ZAPRINAST INCREASES CYCLIC-GMP LEVELS IN PLASMA AND IN AORTIC TISSUE OF RATS

被引:58
作者
DUNDORE, RL
CLAS, DM
WHEELER, LT
HABEEB, PG
BODE, DC
BUCHHOLZ, RA
SILVER, PJ
PAGANI, ED
机构
[1] Department of Vascular and Biochemical Pharmacology, Sterling Winthrop Pharmaceuticals Research Division, Collegeville, PA 19426-0900
关键词
PHOSPHODIESTERASE INHIBITOR; ZAPRINAST; CGMP; BLOOD PRESSURE; SPONTANEOUSLY HYPERTENSIVE RAT (SHR);
D O I
10.1016/0014-2999(93)90525-M
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:293 / 297
页数:5
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