceptor in human adipose tissue, atrium and skeletal muscle [J].
Chamberlain, PD ;
Jennings, KH ;
Paul, F ;
Cordell, J ;
Berry, A ;
Holmes, SD ;
Park, J ;
Chambers, J ;
Sennitt, MV ;
Stock, MJ ;
Cawthorne, MA ;
Young, PW ;
Murphy, GJ .
INTERNATIONAL JOURNAL OF OBESITY, 1999, 23 (10) :1057-1065
[9]  
DEMACKER PNM, 1982, CLIN CHEM, V28, P1765
[10]   DEMONSTRATION OF AN IN-VIVO FUNCTIONAL BETA(3)-ADRENOCEPTOR IN MAN [J].
ENOCKSSON, S ;
SHIMIZU, M ;
LONNQVIST, F ;
NORDENSTROM, J ;
ARNER, P .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (05) :2239-2245