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


     


Am J Physiol Regul Integr Comp Physiol 273: R1117-R1125, 1997;
0363-6119/97 $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 House, W. A.
Right arrow Articles by Wastney, M. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by House, W. A.
Right arrow Articles by Wastney, M. E.

AJP - Regulatory, Integrative and Comparative Physiology, Vol 273, Issue 3 1117-R1125, Copyright © 1997 by American Physiological Society


ARTICLES

Compartmental analysis of zinc kinetics in mature male rats

W. A. House and M. E. Wastney
United States Department of Agriculture-Agriculture Research Service, Plant, Soil, and Nutrition Laboratory, Ithaca, New York 14853, USA.

A compartmental model of zinc kinetics in mature male rats was developed. The model was based on zinc and radioisotopic zinc measured in samples of plasma, skeletal muscle, kidneys, testes, spleen, bone, and intestinal segments collected at various times for up to 4 days after 65Zn was injected intravenously. Zinc intake, excretion of zinc and 65Zn in urine and feces, and the whole body retention of 65Zn were also determined. Other data used to develop the model included published information on zinc concentration and zinc kinetics in tissues that were not sampled. In the model, the intestinal tract was represented by five compartments. Plasma, spleen, kidneys, and testes were each represented by an individual compartment. In contrast, two compartments each were used to represent exchangeable zinc in liver, bone, skeletal muscle, skin, and red blood cells. The present model extends earlier models of zinc kinetics, describes the distribution of zinc in the whole body, and may provide a means to evaluate the influence of either pathophysiological conditions or dietary extremes on the metabolism of zinc.


This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
L. V. Miller, N. F. Krebs, and K. M. Hambidge
Development of a compartmental model of human zinc metabolism: identifiability and multiple studies analyses
Am J Physiol Regulatory Integrative Comp Physiol, November 1, 2000; 279(5): R1671 - R1684.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
M. E. Wastney, W. A. House, R. M. Barnes, and K. N. S. Subramanian
Kinetics of Zinc Metabolism: Variation with Diet, Genetics and Disease
J. Nutr., May 1, 2000; 130(5): 1355S - 1359.
[Abstract] [Full Text]




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