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新型β3肾上腺素能受体激动剂TAK-677对肥胖个体能量代谢无影响:一项双盲、安慰剂对照的随机研究。

Lack of an effect of a novel beta3-adrenoceptor agonist, TAK-677, on energy metabolism in obese individuals: a double-blind, placebo-controlled randomized study.

作者信息

Redman Leanne M, de Jonge Lilian, Fang Xiaobing, Gamlin Betsy, Recker David, Greenway Frank L, Smith Steven R, Ravussin Eric

机构信息

Pennington Biomedical Research Center, Louisiana 70808, USA.

出版信息

J Clin Endocrinol Metab. 2007 Feb;92(2):527-31. doi: 10.1210/jc.2006-1740. Epub 2006 Nov 21.

Abstract

OBJECTIVE

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.

INTERVENTION

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.

OUTCOMES

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

干预措施

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。

观察指标

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。

结果

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。

结论

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。

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