Protective Effects of Flavonoids from Lonicera japonica Thunb. on Hydrogen Peroxide Induced Toxicity in RAW 264.7 Cells

被引:0
|
作者
Luo L. [1 ]
Zhang B. [1 ]
Wei Q. [1 ]
Fan J. [1 ]
Ma L. [1 ]
Guan N. [1 ]
Zhu W. [1 ]
机构
[1] College of Food and Bioengineering, Henan University of Science and Technology, Hennan Agricultural Products Drying Equipment Engineering Technology Research Center, Luoyang
关键词
Antioxidant capacity; Flavonoids; Hydrogen peroxide; Lonicera japonica Thunb; RAW264.7;
D O I
10.16429/j.1009-7848.2019.05.003
中图分类号
学科分类号
摘要
Study on the antioxidant activity of flavonoids from Lonicera japonica Thunb on RAW264.7 cells. The cell damage model was established by H2O2 induced RAW264.7 cell injury, the protective effect of low, middle and high dosage groups of flavonoids from Lonicera japonica Thunb (62.5, 125, 250 mg/mL) on injured cells was studied. The research results show that: Flavonoids at the range of 62.5-250 mg/mL significantly enhanced the proliferation of RAW264.7 cells(P<0.05). In all dose groups of flavonoids from Lonicera japonica Thunb, the total antioxidant capacity in cells and cell culture medium were significantly increased(P<0.05), and the activities of SOD, GSH-Px, CAT and GSH content were significantly increased(P<0.05); the content of MDA was significantly decreased(P<0.05); LDH activity was significantly decreased in cells and was significantly reduced in cell culture medium(P<0.05). Flavonoids from Lonicera japonica Thunb can promote the proliferation of RAW264.7 cells, and the protective effect of H2O2 on RAW264.7 cell injury was dose-dependent. This study provides theoretical basis for the development of Lonicera japonica Thunb functional food and health products. © 2019, Editorial Office of Journal of CIFST. All right reserved.
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页码:18 / 25
页数:7
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共 9 条
  • [1] Inoue M., Free radical theory of life, evolution and disease, The Japanese Journal of Clinical Pathology, 59, 2, pp. 170-171, (2011)
  • [2] Jomova K., Valko M., Importance of iron chelation in free radical-induced oxidative stress and human disease, Current Pharmaceutical Design, 17, 31, pp. 3460-3473, (2011)
  • [3] Halliwell B., Gutteridge J.M.C., Cross C.E., Free-radicals, antioxidants, and human-disease-where are we now, Journal of Laboratory and Clinical Medicine, 119, 6, pp. 598-620, (1992)
  • [4] Geng Y.F., Ge X.F., An experimental study on honeysuckle drying by microwave, Advance Journal of Food Science and Technology, 6, 2, pp. 212-214, (2014)
  • [5] Xue J.Y., Li H.C., Liu F.M., Et al., Vortex-assisted matrix solid-liquid dispersive microextraction for the analysis of triazole fungicides in cotton seed and honeysuckle by gas chromatography, Food Chemistry, 4, 1, pp. 867-876, (2016)
  • [6] Kang O.H., Choi J.G., Lee J.H., Et al., Luteolin isolated from the flowers of Lonicera japonica suppresses inflammatory mediator release by blocking NF-KB and MAPKs activation pathways in HMC-1 Cells, Molecules, 15, 1, pp. 385-398, (2010)
  • [7] Bedoya-Ramirez D., Cilla A., Contreras-Calderon J., Et al., Evaluation of the antioxidant capacity, furan compounds and cytoprotective_cytotoxic effects upon Caco-2 cells of commercial Colombian coffee, Food Chemistry, 219, 15, pp. 364-372, (2017)
  • [8] Wang L., Ding L., Yu Z., Et al., Intracellular ROS scavenging and antioxidant enzyme regulating capacities of corn gluten meal-derived antioxidant peptides in HepG2 cells, Food Research International, 90, pp. 33-41, (2016)
  • [9] Podkopaeva D.A., Miu G., Dubinina G.A., Oxidative stress and antioxidant cell protection systems in the microaerophilic bacterium Spirillum winogradskii, Microbiology, 72, 5, pp. 600-608, (2003)