食品科学 ›› 2021, Vol. 42 ›› Issue (3): 150-157.doi: 10.7506/spkx1002-6630-20200221-227

• 营养卫生 • 上一篇    下一篇

枣花蜜酚类化合物组成及其抗氧化活性分析

杨二林,赵浩安,徐元元,王悦,王银,曹炜   

  1. (1.西北大学食品科学与工程学院,陕西 西安 710069;2.西北大学化工学院,陕西 西安 710069;3.陕西省蜂产品工程技术研究中心,陕西 西安 710065)
  • 发布日期:2021-02-25
  • 基金资助:
    国家自然科学基金面上项目(31871876);陕西省林业科学研究重大专项(2017-01); 陕西省科技厅重点研发计划项目(2018FP2-03)

Phenolic Compounds and Antioxidant Activity of Jujube Honey

YANG Erlin, ZHAO Haoan, XU Yuanyuan, WANG Yue, WANG Yin, CAO Wei   

  1. (1. College of Food Science and Technology, Northwest University, Xi’an 710069, China;2. School of Chemical Engineering, Northwest University, Xi’an 710069, China;3. Bee Product Research Center of Shaanxi Province, Xi’an 710065, China)
  • Published:2021-02-25

摘要: 以陕西佳县、府谷、大荔、渭南4 个地区枣花蜜为研究对象,测定其理化指标、酚类化合物含量、体外抗氧化活性、对·OH诱导的pBR322质粒DNA氧化损伤的保护作用及过氧化氢(H2O2)诱导的小鼠淋巴细胞DNA氧化损伤的保护作用。结果表明,枣花蜜总酚含量为196.55~454.95 mg/kg,总黄酮含量为22.03~39.40 mg/kg;高效液相色谱-电喷雾-四极杆-飞行时间串联质谱分析发现枣花蜜中含有15 种酚类化合物,包括4 种酚酸和11 种黄酮类化合物;体外抗氧化实验表明,枣花蜜具有较强的1,1-二苯基-2-三硝基苯肼自由基清除能力(半抑制浓度为38.03~122.81 mg/mL)、Fe2+络合能力(110.93~158.46 mg/kg)和Fe3+还原力(166.68~365.06 mg/kg);此外,枣花蜜对·OH诱导的pBR322质粒DNA氧化损伤有保护作用且能显著降低H2O2诱导的小鼠淋巴细胞DNA氧化损伤。本实验的研究结果可为枣花蜜资源的开发利用提供理论参考。

关键词: 枣花蜜;抗氧化活性;高效液相色谱-电喷雾-四极杆-飞行时间串联质谱;酚类化合物;DNA损伤

Abstract: In this study, the physicochemical properties, phenolic content, and antioxidant activity in vitro of jujube honeys collected from four regions of Shaanxi province: Jiaxian, Fugu, Dali and Weinan were investigated as well as their effect in protecting plasmid pBR322 against hydroxyl radical-induced oxidative DNA damage and protecting mouse lymphocytes against oxidative DNA damage induced by hydrogen peroxide (H2O2). The results showed that the jujube honeys contained 196.55–454.95 mg/kg of total phenolics, and 22.03–39.40 mg/kg of total flavonoids. By high performance liquid chromatography coupled with electrospray ionization quadrupole time-of-flight mass spectrometry (HPLC/ESI-Q-TOF-MS), a total of 15 phenolic compounds were detected in the samples, including four phenolic acids and 11 flavonoids. In vitro antioxidant test indicated that the jujube honeys had strong 1,1-diphenyl-2-trinitrophenylhydrazine (DPPH) radical scavenging capacity with a half maximal inhibitory concentration (IC50) of 38.03–122.81 mg/mL, ferrous ion chelating activity (110.93–158.45 mg/kg), and ferric reducing power (166.68–365.06 mg/kg). Furthermore, the jujube honeys had a protective effect against oxidative DNA damage in plasmid pBR322 induced by hydroxyl radical and could significantly reduce oxidative DNA damage induced by H2O2 in mouse lymphocytes. The present study provides a theoretical basis for the development and utilization of jujube honey resources.

Key words: jujube honey; antioxidant activity; high performance liquid chromatography coupled with electrospray ionization quadrupole time-of-flight mass spectrometry; phenolics; DNA damage

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