4.5 Article

Role of reactive oxygen species (ROS) in angiotensin II-induced stimulation of the cardiac Na+/HCO3- cotransport

Journal

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
Volume 47, Issue 5, Pages 716-722

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.yjmcc.2009.07.023

Keywords

Sodium/bicarbonate cotransport; Cardiac myocytes; Angiotensin II; Reactive oxygen species; ERK 1/2

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The sarcolemmal Na+/HCO3- cotransporter (NBC) plays an important role in intracellular pH (pH,) regulation in the heart. In the present work we studied, in isolated cat ventricular myocytes, the role of Angiotensin II (Ang II) and reactive oxygen species (RCS) production as potential activators of the NBC. pH, was measured in single cells in a medium with HCO3- using the fluorescent pH indicator BCECF The NH4+ pulse method was used to induce an intracellular acid load and the acid efflux (J(H)) in the presence of the Na+/H+ exchanger blocker HOE642 (10 mu M) was calculated as indicator of NBC activity. The following J(H) data are presented at pH, of 6.8 (* and * indicate p<0.05 after ANOVA vs. control and Ang 11, respectively). The basal J(H) (1.03 +/- 0.12 mM/min, n = 11(#)) was significantly increased in the presence of 100 nM Ang 11 (0.70 +/- 0.15 mM/min. n = 8*) This effect of Ang II was abolished when we added to the extracellular solution 2 mM MPG (RCS scavenger; 0.80 +/- 0.08 mM/min, n = 11#), 300 PM apocynin (NADPH oxidase blocker; 0 80 0 13 mM/min, n = 6#). 500 mu M 5-hydroxidecanoate (mitochondrial ATP dependent K+ channel, mK(ATP). blocker; 0.97 +/- 0.21 mM/min, n = 94). or the inhibitor of the MAP kinase ERK pathway U0126 (10 mu M; 0.56 +/- 0.18 mM/min, n = 6#). We also determined the phosphorylation of ERK clunng the first min of acidosis and we detected that Ang 11 significantly enhanced the ERK phosphorylation levels, an effect that was cancelled by scavenging ROS with MPG. In conclusion, we propose that Ang 11 enhances the production of ROS through the activation of the NADPH oxidase, which in turn triggers mK(ATP) opening and mitochondrial ROS production (ROS-induced ROS-release mechanism). Finally, these mitochondrial ROS stimulate the ERK pathway, leading to the activation of the NBC (C) 2009 Elsevier Inc. All rights reserved.

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