Carlson Olga, Martin Bronwen, Stote Kim S, Golden Erin, Maudsley Stuart, Najjar Samer S, Ferrucci Luigi, Ingram Donald K, Longo Dan L, Rumpler William V, Baer David J, Egan Josephine, Mattson Mark P
Diabetes Section, Laboratory of Clinical Investigation, National Institute on Aging Intramural Research Program, Baltimore, MD, USA.
Metabolism. 2007 Dec;56(12):1729-34. doi: 10.1016/j.metabol.2007.07.018.
An unresolved issue in the field of diet and health is if and how changes in meal frequency affect energy metabolism in humans. We therefore evaluated the influence of reduced meal frequency without a reduction in energy intake on glucose metabolism in normal-weight, healthy male and female subjects. The study was a randomized crossover design, with two 8-week treatment periods (with an intervening 11-week off-diet period) in which subjects consumed all of their calories for weight maintenance distributed in either 3 meals or 1 meal per day (consumed between 4:00 pm and 8:00 pm). Energy metabolism was evaluated at designated time points throughout the study by performing morning oral glucose tolerance tests and measuring levels of glucose, insulin, glucagon, leptin, ghrelin, adiponectin, resistin, and brain-derived neurotrophic factor (BDNF). Subjects consuming 1 meal per day exhibited higher morning fasting plasma glucose levels, greater and more sustained elevations of plasma glucose concentrations, and a delayed insulin response in the oral glucose tolerance test compared with subjects consuming 3 meals per day. Levels of ghrelin were elevated in response to the 1-meal-per-day regimen. Fasting levels of insulin, leptin, ghrelin, adiponectin, resistin, and BDNF were not significantly affected by meal frequency. Subjects consuming a single large daily meal exhibit elevated fasting glucose levels and impaired morning glucose tolerance associated with a delayed insulin response during a 2-month diet period compared with those consuming 3 meals per day. The impaired glucose tolerance was reversible and was not associated with alterations in the levels of adipokines or BDNF.
饮食与健康领域一个尚未解决的问题是,进餐频率的变化是否以及如何影响人体的能量代谢。因此,我们评估了在不减少能量摄入的情况下降低进餐频率对正常体重、健康的男性和女性受试者葡萄糖代谢的影响。该研究采用随机交叉设计,有两个为期8周的治疗期(中间有一个为期11周的非节食期),在此期间,受试者将维持体重所需的所有热量分配为每天3餐或1餐(在下午4点至晚上8点之间进食)。在整个研究过程中的指定时间点,通过进行早晨口服葡萄糖耐量试验并测量葡萄糖、胰岛素、胰高血糖素、瘦素、胃饥饿素、脂联素、抵抗素和脑源性神经营养因子(BDNF)的水平来评估能量代谢。与每天吃3餐的受试者相比,每天吃1餐的受试者早晨空腹血糖水平更高,血浆葡萄糖浓度升高幅度更大且持续时间更长,并且在口服葡萄糖耐量试验中胰岛素反应延迟。胃饥饿素水平因每天1餐的饮食方案而升高。进餐频率对胰岛素、瘦素、胃饥饿素、脂联素、抵抗素和BDNF的空腹水平没有显著影响。与每天吃3餐的受试者相比,在为期2个月的饮食期间,每天吃一顿大餐的受试者空腹血糖水平升高,早晨葡萄糖耐量受损,且胰岛素反应延迟。葡萄糖耐量受损是可逆的,并且与脂肪因子或BDNF水平的改变无关。