Angiotensin II type 1 receptor blockade prevents lethal malignant hypertension - Relation to kidney inflammation | |
Article; Proceedings Paper | |
关键词: MONOCYTE CHEMOATTRACTANT PROTEIN-1; RENOVASCULAR HYPERTENSION; MACROPHAGE INFILTRATION; GENE-EXPRESSION; BLOOD-PRESSURE; RENAL INJURY; HUMAN RENIN; RATS; GLOMERULONEPHRITIS; INHIBITION; | |
DOI : 10.1161/hc3601.095576 | |
来源: SCIE |
【 摘 要 】
Background-Angiotensin II is elevated in malignant hypertension. We tested the hypothesis that angiotensin II type 1 receptor blockade can prevent the development of malignant hypertension even in the absence of a blood pressure-lowering effect. Methods and Results-Two-kidney, 1-clip rats were followed up for 28 days, blood pressure was measured by tail-cuff plethysmography and intra-arterially. After a 2-week run-in phase, rats received valsartan at a dose of 0.3 (n = 14) or 3 (n = 12) mg (.) kg(-1) (.) d(-1) or solvent (n = 27). Only the higher dose of valsartan, but not the lower dose, decreased blood pressure. Both doses of valsartan prevented the development of lethal malignant hypertension. Twenty of 27 solvent-treated renovascular hypertensive rats died, but only 3 of 14 rats treated with the low dose and 1 of 12 rats treated with the high dose of valsartan died. Histological signs of malignant nephrosclerosis were found in all rats examined that had died throughout the study and in 6 of 7 surviving solvent-treated renovascular hypertensive animals. Increased expression of monocyte chemoattractant protein-1 and prominent interstitial influx of macrophages occurred in the nonclipped kidneys exposed to high pressure in solvent-treated rats. These alterations were prevented by valsartan at both doses, irrespective of blood pressure effects. Conclusions-Angiotensin II type I receptor blockade by valsartan prevents lethal malignant hypertension independently of blood pressure. The results suggest that reduction of angiotensin-induced inflammation in the kidney may contribute to the protective effects of valsartan.
【 授权许可】
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