The present study examined renal dopaminergic activity and its response to
high salt (HS) intake in adult (6-month-old) and old (24-month-old) Fischer
344 rats, Daily urinary excretion of L-3,4-dihydroxyphenylalanine (L-DOPA)
, dopamine, and its metabolites 3,4-dihydroxyphenylacetic acid (DOPAC) and
homovanillic acid was similar in adult and old rats; by contrast, daily uri
nary excretion of norepinephrine in old rats was almost twice that in adult
animals. HS intake (1% NaCl) over a period of 24 hours resulted in a 2-fol
d increase in the urinary excretion of dopamine, DOPAC, and norepinephrine
in adult animals but not in old animals, Norepinephrine and L-DOPA plasma l
evels did not change during HS intake and were similar in both groups of ra
ts. The natriuretic response to an HS intake in old rats (from 4.7+/-0.4 to
10.7+/-2.0 nmol . kg(-1) . d(-1); Delta=6.0+/-0.9 nmol . kg(-1) . d(-1)) w
as less than in adult rats (from 5.2+/-0.4 to 13.5+/-2.5 nmol . kg(-1) . d(
-1); Delta=8.3+/-0.8 nmol . kg(-1) . d(-1)). A diuretic response to HS inta
ke was observed in adult rats (from 20.9+/-2.3 to 37.6+/-2.8 mL . kg(-1) .
d(-1)) but not in old rats (from 37.7+/-5.7 to 42.3+/-6.0 mL . kg(-1) . d(-
1)). Dopamine levels and dopamine/L-DOPA ratios in the renal cortex of old
rats were greater than in adult rats. HS intake increased both dopamine lev
els and dopamine/L-DOPA ratios in the renal cortex of adult rats but not in
old rats. Aromatic L-amino acid decarboxylase activity was higher in old r
ats than in adult rats; HS intake increased L-amino acid decarboxylase acti
vity (nmol . mg protein(-1) 15 min(-1)) in adult rats (from 67+/-1 to 93+/-
1) but not in old rats (from 86+/-2 to 87+/-2), Dopamine inhibited Na+,K+-A
TPase activity in proximal tubules obtained from adult rats, but it failed
to exert such an inhibitory effect in old rats. It is concluded that renal
dopaminergic tonus in old rats is higher than in adult rats but fails to re
spond to HS intake as observed in adult rats. This may be due in part to th
e inability of dopamine to inhibit Na+,K+-ATPase activity in old rats.