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J Appl Physiol 93: 463-468, 2002. First published March 22, 2002; doi:10.1152/japplphysiol.00627.2001
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Vol. 93, Issue 2, 463-468, August 2002

Effect of exercise on mRNA expression of select adrenal medullary catecholamine biosynthetic enzymes

S. Remzi Erdem2, Haydar A. Demirel3, Christopher S. Broxson1, Bistra B. Nankova4, Esther L. Sabban4, and Nihal Tümer1,2

1 Geriatric Research, Education and Clinical Center, Malcom Randall Veterans Affairs Medical Center, 2 Department of Pharmacology and Therapeutics, University of Florida College of Medicine, and 3 Center for Exercise Science, University of Florida, Gainesville, Florida 32610; and 4 Department of Biochemistry and Molecular Biology, New York Medical College, Valhalla, New York 10595

The effect of submaximal endurance training (SET) on sympathoadrenal activity is not clear. We tested the hypothesis that SET (90 min/day, 5 days/wk, for 12 wk) elevates mRNA expression of catecholamine (CA) biosynthetic enzymes, tyrosine hydroxylase (TH) and dopamine-beta -hydroxylase (Dbeta H) 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 Dbeta H mRNA expression by 67%. In addition, we examined the effect of SET on Fos-related antigens (FRAs), FRA-2 immunoreactivity, and activator protein (AP)-1 binding activity. SET increased AP-1 binding activity by 78%; however, it did not affect late FRAs and FRA-2 immunoreactivity. Because 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 pretranslational 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.

chronic physical training; tyrosine hydroxylase; activator protein-1; Fos-related antigen-2; neuropeptide Y; dopamine-beta -hydroxylase





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