Effects of baicalin, baicalein, and wogonin on interleukin-6 and interleukin-8 expression, and nuclear factor-κb binding activities induced by interleukin-1β in human retinal pigment epithelial cell line

沃戈宁 黄芩素 黄芩苷 白细胞介素8 白细胞介素 黄芩 化学 细胞培养 分子生物学 木犀草素 药理学 血红素加氧酶 白细胞介素6 促炎细胞因子
作者
Nobuo Nakamura,Seiji Hayasaka,Xueyun Zhang,Yasunori Nagaki,Masayuki Matsumoto,Yoriko Hayasaka,Katsutoshi Terasawa
出处
期刊:Experimental Eye Research [Elsevier BV]
卷期号:77 (2): 195-202 被引量:78
标识
DOI:10.1016/s0014-4835(03)00116-7
摘要

The objective of the study was to investigate the effects of baicalin, baicalein, and wogonin (plant flavonoids) on interleukin-6 (IL-6) and interleukin-8 (IL-8) protein production, mRNA expression, and nuclear factor-κB (NF-κB) binding activities induced by interleukin-1β (IL-1β) in human retinal pigment epithelial cell line (ARPE-19) cells. To induce IL-6 and IL-8 mRNA expression and protein levels, IL-1β was added to serum-free medium of ARPE-19 cells and incubated. The flavonoids were added to the medium. IL-6 and IL-8 in the media were measured using enzyme-linked immunosorbent assay. Both IL-6 and IL-8 mRNA were measured by semiquantitative reverse transcription polymerase chain reaction. The binding activities of the transcription factor NF-κB complexes to IL-6 and IL-8 were measured by electrophoretic mobility shift assay. IL-6 and IL-8 in the culture media of ARPE-19 cells were increased by IL-1β in a dose-dependent manner. Baicalin did not suppress IL-1β-induced IL-6 and IL-8 production, but dexamethasone, baicalein, and wogonin, significantly suppressed IL-6 and IL-8 production. Elevation of IL-6 and IL-8 mRNA was not suppressed by baicalin but was significantly suppressed by dexamethasone, baicalein, and wogonin. NF-κB binding activities were not suppressed by baicalin and baicalein, but was suppressed by wogonin. Wogonin and baicalein inhibited IL-1β-induced IL-6 and IL-8 mRNA and protein production in ARPE-19 cells. The data suggest that wogonin may inhibit IL-6 and IL-8 mRNA expression via the suppression of NF-κB binding activities.

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