Kang Y J, Lee Y S, Lee G W, Lee D H, Ryu J C, Yun-Choi H S, Chang K C
Department of Pharmacology, College of Medicine, Gyeongsang National University, Chinju, Korea.
J Pharmacol Exp Ther. 1999 Oct;291(1):314-20.
Effects of higenamine on nitric oxide (NO) production and inducible NO synthase (iNOS) mRNA expression (RAW 264.7 cells), on vascular reactivity in vitro and in vivo (rats), and on survival rates (mice) and serum nitrite/nitrate levels (rats) were investigated by using last lipopolysaccharide (LPS) plus interferon (IFN)-gamma. Higenamine concentration-dependently inhibited NO production and inducible NO synthase mRNA in RAW 264.7 cells, in which the IC(50) was 53 microM. Higenamine (10 mg/kg i.p.) administered 90 min before LPS (5 mg/kg i.v.) prevented not only LPS-induced hypotension but also pressor response to norepinephrine (1 microgram/kg) in rats. Incubation of thoracic aorta with LPS (300 ng/ml) for 8 h in vitro resulted in suppression of the vasoconstrictor effects to phenylephrine, which was prevented by coincubation with higenamine. The survival rate to endotoxin in mice was significantly (P <.01) increased by the presence of higenamine in the LPS-treated group up to 48 h. Serum nitrite/nitrate levels were significantly (P <.05) reduced by higenamine in LPS-treated rats. Finally, higenamine inhibited the activation of nuclear factor kappaB in RAW 264.7 cells due to LPS + IFN-gamma by mobility shift assays. Taken together, these data strongly suggest that higenamine inhibits iNOS expression by inhibiting nuclear factor kappaB activation by LPS + IFN-gamma, which may be beneficial in inflammatory diseases in which enhanced formation of NO is the main causative factor. Furthermore, due to positive inotropic action, higenamine may be more effective in a condition where myocardial contractility is likely to depress, such as in septic shock and/or endotoxin-induced inflammatory disorders.
通过使用脂多糖(LPS)加干扰素(IFN)-γ,研究了去甲乌药碱对一氧化氮(NO)生成和诱导型一氧化氮合酶(iNOS)mRNA表达(RAW 264.7细胞)、对体外和体内(大鼠)血管反应性以及对存活率(小鼠)和血清亚硝酸盐/硝酸盐水平(大鼠)的影响。去甲乌药碱浓度依赖性地抑制RAW 264.7细胞中NO的生成和诱导型一氧化氮合酶mRNA,其半数抑制浓度(IC50)为53微摩尔。在LPS(5毫克/千克静脉注射)前90分钟腹腔注射去甲乌药碱(10毫克/千克)不仅可预防LPS诱导的低血压,还可预防大鼠对去甲肾上腺素(1微克/千克)的升压反应。在体外将胸主动脉与LPS(300纳克/毫升)孵育8小时会导致对去氧肾上腺素的血管收缩作用受到抑制,而与去甲乌药碱共同孵育可预防这种抑制。在LPS处理组中,去甲乌药碱的存在使小鼠对内毒素的存活率在长达48小时内显著(P<.01)提高。在LPS处理的大鼠中,去甲乌药碱可显著(P<.05)降低血清亚硝酸盐/硝酸盐水平。最后,通过迁移率变动分析,去甲乌药碱抑制了RAW 264.7细胞中因LPS + IFN-γ导致的核因子κB的激活。综上所述,这些数据强烈表明,去甲乌药碱通过抑制LPS + IFN-γ诱导的核因子κB激活来抑制iNOS表达,这在NO生成增加是主要致病因素的炎症性疾病中可能有益。此外,由于具有正性肌力作用,去甲乌药碱在心肌收缩力可能降低的情况下可能更有效,例如在感染性休克和/或内毒素诱导的炎症性疾病中。