Effect of combining an ACE inhibitor and an angiotensin II receptor blocker on plasma and kidney tissue angiotensin II levels

被引:69
作者
Komine, N
Khang, S
Wead, LM
Blantz, RC
Gabbai, FB
机构
[1] VA San Diego Healthcare Syst, Div Nephrol Hypertens, San Diego, CA 92161 USA
[2] Univ Calif San Diego, La Jolla, CA 92093 USA
关键词
angiotensin II (AII); angiotensin-converting enzyme (ACE) inhibitor; anglotensin II receptor blocker (ARB);
D O I
10.1053/ajkd.2002.29909
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Increased angiotensin 11 (All) activity has been recognized as a risk factor for progression of kidney disease. There is increasing clinical evidence that combining an angiotensin-converting enzyme (ACE) inhibitor with an All receptor blocker (ARB) reduces proteinuria and blood pressure in patients with renal disease, although the mechanism of this synergistic effect remains poorly defined. This study tested whether the combination of an ACE inhibitor and an ARB reduces plasma All (Allp) and kidney tissue All (Allk) beyond what is observed with either of these two agents alone. Mean arterial pressure, glomerular filtration rate, Allp, and Allk were measured in four groups of Wistar rats after 2 weeks of a low-salt diet and 1 week of treatment with captopril (2.4 mg/d), losartan (1.7 mg/d), combination captopril+losartan (1.7 mg/d of captopril, 0.7 mg/d of losartan), or no treatment (control). Administration of captopril, losartan, and captopril+losartan produced statistically significant reductions in mean arterial pressure (control, 130 +/- 4 mm Hg; captopril, 92 +/- 5 mm Hg; losartan, 88 +/- 4 mm Hg; captopril+losartan, 104 +/- 5 mm Hg) and mild reductions in glomerular filtration rate (control, 3.1 +/- 0.1 mL/min; captopril, 2.2 +/- 0.3 mL/min; losartan, 1.7 +/- 0.3 mL/min; captopril+losartan, 2.3 +/- 0.3 mL/min) when compared with control rats, but no significant differences were observed among the treated groups. Captopril and captopril +Iosartan reduced Allp significantly when compared with control (captopril, 43 +/- 8 pg/mL; captopril+losartan, 47 +/- 5 pg/mL; control, 134 pg/mL) and with losartan (99 +/- 2 pg/mL). Allk values were reduced in captopril (254 +/- 18 pg/g kidney weight) and losartan (292 +/- 33 pg/g kidney weight) when compared with control (1,235 +/- 79 pg/g kidney weight). Captoprll+losartan (136 +/- 17 pg/g kidney weight) reduced Allk to values significantly lower than captopril or losartan alone. Higher doses of captopril (5 mg/d and 7.5 mg/d) or losartan (4 mg/d and 6 mg/d) alone did not reduce Allk to the levels observed with combination low doses of captopril+losartan. Combining low doses of ACE inhibitor plus ARB reduces Allk more than higher doses of either agent alone. This reduction in Allk with ACE inhibitor plus ARB provides a mechanism to understand the synergism of this combination in reducing proteinuria and blood pressure. The reduction in Allk with ACE inhibitor plus ARB may have important implications in long-term organ protection in hypertension and renal disease. (C) 2002 by the National Kidney Foundation, Inc.
引用
收藏
页码:159 / 164
页数:6
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