Lockette W, McCurdy R, Aronow H, Butler B
Department of Medicine, Wayne State University School of Medicine, Detroit 48201.
Hypertension. 1989 Jun;13(6 Pt 2):865-9. doi: 10.1161/01.hyp.13.6.865.
Endothelium-dependent vasodilators, nitrates, and atrial natriuretic factor relax blood vessels by increasing vascular cyclic guanosine monophosphate (cGMP). The mechanisms by which cGMP relaxes vascular smooth muscle (VSM) are not known. Since contraction of VSM is associated with increased intracellular calcium and pH, we hypothesized that cGMP may decrease vascular tone by lowering ionized, intracellular calcium [( Ca2+]i) and pH. We used microfluorometry to measure cGMP-induced changes in intracellular calcium and pH of cultured A7r5 VSM cells after stimulation with contractile agonists. A cGMP analogue, 8-Br-cGMP, blocked vasopressin- but not thrombin-stimulated increases in [Ca2+]i. High extracellular potassium concentrations [( K+]) increased [Ca2+]i, but the attenuation of [Ca2+]i by 8-Br-cGMP was not statistically significant. 8-Br-cGMP also attenuated vasopressin- but not thrombin-stimulated alkalinization of VSM cells. cGMP may decrease vascular tone by decreasing [Ca2+]i and pH, but these changes are dependent on the contractile agonist studied.
内皮依赖性血管舒张剂、硝酸盐和心房利钠因子通过增加血管环磷酸鸟苷(cGMP)来舒张血管。cGMP舒张血管平滑肌(VSM)的机制尚不清楚。由于VSM的收缩与细胞内钙和pH值的升高有关,我们推测cGMP可能通过降低离子化的细胞内钙[(Ca2+]i)和pH值来降低血管张力。我们使用微量荧光测定法来测量用收缩激动剂刺激后培养的A7r5 VSM细胞内钙和pH值的cGMP诱导变化。一种cGMP类似物8-溴-cGMP可阻断血管加压素刺激的[Ca2+]i升高,但不能阻断凝血酶刺激的[Ca2+]i升高。高细胞外钾浓度[(K+])可增加[Ca2+]i,但8-溴-cGMP对[Ca2+]i的衰减在统计学上不显著。8-溴-cGMP还可减弱血管加压素刺激的VSM细胞碱化,但不能减弱凝血酶刺激的VSM细胞碱化。cGMP可能通过降低[Ca2+]i和pH值来降低血管张力,但这些变化取决于所研究的收缩激动剂。