促炎细胞因子
一氧化氮合酶
化学
一氧化氮
分子生物学
肿瘤坏死因子α
山奈酚
SOD2
免疫印迹
槲皮素
超氧化物歧化酶
生物化学
生物
炎症
氧化应激
免疫学
抗氧化剂
有机化学
基因
作者
Kin Israel Notarte,Mark Tristan J. Quimque,Imee Macaranas,Abbas Khan,Adriel Pastrana,Oliver B. Villaflores,Hans Christian P. Arturo,Delfin Yñigo H. Pilapil,Sophia Morgan Tan,Dong‐Qing Wei,Arlette Wenzel‐Storjohann,Deniz Taşdemir,Chia‐Hung Yen,Seon Yeong Ji,Gi‐Young Kim,Yung Hyun Choi,Allan Patrick G. Macabeo
出处
期刊:ACS omega
[American Chemical Society]
日期:2023-01-31
卷期号:8 (6): 5377-5392
被引量:38
标识
DOI:10.1021/acsomega.2c06451
摘要
Pathologic hyperreactive inflammatory responses occur when there is excessive activation of a proinflammatory NF-κB pathway and a reduced cytoprotective NRF2 cascade. The noncytotoxic, highly selective COX-2 inhibitory flavonol-enriched butanol fraction (UaB) from Uvaria alba (U. alba) was investigated for its inflammatory modulating potential by targeting NF-κB activation and NRF2 activity. Enzyme-linked immunosorbent assay was initially performed to measure levels of proinflammatory mediators [nitric oxide (NO), prostaglandin E2, and reactive oxygen species (ROS)] and cytokines [tumor necrosis factor-alpha (TNF-α), IL-1β, and IL-6], followed by reverse transcription-polymerase chain reaction and western blotting to determine mRNA and protein expression, respectively. Using immunofluorescence staining combined with western blot analysis, the activation of NF-κB was further investigated. NRF2 activity was also measured using a luciferase reporter assay. UaB abrogated protein and mRNA expressions of inducible nitric oxide synthase (iNOS), COX-2, TNF-α, IL-1β, and IL-6 in RAW 264.7 macrophages, thereby suppressing the production of proinflammatory mediators and cytokines. This was further validated when a concentration-dependent decrease in NO and ROS production was observed in zebrafish (Danio rerio) larvae. UaB also increased NRF2 activity in HaCaT/ARE cell line and attenuated NF-κB activation by inhibiting the nuclear translocation of transcription factor p65 in RAW 264.7 macrophages. Nontargeted LC-MS analysis of UaB revealed the presence of the flavonols quercitrin (1), quercetin (2), rutin (3), kaempferol (4), and kaempferol 3-O-rutinoside (5). Molecular docking indicates that major flavonol aglycones have high affinity toward COX-2 NSAID-binding sites, TNF-α, and TNF-α converting enzyme, while the glycosylated flavonoids showed strong binding toward iNOS and IKK-all possessing dynamic stability when performing molecular dynamics simulations at 140 ns. This is the first report to have elucidated the mechanistic anti-inflammatory potential of the Philippine endemic plant U. alba.
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