Nagano C, Wakebe H, Azuma A, Imagawa K, Kikuchi M
Microbiological Research Institute, Otsuka Pharmaceutical Co., Ltd, Tokushima, Japan.
Dig Dis Sci. 1998 Sep;43(9 Suppl):118S-124S.
To investigate the effects of rebamipide, an antigastritis and anti-gastric ulcer drug, on inducible nitric oxide synthase (iNOS), murine macrophage RAW264.7 cells were treated with interferon-gamma (IFN-gamma) in the presence of rebamipide. NO production was stimulated by IFN-gamma, and the level was attenuated by rebamipide in a dose-dependent manner. Therefore, we investigated the possibility that either rebamipide directly inhibited iNOS enzyme activity or that it reduced iNOS mRNA expression. In a cell-free system, rebamipide did not affect iNOS enzyme activity; however, rebamipide inhibited iNOS mRNA and protein expression induced by IFN-gamma. Thus, we concluded that rebamipide inhibited IFN-gamma-induced NO production as a result of its inhibitory action on iNOS mRNA expression.
为研究抗胃炎和抗胃溃疡药物瑞巴派特对诱导型一氧化氮合酶(iNOS)的影响,在瑞巴派特存在的情况下,用γ干扰素(IFN-γ)处理小鼠巨噬细胞RAW264.7细胞。IFN-γ刺激一氧化氮(NO)生成,而瑞巴派特可使其水平呈剂量依赖性降低。因此,我们研究了瑞巴派特是直接抑制iNOS酶活性还是降低iNOS mRNA表达的可能性。在无细胞系统中,瑞巴派特不影响iNOS酶活性;然而,瑞巴派特抑制IFN-γ诱导的iNOS mRNA和蛋白表达。因此,我们得出结论,瑞巴派特通过对iNOS mRNA表达的抑制作用,抑制了IFN-γ诱导的NO生成。