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中国精品科技期刊2020
吴迪, 刘平平, 李萌, 王昌涛, 赵丹, 张佳婵. 葛根水提液及葛根发酵液的体外抗氧化及抗衰老功效评价[J]. 食品工业科技, 2019, 40(12): 285-290,294. DOI: 10.13386/j.issn1002-0306.2019.12.046
引用本文: 吴迪, 刘平平, 李萌, 王昌涛, 赵丹, 张佳婵. 葛根水提液及葛根发酵液的体外抗氧化及抗衰老功效评价[J]. 食品工业科技, 2019, 40(12): 285-290,294. DOI: 10.13386/j.issn1002-0306.2019.12.046
WU Di, LIU Ping-ping, LI Meng, WANG Chang-tao, ZHAO Dan, ZHANG Jia-chan. Evaluation of Antioxidant and Anti-aging Effect of Pueraria Water Extracts and Pueraria Fermentation Broth in Vitro[J]. Science and Technology of Food Industry, 2019, 40(12): 285-290,294. DOI: 10.13386/j.issn1002-0306.2019.12.046
Citation: WU Di, LIU Ping-ping, LI Meng, WANG Chang-tao, ZHAO Dan, ZHANG Jia-chan. Evaluation of Antioxidant and Anti-aging Effect of Pueraria Water Extracts and Pueraria Fermentation Broth in Vitro[J]. Science and Technology of Food Industry, 2019, 40(12): 285-290,294. DOI: 10.13386/j.issn1002-0306.2019.12.046

葛根水提液及葛根发酵液的体外抗氧化及抗衰老功效评价

Evaluation of Antioxidant and Anti-aging Effect of Pueraria Water Extracts and Pueraria Fermentation Broth in Vitro

  • 摘要: 本实验以葛根为研究对象,通过水提取法及微生物发酵法得到葛根水提液(pueraria water extracts,PWE)及葛根发酵液(pueraria fermentation broth,PFB),对其进行有效成分的提取、化学水平清除1,1-二苯基-2-三硝基苯肼(DPPH)自由基能力测定以及细胞水平过氧化氢酶(catalase,CAT)活力、谷胱甘肽过氧化物酶(glutathione peroxidase)活力、基质金属蛋白酶1(matrix metalloproteinase-1,MMP-1)酶活力和I型胶原(Collagen I,COL I)含量分析。结果表明,葛根水提液、葛根发酵液中主要的活性成分为黄酮类物质,葛根水提液黄酮含量为(3.47±0.23) mg/mL,葛根发酵液黄酮含量为(4.80±0.32) mg/mL;二者均具有较为明显的DPPH自由基清除能力,葛根发酵液清除率DPPH自由基的IC50为2.98 mg/mL,葛根水提液清除率DPPH自由基的IC50为3.51 mg/mL,在质量浓度在2.67~4.44 mg/mL间,相同质量浓度下葛根发酵液清除DPPH的作用更为显著(p<0.05);葛根水提液、葛根发酵液在0.05~5.00 mg/mL范围内,对人皮肤成纤维细胞均未表现出强烈的细胞毒性,细胞活力均在85%以上;两种样品刺激细胞后,细胞中过氧化氢酶活力、谷胱甘肽过氧化物酶活力显著(p<0.05)增高,其中葛根水提液比葛根发酵液作用效果更为显著(p<0.05),两种样品刺激细胞后,均能降低细胞内MMP-1的含量,增加细胞中I型胶原的含量,而葛根发酵液相较于葛根水提液,降低MMP-1含量及增加I型胶原含量的作用更为显著(p<0.05)。综上,葛根发酵液的抗氧化性及抗衰老功效强于葛根水提液。

     

    Abstract: In this research,pueraria was used as the research object and extracted by water in the means of microbe extraction methods,then the pueraria water extracts(PWE)and pueraria fermentation broth(PFB)were obtained. The two samples were tested for bioactive components,chemical and cellular antioxidant properties including scavenging capacity against 2,2-diphenyl-1-picrylhydrazyl(DPPH)free radical and catalase activity(CAT),and their effects on glutathione peroxidase activity,matrix metalloproteinase-1(MMP-1)and type I collagen(COLI)contents in the culture supernatants of human skin fibroblast cells were examined. The flavonoid content of PWE was(3.47±0.23) mg/mL,and the flavonoid content of PFB was(4.80±0.32) mg/mL.Both of them had obvious DPPH free radical scavenging ability. The IC50 of DPPH free radical scavenging activity of PWE was 2.98 mg/mL. The IC50 of DPPH free radical scavenging acticity was 3.51 mg/mL. Furthermore,the effect of scavenging DPPH was more significant at the same concentration of 2.67~4.44 mg/mL.(p<0.05). The two samples in the concentration range of 0.05~5.00 mg/mL showed no strong cytotoxicity to human skin fibroblast cells and the cell viability was above 85% in the presence of each sample. Stimulation with the samples significantly(p<0.05)increased catalase activity and glutathione peroxidase activity,and the PWE showed significantly(p<0.05) acticity than PFB. Furthermore,both samples could reduced MMP-1 contents,and increased COL I contents after the stimulation with the samples. PFB showed stronger acticity of reducing MMP-1 and increasing COL I(p<0.05). Therefore,PFB and PWE had potential anti-aging effect.

     

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