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首页> 外文期刊>Inflammation >Protective Effect of Astragaloside IV Against Paraquat-Induced Lung Injury in Mice by Suppressing Rho Signaling
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Protective Effect of Astragaloside IV Against Paraquat-Induced Lung Injury in Mice by Suppressing Rho Signaling

机译:黄芪甲苷IV通过抑制Rho信号转导对百草枯引起的小鼠肺损伤的保护作用

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摘要

The purpose of the present study was to evaluate the protective effects of astragaloside IV (AS IV) against paraquat (PQ)-induced pulmonary injury in vivo. Fifty BALB/C mice were randomized into five groups: (1) control, (2) PQ, (3) PQ + dexamethasone (Dex, 5 mg/kg), (4) PQ + AS IV (50 mg/kg), and (5) PQ + AS IV (100 mg/kg). A single dose of PQ (50 mg/kg, i.p.) was intraperitoneally given to induced acute lung injury. Then, mice were treated with AS IV (50 and 100 mg/kg/day, orally) for 5 days. At the end of the experiment, animals were euthanized; then, the bronchoalveolar lavage fluid (BALF) and lung tissues were collected for histological observation, biochemical assay, and Western blot analysis. Malondialdehyde (MDA), myeloperoxidase (MPO), catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) in lung tissues, and interleukin-6 (IL-6), IL-1 beta, tumor necrosis factor-alpha (TNF-alpha) levels in BALF were determined. Histological examination indicated that AS IV attenuated lung damage caused by PQ. Biochemical results showed that AS IV treatment significantly reduced the levels of MDA, MPO, and inflammatory cytokines while increased the levels of SOD, CAT, and GSH-Px compared with those in PQ group. Western blot results revealed that AS IV attenuated the Txnip/Trx expressions and inhibited Rho/ROCKuclear factor kappaB (NF-kappa B) signaling pathway in PQ-challenged mice. These findings suggested the protective effect of AS IV as a natural product on PQ-induced pulmonary injury.
机译:本研究的目的是评估黄芪甲苷IV(AS IV)在体内对百草枯(PQ)诱导的肺损伤的保护作用。将五十只BALB / C小鼠随机分为五组:(1)对照,(2)PQ,(3)PQ +地塞米松(Dex,5 mg / kg),(4)PQ + AS IV(50 mg / kg), (5)PQ + AS IV(100 mg / kg)。腹膜内给予单剂量的PQ(50 mg / kg,腹腔注射),以诱导急性肺损伤。然后,用AS IV(50和100 mg / kg /天,口服)治疗小鼠5天。实验结束时,对动物实施安乐死;然后,收集支气管肺泡灌洗液(BALF)和肺组织进行组织学观察,生化测定和Western blot分析。肺组织中的丙二醛(MDA),髓过氧化物酶(MPO),过氧化氢酶(CAT),超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GSH-Px)和白细胞介素6(IL-6),IL-1 beta,肿瘤坏死因子测定BALF中的α-α(TNF-α)水平。组织学检查表明,AS IV可减轻PQ引起的肺损伤。生化结果显示,与PQ组相比,AS IV治疗显着降低了MDA,MPO和炎性细胞因子的水平,而增加了SOD,CAT和GSH-Px的水平。蛋白质印迹结果表明,AS IV可以减弱PQ攻击小鼠的Txnip / Trx表达并抑制Rho / ROCK /核因子κB(NF-κB)信号通路。这些发现表明,AS IV作为天然产物对PQ诱发的肺损伤具有保护作用。

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