McMahon E G, Palomo M A, Brown M A, Bertenshaw S R, Carter J S
Department of Cardiovascular Diseases Research, G.D. Searle and Co., St. Louis, Missouri 63167.
Am J Hypertens. 1993 Aug;6(8):667-73. doi: 10.1093/ajh/6.8.667.
We reported previously that the endothelin converting enzyme (ECE) inhibitor phosphoramidon lowers mean arterial pressure (MAP) when infused in conscious, spontaneously hypertensive rats (SHRs). In this study we determined the dose-response relationship for this action in SHRs and in a high-renin hypertensive model, the renal artery-ligated rat. We also determined whether the ETA receptor antagonist BQ-123 (cyclo [D-Trp-D-Asp-Pro-D-Val-Leu]) might lower MAP in hypertensive rats. Phosphoramidon lowered MAP by 9 +/- 4, 31 +/- 4, and 40 +/- 4 mm Hg after 5 h when infused in SHRs at 10, 20, and 40 mg/kg/h. This lowering of MAP was associated with dose-related inhibition of the pressor response to a bolus intravenous injection of big ET (1-39) at 1 nmol/kg. BQ-123 also lowered MAP in SHRs (by 25 +/- 3 mm Hg), but only at a very high dose (50 mg/kg/h for 5 h). At this dose, BQ-123 blocked the pressor response to a bolus intravenous injection of ET-1 (1 nmol/kg), but the blockade was incomplete. Phosphoramidon infused in conscious, renal hypertensive rats lowered MAP by 31 +/- 9, 46 +/- 8, and 54 +/- 1 mm Hg after 5 h at 10, 20, and 40 mg/kg/h, respectively. This lowering of MAP was associated with blockade of the pressor response to big ET (1-39). BQ-123 did not lower MAP in renal hypertensive rats when infused at 30 mg/kg/h for 5 h.(ABSTRACT TRUNCATED AT 250 WORDS)
我们先前报道,内皮素转化酶(ECE)抑制剂磷酰胺素在清醒的自发性高血压大鼠(SHRs)中输注时可降低平均动脉压(MAP)。在本研究中,我们确定了该作用在SHRs和高肾素性高血压模型(肾动脉结扎大鼠)中的剂量反应关系。我们还确定了ETA受体拮抗剂BQ-123(环[D-色氨酸-D-天冬氨酸-脯氨酸-D-缬氨酸-亮氨酸])是否能降低高血压大鼠的MAP。当以10、20和40mg/kg/h的剂量在SHRs中输注5小时后,磷酰胺素使MAP分别降低了9±4、31±4和40±4mmHg。MAP的这种降低与对1nmol/kg大ET(1-39)静脉推注的升压反应的剂量相关抑制有关。BQ-123也降低了SHRs的MAP(降低了25±3mmHg),但仅在非常高的剂量(50mg/kg/h,持续5小时)下。在此剂量下,BQ-123阻断了对1nmol/kg ET-1静脉推注的升压反应,但阻断不完全。在清醒的肾性高血压大鼠中输注磷酰胺素,在10、20和40mg/kg/h的剂量下,5小时后MAP分别降低了31±9、46±8和54±1mmHg。MAP的这种降低与对大ET(1-39)升压反应的阻断有关。当以30mg/kg/h的剂量输注5小时时,BQ-123未降低肾性高血压大鼠的MAP。(摘要截短至250字)