Attenuation of Lipopolysaccharide-Induced Inflammatory Responses through Inhibition of the NF-κB Pathway and the Increased NRF2 Level by a Flavonol-Enriched n-Butanol Fraction from Uvaria alba

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]
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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