Affiliation:
1. From the Department of Physiology and Pharmacology, Federal University of Pelotas (K.R.), Pelotas, Brazil; the Department of Pharmacology and Toxicology, Wright State University School of Medicine (R.P., M.M.), Dayton, Ohio; and the Institute of Normal and Pathological Physiology, Slovak Academy of Sciences (I.B.), Bratislava, Slovak Republic.
Abstract
To explore the role of oxytocin in the regulation of salt appetite and blood pressure, we conducted studies in oxytocin gene–knockout mice and determined (1) blood pressure and heart rate during day and night periods, (2) salt appetite after iso-osmotic volume depletion, and (3) salt appetite and blood pressure after central injection of angiotensin II. Long-term arterial catheters were inserted, and blood pressure and heart rate were recorded for 24 hours. There was a modest decrease in blood pressure and heart rate in knockout mice. Salt appetite was measured with a 2- bottle choice (water and 2% NaCl), with measurement of licking activity. Mice were injected subcutaneously with 30% polyethylene glycol (0.5 mL), and voluntary intakes were measured for 24 hours. Knockout mice consumed 3 times the amount of NaCl than did controls, 276±77 vs 90±38 licks/24 h (
P
<0.05). Water consumption was similar between groups. Angiotensin II (5, 50, and 200 ng/3 μL) injected intracerebroventricularly produced dose-related increases in intake, with no differences between the groups. The 50-ng dose of angiotensin II elicited salt and water intakes of 151±43 vs 160±33 licks and 250±53 vs and 200±51 licks, respectively (control vs knockout). The pressor response to angiotensin II was not different between the groups. Results suggest that oxytocin plays a role in the regulation of blood pressure and salt appetite, specifically as mediated by volume receptors, and that the renin-angiotensin system is not involved in these changes.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Cited by
23 articles.
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