Antonini J M, van Dyke K, DiMatteo M, Reasor M J
Department of Pharmacology and Toxicology, Robert C. Byrd Health Sciences Center of West Virginia University, Morgantown 26506-9223.
Inflammation. 1995 Feb;19(1):9-21. doi: 10.1007/BF01534376.
Chemical alteration of the glucocorticoid, methylprednisolone, has led to the introduction of a new class of compounds called the 21-aminosteroids (21-ASs). The purpose of this study was to investigate the effect of the 21-AS, U74389G, on silica-induced acute lung injury. Male Fischer 344 rats were treated intraperitoneally with saline or U74389G in a total dose of 15 mg/kg divided into three injections of 5 mg/kg separated by 4 h. Following the first treatment, animals from the two groups were intratracheally instilled with silica (10 mg/100 g body wt in 0.5 ml of saline) or saline vehicle (0.5 ml). Twenty-four hours after the instillations, bronchoalveolar lavage (BAL) was performed. In the animals not receiving U74389G, marked increases in total protein, beta-glucuronidase, and lactate dehydrogenase (LDH) activities and number of neutrophils (PMNs) were demonstrated in the BAL fluid of the silica-treated animals compared to their controls. Silica also caused dramatic increases in the luminol-dependent chemiluminescence (CL) of lung tissue and BAL cells. The CL reaction was decreased by superoxide dismutase (SOD) and N-nitro-L-arginine methyl ester hydrochloride (L-NAME), a nitric oxide (NO) synthase inhibitor. In animals treated with U74389G, there was attenuation of the silica-induced increases in biochemical, cellular, and chemiluminescent indices of damage. This study demonstrates that U74389G significantly reduces acute lung injury caused by the intratracheal instillation of silica, and this drug may be of potential value for treatment of lung diseases in which damage caused by reactive oxygen species has been implicated.
糖皮质激素甲泼尼龙的化学结构改变催生了一类名为21-氨基类固醇(21-ASs)的新化合物。本研究旨在探究21-AS U74389G对二氧化硅诱导的急性肺损伤的影响。雄性Fischer 344大鼠腹腔注射生理盐水或U74389G,总剂量为15 mg/kg,分三次注射,每次5 mg/kg,间隔4小时。首次治疗后,两组动物经气管内注入二氧化硅(10 mg/100 g体重,溶于0.5 ml生理盐水中)或生理盐水载体(0.5 ml)。注入后24小时,进行支气管肺泡灌洗(BAL)。在未接受U74389G治疗的动物中,与对照组相比,二氧化硅处理动物的BAL液中总蛋白、β-葡萄糖醛酸酶和乳酸脱氢酶(LDH)活性以及中性粒细胞(PMN)数量显著增加。二氧化硅还导致肺组织和BAL细胞中鲁米诺依赖性化学发光(CL)显著增加。超氧化物歧化酶(SOD)和一氧化氮(NO)合酶抑制剂盐酸N-硝基-L-精氨酸甲酯(L-NAME)可降低CL反应。在用U74389G治疗的动物中,二氧化硅诱导的损伤生化、细胞和化学发光指标增加有所减轻。本研究表明,U74389G可显著减轻气管内注入二氧化硅引起的急性肺损伤,该药物可能对治疗与活性氧引起的损伤有关的肺部疾病具有潜在价值。