Redman Leanne M, de Jonge Lilian, Fang Xiaobing, Gamlin Betsy, Recker David, Greenway Frank L, Smith Steven R, Ravussin Eric
Pennington Biomedical Research Center, Louisiana 70808, USA.
J Clin Endocrinol Metab. 2007 Feb;92(2):527-31. doi: 10.1210/jc.2006-1740. Epub 2006 Nov 21.
Our objective was to test the safety and metabolic effects of a novel beta(3)-adrenoreceptor agonist (TAK-677) in humans.
DESIGN, SETTING, AND PARTICIPANTS: Sixty-five obese (body mass index = 33.9 +/- 2.1 kg/m2, mean +/- se) men and women (31.4 +/- 0.9 yr) participated in a double-blind placebo-controlled study at an institutional research center.
Participants were randomized to 0.1 mg TAK-677 twice daily (BID) (n = 21), 0.5 mg TAK-677 BID (n = 22), or placebo BID (n = 22) for 29 d.
Drug safety, 24-h respiratory quotient (RQ), 24-h energy expenditure (EE), body composition, fat distribution, and fasting plasma concentration of substrates and hormones were assessed. An acute-response study was also conducted.
The drug was well tolerated by all participants; however, heart rate was elevated (9 +/- 2 beats per minute) with the 0.5-mg BID dose. After 28 d of treatment and when compared with placebo, there was no change in 24-h RQ with either 0.1-mg BID (P = 0.1) or 0.5-mg BID (P = 1.0) doses of TAK-677. However, TAK, 0.5 mg BID, resulted in a small increase in 24-h EE that was significantly different from placebo [change from baseline, 13 +/- 17 (0.5 mg BID) vs.-39 +/- 18 (placebo) kcal/d, P < 0.05]. Changes in weight, fat-free mass, and abdominal fat depots (visceral or sc) were not different between the three groups, nor were changes in fasting insulin, free fatty acid, or glucose concentrations.
TAK-677 has no effect on 24-h RQ or fat oxidation but does slightly increase 24-h EE at the highest dose (0.5 mg BID). The acute studies showed large interindividual variability in plasma concentrations of TAK-677 indicating some possible problems with bioavailability and therefore efficacy.
我们的目的是测试一种新型β3-肾上腺素能受体激动剂(TAK-677)在人体中的安全性和代谢效应。
设计、地点和参与者:65名肥胖(体重指数=33.9±2.1kg/m²,均值±标准误)男性和女性(31.4±0.9岁)在一个机构研究中心参与了一项双盲安慰剂对照研究。
参与者被随机分为每日两次服用0.1mg TAK-677(n=21)、每日两次服用0.5mg TAK-677(n=22)或每日两次服用安慰剂(n=22),持续29天。
评估药物安全性、24小时呼吸商(RQ)、24小时能量消耗(EE)、身体成分、脂肪分布以及底物和激素的空腹血浆浓度。还进行了一项急性反应研究。
所有参与者对该药物耐受性良好;然而,0.5mg每日两次的剂量使心率升高(每分钟9±2次)。治疗28天后,与安慰剂相比,0.1mg每日两次(P=0.1)或0.5mg每日两次(P=1.0)剂量的TAK-677对24小时RQ均无影响。然而,0.5mg每日两次的TAK-677使24小时EE略有增加,与安慰剂有显著差异[相对于基线的变化,13±17(0.5mg每日两次)对-39±18(安慰剂)kcal/d,P<0.05]。三组之间体重、去脂体重和腹部脂肪储存(内脏或皮下)的变化无差异,空腹胰岛素、游离脂肪酸或葡萄糖浓度的变化也无差异。
TAK-677对24小时RQ或脂肪氧化无影响,但在最高剂量(0.5mg每日两次)时确实会使24小时EE略有增加。急性研究表明,TAK-677的血浆浓度存在较大的个体间差异,这表明生物利用度以及因此的疗效可能存在一些问题。