Department of Human Biology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Universiteitssingel 50, 6229 ERMaastricht, The Netherlands.
Sensus B.V. (Royal Cosun), Oostelijke Havendijk 15, 4704 RARoosendaal, The Netherlands.
Br J Nutr. 2022 Sep 28;128(6):1072-1081. doi: 10.1017/S0007114521004153. Epub 2021 Oct 18.
Dietary interventions to delay carbohydrate digestion or absorption can effectively prevent hyperglycaemia in the early postprandial phase. L-arabinose can specifically inhibit sucrase. It remains to be assessed whether co-ingestion of L-arabinose with sucrose delays sucrose digestion, attenuates subsequent glucose absorption and impacts hepatic glucose output. In this double-blind, randomised crossover study, we assessed blood glucose kinetics following ingestion of a 200-ml drink containing 50 g of sucrose with 7·5 g of L-arabinose (L-ARA) or without L-arabinose (CONT) in twelve young, healthy participants (24 ± 1 years; BMI: 22·2 ± 0·5 kg/m). Plasma glucose kinetics were determined by a dual stable isotope methodology involving ingestion of (U-C)-glucose-enriched sucrose, and continuous intravenous infusion of (6,6-H)-glucose. Peak glucose concentrations reached 8·18 ± 0·29 mmol/l for CONT 30 min after ingestion. In contrast, the postprandial rise in plasma glucose was attenuated for L-ARA, because peak glucose concentrations reached 6·62 ± 0·18 mmol/l only 60 min after ingestion. The rate of exogenous glucose appearance for L-ARA was 67 and 57 % lower compared with CONT at t = 15 min and 30 min, respectively, whereas it was 214 % higher at t = 150 min, indicating a more stable absorption of exogenous glucose for L-ARA compared with CONT. Total glucose disappearance during the first hour was lower for L-ARA compared with CONT (11 ± 1 . 17 ± 1 g, < 0·0001). Endogenous glucose production was not differentially affected at any time point ( = 0·27). Co-ingestion of L-arabinose with sucrose delays sucrose digestion, resulting in a slower absorption of sucrose-derived glucose without causing adverse effects in young, healthy adults.
饮食干预延迟碳水化合物消化或吸收可以有效预防餐后早期高血糖。L-阿拉伯糖可以特异性抑制蔗糖酶。尚需评估 L-阿拉伯糖与蔗糖共同摄入是否会延迟蔗糖消化,减弱随后的葡萄糖吸收,并影响肝葡萄糖输出。在这项双盲、随机交叉研究中,我们评估了 12 名年轻健康受试者(24 ± 1 岁;BMI:22.2 ± 0.5 kg/m)摄入含 50 g 蔗糖和 7.5 g L-阿拉伯糖(L-ARA)或不含 L-阿拉伯糖(CONT)的 200 ml 饮料后血糖动力学。通过双稳定同位素方法测定血浆葡萄糖动力学,该方法涉及摄入(U-C)-葡萄糖富集蔗糖和(6,6-H)-葡萄糖连续静脉输注。CONT 组在摄入后 30 分钟血糖峰值达到 8.18 ± 0.29 mmol/l。相比之下,L-ARA 组餐后血糖升高减弱,因为血糖峰值仅在摄入后 60 分钟达到 6.62 ± 0.18 mmol/l。L-ARA 在 t = 15 分钟和 30 分钟时,外源性葡萄糖出现率比 CONT 分别低 67%和 57%,而在 t = 150 分钟时则高 214%,表明 L-ARA 比 CONT 更稳定地吸收外源性葡萄糖。与 CONT 相比,L-ARA 组在第一小时内总葡萄糖消失量较低(11 ± 1 ,17 ± 1 g,< 0·0001)。在任何时间点,内源性葡萄糖生成均无差异(= 0·27)。L-阿拉伯糖与蔗糖共同摄入可延迟蔗糖消化,导致蔗糖衍生葡萄糖吸收缓慢,而在年轻健康成年人中不会引起不良反应。