Nakaki T, Nakayama M, Kato R
Department of Pharmacology, Keio University School of Medicine, Tokyo, Japan.
Eur J Pharmacol. 1990 Dec 15;189(6):347-53. doi: 10.1016/0922-4106(90)90031-r.
Effects of nitric oxide (NO) and NO-producing vasodilators such as glyceryl trinitrate and sodium nitroprusside were tested on DNA synthesis in the clonal rat aortic smooth muscle cells, RACS-1. DNA synthesis was estimated by [3H]thymidine incorporation to DNA. NO and NO-producing vasodilators inhibited the DNA synthesis that was induced by 10% fetal calf serum. NO and NO-producing vasodilators also inhibited the basal level of DNA synthesis that occurred possibly as a result of autocrine mechanisms. NO-producing vasodilators also inhibited the fetal calf serum-induced proliferation of cells. Sodium nitroprusside inhibited the endothelin-mediated DNA synthesis. In another mesenchymal cell line, Chinese hamster fibroblast V79 cells, NO and NO-producing vasodilators failed to inhibit DNA synthesis, excluding the possibility of general cell toxicity. An exposure to NO and NO-producing vasodilators resulted in an increase of cyclic GMP (cGMP) content in the RACS-1 cells. A cGMP analog, 8-bromo-cGMP, inhibited DNA synthesis in the RACS-1 cells. These results suggest that EDRF/nitric oxide released from endothelium possibly contributes to inhibition of the DNA synthesis in vascular smooth muscle cells.
研究了一氧化氮(NO)及产生NO的血管舒张剂如硝酸甘油和硝普钠对克隆大鼠主动脉平滑肌细胞RACS-1中DNA合成的影响。通过[3H]胸苷掺入DNA来估计DNA合成。NO及产生NO的血管舒张剂抑制了由10%胎牛血清诱导的DNA合成。NO及产生NO的血管舒张剂也抑制了可能由于自分泌机制而发生的基础水平的DNA合成。产生NO的血管舒张剂还抑制了胎牛血清诱导的细胞增殖。硝普钠抑制了内皮素介导的DNA合成。在另一种间充质细胞系中国仓鼠成纤维细胞V79细胞中,NO及产生NO的血管舒张剂未能抑制DNA合成,排除了一般细胞毒性的可能性。暴露于NO及产生NO的血管舒张剂导致RACS-1细胞中环鸟苷酸(cGMP)含量增加。一种cGMP类似物8-溴-cGMP抑制了RACS-1细胞中的DNA合成。这些结果表明,内皮释放的内皮舒张因子/一氧化氮可能有助于抑制血管平滑肌细胞中的DNA合成。