食品科学 ›› 2026, Vol. 47 ›› Issue (3): 198-209.doi: 10.7506/spkx1002-6630-20250715-126

• 营养卫生 • 上一篇    下一篇

小麦肽性质表征及其对酒精性肝细胞损伤的改善作用与机制

杨程珺,陈亮,王华蕾,王心泽,张酥,谷瑞增,孟甘露,刘文颖   

  1. (1.中国食品发酵工业研究院有限公司,北京市蛋白功能肽工程技术研究中心,北京 100015;2.北京城市学院生物医药学部,北京 100094;3.安徽省功能农业与功能食品重点实验室(安徽科技学院),安徽 滁州 239000;4.浙江省农村实业发展有限公司,浙江 杭州 310000)
  • 出版日期:2026-02-01 发布日期:2026-03-16
  • 基金资助:
    安徽省功能农业与功能食品重点实验室(安徽科技学院)开放课题(iFAST-2024-1); 保利中轻科技创新基金项目(ZQ2023JC-SW04)

Characterization of Wheat Peptides and Their Ameliorative Effects and Mechanism on Alcohol-Induced Damage in Hepatocytes

YANG Chengjun, CHEN Liang, WANG Hualei, WANG Xinze, ZHANG Su, GU Ruizeng, MENG Ganlu, LIU Wenying   

  1. (1. Beijing Engineering Research Center of Protein and Functional Peptides, China National Research Institute of Food & Fermentation Industries, Beijing 100015, China; 2. Department of Biomedical Science, Beijing City University, Beijing 100094, China; 3. Anhui Province Key Laboratory of Functional Agriculture and Functional Food, Anhui Science and Technology University, Chuzhou 239000, China; 4. Zhejiang Rural Industrial Development Co. Ltd., Hangzhou 310000, China)
  • Online:2026-02-01 Published:2026-03-16

摘要: 使用酶解方法将谷朊粉制备为小麦肽,分析其理化性质和稳定性,研究其对人肝癌细胞(HepG2)活性的影响,并探究小麦肽对酒精性肝细胞损伤的改善作用及机制。结果表明,小麦肽分子质量<1 000 Da的组分占比为92.883 2%,酸溶蛋白质量分数达(87.23±1.76)%,必需氨基酸相对含量为(22.70±0.54)%,且在酸碱、高温及体外模拟消化条件下稳定性较好。细胞实验结果表明,0.25~6 mg/mL质量浓度的小麦肽对HepG2细胞无毒性。基于乙醇诱导的HepG2细胞损伤模型,发现2~6 mg/mL质量浓度的小麦肽可显著降低活性氧和丙二醛水平(P<0.05),提升超氧化物歧化酶、过氧化氢酶活性和谷胱甘肽含量(P<0.05),同时抑制炎症因子如肿瘤坏死因子-α、白细胞介素-6的释放,从而达到改善酒精性肝细胞损伤的作用。Western Blot结果显示,小麦肽可激活核因子-红细胞2相关因子2,上调血红素氧合酶1表达,抑制Kelch样ECH相关蛋白1表达,即通过激活该通路改善酒精性肝细胞损伤。

关键词: 小麦肽;抗氧化活性;酒精性肝病;核因子红细胞2相关因子2-Kelch样ECH相关蛋白1-血红素加氧酶?1信号通路

Abstract: To develop natural, low-toxicity functional food ingredients, this study prepared wheat peptides from gluten powder by enzymatic hydrolysis. The physicochemical properties and stability of the peptides were analyzed, their effects on the viability of human hepatoma cells (HepG2) were investigated, and their alleviating effects and underlying mechanisms on alcohol-induced liver cell injury were explored. The results showed that the proportion of wheat peptide components with a molecular mass below 1 000 Da was 92.883 2%, the acid-soluble protein content reached (87.23 ± 1.76)%, and the relative content of essential amino acid was (22.70 ± 0.54)%. The wheat peptides exhibited good stability under acidic, alkaline, high-temperature, and in vitro simulated digestion conditions. Cell experiments indicated that the wheat peptides at mass concentrations of 0.25–6 mg/mL were non-toxic to HepG2 cells. It was also found that the wheat peptides at mass concentrations of 2−6 mg/mL significantly reduced oxygen species (ROS) and malondialdehyde (MDA) levels in ethanol-induced HepG2 cells (P < 0.05), increased superoxide dismutase (SOD) and catalase (CAT) activities as well as glutathione (GSH) content (P < 0.05), and simultaneously inhibited the release of inflammatory factors such as tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), thereby alleviating alcohol-induced liver cell injury. Western blot results demonstrated that the wheat peptides activated nuclear factor erythroid 2-related factor 2 (Nrf2), up-regulated heme oxygenase-1 (HO-1) expression, and suppressed Kelch-like ECH-associated protein 1 (Keap1) expression, indicating that they can ameliorate alcoholic liver injury by activating the Nrf2-Keap1-HO-1 signaling pathway.

Key words: wheat peptides; antioxidant activity; alcoholic liver disease; nuclear factor-erythroid 2-related factor 2-Kelch-like ECH-associated protein 1-heme oxygenase-1 signaling pathway

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