Literature DB >> 25925254

Renal NCC is unchanged in the midpregnant rat and decreased in the late pregnant rat despite avid renal Na+ retention.

Crystal A West1, Alicia A McDonough2, Shyama M E Masilamani3, Jill W Verlander4, Chris Baylis5.   

Abstract

Pregnancy is characterized by plasma volume expansion due to Na(+) retention, driven by aldosterone. The aldosterone-responsive epithelial Na(+) channel is activated in the kidney in pregnancy. In the present study, we investigated the aldosterone-responsive Na(+)-Cl(-) cotransporter (NCC) in mid- and late pregnant rats compared with virgin rats. We determined the abundance of total NCC, phosphorylated NCC (pNCC; pT53, pS71 and pS89), phosphorylated STE20/SPS-1-related proline-alanine-rich protein kinase (pSPAK; pS373), and phosphorylated oxidative stress-related kinase (pOSR1; pS325) in the kidney cortex. We also measured mRNA expression of NCC and members of the SPAK/NCC regulatory kinase network, serum and glucocorticoid-regulated kinase (SGK)1, total with no lysine kinase (WNK)1, WNK3, and WNK4. Additionally, we performed immunohistochemistry for NCC kidneys from virgin and pregnant rats. Total NCC, pNCC, and pSPAK/OSR1 abundance were unchanged in midpregnant versus virgin rats. In late pregnant versus virgin rats, total NCC and pNCC were decreased; however, pSPAK/OSR1 was unchanged. We detected no differences in mRNA expression of NCC, SGK1, total WNK1, WNK3, and WNK4. By immunohistochemistry, NCC was mainly localized to the apical region in virgin rats, and density in the apical region was reduced in late pregnancy. Therefore, despite high circulating aldosterone levels in pregnancy, the aldosterone-responsive transporter NCC is not increased in total or activated (phosphorylated) abundance or in apical localization in midpregnant rats, and all are reduced in late pregnancy. This contrasts to the mineralocorticoid-mediated activation of the epithelial Na(+) channel, which we have previously reported. Why and how NCC escapes aldosterone activation in pregnancy is not clear but may relate to regional differences in aldosterone sensitivity the increased K(+) intake or other undefined mechanisms.
Copyright © 2015 the American Physiological Society.

Entities:  

Keywords:  pregnancy; renal sodium handling; sodium-chloride cotransporter

Mesh:

Substances:

Year:  2015        PMID: 25925254      PMCID: PMC4490381          DOI: 10.1152/ajprenal.00147.2015

Source DB:  PubMed          Journal:  Am J Physiol Renal Physiol        ISSN: 1522-1466


  52 in total

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5.  Conservation of Na+ vs. K+ by the rat cortical collecting duct.

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10.  Activation of the renal Na+:Cl- cotransporter by angiotensin II is a WNK4-dependent process.

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1.  Sexual Dimorphic Pattern of Renal Transporters and Electrolyte Homeostasis.

Authors:  Luciana C Veiras; Adriana C C Girardi; Joshua Curry; Lei Pei; Donna L Ralph; An Tran; Regiane C Castelo-Branco; Nuria Pastor-Soler; Cristina T Arranz; Alan S L Yu; Alicia A McDonough
Journal:  J Am Soc Nephrol       Date:  2017-08-03       Impact factor: 10.121

Review 2.  The enigma of continual plasma volume expansion in pregnancy: critical role of the renin-angiotensin-aldosterone system.

Authors:  Crystal A West; Jennifer M Sasser; Chris Baylis
Journal:  Am J Physiol Renal Physiol       Date:  2016-10-05

3.  Renal and colonic potassium transporters in the pregnant rat.

Authors:  Crystal A West; Paul A Welling; David A West; Richard A Coleman; Kit-Yan Cheng; Chao Chen; Thomas D DuBose; Jill W Verlander; Chris Baylis; Michelle L Gumz
Journal:  Am J Physiol Renal Physiol       Date:  2017-10-18

4.  Time course of renal sodium transport in the pregnant rat.

Authors:  Crystal A West; Steven D Beck; Shyama M E Masilamani
Journal:  Curr Res Physiol       Date:  2021-10-23

5.  The chloride-bicarbonate exchanger pendrin is increased in the kidney of the pregnant rat.

Authors:  Crystal A West; Jill W Verlander; Susan M Wall; Chris Baylis
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  5 in total

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