Chukwuma Chika Ifeanyi, Islam Md Shahidul
Department of Biochemistry, School of Life Sciences, University of KwaZulu-Natal (Westville Campus), Durban 4000, South Africa.
Food Funct. 2015 Mar;6(3):955-62. doi: 10.1039/c4fo00994k.
The present study investigated the possible mechanism(s) behind the effects of xylitol on carbohydrate digesting enzymes activity, muscle glucose uptake and intestinal glucose absorption using in vitro, ex vivo and in vivo experimental models. The effects of increasing concentrations of xylitol (2.5%-40% or 164.31 mM-2628.99 mM) on alpha amylase and alpha glucosidase activity in vitro and intestinal glucose absorption and muscle glucose uptake were investigated under ex vivo conditions. Additionally, the effects of an oral bolus dose of xylitol (1 g per kg BW) on gastric emptying and intestinal glucose absorption and digesta transit in the different segments of the intestinal tract were investigated in normal and type 2 diabetic rats at 1 hour after dose administration, when phenol red was used as a recovery marker. Xylitol exhibited concentration-dependent inhibition of alpha amylase (IC₅₀ = 1364.04 mM) and alpha glucosidase (IC₅₀ = 1127.52 mM) activity in vitro and small intestinal glucose absorption under ex vivo condition. Xylitol also increased dose dependent muscle glucose uptake with and without insulin, although the uptake was not significantly affected by the addition of insulin. Oral single bolus dose of xylitol significantly delayed gastric emptying, inhibited intestinal glucose absorption but increased the intestinal digesta transit rate in both normal and diabetic rats compared to their respective controls. The data of this study suggest that xylitol reduces intestinal glucose absorption via inhibiting major carbohydrate digesting enzymes, slowing gastric emptying and fastening the intestinal transit rate, but increases muscle glucose uptake in normal and type 2 diabetic rats.
本研究使用体外、离体和体内实验模型,探究了木糖醇对碳水化合物消化酶活性、肌肉葡萄糖摄取和肠道葡萄糖吸收影响背后的可能机制。在离体条件下,研究了木糖醇浓度增加(2.5%-40%或164.31 mM-2628.99 mM)对体外α淀粉酶和α葡萄糖苷酶活性以及肠道葡萄糖吸收和肌肉葡萄糖摄取的影响。此外,在正常大鼠和2型糖尿病大鼠中,以酚红作为回收标记物,研究了口服大剂量木糖醇(1 g/kg体重)在给药后1小时对胃排空、肠道葡萄糖吸收以及肠道不同节段食糜转运的影响。木糖醇在体外对α淀粉酶(IC₅₀ = 1364.04 mM)和α葡萄糖苷酶(IC₅₀ = 1127.52 mM)活性以及离体条件下的小肠葡萄糖吸收表现出浓度依赖性抑制作用。木糖醇还在有或无胰岛素的情况下增加了剂量依赖性的肌肉葡萄糖摄取,尽管胰岛素的添加对摄取没有显著影响。与各自的对照组相比,口服单次大剂量木糖醇在正常大鼠和糖尿病大鼠中均显著延迟胃排空、抑制肠道葡萄糖吸收,但提高了肠道食糜转运速率。本研究数据表明,木糖醇通过抑制主要碳水化合物消化酶、减缓胃排空和加快肠道转运速率来减少肠道葡萄糖吸收,但增加了正常大鼠和2型糖尿病大鼠的肌肉葡萄糖摄取。