The nonpeptide angiotensin-(1-7) receptor Mas agonist AVE-0991 attenuates heart failure induced by myocardial infarction

被引:89
作者
Ferreira, Anderson J.
Jacoby, Bruno A.
Araujo, Cicero A. A.
Macedo, Filipe A. F. F.
Silva, Gerluza A. B.
Almeida, Alvair P.
Caliari, Marcelo V.
Santos, Robson A. S.
机构
[1] Univ Fed Minas Gerais, Dept Fisiol & Biofis, Inst Biol Sci, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Morphol, Inst Biol Sci, BR-31270901 Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Dept Pathol, Inst Biol Sci, BR-31270901 Belo Horizonte, MG, Brazil
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2007年 / 292卷 / 02期
关键词
angiotensin II; renin-angiotensin system; A-779; angiotensin converting enzyme 2;
D O I
10.1152/ajpheart.00828.2006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The nonpeptide angiotensin(1-7) receptor Mas agonist AVE-0991 attenuates heart failure induced by myocardial infarction. Am J Physiol Heart Circ Physiol 292: H1113-H1119, 2007. First published October 20, 2006; doi:10.1152/ajpheart.00828.2006. -The nonpeptide AVE-0991, which has been reported as a selective ligand for the angiotensin-(1-7) [ANG-(1-7)] receptor Mas, has actions similar to those attributed to the cardioprotective product of the renin-angiotensin system, ANG(1-7). In this study, we evaluated the cardiac effects of AVE-0991 in normal and infarcted male Wistar rats. Myocardial infarction was induced by left coronary artery ligation. At the end of the treatment, the Langendorff technique was used to analyze cardiac function. Left ventricle serial sections were dyed with Gomori trichrome stain to quantify the infarcted area. In normal hearts, AVE-0991 produced a significant decrease in perfusion pressure and an increase in systolic tension, rate of tension rise and fall (+/- dT/dt), and heart rate. These effects were completely blocked by the perfusion of the hearts with a solution containing the selective ANG-(1-7) antagonist A-779. N-G-nitro-L-arginine methyl ester treatment abolished the AVE-0991-induced vasodilation in isolated hearts. AVE-0991 significantly attenuated the decrease in systolic tension ( sham operated, 13.00 +/- 1.02 g; infarction, 7.18 +/- 0.66 g; AVE treated, 9.23 +/- 1.05 g, n = 5), +dT/dt, -dT/dt, and heart rate induced by myocardial infarction. Infarction-induced vasoconstriction was completely prevented by AVE-0991 treatment. Furthermore, AVE-0991 significantly decreased the infarcted area (6.98 +/- 1.01 vs. 3.94 +/- 1.04 mm(2) in AVE-treated rats). These data indicate that the compound AVE-0991 produces beneficial effects in isolated perfused rat hearts involving the ANG-(1-7) receptor Mas and the release of nitric oxide. In addition, our results indicate that AVE-0991 attenuates postischemic heart failure.
引用
收藏
页码:H1113 / H1119
页数:7
相关论文
共 25 条
[21]   Impairment of in vitro and in vivo heart function in angiotensin-(1-7) receptor Mas knockout mice [J].
Santos, RAS ;
Castro, CH ;
Gava, E ;
Pinheiro, SVB ;
Almeida, AP ;
de Paula, RD ;
Cruz, JS ;
Ramos, AS ;
Rosa, KT ;
Irigoyen, MC ;
Bader, M ;
Alenina, N ;
Kitten, GT ;
Ferreira, AJ .
HYPERTENSION, 2006, 47 (05) :996-1002
[22]   Expression of an angiotensin-(1-7)-producing fusion protein produces cardioprotective effects in rats [J].
Santos, RAS ;
Ferreira, AJ ;
Nadu, AP ;
Braga, ANG ;
de Almeida, AP ;
Campagnole-Santos, MJ ;
Baltatu, O ;
Iliescu, R ;
Reudelhuber, TL ;
Bader, M .
PHYSIOLOGICAL GENOMICS, 2004, 17 (03) :292-299
[23]   A human homolog of angiotensin-converting enzyme - Cloning and functional expression as a captopril-insensitive carboxypeptidase [J].
Tipnis, SR ;
Hooper, NM ;
Hyde, R ;
Karran, E ;
Christie, G ;
Turner, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (43) :33238-33243
[24]   Inhibition of endogenous nitric oxide in the heart enhances matrix metalloproteinase-2 release [J].
Wang, WJ ;
Viappiani, S ;
Sawicka, J ;
Schulz, R .
BRITISH JOURNAL OF PHARMACOLOGY, 2005, 145 (01) :43-49
[25]   AVE 0991, a nonpeptide mimic of the effects of angiotensin-(1-7) on the endothelium [J].
Wiemer, G ;
Dobrucki, LW ;
Louka, FR ;
Malinski, T ;
Heitsch, H .
HYPERTENSION, 2002, 40 (06) :847-852