Kim Min Jeong, Lee Hye Hyeon, Jeong Jin Woo, Seo Min Jeong, Kang Byoung Won, Park Jeong Uck, Kim Kyoung-Sook, Cho Young-Su, Seo Kwon-Il, Kim Gi-Young, Kim Jung-In, Choi Yung Hyun, Jeong Yong Kee
Department of Biotechnology, Dong-A University, Saha‑gu, Busan 604-714, Republic of Korea.
Center for Core Research Facilities, Daegu Gyeongbuk Institute of Science and Technology, Dalseong‑gun, Daegu 711-873, Republic of Korea.
Mol Med Rep. 2014 Apr;9(4):1197-203. doi: 10.3892/mmr.2014.1922. Epub 2014 Jan 28.
The anti-inflammatory mechanism of 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone (5HHMF), a polyhydroxyflavone isolated from the marine algae Hizikia fusiforme, was investigated in RAW 264.7 murine macrophage cells. Western blot and reverse transcriptase PCR analyses indicated that adding 5HHMF to cultured cells significantly reduced the production of nitric oxide and prostaglandin E2 and downregulated inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) expression in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. In addition, 5HHMF inhibited the release of pro-inflammatory cytokines, such as tumor necrosis factor-α and interleukin-1β, and decreased the transcriptional levels. In particular, 5HHMF significantly inhibited the LPS-induced nuclear factor-κB (NF-κB) translocation from the cytosol to the nucleus, which was associated with the abrogation of inhibitory IκBα degradation and subsequent decreases in nuclear p65 levels. In conclusion, these results suggested that the anti-inflammatory activities of 5HHMF may be attributed to the inhibition of iNOS, COX-2 and cytokine expression by attenuating NF-κB activation via IκBα degradation in macrophages.
对从羊栖菜中分离得到的多羟基黄酮5-羟基-3,6,7,8,3',4'-六甲氧基黄酮(5HHMF)的抗炎机制,在RAW 264.7小鼠巨噬细胞中进行了研究。蛋白质免疫印迹法和逆转录聚合酶链反应分析表明,向培养细胞中添加5HHMF可显著降低一氧化氮和前列腺素E2的产生,并下调脂多糖(LPS)刺激的RAW 264.7细胞中诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达。此外,5HHMF抑制促炎细胞因子如肿瘤坏死因子-α和白细胞介素-1β的释放,并降低转录水平。特别地,5HHMF显著抑制LPS诱导的核因子-κB(NF-κB)从细胞质向细胞核的转位,这与抑制性IκBα降解的消除以及随后细胞核p65水平的降低有关。总之,这些结果表明,5HHMF的抗炎活性可能归因于通过巨噬细胞中IκBα降解减弱NF-κB激活,从而抑制iNOS、COX-2和细胞因子的表达。