Jf. Hyde et al., BILATERAL CHANGES IN STRIATAL DOPAMINE METABOLISM AFTER UNILATERAL INTRACAROTID AND INTRASTRIATAL ADMINISTRATION OF APOMORPHINE, Brain research, 655(1-2), 1994, pp. 83-90
Following cannulation of the common carotid artery of female Sprague-D
awley rats, 3 mu Ci (10 mu g) of [H-3]apomorphine were infused. At var
ious time intervals, drug concentrations were determined in the right
and left striata, anterior forebrains, posterior forebrains and cerebe
lla. One minute following intracarotid infusion of apomorphine, approx
imately a 65-fold right/left difference in apomorphine concentrations
was attained in all forebrain structures, and this difference steadily
diminished with time as a result of declining drug levels in the infu
sed hemisphere. The concentrations of dopamine and its metabolites (DO
PAC, HVA and 3-MT) were quantified by gas chromatography-mass spectrom
etry in the right and left striata at 5 and 15 min after unilateral in
tracarotid infusion of 1 mu g apomorphine. At both time intervals and
regardless of the side infused, the metabolites of dopamine increased
ipsilateral to the side of infusion. Moreover, 3-MT levels were signif
icantly decreased in the contralateral striatum. After direct intrastr
iatal injection of either 0.1 or 1.0 mu g apomorphine into the right s
triatum, the levels of dopamine metabolites were again increased in th
e ipsilateral striatum. 3-MT levels were also decreased significantly
in the left striatum. In contrast to the effects observed after system
ic administration of apomorphine, these results demonstrate that dopam
ine release in the striatum is increased by selectively delivering hig
her concentrations of apomorphine to the nerve terminals of the nigros
triatal neurons. The effects of unilateral apomorphine on dopamine met
abolism in the contralateral striatum are most likely the effect of in
terhemispheric communication.