NutritionMetabolism and Diabetes Research Group, Faculty of Health and Medical Sciences, University of Surrey, Leggett Building, Guildford, Surrey GU2 7WG, UK Metabolic and Molecular Imaging GroupMRC Clinical Sciences Centre, Imperial College, London W12 0HS, UK Department of Food and Nutritional SciencesUniversity of Reading, Whiteknights Campus, Reading RG6 6AP, UK.
Endocr Connect. 2014 Apr 15;3(2):75-84. doi: 10.1530/EC-14-0036. Print 2014.
Resistant starch (RS) has been shown to beneficially affect insulin sensitivity in healthy individuals and those with metabolic syndrome, but its effects on human type 2 diabetes (T2DM) are unknown. This study aimed to determine the effects of increased RS consumption on insulin sensitivity and glucose control and changes in postprandial metabolites and body fat in T2DM. Seventeen individuals with well-controlled T2DM (HbA1c 46.6±2 mmol/mol) consumed, in a random order, either 40 g of type 2 RS (HAM-RS2) or a placebo, daily for 12 weeks with a 12-week washout period in between. AT THE END OF EACH INTERVENTION PERIOD, PARTICIPANTS ATTENDED FOR THREE METABOLIC INVESTIGATIONS: a two-step euglycemic-hyperinsulinemic clamp combined with an infusion of [6,6-(2)H2] glucose, a meal tolerance test (MTT) with arterio-venous sampling across the forearm, and whole-body imaging. HAM-RS2 resulted in significantly lower postprandial glucose concentrations (P=0.045) and a trend for greater glucose uptake across the forearm muscle (P=0.077); however, there was no effect of HAM-RS2 on hepatic or peripheral insulin sensitivity, or on HbA1c. Fasting non-esterified fatty acid (NEFA) concentrations were significantly lower (P=0.004) and NEFA suppression was greater during the clamp with HAM-RS2 (P=0.001). Fasting triglyceride (TG) concentrations and soleus intramuscular TG concentrations were significantly higher following the consumption of HAM-RS2 (P=0.039 and P=0.027 respectively). Although fasting GLP1 concentrations were significantly lower following HAM-RS2 consumption (P=0.049), postprandial GLP1 excursions during the MTT were significantly greater (P=0.009). HAM-RS2 did not improve tissue insulin sensitivity in well-controlled T2DM, but demonstrated beneficial effects on meal handling, possibly due to higher postprandial GLP1.
抗性淀粉(RS)已被证明有益于改善健康人群和代谢综合征人群的胰岛素敏感性,但它对 2 型糖尿病(T2DM)患者的影响尚不清楚。本研究旨在确定增加 RS 摄入量对 T2DM 患者胰岛素敏感性和血糖控制的影响,以及餐后代谢物和体脂的变化。17 名血糖控制良好的 T2DM 患者(HbA1c 46.6±2mmol/mol)以随机顺序每天摄入 40g 2 型 RS(HAM-RS2)或安慰剂,两种干预方式之间间隔 12 周洗脱期。在每个干预期结束时,参与者进行了三次代谢研究:两步法正葡萄糖-高胰岛素钳夹试验联合[6,6-(2)H2]葡萄糖输注、前臂动静脉采样的口服糖耐量试验(MTT)和全身成像。HAM-RS2 导致餐后血糖浓度显著降低(P=0.045),前臂肌肉葡萄糖摄取量呈增加趋势(P=0.077);然而,HAM-RS2 对肝或外周胰岛素敏感性或 HbA1c 没有影响。空腹非酯化脂肪酸(NEFA)浓度显著降低(P=0.004),且 HAM-RS2 钳夹时 NEFA 抑制作用更强(P=0.001)。HAM-RS2 干预后空腹甘油三酯(TG)浓度和比目鱼肌内 TG 浓度显著升高(P=0.039 和 P=0.027)。尽管 HAM-RS2 干预后空腹 GLP1 浓度显著降低(P=0.049),但 MTT 期间餐后 GLP1 反应明显更大(P=0.009)。HAM-RS2 并未改善血糖控制良好的 T2DM 患者的组织胰岛素敏感性,但在餐食处理方面表现出有益作用,可能是由于餐后 GLP1 升高。