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Effects of nitric oxide synthase inhibitor on acid aspiration-induced lung injury in rats.

机译:一氧化氮合酶抑制剂对大鼠酸吸入性肺损伤的影响。

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The current study was designed to determine the effects of nitric oxide synthase (NOS) in the development of acid aspiration-induced lung injury in rats. Hydrochloric acid (HCl, 0.1N; 2ml/kg) or normal saline (NS, 2ml/kg) was instilled into the lung of anesthetized, ventilated Sprague-Dawley rats. NG-monomethyl-l-arginine (l-NMMA, 20mgkg(-1)) and a selective inducible nitric oxide synthase (iNOS) inhibitor, ONO-1714 (0.1 and 0.3mgkg(-1)), were used to block NOS. Bronchoalveolar lavage fluid (BALF) and wet and dry measurements of lung (W/D) were obtained 5h after HCl or NS instillation. Unlike the control group, rats instilled with HCl showed significant increases in total nuclear cell counts (NCC), neutrophil counts, concentrations of albumin, tumor necrosis factor-alpha (TNF-alpha), interleukine-6 (IL-6) and nitritesitrates (NO(x)) in BALF. These parameters were associated with the significantly increased W/D in the HCl group compared with the NS group. ONO-1714 (0.1mgkg(-1)) significantly preventedthe increases in all these parameters. Its inhibitory effects were superior to those of l-NMMA and 0.3mgkg(-1) of ONO-1714. NOS plays an important role in the pathogenesis of acid aspiration-induced lung injury. Furthermore, selective iNOS inhibition at the optimal dose was most effective in improving lung injury induced by acid aspiration in rats.
机译:当前的研究旨在确定一氧化氮合酶(NOS)在酸吸入性肺损伤大鼠发展中的作用。将盐酸(HCl,0.1N; 2ml / kg)或生理盐水(NS,2ml / kg)滴入麻醉,通风的Sprague-Dawley大鼠的肺中。 NG单甲基-1-精氨酸(1-NMMA,20mgkg(-1))和选择性诱导型一氧化氮合酶(iNOS)抑制剂ONO-1714(0.1和0.3mgkg(-1))用于阻断NOS。滴注HCl或NS后5小时,获得支气管肺泡灌洗液(BALF)和肺干湿测量(W / D)。与对照组不同,滴注HCl的大鼠的总核细胞计数(NCC),中性粒细胞计数,白蛋白浓度,肿瘤坏死因子α(TNF-alpha),白细胞介素6(IL-6)和亚硝酸盐/ BALF中的硝酸盐(NO(x))。与NS组相比,这些参数与HCl组的W / D显着增加有关。 ONO-1714(0.1mgkg(-1))显着阻止了所有这些参数的增加。它的抑制作用优于1-NMMA和0.3mgkg(-1)的ONO-1714。 NOS在酸吸入引起的肺损伤的发病机理中起重要作用。此外,最佳剂量的选择性iNOS抑制作用最有效地改善了大鼠因酸吸入引起的肺损伤。

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