食品科学 ›› 2024, Vol. 45 ›› Issue (21): 10-19.doi: 10.7506/spkx1002-6630-20240418-173

• 蛋品科学与加工专栏 • 上一篇    下一篇

蛋清水解物降血脂功效的体内/体外评价及其活性肽的筛选与鉴定

陈航, 王玉林, 蔡朝霞, 刘美玉, 黄茜   

  1. (1.华中农业大学食品科学技术学院,农业农村部蛋品加工重点实验室,湖北 武汉 430000;2.河北工程大学生命科学与食品工程学院,河北 邯郸 056038)
  • 出版日期:2024-11-15 发布日期:2024-11-05
  • 基金资助:
    国家自然科学基金面上项目(32072237);河北省现代农业产业技术体系建设专项(HBCT2024260208)

In Vivo and in Vitro Hypolipidemic Efficacy of Egg White Hydrolysate and Screening and Characterization of Active Peptides from It

CHEN Hang, WANG Yulin, CAI Zhaoxia, LIU Meiyu, HUANG Xi   

  1. (1. Key Laboratory of Egg Processing, Ministry of Agriculture and Rural Affairs, College of Food Science and Technology, Huazhong Agricultural University, Wuhan 430000, China; 2. School of Life Sciences and Food Engineering, Hebei University of Engineering, Handan 056038, China)
  • Online:2024-11-15 Published:2024-11-05

摘要: 建立高脂小鼠模型,以辛伐他汀和市售醋蛋液水解物作为药品和食品阳性对照组,综合评价肽酶433P酶解蛋清获得蛋清水解物(egg white hydrolysate,EWH)的体内降血脂效果。结果表明,EWH可以显著抑制小鼠体质量增长,调节血脂异常,减轻肝脏脂质异常与炎症损伤,抑制肝脏脂肪细胞的积累、变性和脂肪组织甘油三酯的堆积。之后研究了胃肠消化对EWH血脂调节活性影响,结果发现,经胃肠消化后EWH的胆固醇胶束溶解度抑制率下降,但胆汁酸结合率和胰脂肪酶抑制率基本无明显变化。最后通过质谱鉴定及分子对接,得到了3 个潜在的胰脂肪酶抑制活性肽,其氨基酸序列分别为LWVPSVY、YPILPEYLQ和WNIPIGTL,上述肽段可以通过氢键、疏水相互作用和静电相互作用等作用力与受体蛋白1ETH相互作用,从而发挥降血脂作用。

关键词: 降血脂, 蛋清水解物, 高脂动物模型, 体外胃肠消化, 分子对接

Abstract: The hypolipidemic effect of egg white hydrolysate (EWH), which was prepared using peptidase 433P, in high-fat diet-fed mice was evaluated using simvastatin and commercially available vinegar-egg hydrolysate as positive controls. The results demonstrated that EWH markedly inhibited body mass gain, regulated dyslipidemia, reduced hepatic lipid abnormalities and inflammatory damage, and inhibited the degeneration and formation of adipocytes and the accumulation of triglycerides in adipose tissue. Afterwards, the effect of gastrointestinal digestion on the blood lipid regulatory activity of EWH was studied. The results showed that the inhibitory effect of EWH on the solubility of cholesterol-rich micelles decreased after gastrointestinal digestion, while the bile acid binding capacity and pancreatic lipase inhibitory activity showed no significant change. At last, three putative pancreatic lipase inhibitory peptides with amino acid sequences of LWVPSVY, YPILPEYLQ and WNIPIGTL were identified by mass spectrometry (MS) and molecular docking. Each of these peptides could interact with the receptor protein 1ETH through hydrogen bonds, electrostatic interactions and hydrophobic interactions, thus exerting hypolipidemic activity.

Key words: hypolipidemic, egg white hydrolysate, hyperlipidemic animal model, in vitro gastrointestinal digestion, molecular docking

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