Dundore R L, Clas D M, Wheeler L T, Habeeb P G, Bode D C, Buchholz R A, Silver P J, Pagani E D
Department of Vascular and Biochemical Pharmacology, Sterling Winthrop Pharmaceuticals Research Division, Collegeville, PA 19426-0900.
Eur J Pharmacol. 1993 Nov 16;249(3):293-7. doi: 10.1016/0014-2999(93)90525-m.
The purpose of this study was to determine if significant relationships exist between plasma and aortic cyclic GMP (cGMP) levels and pharmacodynamic effect after the i.v. administration of the cGMP-selective phosphodiesterase inhibitor zaprinast to conscious, spontaneously hypertensive rats. Zaprinast dose-dependently increased plasma and aortic cGMP levels at 10, 18 and 30 mg/kg and decreased mean arterial blood pressure (MAP) at 18 and 30 mg/kg. The concentrations of cGMP in the plasma and in the aorta were significantly correlated (r = 0.765, P < 0.0001). The changes in MAP were significantly correlated to aortic (r = -0.750, P < 0.0001) and plasma (r = -0.762, P < 0.0001) cGMP levels. We conclude that plasma cGMP may be an index of cGMP-selective phosphodiesterase inhibition in vivo.
本研究的目的是确定在清醒的自发性高血压大鼠静脉注射环鸟苷酸(cGMP)选择性磷酸二酯酶抑制剂扎普司特后,血浆和主动脉中cGMP水平与药效学效应之间是否存在显著关系。扎普司特在剂量为10、18和30mg/kg时可剂量依赖性地增加血浆和主动脉中的cGMP水平,并在剂量为18和30mg/kg时降低平均动脉血压(MAP)。血浆和主动脉中cGMP的浓度显著相关(r = 0.765,P < 0.0001)。MAP的变化与主动脉(r = -0.750,P < 0.0001)和血浆(r = -0.762,P < 0.0001)中的cGMP水平显著相关。我们得出结论,血浆cGMP可能是体内cGMP选择性磷酸二酯酶抑制作用的一个指标。