Bracale Renata, Petroni Maria Letizia, Davinelli Sergio, Bracale Umberto, Scapagnini Giovanni, Carruba Michele O, Nisoli Enzo
Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
Clinical Nutrition Laboratory, IRCCS Institute Auxologico Italiano, Piancavallo (Verbania), Italy.
PLoS One. 2014 Jun 6;9(6):e98244. doi: 10.1371/journal.pone.0098244. eCollection 2014.
Ephedrine/caffeine combination (EC) has been shown to induce a small-to-moderate weight loss in obese patients. Several mechanisms have been proposed, among which an increased thermogenic capacity of skeletal muscle consequent to the EC-induced up-regulation of uncoupling protein 3 (UCP3) gene expression. We did a parallel group double-blind, placebo-controlled, 4-week trial to investigate this hypothesis. Thirteen morbidly obese women (25-52 years of age, body-mass index 48.0±4.0 kg/m2, range 41.1-57.6) were randomly assigned to EC (200/20 mg, n = 6) or to placebo (n = 7) administered three times a day orally, before undergoing bariatric surgery. All individuals had an energy-deficit diet equal to about 70% of resting metabolic rate (RMR) diet (mean 5769±1105 kJ/day). The RMR analysed by intention to treat and the UCP3 (long and short isoform) mRNA levels in rectus abdominis were the primary outcomes. Body weight, plasma levels of adrenaline, noradrenaline, triglycerides, free fatty acids, glycerol, TSH, fT4, and fT3 were assessed, as well as fasting glucose, insulin and HOMA index, at baseline and at the end of treatments. Body weight loss was evident in both groups when compared to baseline values (overall -5.2±3.2%, p<0.0001) without significant differences between the treated groups. EC treatment increased the RMR (+9.2±6.8%, p = 0.020), differently from placebo which was linked to a reduction of RMR (-7.6±6.5%, p = 0.029). No significant differences were seen in other metabolic parameters. Notably, no changes of either UCP3 short or UCP3 long isoform mRNA levels were evident between EC and placebo group. Our study provides evidence that 4-week EC administration resulted in a pronounced thermogenic effect not related to muscle UCP3 gene expression and weight loss in morbidly obese females under controlled conditions.
ClinicalTrials.gov NCT02048215.
麻黄碱/咖啡因组合(EC)已被证明可使肥胖患者出现轻度至中度体重减轻。已提出多种机制,其中一种是EC诱导解偶联蛋白3(UCP3)基因表达上调,从而增加骨骼肌的产热能力。我们进行了一项平行组双盲、安慰剂对照的4周试验来研究这一假设。13名病态肥胖女性(年龄25 - 52岁,体重指数48.0±4.0 kg/m²,范围41.1 - 57.6)在接受减肥手术前,被随机分配至EC组(200/20 mg,n = 6)或安慰剂组(n = 7),每天口服三次。所有个体均采用能量亏空饮食,约为静息代谢率(RMR)饮食的70%(平均5769±1105 kJ/天)。按意向性分析的RMR以及腹直肌中UCP3(长亚型和短亚型)mRNA水平为主要观察指标。在基线和治疗结束时,评估体重、血浆肾上腺素、去甲肾上腺素、甘油三酯、游离脂肪酸、甘油、促甲状腺激素、游离甲状腺素(fT4)和游离三碘甲状腺原氨酸(fT3)水平,以及空腹血糖、胰岛素和稳态模型评估胰岛素抵抗指数(HOMA指数)。与基线值相比,两组体重均明显下降(总体下降 -5.2±3.2%,p<0.0001),治疗组之间无显著差异。与安慰剂组使RMR降低(-7.6±6.5%,p = 0.029)不同,EC治疗使RMR增加(+9.2±6.8%,p = 0.020)。其他代谢参数未见显著差异。值得注意的是,EC组和安慰剂组之间UCP3短亚型或UCP3长亚型mRNA水平均无明显变化。我们的研究提供了证据,即在受控条件下,4周的EC给药可产生明显的产热效应,且与病态肥胖女性的肌肉UCP3基因表达和体重减轻无关。
ClinicalTrials.gov NCT02048215。