Renal cyclic 3 ',5 '-guanosine monophosphate and sodium excretion in Dahl salt-resistant and Dahl salt-sensitive rats: comparison of the roles of bradykinin and nitric oxide
Lj. Millatt et Hm. Siragy, Renal cyclic 3 ',5 '-guanosine monophosphate and sodium excretion in Dahl salt-resistant and Dahl salt-sensitive rats: comparison of the roles of bradykinin and nitric oxide, J HYPERTENS, 18(10), 2000, pp. 1491-1496
Citations number
32
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objective The purpose of this study was to determine the relative importanc
e of bradykinin and nitric oxide (NO) in mediating renal responses to alter
ed sodium intake in Dahl salt-resistant (Dahl-SR) and salt-sensitive (Dahl-
SS) rats.
Design and methods Dahl-SR and Dahl-SS rats consumed a diet containing 0.15
% (low) or 4.0% (high) sodium chloride for 10 days. A microdialysis techniq
ue was then used to measure renal cortical interstitial fluid (RIF) cyclic
3',5'-guanosine monophosphate (cGMP) production in anesthetized rats, under
baseline conditions and during acute cortical infusion of either the brady
kinin B-2 receptor antagonist icatibant or the NO synthase inhibitor nitro-
L-arginine methyl ester (L-NAME). Urine sodium excretion was monitored simu
ltaneously by ureter cannulation.
Results Baseline sodium excretion was similar in the two types of rats, but
RIF cGMP was significantly elevated in Dahl-SR compared to Dahl-SS rats on
both low and high sodium diets. Icatibant infusion significantly reduced b
oth RIF cGMP and sodium excretion in Dahl-SR rats during low sodium intake,
but had no effect in Dahl-SS rats on either diet L-NAME infusion significa
ntly reduced sodium excretion in Dahl-SR and Dahl-SS rats, during both low
and high sodium intake. L-NAME infusion caused a significant reduction in R
IF cGMP in Dahl-SR and Dahl-SS rats on low sodium diet, but reduced RIF cGM
P only in Dahl-SR rats on high sodium diet.
Conclusion These data suggest a potential role for cortical bradykinin, but
not NO, in mediating the differences in the renal response to low sodium i
ntake between Dahl-SR and Dahl-SS rats. J Hypertens 18:1491-1496 (C) 2000 L
ippincott Williams & Wilkins.