Lin Po-Ju, Borer Katarina T
School of Kinesiology, University of Michigan, Ann Arbor, Michigan, United States of America.
PLoS One. 2016 Oct 31;11(10):e0165378. doi: 10.1371/journal.pone.0165378. eCollection 2016.
Postprandial hyperinsulinemia, hyperglycemia, and insulin resistance increase the risk of type 2 diabetes (T2D) and cardiovascular disease mortality. Postprandial hyperinsulinemia and hyperglycemia also occur in metabolically healthy subjects consuming high-carbohydrate diets particularly after evening meals and when carbohydrate loads follow acute exercise. We hypothesized the involvement of dietary carbohydrate load, especially when timed after exercise, and mediation by the glucose-dependent insulinotropic peptide (GIP) in this phenomenon, as this incretin promotes insulin secretion after carbohydrate intake in insulin-sensitive, but not in insulin-resistant states.
Four groups of eight metabolically healthy weight-matched postmenopausal women were provided with three isocaloric meals (a pre-trial meal and two meals during the trial day) containing either 30% or 60% carbohydrate, with and without two-hours of moderate-intensity exercise before the last two meals. Plasma glucose, insulin, glucagon, GIP, glucagon-like peptide 1 (GLP-1), free fatty acids (FFAs), and D-3-hydroxybutyrate concentrations were measured during 4-h postprandial periods and 3-h exercise periods, and their areas under the curve (AUCs) were analyzed by mixed-model ANOVA, and insulin resistance during fasting and meal tolerance tests within each diet was estimated using homeostasis-model assessment (HOMA-IR).
The third low-carbohydrate meal, but not the high-carbohydrate meal, reduced: (1) evening insulin AUC by 39% without exercise and by 31% after exercise; (2) GIP AUC by 48% without exercise and by 45% after exercise, and (3) evening insulin resistance by 37% without exercise and by 24% after exercise. Pre-meal exercise did not alter insulin-, GIP- and HOMA-IR- lowering effects of low-carbohydrate diet, but exacerbated evening hyperglycemia.
Evening postprandial insulin and GIP responses and insulin resistance declined by over 30% after three meals that limited daily carbohydrate intake to 30% compared to no such changes after three 60%-carbohydrate meals, an effect that was independent of pre-meal exercise. The parallel timing and magnitude of postprandial insulin and GIP changes suggest their dependence on a delayed intestinal adaptation to a low-carbohydrate diet. Pre-meal exercise exacerbated glucose intolerance with both diets most likely due to impairment of insulin signaling by pre-meal elevation of FFAs.
餐后高胰岛素血症、高血糖和胰岛素抵抗会增加2型糖尿病(T2D)和心血管疾病死亡风险。餐后高胰岛素血症和高血糖也会出现在食用高碳水化合物饮食的代谢健康受试者中,尤其是晚餐后以及碳水化合物负荷紧跟急性运动之后。我们推测饮食中的碳水化合物负荷,特别是运动后摄入时,以及葡萄糖依赖性促胰岛素多肽(GIP)在这一现象中起到介导作用,因为这种肠促胰岛素在胰岛素敏感状态下会促进碳水化合物摄入后的胰岛素分泌,但在胰岛素抵抗状态下则不然。
四组每组八名体重匹配的代谢健康绝经后女性,分别提供三种等热量膳食(一种试验前膳食和试验日的两顿膳食),碳水化合物含量分别为30%或60%,其中两组在最后两顿膳食前有两小时的中等强度运动,另外两组没有。在餐后4小时和运动3小时期间测量血浆葡萄糖、胰岛素、胰高血糖素、GIP、胰高血糖素样肽1(GLP-1)、游离脂肪酸(FFA)和D-3-羟基丁酸浓度,并通过混合模型方差分析其曲线下面积(AUC),使用稳态模型评估(HOMA-IR)估计每种饮食在空腹和糖耐量试验期间的胰岛素抵抗。
第三顿低碳水化合物膳食,而非高碳水化合物膳食,降低了:(1)无运动时夜间胰岛素AUC 39%,运动后降低31%;(2)无运动时GIP AUC 48%,运动后降低45%,以及(3)无运动时夜间胰岛素抵抗37%,运动后降低24%。餐前运动并未改变低碳水化合物饮食对胰岛素、GIP和HOMA-IR的降低作用,但加剧了夜间高血糖。
与三餐碳水化合物含量为60%时无此类变化相比,将每日碳水化合物摄入量限制在30%的三餐后,夜间餐后胰岛素和GIP反应以及胰岛素抵抗下降超过30%,这一效应与餐前运动无关。餐后胰岛素和GIP变化的平行时间和幅度表明它们依赖于肠道对低碳水化合物饮食的延迟适应。餐前运动在两种饮食中均加剧了葡萄糖不耐受,最可能的原因是餐前FFA升高损害了胰岛素信号传导。