Ikeda U, Yamamoto K, Ichida M, Ohkawa F, Murata M, Iimura O, Kusano E, Asano Y, Shimada K
Department of Cardiology, Jichi Medical School, Tochigi, Japan.
J Mol Cell Cardiol. 1996 Apr;28(4):789-95. doi: 10.1006/jmcc.1996.0073.
We investigated the effect of adenosine 3', 5'-cyclic monophosphate (cAMP) on inducible nitric oxide synthase (iNOS) expression in cultured neonatal rat cardiac myocytes. Incubation of cardiac myocytes for 24 h with interleukin-1 beta (IL-1 beta) caused a significant increase in the production of nitrite, a stable metabolite of nitric oxide. Dibutyl cAMP (db-cAMP) significantly augmented nitrite production by IL-1 beta-stimulated, but not by unstimulated cells, in a dose-dependent manner. db-cAMP also dose dependently increased nitrite production by tumor necrosis factor-alpha(TNF-alpha)-stimulated cells. Simultaneous incubation with NG-monomethyl-L-arginine completely inhibited the effect of db-cAMP on nitrite production. cAMP-induced nitrite production by cytokine-stimulated cells was accompanied by increased iNOS mRNA accumulation. The synergistic effect of cAMP on IL-1 beta-induced nitrite accumulation was mimicked by cAMP-generating agonists forskolin and isoproterenol. These results indicate that cAMP upregulates cytokine-induced iNOS expression in cardiac myocytes.
我们研究了3',5'-环磷酸腺苷(cAMP)对培养的新生大鼠心肌细胞中诱导型一氧化氮合酶(iNOS)表达的影响。用白细胞介素-1β(IL-1β)孵育心肌细胞24小时,可使一氧化氮的稳定代谢产物亚硝酸盐的生成显著增加。二丁酰cAMP(db-cAMP)以剂量依赖的方式显著增强了IL-1β刺激的细胞(而非未刺激的细胞)的亚硝酸盐生成。db-cAMP还剂量依赖性地增加了肿瘤坏死因子-α(TNF-α)刺激的细胞的亚硝酸盐生成。与NG-单甲基-L-精氨酸同时孵育完全抑制了db-cAMP对亚硝酸盐生成的作用。细胞因子刺激的细胞中cAMP诱导的亚硝酸盐生成伴随着iNOS mRNA积累的增加。cAMP生成激动剂福斯可林和异丙肾上腺素模拟了cAMP对IL-1β诱导的亚硝酸盐积累的协同作用。这些结果表明,cAMP上调了心肌细胞中细胞因子诱导的iNOS表达。