Yasunari K, Kohno M, Yokokawa K, Horio T, Takeda T
First Department of Internal Medicine, Osaka City University Medical School, Japan.
Am J Physiol. 1994 Sep;267(3 Pt 2):R628-34. doi: 10.1152/ajpregu.1994.267.3.R628.
The modulation of dopamine DA1 receptors of cultured rat renal arterial smooth muscle cells by glucocorticoid and sodium chloride was studied. At a concentration of 10 nM, the synthetic glucocorticoid dexamethasone increased maximum receptor binding but had no effect on the dissociation constant. However, the maximum binding of [3H]Sch-23390 in cells treated with 100 mM sodium chloride did not change. However, the dissociation constant for DA1 receptor was increased by adding sodium chloride. The glucocorticoid effect on DA1 of arterial smooth muscle cells became apparent after hours of incubation in the presence of the steroid and was significantly inhibited by cycloheximide (10 micrograms/ml) or by the glucocorticoid receptor antagonist RU-38486, indicating that the effect required protein synthesis through glucocorticoid receptors. Treatment of cells with 1 microM dexamethasone for 24 h increased basal and DA1-stimulated adenylate cyclase activity. Basal adenylate cyclase was decreased by sodium chloride in a dose-dependent manner. These results suggest differential control of DA1 receptors on vascular smooth muscle cells by glucocorticoid or sodium chloride.
研究了糖皮质激素和氯化钠对培养的大鼠肾动脉平滑肌细胞多巴胺DA1受体的调节作用。在10 nM的浓度下,合成糖皮质激素地塞米松增加了最大受体结合,但对解离常数没有影响。然而,用100 mM氯化钠处理的细胞中,[3H]Sch-23390的最大结合没有变化。然而,添加氯化钠会增加DA1受体的解离常数。在类固醇存在下孵育数小时后,糖皮质激素对动脉平滑肌细胞DA1的作用变得明显,并且被环己酰亚胺(10微克/毫升)或糖皮质激素受体拮抗剂RU-38486显著抑制,表明该作用需要通过糖皮质激素受体进行蛋白质合成。用1 microM地塞米松处理细胞24小时会增加基础和DA1刺激的腺苷酸环化酶活性。基础腺苷酸环化酶被氯化钠以剂量依赖的方式降低。这些结果表明糖皮质激素或氯化钠对血管平滑肌细胞上的DA1受体有不同的控制作用。