Adrenal-dependent modulation of the catalytic subunit isoforms of the Na+-K+-ATPase in aorta

Michea, L.; Valenzuela, V.; Bravo, I; Schuster, A; Marusic E.T.

Keywords: acetate, model, catalysis, rat, enzyme, animals, expression, rats, gene, gland, site, experiment, male, regulation, atpase, aorta, hormones, isoenzymes, isoenzyme, glands, tissue, rna, cortex, adrenalectomy, adenosine, active, article, concentration, controlled, animal, study, adrenal, priority, nonhuman, journal, triphosphatase, Rats,, Sprague-Dawley, Messenger, (potassium, sodium), Na(+)-K(+)-Exchanging, Osmolar, deoxycorticosterone, Desoxycorticosterone

Abstract

Na+-K+-ATPase gene expression and activity were studied in aortas from adrenalectomized (ADX) rats and ADX rats with deoxycorticosterone supplement (ADX-DOCA). Northern analysis of RNA from ADX rats revealed a significant decrease in ?2-mRNA levels (38.5 ± 8.3% of control, P < 0.01) that was prevented by DOCA (P < 0.05). A decrease to 55.8 ± 7.7% in ?2-isoform protein was observed 8 days after adrenal removal (P < 0.05); DOCA reversed this effect (90.8 ± 10.5%). Adrenalectomy induced a decrease of 68.5 ± 4.5% in ?-mRNA (P < 0.01) and 52.7 ± 8.3% in ADX-DOCA rats (P < 0.01). Also, a reduction in ?1-isoform protein that was not prevented by DOCA was detected after adrenalectomy (47.1 ± 11%, P < 0.01). In contrast, no differences in ?1-mRNA or -protein levels were observed. Vascular sodium pump activity was reduced to 59.8 ± 4.6% of control values after adrenalectomy (P < 0.01); this reduction was reversed by DOCA. Our data indicate that corticosteroids regulate Na+-K+-ATPase isoform expression and activity in vascular tissue in vivo, suggesting a mineralocorticoid-dependent modulation of ?2-Na+- K+-ATPase gene expression in aorta, with ?1-isoform expression dependent on the presence of glucocorticoids.

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Título de la Revista: AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
Volumen: 275
Número: 6 38-6
Editorial: AMER PHYSIOLOGICAL SOC
Fecha de publicación: 1998
URL: http://www.scopus.com/inward/record.url?eid=2-s2.0-0032427185&partnerID=q2rCbXpz