Spiraea prunifolia var. simpliciflora Attenuates Oxidative Stress and Inflammatory Responses in a Murine Model of Lipopolysaccharide-Induced Acute Lung Injury and TNF-α-Stimulated NCI-H292 Cells

氧化应激 肿瘤坏死因子α 脂多糖 活性氧 炎症 化学 支气管肺泡灌洗 NF-κB 促炎细胞因子 药理学 免疫学 分子生物学 生物 医学 生物化学 内科学
作者
Ba-Wool Lee,Ji-Hye Ha,Han-Gyo Shin,Seong-Hun Jeong,Da-Bin Jeon,Ju‐Hong Kim,Jiyoung Park,Hyung‐Jun Kwon,Kyungsook Jung,Woo-Song Lee,Hyeon-Young Kim,Sung‐Hwan Kim,Hyun‐Jae Jang,Young Bae Ryu,In‐Chul Lee
出处
期刊:Antioxidants [Multidisciplinary Digital Publishing Institute]
卷期号:9 (3): 198-198 被引量:19
标识
DOI:10.3390/antiox9030198
摘要

Spiraea prunifolia var. simpliciflora (SP) is traditionally used as an herbal remedy to treat fever, malaria, and emesis. This study aimed to evaluate the anti-oxidative and anti-inflammatory properties of the methanol extract of SP leaves in tumor necrosis factor (TNF)-α-stimulated NCI-H292 cells and in a lipopolysaccharide (LPS)-induced acute lung injury (ALI) mouse model. SP decreased the number of inflammatory cells and the levels of TNF-α, interleukin (IL)-1β, and IL-6 in the bronchoalveolar lavage fluid, and inflammatory cell infiltration in the lung tissues of SP-treated mice. In addition, SP significantly suppressed the mRNA and protein levels of TNF-α, IL-1β, and IL-6 in TNF-α-stimulated NCI-H292 cells. SP significantly suppressed the phosphorylation of the mitogen-activated protein kinases (MAPKs) and p65-nuclear factor-kappa B (NF-κB) in LPS-induced ALI mice and TNF-α-stimulated NCI-H292 cells. SP treatment enhanced the nuclear translocation of nuclear factor erythroid 2-related factor (Nrf2) with upregulated antioxidant enzymes and suppressed reactive oxygen species (ROS)-mediated oxidative stress in the lung tissues of LPS-induced ALI model and TNF-α-stimulated NCI-H292 cells. Collectively, SP effectively inhibited airway inflammation and ROS-mediated oxidative stress, which was closely related to its ability to induce activation of Nrf2 and inhibit the phosphorylation of MAPKs and NF-κB. These findings suggest that SP has therapeutic potential for the treatment of ALI.
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