食品科学 ›› 2024, Vol. 45 ›› Issue (6): 97-104.doi: 10.7506/spkx1002-6630-20221220-203

• 营养卫生 • 上一篇    下一篇

两种生育酚酯衍生物对D-半乳糖致衰老小鼠的抗衰老作用

陈炜莉,贝翎,杨扬,王璧莹,李家旭,阚绪甜,李文治,杜冰   

  1. (1.华南农业大学食品学院,广东 广州 510642;2.无限极(中国)有限公司研发中心,广东 广州 510623)
  • 出版日期:2024-03-25 发布日期:2024-04-03
  • 基金资助:
    财政部和农业农村部:国家现代农业产业技术体系建设专项(CARS-21)

Anti-Aging Effects of Two Tocopherol Ester Derivatives on D-Galactose-Induced Aging in Mice

CHEN Weili, BEI Ling, YANG Yang, WANG Biying, LI Jiaxu, KAN Xutian, LI Wenzhi, DU Bing   

  1. (1. College of Food Science, South China Agriculture University, Guangzhou 510642, China;2. Research and Development Centre of Infinitus (China), Guangzhou 510623, China)
  • Online:2024-03-25 Published:2024-04-03

摘要: 为探究两种生育酚酯衍生物(D-α-生育酚醋酸酯和DL-α-生育酚醋酸酯)的抗衰老作用,本实验测定其体外抗氧化能力,并采用D-半乳糖构建衰老小鼠模型,同时用两种生育酚酯衍生物干预42 d,分析衰老相关指标变化规律。结果表明:在0.1~0.3 mg/mL质量浓度范围内,两种生育酚酯衍生物的羟自由基清除能力、2,2’-联氮双(3-乙基苯并噻唑啉-6-磺酸)阳离子自由基清除能力、Fe2+螯合能力、总还原能力均优于VC。与衰老模型组相比,经过生育酚酯衍生物干预后,小鼠血清中丙二醛含量显著下降(P<0.05,P<0.01,P<0.001,P<0.000 1),谷胱甘肽过氧化物酶和总抗氧化能力显著升高(P<0.05,P<0.01,P<0.001,P<0.000 1);血清中炎症因子白细胞介素-6、白细胞介素-1β、肿瘤坏死因子-α和肝功能指标天冬氨酸氨基转移酶、丙氨酸氨基转移酶水平显著降低(P<0.05,P<0.01,P<0.001,P<0.000 1);小鼠肝脏中核因子-E2-相关因子(nuclear factor E2 related factor 2,Nrf2)、醌氧化还原酶1(quinone oxidoreductase,NQO1)、血红素氧合酶1(heme oxygenase-1,HO-1)的mRNA及蛋白相对表达量提升,其中DL-α-生育酚醋酸酯的Nrf2、NQO1、HO-1 mRNA相对表达量分别增加了514.08%、461.78%、515.32%,蛋白相对表达量分别增加了620.00%、988.89%、1 200.00%(P<0.000 1)。综上所述,两种生育酚酯衍生物对D-半乳糖致衰老小鼠具有抗衰老作用,且DL-α-生育酚醋酸酯效果更好,二者抗衰老作用可能与调控Nrf2信号通路相关。

关键词: 生育酚酯衍生物;D-半乳糖;抗氧化;抗衰老;核因子-E2-相关因子

Abstract: In order to explore the anti-aging effects of two tocopherol ester derivatives, the in vitro antioxidant capacity of D-α-tocopherol acetate and DL-α-tocopherol acetate was determined. A mouse model of D-galactose-induced was created and intervened with each of the tocopherol ester derivatives for 42 days. Changes in aging related indicators were analyzed. The results showed that the hydroxyl radical scavenging capacity, and the 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) cation radical scavenging capacity, Fe2+ chelating capacity, and total reducing power of the two tocopherol ester derivatives were better than those of vitamin C in the concentration range of 0.1 to 0.3 mg/mL. Compared with the aging model group, after intervention with tocopherol ester derivatives, the content of malondialdehyde (MDA) in serum decreased significantly (P < 0.05, P < 0.01, P < 0.001, and P < 0.000 1), and glutathione peroxidase (GSH-Px) activity and total antioxidant capacity (T-AOC) increased significantly (P < 0.05, P < 0.01, P < 0.001, and P < 0.000 1). The serum levels of inflammatory cytokines such as interleukin-6 (IL-6), interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α), and liver function indexes including aspartate aminotransferase (AST) and alanine aminotransferase (ALT) decreased significantly (P < 0.05, P < 0.01, P < 0.001, and P < 0.001). Moreover, the relative mRNA and protein expression levels of nuclear factor-E2-related factors (Nrf2), quinone oxidoreductase (NQO1) and heme oxygenase 1 (HO-1) in the mouse liver were enhanced. DL-α-tocopherol acetate increased the relative mRNA expression of Nrf2, NQO1 and HO-1 by 514.08%, 461.78% and 515.32%, respectively, and their relative protein expression by 620.00%, 988.89% and 1 200.00%, respectively (P < 0.000 1). To sum up, the two tocopherol ester derivatives have anti-aging effects on D-galactose-induced aging in mice, DL-α-tocopherol acetate being more effective than D-α-tocopherol acetate, and their anti-aging effects may be related to the regulation of the Nrf2 signaling pathway.

Key words: tocopherol ester derivatives; D-galactose; antioxidant; anti-aging; nuclear factor E2 related factor 2

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