石榴汁和籽提取物对百草枯致急性肺损伤小鼠氧化应激、炎症和erk1/2磷酸化的影响

S. Fathy, Heba A. El‐dash, N. Salim
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引用次数: 0

摘要

肺纤维化被认为是百草枯(PQ)中毒最显著的特征。炎症和氧化应激在pq诱导的肺纤维化发病机制中起重要作用。目前的研究旨在评估石榴汁(PJ)和石榴籽提取物(PSE)补充对pq诱导的肺纤维化小鼠模型的疗效。雄性小鼠(小家鼠)随机分为4个实验组,每组8只。1组(对照组)仅给予0.9%生理盐水;2组腹腔单次注射PQ (30 mg/kg);3、4组分别于PQ注射前1周灌胃PJ (5 mL, 1:40稀释)或PSE (500 mg/kg体重,悬浮于蒸馏水中),连续灌胃3周。与对照组相比,PQ显著增加肺组织中羟脯氨酸、减少的烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶4 (NOX4)、一氧化氮(NO)、丙二醛(MDA)和细胞外信号调节激酶1/2 (ERK1/2)的水平。此外,PQ注射后肺组织中白细胞介素(IL-6、IL-17)、转化生长因子(TGF)-β1、CC趋化因子配体2 (CCL2)水平显著升高。PJ或PSE可明显减轻PQ所致肺生化改变。此外,补充PJ和PSE降低了pq处理小鼠IL-6、IL-17、TGF-β1和CCL2的水平,并显著降低了磷酸化的(p)-ERK1/2。综上所述,PJ和PSE通过调节炎症、氧化应激和纤维化,有效地减轻了pq诱导的小鼠肺损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EFFECTS OF JUICE AND SEED EXTRACT OF POMEGRANATE ON OXIDATIVE STRESS, INFLAMMATION, AND PHOSPHORYLATION OF ERK1/2 IN PARAQUAT-INDUCED ACUTE LUNG INJURY IN MICE
Pulmonary fibrosis is considered the most distinctive feature of paraquat (PQ) poisoning. Inflammation and oxidative stress play crucial roles in the pathogenesis of PQ-induced pulmonary fibrosis. The current study was designed to assess the efficacy of pomegranate juice (PJ) and pomegranate seed extract (PSE) supplementation against PQ-induced pulmonary fibrosis in a mouse model. Male mice (Mus musculus) were randomly divided into four experimental groups (n=8). Group 1 (control group) received 0.9% saline only; group 2 received a single intraperitoneal injection of PQ (30 mg/kg); and groups 3 and 4 were daily treated with PJ (5 mL, 1:40 dilution) or PSE (500 mg/kg body weight, suspended in distilled water), respectively, by gavage one week before the PQ injection, then continued for 3 weeks. PQ increased significantly the levels of hydroxproline, reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 4 (NOX4), nitric oxide (NO), malondialdehyde (MDA), and extracellular signal-regulated kinase 1/2 (ERK1/2) in the lung tissue compared with the control group. Furthermore, the levels of interleukins (IL-6 and IL-17), transforming growth factor (TGF)-β1, and CC chemokine ligand 2 (CCL2) elevated significantly in the lung tissue due to PQ injection. Administration of PJ or PSE alleviated markedly the biochemical lung alterations caused by PQ injection. Additionally, PJ and PSE supplementation decreased the levels of IL-6, IL-17, TGF-β1, and CCL2, as well as reduced significantly the phosphorylated (p)-ERK1/2, in PQ-treated mice. In conclusion, administration of PJ and PSE attenuated effectively PQ-induced lung injury in mice by modulating inflammation, oxidative stress, and fibrosis.
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