School of Pharmacy, Xi'an Jiaotong University, No. 76 Western Yanta Road, Xi'an City, 710061, Shaanxi Province, People's Republic of China.
Queen Mary College, Nanchang University, Nanchang, 330019, People's Republic of China.
Inflammation. 2018 Jun;41(3):996-1007. doi: 10.1007/s10753-018-0753-3.
Nobiletin (NOB), a citrus polymethoxy flavonoid, has been reported to exhibit anti-inflammatory, anti-cancer, and anti-insulin resistance activities. Although the anti-inflammatory activity of NOB already reported, its involvement in lung protection has not been reported. Thus, this study aimed to investigate the anti-inflammatory response of NOB in lipopolysaccharide (LPS)-stimulated A549 cells and LPS-induced acute lung injury (ALI) in mice. The animals were pre-treated with NOB (5, 10, and 20 mg/kg) or DEX (5 mg/kg) at 12 and 1 h before intranasal instillation of LPS. The severity of pulmonary injury was evaluated 6 h after LPS administration. Results suggested that treatment with NOB dramatically attenuated lung histopathological changes, wet-to-dry (W/D) ratio, myeloperoxidase (MPO) activity, the numbers of inflammatory cells, and TNF-α, IL-6, and NO in BALF induced by LPS. Furthermore, NOB also significantly inhibited the expression of iNOS and the phosphorylation of NF-κBp65 and IκBα. In vitro, NOB inhibited NF-κB activation and TNF-α, IL-6 production in LPS-stimulated A549 cells. Taken together, these results indicated that NOB exhibited a protective effect on ALI, and the possible mechanism is involved in inhibiting NF-κB activation, subsequently inhibiting LPS-induced inflammatory response.
川陈皮素(NOB)是一种柑橘类多甲氧基黄酮类化合物,具有抗炎、抗癌和抗胰岛素抵抗活性。尽管已经报道了 NOB 的抗炎活性,但它在肺保护中的作用尚未被报道。因此,本研究旨在探讨 NOB 在脂多糖(LPS)刺激的 A549 细胞中的抗炎反应和 LPS 诱导的小鼠急性肺损伤(ALI)中的作用。动物在 LPS 鼻内滴注前 12 和 1 小时用 NOB(5、10 和 20 mg/kg)或 DEX(5 mg/kg)预处理。在 LPS 给药后 6 小时评估肺损伤的严重程度。结果表明,NOB 处理可显著减轻 LPS 诱导的肺组织病理学变化、湿重/干重(W/D)比、髓过氧化物酶(MPO)活性、炎症细胞数量以及 BALF 中的 TNF-α、IL-6 和 NO。此外,NOB 还显著抑制了 iNOS 的表达和 NF-κBp65 和 IκBα的磷酸化。在体外,NOB 抑制了 LPS 刺激的 A549 细胞中 NF-κB 的激活和 TNF-α、IL-6 的产生。综上所述,这些结果表明,NOB 对 ALI 具有保护作用,其可能的机制涉及抑制 NF-κB 激活,进而抑制 LPS 诱导的炎症反应。