Pm. Beardsley et Rl. Balster, THE EFFECTS OF DELAY OF REINFORCEMENT AND DOSE ON THE SELF-ADMINISTRATION OF COCAINE AND PROCAINE IN RHESUS-MONKEYS, Drug and alcohol dependence, 34(1), 1993, pp. 37-43
Delays of reinforcement were imposed while three rhesus monkeys intrav
enously self-administered either cocaine or procaine to determine whet
her the magnitude of delay-induced reductions in infusion frequency we
re dose- or drug-dependent. Drug-maintained baselines demonstrating th
e greatest resistance to change under delay conditions might be concep
tualized as involving the greatest strength of responding and include
drug reinforcers with the greatest efficacy. Under baseline conditions
, cocaine or procaine was infused contingent upon lever pressing accor
ding to fixed ratio 10 schedules during daily, 1-h experimental sessio
ns. Under delay conditions, a 120-s delay of reinforcement was inserte
d between the completion of each fixed ratio contingency and infusion
delivery. Tests under baseline and delay conditions alternated until s
everal doses of cocaine (3, 10, 33, 100, and 300 mu g/kg), and subsequ
ently, of procaine (33, 100, 300, 1000, and 3000 mu g/kg) were tested.
The results indicated that during both baseline and delay conditions
increases in dose of either drug resulted in increases followed by dec
reases in the number of infusions obtained. Introducing delays of rein
forcement resulted in decreases in the number of infusions obtained at
a given dose. Generally, however, when reinforcement delays were impo
sed the decreases in infusion number, as a percentage of baseline numb
er, were less at the higher doses of both drugs. The doses of procaine
which were maximally effective as reinforcers (i.e. during which infu
sion number was minimally reduced by delay) were as effective as the m
aximally effective doses of cocaine: These results suggest that drug p
reparations and routes of administration which, in fact, maximize unit
dose delivery would also maximize the likelihood that drug-maintained
behavior will be; resistant to theraputic intervention.