Document Detail


Renal, intestinal, and adrenal responses to sodium loading in Dahl-Iwai salt-sensitive and salt-resistant rats.
MedLine Citation:
PMID:  9601487     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
This study compared renal and intestinal handling of sodium in Dahl-Iwai salt-sensitive (S) and salt-resistant (R) rats given a normal-salt diet (0.3% NaCl) and a high-salt diet (4.0% NaCl). Six-week-old female S and R rats (n = 7 each) were given a normal-salt diet for 14 days followed by a high-salt diet for 3 weeks. Systolic blood pressure was significantly higher in the S rats than in the R rats only at the end of the high-salt diet period (170 +/- 5, mean +/- SEM, vs 152 +/- 1 mmHg, p < 0.01). Daily sodium intake, water intake, urine volume, and urinary and fecal excretions did not significantly differ between the R and the S rats during the normal- and high-salt diets, except for a slight, although significant, decrease in fecal sodium excretion in the S rats as compared with the R rats in the 2nd week of the high-salt diet period. After switching from the normal-salt diet to the high-salt diet, urinary sodium excretion increased by 17- to 18-fold and fecal sodium excretion increased by about 5-fold in the 1st week of salt loading. The changes in urinary and fecal sodium excretions did not differ significantly between the groups. Cumulative sodium retention was similar in the two groups. The aldosterone/creatinine ratio in 24-hr urine, which was significantly lower in the S than in the R rats during the normal-salt diet, decreased to similar levels in both groups after salt loading, indicating a blunted response of aldosterone in the S rats. Thus, there were no discernible differences in renal and intestinal handling of sodium between the S and the R rats, except for a slight, but significant, difference in fecal sodium excretion in the 2nd week of the high-salt period. The results indicate that inappropriate suppression of aldosterone or some other mechanism induced by salt loading may be involved in blood pressure elevation in Dahl-Iwai S rats.
Authors:
Y Katoh; S Umemura; K Sugimoto; M Tomiyama; Y Abe; N Hirawa; M Ishii
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Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  Japanese heart journal     Volume:  39     ISSN:  0021-4868     ISO Abbreviation:  Jpn Heart J     Publication Date:  1998 Jan 
Date Detail:
Created Date:  1998-06-01     Completed Date:  1998-06-01     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0401175     Medline TA:  Jpn Heart J     Country:  JAPAN    
Other Details:
Languages:  eng     Pagination:  109-19     Citation Subset:  IM    
Affiliation:
Second Department of Internal Medicine, Yokohama City University School of Medicine, Japan.
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MeSH Terms
Descriptor/Qualifier:
Adrenal Glands / drug effects*,  physiology
Aldosterone / physiology,  urine
Animals
Blood Pressure / drug effects*
Creatinine / urine
Drinking
Drug Resistance
Female
Intestines / drug effects*,  physiology
Kidney / drug effects*,  physiology
Natriuresis
Rats
Rats, Inbred Strains
Sodium, Dietary / administration & dosage*,  pharmacology,  urine
Chemical
Reg. No./Substance:
0/Sodium, Dietary; 52-39-1/Aldosterone; 60-27-5/Creatinine

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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