The expression of the biogenic amine degrading enzyme monoamine oxidases-A
and -B depends on several factors including regional distribution, developm
ent and hormonal environment. In the present study. we investigated the exp
ression of monoamine oxidases in developing kidney and their regulation by
dexamethasone treatment. Immunoblots and enzyme assays, performed using [C-
14]S-hydroxytriptamine and C-14]beta -phenylethylamine as substrates for mo
noamine oxidases-A and -B, respectively, showed that monoamine oxidase-A is
the isoenzyme largely predominant in 9-day-old rats renal cortex. Experime
nts performed in 5-week-old rats showed an increase in monoamine oxidase-B
activity and a decrease in monoamine oxidase-A activity and substrate affin
ity. The changes of monoamine oxidase-A activity and affinity were mimicked
by dexamethasone treatment (0.60 mg/kg body weight injected subcutaneously
three times at intervals of 24 h) of 9-day-old rats. In contrast, dexameth
asone administration induced a modification of monoamine oxidase-B activity
opposite to that found between 9-day- and 5-week-old rats. Dexamethasone t
reatment did not modify immunoreactivity and mRNA corresponding to monoamin
e oxidases-A and -B indicating that changes of enzyme activities were unrel
ated to regulation of protein synthesis and mRNA turnover. These results sh
ow that monoamine oxidases-A and -B are differently expressed in developing
renal cortex and are regulated by dexamethasone treatment. (C) 2001 Publis
hed by Elsevier Science B.V.