AJP - Endo Watch the video to learn how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Endocrinol Metab 264: E456-E464, 1993;
0193-1849/93 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gogerly, R. L.
Right arrow Articles by McDougall, J. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gogerly, R. L.
Right arrow Articles by McDougall, J. G.

AJP - Endocrinology and Metabolism, Vol 264, Issue 3 E456-E464, Copyright © 1993 by American Physiological Society


ARTICLES

Two-compartment model of acute stimulation of aldosterone secretion in vivo by angiotensin II

R. L. Gogerly, J. P. Coghlan, P. Morgenroth and J. G. McDougall
Howard Florey Institute of Experimental Physiology and Medicine, University of Melbourne, Parkville, Victoria, Australia.

Sheep with a cervical adrenal autotransplant were used to establish the relationship between acute change in angiotensin II (ANG II) concentration and acute change in aldosterone secretion rate (ASR). The kinetics of 131I-labeled ANG II and unlabeled ANG II across the adrenal were consistent with distribution within a two-compartment model. ASR was found to be a linear function of the ANG II concentration predicted to occur in the second compartment, indicating that acute change in ASR is determined to a large degree by the rate of exchange of ANG II between the first and second compartments. The time required for ANG II concentration to reach 50 and 95% of steady state was estimated to be approximately 5 and 45 min, respectively. The time course for agonist distribution within the adrenal may be an important factor to consider in both the design and interpretation of experimental studies that involve the stimulation (or inhibition) of adrenocortical cells.


This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
M. J. McKinley, M. D. Evered, and M. L. Mathai
Renal Na excretion in dehydrated and rehydrated adrenalectomized sheep maintained with aldosterone
Am J Physiol Regulatory Integrative Comp Physiol, July 1, 2000; 279(1): R17 - R24.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online