Vol. 283, Issue 5, E1067-E1075, November 2002
Effect of treatment of diabetic rats with
dehydroepiandrosterone on vascular and neural
function
Mark A.
Yorek,
Lawrence J.
Coppey,
Jill S.
Gellett,
Eric P.
Davidson,
Xinyu
Bing,
Donald D.
Lund, and
Joseph S.
Dillon
Veterans Affairs Medical Center, Diabetes Endocrinology
Research Center, and Department of Internal Medicine, University of
Iowa, Iowa City, Iowa 52246
Nutritional supplementation
with dehydroepiandrosterone (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 myoinositol 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.
diabetic neuropathy; vascular reactivity; oxidative stress; superoxide