Okamoto T, Masuda Y, Kawasaki T, Shinohara M, Matsuzaki K
Research Laboratories, Nippon Chemiphar Co., Ltd., 1-22 Hikokawato, Saitama 341-0005, Misato, Japan.
Eur J Pharmacol. 2000 May 19;396(2-3):125-30. doi: 10.1016/s0014-2999(00)00186-2.
Aminoguanidine is an inhibitor of the inducible form of nitric oxide synthase (iNOS). In the present study, the effect of aminoguanidine on concanavalin A-induced hepatitis was examined. Treatment of mice with concanavalin A (10 mg/kg, i.v.) induced interferon-gamma and iNOS mRNA expression in the liver before the elevation of plasma alanine aminotransferase activity. Immunohistochemical study showed the induction of iNOS protein expression in the area of necrosis. Aminoguanidine (1, 3 and 10 mg/kg, i.p.) inhibited the concanavalin A-induced elevation of alanine aminotransferase activity. Aminoguanidine (10 mg/kg, i.p.) did not inhibit concanavalin A-induced interleukin-2, interferon-gamma, tumor necrosis factor-alpha or iNOS mRNA expression in the liver. The plasma nitrite/nitrate level was elevated at 6 and 24 h after concanavalin A treatment. The elevation of nitrite/nitrate was inhibited by aminoguanidine (10 mg/kg, i.p.). From these results, we conclude that nitric oxide formed by iNOS may be involved in the development of concanavalin A-induced hepatitis.
氨基胍是诱导型一氧化氮合酶(iNOS)的抑制剂。在本研究中,检测了氨基胍对伴刀豆球蛋白A诱导的肝炎的影响。用伴刀豆球蛋白A(10mg/kg,静脉注射)处理小鼠,在血浆丙氨酸转氨酶活性升高之前,诱导肝脏中γ干扰素和iNOS mRNA表达。免疫组织化学研究显示坏死区域iNOS蛋白表达增加。氨基胍(1、3和10mg/kg,腹腔注射)抑制伴刀豆球蛋白A诱导的丙氨酸转氨酶活性升高。氨基胍(10mg/kg,腹腔注射)不抑制伴刀豆球蛋白A诱导的肝脏中白细胞介素-2、γ干扰素、肿瘤坏死因子-α或iNOS mRNA表达。伴刀豆球蛋白A处理后6小时和24小时血浆亚硝酸盐/硝酸盐水平升高。氨基胍(10mg/kg,腹腔注射)抑制亚硝酸盐/硝酸盐的升高。从这些结果,我们得出结论,iNOS产生的一氧化氮可能参与伴刀豆球蛋白A诱导的肝炎的发生。