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Articles in PresS, published online ahead of print March 22, 2002
J Appl Physiol, 10.1152/jap.00627.2001
Submitted on June 18, 2001
Accepted on March 13, 2002
1 Department of Pharmacology/Therapeutics, University of Florida, Gainesville, Florida, USA
2 Center for Exercise Science, University of Florida, Gainesville, Florida, USA
3 Geriatric Research and Clinical Center, Malcom Randall VA Medical Center, Gainesville, Florida, USA
4 Department of Biochemstry and Molecular Biology, New York Medical College, Valhalla, New York, USA
5 Geriatric Research and Clinical Center, Malcom Randall VA Medical Center, Gainesville, Florida, USA; Department of Pharmacology/Therapeutics, University of Florida, Gainesville, Florida, USA
* To whom correspondence should be addressed. E-mail: rerdem{at}ufl.edu.
The effect of submaximal endurance training (SET) on sympathoadrenal activity is not clear. We tested the hypothesis that SET (90 min/day, 5 days/week, 12 weeks) elevates mRNA expression of catecholamine (CA) biosynthetic enzymes, tyrosine hydroxylase (TH) and dopamine ß hydroxylase (DßH) in the adrenal medullae of adult, female Sprague-Dawley rats. SET increased TH protein level by 35%, TH activity by 62%, TH mRNA expression by 40%, and DßH mRNA expression by 67%. In addition, we examined the effect of SET on Fos-related antigens (Fras), Fra-2 immunoreactivity, and activator protein-1 (AP-1) binding activity. SET increased AP-1 binding activity by 78%, however it did not affect late Fras and Fra-2 immunoreactivity. Since the regulation of neuropeptide Y (NPY) often parallels that of CAs, we also examined the effect of SET on NPY mRNA expression. Indeed, SET elevated NPY mRNA expression as well. We conclude that 1) SET elicits a pre-translational stimulatory effect on adrenomedullary CA biosynthetic enzymes, 2) another immediate early mRNA product, rather than Fra-2, may contribute to the increase in AP-1 binding activity in response to SET, and 3) SET increases NPY mRNA expression.
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