AJP - Endo Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Am J Physiol Endocrinol Metab (July 30, 2002). doi:10.1152/ajpendo.00173.2002
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
283/5/E1067    most recent
00173.2002v1
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 Web of Science
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 Web of Science (15)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yorek, M. A
Right arrow Articles by Dillon, J. S
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yorek, M. A
Right arrow Articles by Dillon, J. S

Articles in PresS, published online ahead of print July 28, 2002
Am J Physiol Endocrinol Metab, 10.1152/ajpendo.00173.2002
Submitted on April 26, 2002
Accepted on July 23, 2002

Effect of treatment of diabetic rats with Dehydroepiandrosterone (DHEA) on vascular and neural function

Mark A Yorek1*, Lawrence J Coppey1, Jill S Gellett1, Eric P Davidson1, Xinyu Bing1, Donald D Lund1, and Joseph S Dillon1

1 Department of Internal Medicine, University of Iowa, Veterans Affairs Medical Center, Iowa City, IA, USA

* To whom correspondence should be addressed. E-mail: myorek{at}icva.gov.

Nutritional supplementation with DHEA may be a candidate for treating diabetes-induced vascular and neural dysfunction. DHEA is a naturally occurring adrenal androgen that has antioxidant properties and is reportedly reduced in diabetes. Using a prevention protocol we found that dietary supplementation of streptozotocin-induced diabetic rats with 0.1, 0.25 or 0.5% DHEA caused a concentration-dependent prevention in the development of motor nerve conduction velocity and endoneurial blood flow impairment, which are decreased in diabetes. At 0.25%, DHEA significantly prevented the diabetes-induced increase in serum thiobarbituric acid reactive substances and sciatic nerve conjugated diene levels. This treatment also reduced the production of superoxide by epineurial arterioles of the sciatic nerve. DHEA treatment (0.25%) significantly improved vascular relaxation mediated by acetylcholine in epineurial vessels of diabetic rats. Sciatic nerve Na+/K+ ATPase activity and myo-inositol content was also improved by DHEA treatment, whereas sorbitol and fructose content remained elevated. These studies suggest that DHEA, by preventing oxidative stress and perhaps improving sciatic nerve Na+/K+ ATPase activity, may improve vascular and neural dysfunction in diabetes.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2002 by the American Physiological Society.