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中国精品科技期刊2020
杨秋变,张笑莹,陈沛航,等. 基于体外化学、细胞和线虫模型评价小黄姜提取物及其复配物的协同降血糖活性J. 食品工业科技,2026,47(11):1−12. doi: 10.13386/j.issn1002-0306.2025040217.
引用本文: 杨秋变,张笑莹,陈沛航,等. 基于体外化学、细胞和线虫模型评价小黄姜提取物及其复配物的协同降血糖活性J. 食品工业科技,2026,47(11):1−12. doi: 10.13386/j.issn1002-0306.2025040217.
YANG Qiubian, ZHANG Xiaoying, CHEN Peihang, et al. Evaluation of Synergistic Hypoglycemic Small Yellow Ginger Extract and and Its Complexes Based on In Vitro Chemical, Cellular, and Nematode ModelsJ. Science and Technology of Food Industry, 2026, 47(11): 1−12. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025040217.
Citation: YANG Qiubian, ZHANG Xiaoying, CHEN Peihang, et al. Evaluation of Synergistic Hypoglycemic Small Yellow Ginger Extract and and Its Complexes Based on In Vitro Chemical, Cellular, and Nematode ModelsJ. Science and Technology of Food Industry, 2026, 47(11): 1−12. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025040217.

基于体外化学、细胞和线虫模型评价小黄姜提取物及其复配物的协同降血糖活性

Evaluation of Synergistic Hypoglycemic Small Yellow Ginger Extract and and Its Complexes Based on In Vitro Chemical, Cellular, and Nematode Models

  • 摘要: 为开发具有协同降血糖作用的天然产物复配物,本研究以小黄姜提取物为主体原料,陈皮和山楂提取物为辅料,采用α-葡萄糖苷酶活性抑制实验、等效线图解法与Chou-Talalay联合指数方法相结合,对小黄姜、陈皮和山楂提取物单独和复配的α-葡萄糖苷酶抑制能力和联合指数进行分析评价,具有协同降血糖作用的复配组合通过IR-HepG2细胞模型和线虫高糖模型进行进一步的降血糖研究。结果显示,小黄姜-陈皮复配物(GE-DTPE1:2)、小黄姜-山楂复配物(GE-CPE1:2)和小黄姜-山楂复配物(GE:CPE1:3)(CI=0.759、0.837和0.861)具有协同降血糖效果;在IR-HepG2细胞实验中,当样品浓度400 μg/mL时,GE、GE-DTPE(1:2)、GE-CPE(1:2)、GE-CPE(1:3)和阿卡波糖组可使IR-HepG2细胞的葡萄糖消耗量分别增加16.86%、18.09%、22.51%、18.97%和40.57%,糖原合成量分别增加13.18%、14.90%、17.10%、15.67%和24.60%;在线虫高糖模型中,相较于高糖模型组,当样品浓度200 μg/mL时,GE-CPE(1:2)显示出最佳降糖潜力,可使GSH和SOD分别提高69.89%和46.99%,而MDA、体内葡萄糖、甘油三酯和脂质积累量分别降低37.43%、66.10%、56.43%和47.35%。该研究为小黄姜提取物系列协同降血糖活性的研究以及开发复合降糖功能食品提供了理论参考。

     

    Abstract: To develop natural product complexes with synergistic hypoglycemic effects, small yellow ginger extract (GE) was used as the main material with dried tangerine peel (Citrus reticulata Blanco) and hawthorn (Crataegus pinnatifida Bge.) extracts (DTPE and CPE) as auxiliary materials. The α-glucosidase activity inhibition assay was integrated with the isobologram method and Chou-Talalay combination index method to comprehensively analyze and evaluate the α-glucosidase inhibitory activities and combination indices of the individual and combined extracts of small yellow ginger, dried tangerine peel, and hawthorn. Subsequently, the complex combinations exhibiting synergistic hypoglycemic effects were further investigated for their hypoglycemic activities using an insulin-resistant HepG2 (IR-HepG2) cell model and a Caenorhabditis elegans (C. elegans) hyperglycemic model. The results showed that GE-DTPE (1:2), GE-CPE (1:2) and GE-CPE (1:3) combinations exhibited synergistic hypoglycaemic effects (CI: 0.759, 0.837, and 0.861, respectively). In the IR-HepG2 cell experiments, when the sample concentration was 400 μg/mL, the GE, GE-DTPE (1:2), GE-CPE (1:2), GE-CPE (1:3), and acarbose increased IR-HepG2 cell glucose consumption by 16.86%, 18.09%, 22.51%, 18.97%, and 40.57%, and boosted glycogen synthesis by 13.18%, 14.90%, 17.10%, 15.67%, and 24.60%, respectively. In the high-glucose C. elegans model, GE-CPE (1:2) at a sample concentration of 200 μg/mL exhibited the strongest hypoglycemic potential compared to the high-glucose control group. It increased GSH and SOD levels by 69.89% and 46.99%, respectively, while reducing MDA, intracellular glucose, triglyceride, and lipid accumulation by 37.43%, 66.10%, 56.43%, and47.35%, respectively. This study provides a theoretical reference for the study of synergistic hypoglycaemic activity of small yellow ginger extract series and the development of compound hypoglycaemic functional foods.

     

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