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中国精品科技期刊2020
金雅丽,李佳,徐梦,等. 紫薯多酚蛋白复合物酶解产物的降血糖活性J. 食品工业科技,2026,47(12):1−8. doi: 10.13386/j.issn1002-0306.2025050072.
引用本文: 金雅丽,李佳,徐梦,等. 紫薯多酚蛋白复合物酶解产物的降血糖活性J. 食品工业科技,2026,47(12):1−8. doi: 10.13386/j.issn1002-0306.2025050072.
JIN Yali, LI Jia, XU Meng, et al. Hypoglycemic Activity of Enzymatic Hydrolyzed Purple Sweet Potato Polyphenol-Protein ComplexesJ. Science and Technology of Food Industry, 2026, 47(12): 1−8. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025050072.
Citation: JIN Yali, LI Jia, XU Meng, et al. Hypoglycemic Activity of Enzymatic Hydrolyzed Purple Sweet Potato Polyphenol-Protein ComplexesJ. Science and Technology of Food Industry, 2026, 47(12): 1−8. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025050072.

紫薯多酚蛋白复合物酶解产物的降血糖活性

Hypoglycemic Activity of Enzymatic Hydrolyzed Purple Sweet Potato Polyphenol-Protein Complexes

  • 摘要: 紫薯多酚蛋白复合物(Purple sweet potato polyphenol-protein complexes,PPPCs)的酶解物在降血糖功能方面具有潜在应用价值。本研究以PPPCs为原料,采用木瓜蛋白酶和碱性蛋白酶协同酶解,并通过3 kDa和10 kDa超滤膜分离获得三组不同分子量的活性肽段(组分1:<3 kDa,组分2:3~10 kDa,组分3:>10 kDa)。利用高脂饲养联合腹腔注射链脲佐菌素(Streptozotocin,STZ)诱导的糖尿病小鼠模型,评估各肽段组分对糖尿病小鼠的降糖活性。采用凝胶渗透色谱对降糖活性最显著的肽段进行分离,并利用HepG2细胞胰岛素抵抗模型评估其对葡萄糖的促消耗能力。结果显示,给药组中组分1高剂量组(D+H1)的降血糖效果最佳,与建模未给药组(D+HF)相比,小鼠空腹血糖水平显著降低(P<0.05),葡萄糖耐受量显著提高(P<0.05),糖尿病引起的体重减轻及肝脏、肾脏和心脏损伤显著改善(P<0.05),血清中总胆固醇(Total cholesterol,TC)、甘油三酯(Triglycerides,TG)、低密度脂蛋白胆固醇(Low density lipoprotein cholesterol,LDL-C)含量均显著降低(P<0.05),高密度脂蛋白胆固醇(High density lipoprotein cholesterol,HDL-C)含量显著提高(P<0.05)。其亚组分1(峰1)在0.1 mg/mL浓度下可使胰岛素抵抗HepG2细胞的葡萄糖消耗量提升至16.20%。本研究证实了PPPCs酶解产物具有显著的降血糖活性功能。其中<3 kDa肽段降血糖效果最好且具有一定的剂量依赖性,其降血糖活性主要来源于其亚组分1。此研究结果为紫薯活性肽的开发及糖尿病群体营养干预策略提供了理论依据,同时,为农产品高值化加工和综合利用带来新机遇。

     

    Abstract: Enzymatic hydrolysates of purple sweet potato polyphenol-protein complexes (PPPCs) exhibited potential hypoglycemic activity. In this study, PPPCs were synergistically hydrolyzed using papain and alkaline protease, followed by fractionation through 3 kDa and 10 kDa ultrafiltration membranes to obtain three peptide fractions (fraction 1: <3 kDa, fraction 2: 3~10 kDa, and fraction 3: >10 kDa). The hypoglycemic effects of these fractions were evaluated in a diabetic mice model induced by a high-fat diet and streptozotocin (STZ) injection. The most active peptide fraction was further purified by gel chromatography, and its glucose uptake-enhancing activity was assessed using an insulin-resistant HepG2 cell model. Results showed that the group of high-dose fraction 1 (D+H1) in the treatment groups exhibited the most potent hypoglycemic effect. Compared with the modeling group without treatment (D+HF), mice in this group demonstrated significantly reduced fasting blood glucose levels (P<0.05), markedly improved glucose tolerance (P<0.05), and significant amelioration of diabetes-induced weight loss and damage to the liver, kidneys, and heart (P<0.05). Levels of total cholesterol (TC), triglycerides (TG), and low-density lipoprotein cholesterol (LDL-C) in serum were significantly reduced (P<0.05), while high-density lipoprotein cholesterol (HDL-C) levels were significantly elevated (P<0.05). Notably, its subfraction 1 (Peak 1) significantly increased glucose consumption in insulin-resistant HepG2 cells by 16.20% at a concentration of 0.1 mg/mL (P<0.05). This study confirmed that enzymatic hydrolysates of PPPCs possessed potent hypoglycemic properties. Among them, the <3 kDa peptide fraction had the best hypoglycemic effect and exhibited a certain degree of dose dependency, and its hypoglycemic activity primarily originated from its subfraction 1. These findings provide a theoretical foundation for developing purple sweet potato-derived bioactive peptides as nutritional interventions for diabetes. Additionally, this study highlights the potential for high-value utilization of agricultural byproducts in functional food applications.

     

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