Obesity and Diabetes Clinical Research Section, Phoenix Epidemiology and Clinical Research Branch, Department of Health and Human Services, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Phoenix, Arizona, USA.
Endocrinology Division, Medicine Department, Phoenix VA Health Care System, Phoenix, Arizona, USA.
Obesity (Silver Spring). 2023 Jan;31(1):139-149. doi: 10.1002/oby.23584. Epub 2022 Dec 5.
This study investigated whether interindividual variance in diet-induced metabolic flexibility is explained by differences in gut hormone concentrations.
A total of 69 healthy volunteers with normal glucose regulation underwent 24-hour assessments of respiratory quotient (RQ) in a whole-room indirect calorimeter during eucaloric feeding (EBL; 50% carbohydrate, 30% fat) and then, in a crossover design, during 24-hour fasting and three normal-protein (20%) overfeeding diets (200% energy requirements). Metabolic flexibility was defined as the change in 24-hour RQ from EBL during standard (50% carbohydrate), high-fat (60%), and high-carbohydrate (75%) overfeeding diets. Plasma concentrations of glucagon-like peptide-1 (GLP-1) and peptide YY (PYY) after an overnight fast were measured prior to and after each diet.
Compared with EBL, on average, 24-hour RQ decreased by ~4% during high-fat overfeeding, whereas it increased by ~4% during standard overfeeding and by ~9% during high-carbohydrate overfeeding. During high-carbohydrate overfeeding, but not during any other overfeeding diet or fasting, increased GLP-1 concentration was associated with increased RQ (r = 0.44, p < 0.001), higher/lower carbohydrate/lipid oxidation rates (r = 0.34 and r = -0.51, both p < 0.01), respectively, and increased plasma insulin concentration (r = 0.38, p = 0.02).
Increased GLP-1 concentration following high-carbohydrate overfeeding associated with a greater shift to carbohydrate oxidation, suggesting that GLP-1 may be implicated in diet-induced metabolic flexibility to carbohydrate overload.
本研究旨在探讨个体间饮食诱导代谢灵活性的差异是否可以用肠激素浓度的差异来解释。
共有 69 名血糖正常的健康志愿者在整个房间间接测热仪中接受 24 小时的呼吸商(RQ)评估,在能量平衡饮食(EBL;50%碳水化合物,30%脂肪)期间,然后以交叉设计的方式在 24 小时禁食和三种正常蛋白质(20%)过食饮食(200%能量需求)期间进行。代谢灵活性定义为 EBL 期间标准(50%碳水化合物)、高脂肪(60%)和高碳水化合物(75%)过食饮食期间 24 小时 RQ 的变化。在每个饮食之前和之后,测量禁食一夜后的血浆胰高血糖素样肽-1(GLP-1)和肽 YY(PYY)浓度。
与 EBL 相比,平均而言,高脂肪过食期间 24 小时 RQ 下降约 4%,而标准过食期间增加约 4%,高碳水化合物过食期间增加约 9%。在高碳水化合物过食期间,但不在任何其他过食饮食或禁食期间,增加的 GLP-1 浓度与增加的 RQ 相关(r=0.44,p<0.001),分别与更高/更低的碳水化合物/脂质氧化率相关(r=0.34 和 r=-0.51,均 p<0.01),并与增加的血浆胰岛素浓度相关(r=0.38,p=0.02)。
高碳水化合物过食后 GLP-1 浓度增加与碳水化合物氧化的更大转变相关,表明 GLP-1 可能与碳水化合物过载诱导的代谢灵活性有关。