Increased renal α-epithelial sodium channel (ENAC) protein and increased ENAC activity in normal pregnancy
Autor: | Geoffrey Ecker, Crystal A. West, Zheng Zhang, Shyama M. E. Masilamani |
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Rok vydání: | 2010 |
Předmět: |
Proteomics
inorganic chemicals Epithelial sodium channel medicine.medical_specialty Physiology Immunoblotting Natriuresis Spironolactone Kidney Amiloride Rats Sprague-Dawley chemistry.chemical_compound Mineralocorticoid receptor Pregnancy Mineralocorticoids Physiology (medical) Internal medicine Benzamil Epithelial Sodium Channel Blockers medicine Animals Plasma Volume Epithelial Sodium Channels Mineralocorticoid Receptor Antagonists urogenital system Sodium Kidney metabolism Articles respiratory system Eplerenone Rats Up-Regulation Endocrinology medicine.anatomical_structure chemistry Female hormones hormone substitutes and hormone antagonists Sodium Channel Blockers medicine.drug |
Zdroj: | American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 299:R1326-R1332 |
ISSN: | 1522-1490 0363-6119 |
Popis: | Pregnancy-mediated sodium (Na) retention is required to provide an increase in plasma volume for the growing fetus. The mechanisms responsible for this Na retention are not clear. We first used a targeted proteomics approach and found that there were no changes in the protein abundance compared with virgin rats of the β or γ ENaC, type 3 Na+/H+exchanger (NHE3), bumetanide-sensitive cotransporter (NKCC2), or NaCl cotransporter (NCC) in mid- or late pregnancy. In contrast, we observed marked increases in the abundance of the α-ENaC subunit. The plasma volume increased progressively during pregnancy with the greatest plasma volume being evident in late pregnancy. ENaC inhibition abolished the difference in plasma volume status between virgin and pregnant rats. To determine the in vivo activity of ENaC, we conducted in vivo studies of rats in late pregnancy ( days 18–20) and virgin rats to measure the natriuretic response to ENaC blockade (with benzamil). The in vivo activity of ENaC (UNaV postbenzamil-UNaV postvehicle) was markedly increased in late pregnancy, and this difference was abolished by pretreatment with the mineralocorticoid receptor antagonist, eplerenone. These findings demonstrate that the increased α-ENaC subunit of pregnancy is associated with an mineralocorticoid-dependent increase in ENaC activity. Further, we show that ENaC activity is a major contributor of plasma volume status in late pregnancy. These changes are likely to contribute to the renal sodium retention and plasma volume expansion required for an optimal pregnancy. |
Databáze: | OpenAIRE |
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