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  3. Physiological and Molecular Responses to Altered Sodium Intake in Rat Pregnancy.

Physiological and Molecular Responses to Altered Sodium Intake in Rat Pregnancy.

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DOI
10.7892/boris.122223
Publisher DOI
10.1161/JAHA.117.008363
PubMed ID
30371243
Abstract
Background In pregnancy, a high plasma volume maintains uteroplacental perfusion and prevents placental ischemia, a condition linked to elevated maternal blood pressure ( BP ). Reducing BP by increasing Na intake via plasma volume expansion appears contra-intuitive. We hypothesize that an appropriate Na intake in pregnancy reduces maternal BP and adapts the renin-angiotensin system in a pregnancy-specific manner. Methods and Results BP was measured by implanted telemetry in Sprague-Dawley rats before and throughout pregnancy. Pregnant and nonpregnant animals received either a normal-salt (0.4%; NS ), high-salt (8%; HS ), or low-salt (0.01%; LS ) diet, or HS (days 1-14) followed by LS (days 14-20) diet ( HS / LS ). Before delivery (day 20), animals were euthanized and organs collected. Food, water, and Na intake were monitored in metabolic cages, and urinary creatinine and Na were analyzed. Na intake and retention increased in pregnancy ( NS , LS ), leading to a positive Na balance ( NS , LS ). BP was stable during LS , but reduced in HS conditions in pregnancy. The renin-angiotensin system was adapted as expected. Activating cleavage of α- and γ-subunits of the renal epithelial Na channel and expression of-full length medullary β-subunits, accentuated further in all LS conditions, were upregulated in pregnancy. Conclusions Pregnancy led to Na retention adapted to dietary changes. HS exposure paradoxically reduced BP . Na uptake while only modestly linked to the renin-angiotensin system is enhanced in the presence of posttranslational renal epithelial Na channel modifications. This suggests (1) storage of Na in pregnancy upon HS exposure, bridging periods of LS availability; and (2) that potentially non-renin-angiotensin-related mechanisms participate in EN aC activation and consecutive Na retention.
Date Issued
2018-08-07
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Subjects
ion transport kidney physiology pregnancy renin angiotensin system
Language(s)
en
Author(s)
Eisele, Nicole  
Universitätsklinik für Nephrologie und Hypertonie  
Department for BioMedical Research, Forschungsgruppe Nephrologie / Hypertonie  
Klossner, Rahel  
Department for BioMedical Research, Forschungsgruppe Nephrologie / Hypertonie  
Escher, Geneviève  
Department for BioMedical Research, Forschungsgruppe Nephrologie / Hypertonie  
Universitätsklinik für Nephrologie und Hypertonie  
Rudloff, Stefan  
Department for BioMedical Research, Forschungsgruppe Nephrologie / Hypertonie  
Universitätsklinik für Nephrologie und Hypertonie  
Larionov, Alexey
Theilig, Franziska
Mohaupt, Markus  
Department for BioMedical Research, Forschungsgruppe Nephrologie / Hypertonie  
Mistry, Hiten Dhirubhai  
Department for BioMedical Research, Forschungsgruppe Nephrologie / Hypertonie  
Gennari, Carine  
Department for BioMedical Research, Forschungsgruppe Nephrologie / Hypertonie  
Additional Credits
Department for BioMedical Research, Forschungsgruppe Nephrologie / Hypertonie  
Universitätsklinik für Nephrologie und Hypertonie  
Journal
Journal of the American Heart Association
Publisher
American Heart Association
ISSN
2047-9980
Access(Rights)
open.access
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