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Am J Physiol Regul Integr Comp Physiol 283: R1070-R1078, 2002. First published July 25, 2002; doi:10.1152/ajpregu.00248.2002
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Vol. 283, Issue 5, R1070-R1078, November 2002

Synergy between angiotensin and aldosterone in evoking sodium appetite in baboons

R. E. Shade1,2, J. R. Blair-West1,2,3, K. D. Carey1,2, L. J. Madden1, R. S. Weisinger4, and D. A. Denton1,4

1 Department of Physiology and Medicine and 2 Southwest National Primate Research Center, Southwest Foundation for Biomedical Research, San Antonio, Texas 78245-0549; 3 Department of Physiology and 4 Howard Florey Institute of Experimental Physiology and Medicine, University of Melbourne, Victoria 3010, Australia

The synergy between ANG II and aldosterone (Aldo) in the induction of salt appetite, extensively studied in rats, has been tested in baboons. ANG II was infused intracerebroventricularly at 0.5 or 1.0 µg/h; Aldo was infused subcutaneously at 20 µg/h. Separate infusions over 7 days had no significant effect on the daily intake of 300 mM NaCl. Concurrent infusions, however, increased daily NaCl intake ~10-fold and daily water intake ~2.5-fold. In addition, the combined infusions caused 1) a reduction in daily food intake, 2) changes in blood composition indicative of increased vasopressin release, and 3) changes of urinary excretion rates of cortisol and Aldo indicative of increased ACTH release. Arterial blood pressure, measured in two baboons, rose during concurrent ANG II and Aldo treatment. These results indicate a potent synergy between central ANG II and peripheral Aldo in stimulating salt appetite in baboons. At the same time, other ANG II-specific brain mechanisms concerned with water intake, food intake, vasopressin release, ACTH release, and blood pressure regulation appear to have been activated by the same type of synergy. These central enhancement processes have never been previously demonstrated in primates.

salt; thirst; food intake; adrenocorticotropic hormone release; blood pressure


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