Effect of chronic inhibition of converting enzyme on proximal tubule acidification
| Autor: | C. Amorena, Stella M. Dieguez, Mariana Fiori, Mariano L. Lopardo, Paula L. Diaz-Sylvester, Angélica Muller |
|---|---|
| Rok vydání: | 2008 |
| Předmět: |
Male
Vacuolar Proton-Translocating ATPases medicine.medical_specialty Sodium-Hydrogen Exchangers Physiology Urinary system Angiotensin-Converting Enzyme Inhibitors Peptidyl-Dipeptidase A Arginine Nitric Oxide Nitric oxide Kidney Tubules Proximal chemistry.chemical_compound Enalapril Physiology (medical) Internal medicine Renin–angiotensin system medicine Animals Rats Wistar chemistry.chemical_classification Kidney Sodium-Hydrogen Exchanger 3 Chemistry Rats Sodium–hydrogen antiporter Enzyme Convoluted tubule Endocrinology medicine.anatomical_structure Citrulline Oxidation-Reduction medicine.drug |
| Zdroj: | American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 294:R2014-R2020 |
| ISSN: | 1522-1490 0363-6119 |
| DOI: | 10.1152/ajpregu.00589.2007 |
| Popis: | The acute effect of angiotensin-converting enzyme inhibition (ACEi) on proximal convoluted tubule (PCT) function is well documented. However, the effect of chronic treatment is less known. The aim of this work was to evaluate the effect of chronic ACEi on PCT acidification (JHCO3−). Rats received enalapril (10 mg·kg−1·day−1, added to the drinking water) during 3 mo. Micropuncture experiments were performed to measure the effect of chronic ACEi on JHCO3−. Nitric oxide (NO·) synthesis in kidney cortex homogenates was assessed by quantifying the conversion of [14C]-l-arginine to [14C]-l-citrulline. Western blot analysis was performed to determine the abundances of V-H+ATPase and NHE3 isoform of the Na+/H+exchanger in proximal brush-border membrane vesicles (BBMV). Enalapril treatment induced a ∼50% increase in JHCO3−. Luminal perfusion with ethyl-isopropyl amiloride (EIPA) 10−4M or bafilomycin 10−6M decreased JHCO3−by ∼60% and ∼30%, respectively, in both control and enalapril-treated rats. The effect of EIPA and bafilomycin on absolute JHCO3−was larger in enalapril-treated than in control rats. Acute inhibition of NO·synthesis with NG-nitro-l-arginine methyl esther abolished the enalapril-induced increase in JHCO3−. Cortex homogenates from enalapril-treated rats displayed a 46% increase in nitric oxide synthase (NOS) activity compared with those from untreated animals. Enalapril treatment did not affect the abundances of NHE3 and V-H+ATPase in BBMV. Our results suggest that PCT acidification is increased during chronic ACEi probably due to an increase in NO·synthesis, which would stimulate Na+/H+exchange and electrogenic proton transport. |
| Databáze: | OpenAIRE |
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