CONDITIONED CHANGES IN DOPAMINE OXIDATION CURRENTS IN THE NUCLEUS-ACCUMBENS OF RATS BY STIMULI PAIRED WITH SELF-ADMINISTRATION OR YOKED-ADMINISTRATION OF D-AMPHETAMINE
P. Diciano et al., CONDITIONED CHANGES IN DOPAMINE OXIDATION CURRENTS IN THE NUCLEUS-ACCUMBENS OF RATS BY STIMULI PAIRED WITH SELF-ADMINISTRATION OR YOKED-ADMINISTRATION OF D-AMPHETAMINE, European journal of neuroscience, 10(3), 1998, pp. 1121-1127
In vivo chronoamperometry was used to monitor changes in dopamine oxid
ation currents corresponding to dopamine efflux in the nucleus accumbe
ns of rats after presentation of a conditioned light stimulus repeated
ly paired with either yoked-or self-administered intravenous injection
s of the psychostimulant d-amphetamine. Daily conditioning trials bega
n with a non-contingent drug injection, paired with a conditioned stim
ulus consisting of a 5 s flashing light and 30 s lights out, after whi
ch a house light was illuminated during the 3 h session, signalling dr
ug availability. Each subsequent injection of d-amphetamine was paired
with the conditioned stimulus. Electrochemical measures were taken on
conditioning trials 4-7, and on each trial, intravenous d-amphetamine
(0.25 mg/kg per injection) self-administration produced a significant
maximal increase in mean dopamine oxidation currents of approximate t
o 8 nA above baseline. Dopamine oxidation currents in rats receiving y
oked d-amphetamine were approximate to 5 nA above baseline by the four
th day of drug administration and reached approximate to 8 nA on the s
eventh and final day of drug administration. On day 9 the first presen
tation of the vehicle injection and conditioned stimulus, in combinati
on with illumination of the house lights, induced an immediate increas
e in nucleus accumbens dopamine oxidation currents in all rats that ha
d previously received d-amphetamine. Subsequent presentations of the c
onditioned stimulus at 30 min intervals induced further increases in e
xtracellular dopamine oxidation currents in both drug-treated groups.
By the end of the 3 h session, both groups had similar maximal conditi
oned increases in dopamine oxidation currents of approximate to 6 nA.
These data are discussed with relation to the neurochemistry of drug c
raving.