Farivar R S, Brecher P
Department of Pathology, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts 02118, USA.
J Biol Chem. 1996 Dec 6;271(49):31585-92. doi: 10.1074/jbc.271.49.31585.
We have previously reported that salicylate inhibits the inducible NO synthase (NOS 2) in cytokine-induced cardiac fibroblasts (Farivar, R. S., Chobanian, A. V., and Brecher, P. (1996) Circ. Res. 78, 759-768). To define further the mechanism of inhibition of NOS 2 by salicylate, we investigated NOS 2 mRNA induction by cytokines and determined the kinetics of inhibition by salicylate as compared to dexamethasone. Interferon-gamma plus tumor necrosis factor-alpha induced NOS 2 mRNA synergistically in a time- and dose-dependent manner. Both dexamethasone and salicylate equally inhibited the induction of NOS 2 mRNA in a time- and dose-dependent fashion, both before and after cytokine induction. Salicylate also inhibited interferon-gamma plus interleukin-1beta-induced NOS 2 mRNA. After 24 h of cytokine stimulation, salicylate stopped the induction of NOS 2 mRNA, whereas dexamethasone delayed the accumulation of transcript. In half-life experiments of NOS 2 mRNA, we found that dexamethasone reduced the half-life of NOS 2 mRNA from 7 to 4 h, whereas salicylate had no effect on mRNA stability. Tumor necrosis factor-alpha and interferon-gamma induced NF-kappaB (p50/p65) and STAT-1, respectively, as assessed by gel shift assays. Salicylate did not inhibit the cytokine induction of NF-kappaB or STAT-1. This study suggests that the anti-inflammatory mechanism of salicylate involves inhibition of NOS 2 transcription and shows that the effect is independent of NF-kappaB activation.
我们之前曾报道,水杨酸盐可抑制细胞因子诱导的心脏成纤维细胞中的诱导型一氧化氮合酶(NOS 2)(Farivar, R. S., Chobanian, A. V., and Brecher, P. (1996) Circ. Res. 78, 759 - 768)。为了进一步明确水杨酸盐抑制NOS 2的机制,我们研究了细胞因子对NOS 2 mRNA的诱导作用,并确定了与地塞米松相比水杨酸盐的抑制动力学。干扰素-γ加肿瘤坏死因子-α以时间和剂量依赖性方式协同诱导NOS 2 mRNA。地塞米松和水杨酸盐均以时间和剂量依赖性方式同等程度地抑制细胞因子诱导前后的NOS 2 mRNA诱导。水杨酸盐还抑制干扰素-γ加白细胞介素-1β诱导的NOS 2 mRNA。细胞因子刺激24小时后,水杨酸盐停止了NOS 2 mRNA的诱导,而地塞米松延迟了转录本的积累。在NOS 2 mRNA的半衰期实验中,我们发现地塞米松将NOS 2 mRNA的半衰期从7小时缩短至4小时,而水杨酸盐对mRNA稳定性没有影响。通过凝胶迁移试验评估,肿瘤坏死因子-α和干扰素-γ分别诱导了NF-κB(p50/p65)和STAT-1。水杨酸盐不抑制细胞因子对NF-κB或STAT-1的诱导。本研究表明,水杨酸盐的抗炎机制涉及抑制NOS 2转录,并表明该作用独立于NF-κB激活。