AJP Legacy 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 205: 322-324, 1963;
0002-9513/63 $5.00
This Article
Right arrow Full Text (PDF)
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 Google Scholar
Google Scholar
Right arrow Articles by Hardwick, D. F.
Right arrow Articles by Misrahy, G. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hardwick, D. F.
Right arrow Articles by Misrahy, G. A.

Kidney oxygen availability

D. F. Hardwick 1, J. Strauss 1, and G. A. Misrahy 1

1 Developmental and Sensory Physiology Laboratory, Childrens Hospital of Los Angeles, Los Angeles, California

Mean oxygen availability (aO2) was measured in the kidney cortex and bone marrow of cats by polarographic technique. O2, CO2, and Apresoline increased the mean aO2, whereas N2, Amobarbital, Pitressin, Adrenalin, Methacholine, venesection, and spinal anesthesia decreased it with varied effects on the cyclic fluctuations in mean aO2. These results suggest that the regulation of kidney aO2 is intermediate between brain and bone marrow oxygen and that kidney hypoxia is not the only factor responsible for erythropoietic stimulation.

Submitted on February 4, 1963







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 1963 by the American Physiological Society.