Potter G S, Johnson R J, Fink G D
Department of Pharmacology and Toxicology, Michigan State University, East Lansing 48824-1317, USA.
Hypertension. 1997 Dec;30(6):1578-84. doi: 10.1161/01.hyp.30.6.1578.
Surgical ablation of renal mass leads to a reduction in kidney function and commonly to the development of hypertension and chronic renal failure (CRF) in rats. The objective of this study was to determine whether endothelin (ET)-1 is involved in the maintenance of the hypertension that accompanies loss of renal mass. First, we demonstrated the antihypertensive efficacy of PD 155080, a selective, orally active ET(A) receptor antagonist, in a group of rats made hypertensive by continuous intravenous infusion of ET-1 (2.5 pmol x kg(-1) x min[-1]) for 7 days. ET-1 produced a sustained hypertension and PD 155080 (56.4 micromol/kg [25mg/kg] BID PO) normalized blood pressure (BP) during the 5 days of drug administration. In a second experiment, Sprague-Dawley rats underwent a 5/6 reduction in renal mass (RRM); 4 weeks later, PD 155080 administered for 7 days resulted in a sustained reduction in BP. Sham-operated rats also showed a slight hypotensive response to PD 155080 administration. Plasma urea nitrogen, plasma creatinine, urinary protein excretion, and creatinine clearance were not altered by PD 155080 administration in RRM or sham rats. In a third experiment, we investigated the contribution of the renin-angiotensin system to BP control in RRM rats given PD 155080. In these rats, PD 155080 reduced BP during 5 treatment days, and this antihypertensive effect was not altered by coadministration of the angiotensin-converting enzyme inhibitor enalapril in the drinking water (508 micromol/L [250 mg/L]). These results demonstrate that (1) ET-1 plays a role in established RRM hypertension through activation of the ET(A) receptor subtype, (2) lowering blood pressure with PD 155080 in RRM rats does not adversely affect renal function, and 3) the antihypertensive effect of ET(A) receptor antagonism is not opposed by the renin-angiotensin system.
肾肿块的手术切除会导致大鼠肾功能下降,并通常会引发高血压和慢性肾衰竭(CRF)。本研究的目的是确定内皮素(ET)-1是否参与了肾质量丧失伴随的高血压的维持。首先,我们在一组通过连续静脉输注ET-1(2.5 pmol·kg⁻¹·min⁻¹)7天而高血压的大鼠中,证明了选择性口服活性ET(A)受体拮抗剂PD 155080的降压效果。ET-1产生了持续性高血压,而PD 155080(56.4 μmol/kg [25mg/kg],每日两次,口服)在给药的5天内使血压(BP)恢复正常。在第二个实验中,Sprague-Dawley大鼠接受了5/6肾质量减少(RRM);4周后,给予PD 155080 7天导致血压持续降低。假手术大鼠对PD 155080给药也表现出轻微的降压反应。在RRM大鼠或假手术大鼠中,给予PD 155080并未改变血浆尿素氮、血浆肌酐、尿蛋白排泄和肌酐清除率。在第三个实验中,我们研究了肾素-血管紧张素系统对给予PD 155080的RRM大鼠血压控制的作用。在这些大鼠中,PD 155080在5天的治疗期间降低了血压,并且这种降压作用在饮用水中同时给予血管紧张素转换酶抑制剂依那普利(508 μmol/L [250 mg/L])时并未改变。这些结果表明:(1)ET-1通过激活ET(A)受体亚型在已建立的RRM高血压中起作用;(2)在RRM大鼠中用PD 155080降低血压不会对肾功能产生不利影响;(3)ET(A)受体拮抗的降压作用不受肾素-血管紧张素系统的对抗。