杨梅素
马来西亚令吉
体外
化学
儿茶素
免疫印迹
炎症
伤口愈合
药理学
类黄酮
促炎细胞因子
抗氧化剂
传统医学
生物化学
生物
多酚
医学
免疫学
基因组
基因
山奈酚
作者
Renáta Sklenářová,Marika Svrčková,Petr Hodek,Jitka Ulrichová,Jana Franková
标识
DOI:10.32725/jab.2021.017
摘要
Myricetin (MYR) and dihydromyricetin (DHM) are classified as natural flavonoids. Both substances are known for their anti-inflammatory and antioxidant properties. In this study, an in vitro model of inflammation was demonstrated on monolayers of scratched fibroblasts or keratinocytes exposed to LPS from Pseudomonas aeruginosa for six hours. MYR and DHM were subsequently applied to the cells for 24 hours at sub toxic concentrations (5-15 µM). Inflammatory parameters were analysed in collected cell medium and lysate after the incubation period using the Enzyme-Linked ImmuneSorbent Assay (ELISA) and Western blot. Both flavonoids inhibit the production of pro-inflammatory cytokines (IL-6, IL-8) in LPS-stimulated skin cells as well as the decreased level of MMP-1 in fibroblasts. However, the application of MYR and DHM dose dependently increased the level of MMP-1 in keratinocytes. In our experiments, we focused on the anti-glycation activity of MYR and DHM, where the higher concentration of MYR seems to be more effective.
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