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首页> 外文期刊>International immunopharmacology >Amelioration of bleomycin-induced lung fibrosis in rats by valproic acid and butyrate: Role of nuclear factor kappa-B, proinflammatory cytokines and oxidative stress
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Amelioration of bleomycin-induced lung fibrosis in rats by valproic acid and butyrate: Role of nuclear factor kappa-B, proinflammatory cytokines and oxidative stress

机译:丙戊酸和丁酸酯改善博来霉素诱导的大鼠肺纤维化:核因子κB,促炎细胞因子和氧化应激的作用

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Bleomycin is one of the anticancer agents used frequently in management of various types of tumors. Pulmonary fibrosis is the major limiting factor for the use of bleomycin. Mechanisms of fibrosis may include disordered wound healing, infiltration with inflammatory cells and fibroblasts and release of reactive oxygen species and growth factors. The aim of this study was to investigate the effect of valproic acid and butyrate on lung fibrosis induced by bleomycin, and to clarify their mechanisms of action. Fifty male Wistar rats were divided into 5 equal groups as follows: control group; bleomycin group; bleomycin + valproic acid group; bleomycin + butyrate group and bleomycin + valproic acid + butyrate group. Weight of rats, lung tissue hydroxyproline, malondialdehyde, superoxide dismutase and catalase were measured. Also, bronchoalveolar lavage (BAL) was analyzed for total and differential leukocytic count, tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and transforming growth factor-beta 1 (TGF-beta 1). Lung tissue was examined histopathologically and immunostained for nuclear factor kappa B (NF-kappa B). Valproic acid and/or butyrate resulted in significant improvement of the body weight gain, oxidative stress, TGF-beta 1, IL-6, TNF-alpha, hydroxyproline and BAL cellularity together with significant improvement of the histopathological and immunohistochemical picture. The use of valproic acid/butyrate combination was better than the use of each of these drugs alone in bleomycin-induced pulmonary fibrosis. In conclusion, valproic acid/butyrate combination may be used prophylactically for amelioration of bleomycin-induced pulmonary fibrosis. (C) 2016 Elsevier B.V. All rights reserved.
机译:博来霉素是在治疗各种类型的肿瘤中经常使用的抗癌药之一。肺纤维化是博来霉素使用的主要限制因素。纤维化的机制可能包括伤口愈合不良,炎性细胞和成纤维细胞浸润以及活性氧和生长因子的释放。这项研究的目的是研究丙戊酸和丁酸对博来霉素诱导的肺纤维化的作用,并阐明其作用机理。将五十只雄性Wistar大鼠分成5个相等的组,如下:对照组;和对照组。博来霉素组;博来霉素+丙戊酸组;博来霉素+丁酸酯组和博来霉素+丙戊酸+丁酸酯组。测量大鼠体重,肺组织羟脯氨酸,丙二醛,超氧化物歧化酶和过氧化氢酶。此外,分析了支气管肺泡灌洗(BAL)的总白细胞计数和差异白细胞计数,肿瘤坏死因子-α(TNF-α),白介素6(IL-6)和转化生长因子-β1(TGF-β1)。对肺组织进行组织病理学检查并免疫染色核因子κB(NF-κB)。丙戊酸和/或丁酸盐可显着改善体重增加,氧化应激,TGF-β1,IL-6,TNF-α,羟脯氨酸和BAL细胞性,并显着改善组织病理学和免疫组织化学图像。在博来霉素诱导的肺纤维化中,丙戊酸/丁酸酯的组合优于单独使用这些药物。总之,丙戊酸/丁酸酯的组合可预防性地用于博来霉素诱导的肺纤维化的改善。 (C)2016 Elsevier B.V.保留所有权利。

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