Primary role of angiotensin-converting enzyme-2 in cardiac production of anglotensin-(1-7) in transgenic Ren-2 hypertensive rats

被引:43
作者
Trask, Aaron J. [1 ]
Averill, David B.
Ganten, Detlev
Chappell, Mark C.
Ferrario, Carlos M.
机构
[1] Wake Forest Univ, Sch Med, Hypertens & Vasc Res Ctr, Winston Salem, NC 27109 USA
[2] Univ Med Berlin, Charite, Berlin, Germany
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2007年 / 292卷 / 06期
关键词
angiotensin II; hypertension; isolated heart;
D O I
10.1152/ajpheart.01198.2006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary role of angiotensin-converting enzyme 2 in cardiac production of angiotensin-(1-7) in transgenic Ren-2 hypertensive rats. Am J Physiol Heart Circ Physiol 292: H3019-H3024. 2007. First published February 16, 2007: doi: 10.1152/ajplicart.01198.2006. - Angiotensin-converting enzyme-2 (ACE2) converts angiotensin 11 (ANG 11) to angiotensin-(1-7) [ANG-(1-7)], and this enzyme may serve as a key regulatory juncture in various tissues. Although the heart expresses ACE2, the extent that the enzyme participates in the cardiac processing of ANG 11 and ANG-(1-7) is equivocal. Therefore. we utilized the Langendorff preparation to characterize the ACE2 pathway in isolated hearts from male normotensive Sprague-Dawley [Tg((-))] and hypertensive [mRen2]27 [TL(+)] rats. During a 60-min recirculation period with 10 nM ANG II. he presence of ANG-(1-7) was assessed in the cardiac effluent. ANG-(1-7) generation from ANG 11 was similar in both the normal and hypertensive hearts [Tg(-) : 510 +/- 55 pM, n = 20 vs. Tg((+)): 497 +/- 63 pM, n = 14] with peak levels occurring at 30 min after administration of the peptide. ACE2 inhibition (MLN-4760, I LM) sianificantly reduced ANG-(1-7) production by 83% (57 +/- 19 pM,. P < 0.01. n = 7) in the Tg((+)) rats. whereas the inhibitor had no significant effect in the TL, -) rats (285 +/- 53 pM, P > 0.05, n = 10). ACE2 activity was found in the effluent of perfused Tg((-)) and Tg((+)) hearts. and it was highly associated with ACE2 protein expression (r = 0.78). This study is the first demonstration for a direct role of ACE2 in the metabolism of cardiac ANG 11 in the hypertrophic heart of hypertensive rats. We Conclude that predominant expression of cardiac ACE2 activity in the Tg((+)) may be a compensatory response to the extensive cardiac remodeling in this strain.
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收藏
页码:H3019 / H3024
页数:6
相关论文
共 32 条
[1]  
Agirregoitia N, 2003, J GERONTOL A-BIOL, V58, P792
[2]   ANTIHYPERTENSIVE ACTIONS OF ANGIOTENSIN-(1-7) IN SPONTANEOUSLY HYPERTENSIVE RATS [J].
BENTER, IF ;
FERRARIO, CM ;
MORRIS, M ;
DIZ, DI .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 269 (01) :H313-H319
[3]   Myocardial infarction increases ACE2 expression in rat and humans [J].
Burrell, LM ;
Risvanis, J ;
Kubota, E ;
Dean, RG ;
MacDonald, PS ;
Lu, S ;
Tikellis, C ;
Grant, SL ;
Lew, RA ;
Smith, AI ;
Cooper, ME ;
Johnston, CI .
EUROPEAN HEART JOURNAL, 2005, 26 (04) :369-375
[4]   PROCESSING OF ANGIOTENSIN PEPTIDES BY NG108-15 NEUROBLASTOMA X GLIOMA HYBRID CELL-LINE [J].
CHAPPELL, MC ;
TALLANT, EA ;
BROSNIHAN, KB ;
FERRARIO, CM .
PEPTIDES, 1990, 11 (02) :375-380
[5]  
CHAPPELL MC, 1989, J BIOL CHEM, V264, P16518
[6]   Angiotensin-converting enzyme 2 is an essential regulator of heart function [J].
Crackower, MA ;
Sarao, R ;
Oudit, GY ;
Yagil, C ;
Kozieradzki, I ;
Scanga, SE ;
Oliveira-dos-Santos, AJ ;
da Costa, J ;
Zhang, LY ;
Pei, Y ;
Scholey, J ;
Ferrario, CM ;
Manoukian, AS ;
Chappell, MC ;
Backx, PH ;
Yagil, Y ;
Penninger, JM .
NATURE, 2002, 417 (6891) :822-828
[7]   Substrate-based design of the first class of angiotensin-converting enzyme-related carboxypeptidase (ACE2) inhibitors [J].
Dales, NA ;
Gould, AE ;
Brown, JA ;
Calderwood, EF ;
Guan, B ;
Minor, CA ;
Gavin, JM ;
Hales, P ;
Kaushik, VK ;
Stewart, M ;
Tummino, PJ ;
Vickers, CS ;
Ocain, TD ;
Patane, MA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (40) :11852-11853
[8]   Angiotensin (1-7) re-establishes impulse conduction in cardiac muscle during ischaemia-reperfusion. The role of the sodium pump [J].
De Mello, WC .
JOURNAL OF THE RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM, 2004, 5 (04) :203-208
[9]   Products of angiotensin I hydrolysis by human cardiac enzymes potentiate Bradykinin [J].
Erdös, EG ;
Jackman, HL ;
Brovkovych, V ;
Tan, FL ;
Deddish, PA .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2002, 34 (12) :1569-1576
[10]   Short-term angiotensin(1-7) receptor Mas stimulation improves endothelial function in normotensive rats [J].
Faria-Silva, R ;
Duarte, FV ;
Santos, RAS .
HYPERTENSION, 2005, 46 (04) :948-952