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首页> 外文期刊>Journal of Agricultural and Food Chemistry >Protein-Bound Anthocyanin Compounds of Purple Sweet Potato Ameliorate Hyperglycemia by Regulating Hepatic Glucose Metabolism in High-Fat Diet/Streptozotocin-Induced Diabetic Mice
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Protein-Bound Anthocyanin Compounds of Purple Sweet Potato Ameliorate Hyperglycemia by Regulating Hepatic Glucose Metabolism in High-Fat Diet/Streptozotocin-Induced Diabetic Mice

机译:紫色甘薯的蛋白质结合的花青素化合物通过调节高脂饮食/链脲佐菌素诱导的糖尿病小鼠来调节肝葡萄糖代谢来改善高血糖症

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摘要

Purple sweet potato is known as a rich source of protein and anthocyanins. Anthocyanins can form complexes with protein present in food products through non-covalent forces or covalent bonds during processing, transportation, and storage as their protein affinity. We evaluated the hypoglycemic effects of protein-bound anthocyanin compounds of purple sweet potato (p-BAC-PSP) and free anthocyanin compounds of purple sweet potato (FAC-PSP) in high-fat diet/streptozotocin-induced diabetic mice. The results showed that administration of both p-BAC-PSP and FAC-PSP improved diabetic condition, as evidenced by the improvement of glucose tolerance and lipid metabolism, and the decrease of oxidative stress and liver damage. For the mechanism study, we have found that p-BAC-PSP and FAC-PSP induced the expression of AMP-activated protein kinase in liver. With p-BAC-PSP or FAC-PSP treatment, glucose transporter type 2, the protein levels of glucokinase, and insulin receptor alpha were found to be improved significantly (p < 0.05). Glycolysis key genes, phosphofructokinase and pyruvate kinase, were upregulated in two treatment groups, while gluconeogenic genes, glucose-6-phosphatase and phosphoenolpyruvate carboxykinase, were downregulated. Our findings suggested that p-BAC-PSP has great potential as a dietary supplement with hypoglycemic activity for general, pre-diabetic, and diabetic population.
机译:紫色甘薯被称为丰富的蛋白质和花青素。花青素可以通过加工,运输和储存期间的非共价力或共价键在食品中存在与食品中存在的蛋白质的复合物作为其蛋白质亲和力。我们评估了紫色甘薯(P-BAC-PSP)蛋白结合的花青素化合物的低血糖作用,以及在高脂饮食/链脲佐菌素诱导的糖尿病小鼠中的紫色甘薯(FAC-PSP)的游离花青素化合物。结果表明,P-BAC-PSP和FAC-PSP的施用改善了糖尿病病症,如葡萄糖耐量和脂质代谢的改善所证明,以及氧化应激和肝损伤的降低。对于机制研究,我们发现P-BAC-PSP和FAC-PSP诱导肝脏中AMP活化蛋白激酶的表达。用P-BAC-PSP或FAC-PSP处理,发现葡萄糖转运蛋白型,葡萄糖酮酶的蛋白质水平和胰岛素受体α进行显着改善(P <0.05)。糖酵解键基因,磷化氢酶和丙酮酸激酶,在两个处理基团中上调,而葡糖来基因,葡萄糖基因,葡萄糖-6-磷酸酶和磷酸丙酮酸羧基酶进行下调。我们的研究结果表明,P-BAC-PSP具有较大的潜力,作为一般,糖尿病患者和糖尿病群的低血糖活性膳食补充剂。

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