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磷酰胺(内皮素转化酶抑制剂)和BQ - 123(内皮素A受体亚型拮抗剂)对高血压大鼠血压的影响。

Effect of phosphoramidon (endothelin converting enzyme inhibitor) and BQ-123 (endothelin receptor subtype A antagonist) on blood pressure in hypertensive rats.

作者信息

McMahon E G, Palomo M A, Brown M A, Bertenshaw S R, Carter J S

机构信息

Department of Cardiovascular Diseases Research, G.D. Searle and Co., St. Louis, Missouri 63167.

出版信息

Am J Hypertens. 1993 Aug;6(8):667-73. doi: 10.1093/ajh/6.8.667.

Abstract

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)

摘要

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)

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