Soto Dany Alexis Sobarzo, Pérez Diego Ignácio Valenzuela, Souza Mateus Rossow de, Reis Milena Leite Garcia, Almeida Naiara Ribeiro, Miarka Bianca, Aedo-Muñoz Esteban, Oyarzo Armin Isael Alvarado, Sillero-Quintana Manuel, Queiroz Andreia Cristiane Carrenho, Brito Ciro José
Department of Physical Education, Federal University of Juiz de Fora, Governador Valadares 35010-900, Brazil.
Escuela de Kinesiología, Facultad de Salud, Universidad Santo Tomás, Santiago 8320000, Chile.
Metabolites. 2025 Aug 1;15(8):517. doi: 10.3390/metabo15080517.
To investigate acute caffeine (CAF: 375 mg, ≈4.8 mg/kg body mass) effects on energy expenditure (EE) and substrate kinetics during high-intensity interval exercise in individuals with high (HBAT) versus low (LBAT) brown adipose tissue activity using time-trend polynomial modeling. : This is a randomized, double-blind crossover study in which 35 highly-trained males [HBAT-CAF, HBAT-PLA (Placebo), LBAT-CAF, LBAT-PLA] performed 30-min treadmill HIIE. Infrared thermography (IRT) assessed BAT activity by measuring supraclavicular skin temperature (SST). Breath-by-breath ergospirometry measured EE (kcal/min) and carbohydrate (CHO), lipid (LIP), and protein (PTN) oxidation. We applied second- and third-order polynomial regression models to depict the temporal trajectories of metabolic responses. : HBAT groups showed 25% higher sustained EE versus LBAT ( < 0.001), amplified by CAF. CHO oxidation exhibited biphasic kinetics: HBAT had 40% higher initial rates (0.75 ± 0.05 vs. 0.45 ± 0.04 g/min; < 0.001) with accelerated decline (k = -0.21 vs. -0.15/min; = 0.01). LIP oxidation peaked later in LBAT (40 vs. 20 min in HBAT), with CAF increasing oxidation by 18% in LBAT ( = 0.01). HBAT-CAF uniquely showed transient PTN catabolism (peak: 0.045 g/min at 10 min; k = -0.0033/min; < 0.001). : BAT status determines EE magnitude and substrate-specific kinetic patterns, while CAF exerts divergent modulation, potentiating early glycogenolysis in HBAT and lipolysis in LBAT. The HBAT-CAF synergy triggers acute proteolysis, revealing BAT-mediated metabolic switching.
使用时间趋势多项式模型,研究急性咖啡因(CAF:375毫克,约4.8毫克/千克体重)对高棕色脂肪组织活性(HBAT)与低棕色脂肪组织活性(LBAT)个体在高强度间歇运动期间能量消耗(EE)和底物动力学的影响。:这是一项随机、双盲交叉研究,35名训练有素的男性[HBAT - CAF、HBAT - PLA(安慰剂)、LBAT - CAF、LBAT - PLA]进行了30分钟的跑步机高强度间歇运动(HIIE)。红外热成像(IRT)通过测量锁骨上皮肤温度(SST)评估棕色脂肪组织活性。逐次呼吸气体代谢测定法测量EE(千卡/分钟)以及碳水化合物(CHO)、脂质(LIP)和蛋白质(PTN)氧化。我们应用二阶和三阶多项式回归模型来描绘代谢反应的时间轨迹。:HBAT组的持续EE比LBAT组高25%(<0.001),咖啡因使其增强。CHO氧化呈现双相动力学:HBAT组的初始速率高40%(0.75±0.05对0.45±0.04克/分钟;<0.001),下降加速(k = -0.21对-0.15/分钟;=0.01)。LIP氧化在LBAT组中达到峰值的时间更晚(HBAT组为20分钟,LBAT组为40分钟),咖啡因使LBAT组的氧化增加18%(=0.01)。HBAT - CAF组独特地显示出短暂的PTN分解代谢(峰值:10分钟时为0.045克/分钟;k = -0.0033/分钟;<0.001)。:棕色脂肪组织状态决定EE大小和底物特异性动力学模式,而咖啡因发挥不同的调节作用,增强HBAT组早期糖原分解和LBAT组脂肪分解。HBAT - CAF协同作用引发急性蛋白水解,揭示棕色脂肪组织介导的代谢转换。