Characterization of angiotensin-(1-7) receptor subtype in mesenteric arteries

被引:30
作者
Neves, LAA
Averill, DB
Ferrario, CM
Chappell, MC
Aschner, JL
Walkup, MP
Brosnihan, KB
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Hypertens & Vasc Dis Ctr, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Pediat, Winston Salem, NC 27157 USA
关键词
hypertension; renin-angiotensin system; vasodilation; angiotensin receptors;
D O I
10.1016/S0196-9781(03)00062-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mesenteric arteries from male Sprague-Dawley rats were mounted in a pressurized myograph system. Ang-(1-7) concentration-dependent responses were determined in arteries preconstricted with endothelin-1 (10(-7) M). The receptor(s) mediating the Ang-(1-7) evoked dilation were investigated by pretreating the mesenteric arteries with specific antagonists of Ang-(1-7), AT(1) or AT(2) receptors. The effects of Ang-(3-8) and Ang-(3-7) were also determined. Ang-(1-7) caused a concentration-dependent dilation (EC50: 0.95 nM) that was blocked by the selective Ang-(1-7) receptor antagonist D-[Ala(7)]-Ang-(1-7). Administration of a specific antagonist to the AT(2) receptor (PD123319) had no effect. On the other hand, losartan and CV-11974 attenuated the Ang-(1-7) effect. These results demonstrate that Ang-(1-7) elicits potent dilation of mesenteric resistance vessels mediated by a D-[Ala(7)]-Ang-(1-7) sensitive site that is also sensitive to losartan and CV-11974. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:455 / 462
页数:8
相关论文
共 43 条
[1]   Possible role of P-450 metabolite of arachidonic acid in vasodilator mechanism of angiotensin II type 2 receptor in the isolated microperfused rabbit afferent arteriole [J].
Arima, S ;
Endo, Y ;
Yaoita, H ;
Omata, K ;
Ogawa, S ;
Tsunoda, K ;
Abe, M ;
Takeuchi, K ;
Abe, K ;
Ito, S .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (11) :2816-2823
[2]   Effect of selective angiotensin antagonists on the antidiuresis produced by angiotensin-(1-7) in water-loaded rats [J].
Baracho, NCV ;
Simoes-e-Silva, AC ;
Khosla, MC ;
Santos, RAS .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1998, 31 (09) :1221-1227
[3]   PRESSOR AND REFLEX SENSITIVITY IS ALTERED IN SPONTANEOUSLY HYPERTENSIVE RATS TREATED WITH ANGIOTENSIN-(1-7) [J].
BENTER, IF ;
DIZ, DI ;
FERRARIO, CM .
HYPERTENSION, 1995, 26 (06) :1138-1144
[4]   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
[5]   Angiotensin-(1-7) dilates canine coronary arteries through kinins and nitric oxide [J].
Brosnihan, KB ;
Li, P ;
Ferrario, CM .
HYPERTENSION, 1996, 27 (03) :523-528
[6]   RETENTION OF CEREBROVASCULAR DILATION AFTER CORTICAL SPREADING DEPRESSION IN ANESTHETIZED RABBITS [J].
BUSIJA, DW ;
MENG, W .
STROKE, 1993, 24 (11) :1740-1745
[7]   DIFFERENTIAL BARORECEPTOR REFLEX MODULATION BY CENTRALLY INFUSED ANGIOTENSIN PEPTIDES [J].
CAMPAGNOLESANTOS, MJ ;
HERINGER, SB ;
BATISTA, EN ;
KHOSLA, MC ;
SANTOS, RAS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01) :R89-R97
[8]   Analysis of the effects of candesartan in the mesenteric vascular bed of the cat [J].
Champion, HC ;
Kadowitz, PJ .
HYPERTENSION, 1997, 30 (05) :1260-1266
[9]   CHARACTERIZATION OF ANGIOTENSIN-II RECEPTOR SUBTYPES IN PANCREATIC ACINAR AR42J CELLS [J].
CHAPPELL, MC ;
JACOBSEN, DW ;
TALLANT, EA .
PEPTIDES, 1995, 16 (04) :741-747
[10]  
Chappell MC, 2000, V CH MO CAR, V1, P3