Ang-(3-4) suppresses inhibition of renal plasma membrane calcium pump by Ang II

被引:20
作者
Axelband, Flavia [1 ]
Assuncao-Miranda, Iranaia [2 ]
de Paula, Isabela R. [1 ]
Ferrao, Fernanda M. [1 ]
Dias, Juliana [1 ]
Miranda, Antonio [3 ]
Miranda, Filipe [1 ]
Lara, Lucienne S. [4 ]
Vieyra, Adalberto [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, BR-21941 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Inst Bioquim Med, Rio De Janeiro, Brazil
[3] Univ Fed Sao Paulo, Dept Biofis, Sao Paulo, Brazil
[4] Univ Fed Rio de Janeiro, Inst Ciencias Biomed, Rio De Janeiro, Brazil
基金
巴西圣保罗研究基金会;
关键词
Renin-angiotensin system; Ang-(3-4); Angiotensin receptors; Active calcium transport; Kidney cells; Basolateral membranes; INTERSTITIAL FLUID ANGIOTENSIN; TUBULE NA+-ATPASE; VAL-TYR; ANTIHYPERTENSIVE DIPEPTIDE; PROXIMAL TUBULES; CA2+ ATPASE; RECEPTOR; TRANSPORT; METABOLISM; PATHWAYS;
D O I
10.1016/j.regpep.2009.03.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We previously demonstrated that Ang II inhibits the renal plasma membrane Ca2+-ATPase. In the present work we have studied the effect of Ang II, at concentrations similar to those found in the renal interstitium, on the Ca2+-ATPase from proximal tubule cells. High Ang II concentration (5 x 10(-7) mol/L) led to the recovery of Ca2+-ATPase activity previously inhibited by 50% at low Ang II concentration (10(-10) mol/L). Reacdvation occurred in parallel with: (i) formation of only two dead-end metabolites [Ang-(3-4) and Tyr] after incubation of isolated membranes with micromolar Ang II; and (ii) dissociation of constitutive AT(1)R/AT(2)R heterodimers, which are preserved with 10(-10) mol/LAng II. When the membranes were incubated with 10(-14) mol/LAng-(3-4), inhibition by 10(-10) mol/L Ang II was no longer observed. The counteracting effect of Ang-(3-4) was abolished by PD123319, an antagonist of AT(2)R, and mimicked by CGP42112A, an agonist of AT(2)R. Ang-(1-7) is an intermediate in the formation of Ang(3-4) via a pathway involving angiotensin-converting enzyme (ACE), and complete dipeptide breakdown to Tyr and Val is impaired by low Ang II. We conclude that Ang-(3-4) may be a physiological regulator of active Ca2+ fluxes in renal proximal cells by acting within the renin-angiotensin axis. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:81 / 90
页数:10
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