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首页> 外文期刊>Pulmonary pharmacology & therapeutics >N-acetylcysteine attenuates the acute lung injury caused by phorbol myristate acetate in isolated rat lungs.
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N-acetylcysteine attenuates the acute lung injury caused by phorbol myristate acetate in isolated rat lungs.

机译:N-乙酰半胱氨酸减轻了离体大鼠肺中由佛波醇肉豆蔻酸酯乙酸盐引起的急性肺损伤。

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Acute lung injury (ALI) caused by phorbol myristate acetate (PMA) is characterized by pulmonary edema and inflammatory cells infiltration. PMA-activated neutrophils in vivo and in vitro to release free radicals, pro-inflammatory cytokines, nitric oxide (NO) and other mediators. These mediators may be the causes of pulmonary hypertension and increased microvascular permeability. In the present study, we used isolated perfused rat lungs from Sprague-Dawley (SD) rats. The purpose was to evaluate the effects of pretreatment of N-acetylcysteine (NAC) on the PMA-induced ALI and associated changes. PMA (2mugkg(-1)) was introduced into the lung perfusate. NAC (150mgkg(-1)) was administered 10min before PMA. Thirty isolated lungs were randomly assigned to receive vehicle (dimethyl sulfoxide, DMSO, the solvent for PMA, 100mugg(-1)), PMA alone and PMA with NAC pretreatment. There were 10 lungs in each group. We measured the lung weight (LW) to body weight (BW) ratio (LW/BW), LW gain (LWG), exhaled nitric oxide (NO) and protein concentration in bronchoalveolar lavage (PCBAL). The pulmonary arterial pressure (PAP) and microvascular permeability (K(fc)) were assessed. The concentration of nitrateitrite, methyl guanidine (MG), tumor necrosis factor(alpha) (TNF(alpha)) and interleukin-1(beta) (IL-1(beta)) in lung perfusate were determined. In addition, we also evaluate the lung injury by histopathological examination and by grading system for the lung injury score (LIS). PMA caused severe ALI as evidenced by the marked increases in LW changes, exhaled NO, PCBAL, histopathological changes, and LIS. It also increased the nitrateitrite, MG, TNF(alpha), and IL-1(beta) in lung perfusate. Pretreatment with NAC significantly attenuated these changes and abrogated the extent of ALI. Our results suggest that NAC exerts strong protective effects on the PMA-induced ALI and associated alterations. The mechanisms are possibly attributable to its antioxidant actions, inhibition of pro-inflammatory cytokines, and restoration of glutathione enzymes.
机译:佛波肉豆蔻酸酯乙酸盐(PMA)引起的急性肺损伤(ALI)的特征是肺水肿和炎性细胞浸润。 PMA激活的中性粒细胞在体内和体外释放自由基,促炎性细胞因子,一氧化氮(NO)和其他介质。这些介质可能是肺动脉高压和微血管通透性增加的原因。在本研究中,我们使用了来自Sprague-Dawley(SD)大鼠的分离的灌注大鼠肺。目的是评估N-乙酰半胱氨酸(NAC)预处理对PMA诱导的ALI及其相关变化的影响。将PMA(2mugkg(-1))引入肺灌注液中。 NAC(150mgkg(-1))在PMA前10分钟给药。随机分配三十只分离的肺,以接受媒介物(二甲亚砜,DMSO,PMA的溶剂,100mugg(-1)),单独的PMA和经过NAC预处理的PMA。每组有10个肺。我们测量了肺重量(LW)与体重(BW)的比率(LW / BW),LW增益(LWG),呼出气一氧化氮(NO)和支气管肺泡灌洗液(PCBAL)中的蛋白质浓度。评估肺动脉压(PAP)和微血管通透性(K(fc))。确定了肺灌注液中硝酸盐/亚硝酸盐,甲基胍(MG),肿瘤坏死因子α(TNFα)和白介素1β(IL-1β)的浓度。此外,我们还通过组织病理学检查和肺损伤评分(LIS)评分系统评估肺损伤。 PMA引起严重的ALI,如LW变化,呼出NO,PCBAL,组织病理学变化和LIS明显增加所证明。它还增加了肺灌注液中的硝酸盐/亚硝酸盐,MG,TNFα和IL-1β。用NAC预处理可显着减弱这些变化并消除ALI的程度。我们的结果表明,NAC对PMA诱导的ALI及其相关改变具有强大的保护作用。该机制可能归因于其抗氧化作用,抑制促炎性细胞因子和恢复谷胱甘肽酶。

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