University of Aberdeen, Rowett Institute, School of Medicine, Medical Sciences and Nutrition, Aberdeen, AB25 2ZD, United Kingdom.
University of Aberdeen, Rowett Institute, School of Medicine, Medical Sciences and Nutrition, Aberdeen, AB25 2ZD, United Kingdom.
J Nutr Biochem. 2020 Apr;78:108325. doi: 10.1016/j.jnutbio.2019.108325. Epub 2019 Dec 26.
The hypoglycaemic effects of two Ribes sp. i.e., anthocyanin-rich black currants (BC) were compared to green currants (GC), which are low in anthocyanins to establish which compounds are involved in the regulation of postprandial glycaemia. We determined the effect of the currants on inhibiting carbohydrate digestive enzymes (α-amylase, α-glucosidase), intestinal sugar absorption and transport across CaCo-2 cells. The digestion of these currants was modelled using in vitro gastrointestinal digestion (IVGD) to identify the metabolites present in the digested extracts by LC-MS/MS. Freeze-dried BC and IVDG extracts inhibited yeast α-glucosidase activity (P<.0001) at lower concentrations than acarbose, whereas GC and IVDG GC at the same concentrations showed no inhibition. BC and GC both showed significant inhibitory effects on salivary α-amylase (P<.0001), glucose uptake (P<.0001) and the mRNA expression of sugar transporters (P<.0001). Taken together this suggests that the anthocyanins which are high in BC have their greatest effect on postprandial hyperglycaemia by inhibiting α-glucosidase activity. Phytochemical analysis identified the phenolics in the currants and confirmed that freeze-dried BC contained higher concentrations of anthocyanins compared to GC (39.80 vs. 9.85 g/kg dry weight). Specific phenolics were also shown to inhibit salivary α-amylase, α-glucosidase, and glucose uptake. However, specific anthocyanins identified in BC which were low in GC were shown to inhibit α-glucosidase. In conclusion the anthocyanins in BC appear to regulate postprandial hyperglycaemia primarily but not solely by inhibiting α-glucosidase while other phenolics modulate salivary α-amylase, glucose uptake and sugar transporters which together could lower the associated risk of developing type-2 diabetes.
两种黑穗醋栗(富含花色苷)和绿穗醋栗(花色苷含量低)的降血糖作用进行了比较,以确定调节餐后血糖的化合物。我们确定了醋栗对抑制碳水化合物消化酶(α-淀粉酶、α-葡萄糖苷酶)、肠道糖吸收和 CaCo-2 细胞跨膜转运的影响。使用体外胃肠消化(IVGD)模拟这些醋栗的消化,通过 LC-MS/MS 鉴定消化提取物中存在的代谢物。与阿卡波糖相比,冻干黑穗醋栗和 IVGD 提取物在较低浓度下即可抑制酵母α-葡萄糖苷酶活性(P<.0001),而相同浓度的绿穗醋栗和 IVGD 绿穗醋栗则没有抑制作用。黑穗醋栗和绿穗醋栗均对唾液α-淀粉酶(P<.0001)、葡萄糖摄取(P<.0001)和糖转运体的 mRNA 表达有显著抑制作用(P<.0001)。总的来说,这表明黑穗醋栗中高含量的花色苷通过抑制α-葡萄糖苷酶活性对餐后高血糖有最大的影响。植物化学分析确定了醋栗中的酚类物质,并证实冻干黑穗醋栗中花色苷的浓度高于绿穗醋栗(39.80 与 9.85 g/kg 干重)。还表明特定的酚类物质可抑制唾液α-淀粉酶、α-葡萄糖苷酶和葡萄糖摄取。然而,在黑穗醋栗中发现的低绿穗醋栗含量的特定花色苷被证明可抑制α-葡萄糖苷酶。总之,黑穗醋栗中的花色苷似乎主要通过抑制α-葡萄糖苷酶来调节餐后高血糖,但不仅仅是通过抑制α-葡萄糖苷酶,而其他酚类物质则调节唾液α-淀粉酶、葡萄糖摄取和糖转运体,共同降低患 2 型糖尿病的风险。