TY - JOUR
T1 - CONCURRENT PHENCYCLIDINE AND SACCHARIN ACCESS
T2 - PRESENTATION OF AN ALTERNATIVE REINFORCER REDUCES DRUG INTAKE
AU - Carroll, Marilyn E.
PY - 1985/1
Y1 - 1985/1
N2 - Six monkeys self‐administered orally delivered phencyclidine (“angel dust”) and saccharin under concurrent fixed‐ratio 16 schedules during daily three‐hour sessions. Liquid deliveries were contingent upon lip‐contact responses on solenoid‐operated drinking spouts. Three saccharin concentrations (0.003%, 0.03% and 0.3%, wt/vol) were tested in a nonsystematic order. For each saccharin concentration, the following series of phencyclidine concentrations (mg/ml) was presented: 0.25, 0.5, 1, 0.25 (retest), 0.125, 0.0625, 0.0312, 0.25 (retest) and 0 (water with stimuli signaling phencyclidine). As the saccharin concentration increased, the number of drug deliveries decreased, and the peaks of the concentration‐response functions were shifted to the right. The lowest saccharin concentration (0.003%, wt/vol) maintained responding in excess of phencyclidine levels in only one monkey. The two higher saccharin concentrations maintained behavior far in excess of phencyclidine, but saccharin deliveries decreased in some monkeys as phencyclidine concentration and intake (mg/kg) increased. The time course and patterns of phencyclidine‐reinforced responding were also altered when saccharin was concurrently available. The results are discussed in terms of strategies to reduce drug‐reinforced behavior, preference between different reinforcers, and measures of reinforcing efficacy. 1985 Society for the Experimental Analysis of Behavior
AB - Six monkeys self‐administered orally delivered phencyclidine (“angel dust”) and saccharin under concurrent fixed‐ratio 16 schedules during daily three‐hour sessions. Liquid deliveries were contingent upon lip‐contact responses on solenoid‐operated drinking spouts. Three saccharin concentrations (0.003%, 0.03% and 0.3%, wt/vol) were tested in a nonsystematic order. For each saccharin concentration, the following series of phencyclidine concentrations (mg/ml) was presented: 0.25, 0.5, 1, 0.25 (retest), 0.125, 0.0625, 0.0312, 0.25 (retest) and 0 (water with stimuli signaling phencyclidine). As the saccharin concentration increased, the number of drug deliveries decreased, and the peaks of the concentration‐response functions were shifted to the right. The lowest saccharin concentration (0.003%, wt/vol) maintained responding in excess of phencyclidine levels in only one monkey. The two higher saccharin concentrations maintained behavior far in excess of phencyclidine, but saccharin deliveries decreased in some monkeys as phencyclidine concentration and intake (mg/kg) increased. The time course and patterns of phencyclidine‐reinforced responding were also altered when saccharin was concurrently available. The results are discussed in terms of strategies to reduce drug‐reinforced behavior, preference between different reinforcers, and measures of reinforcing efficacy. 1985 Society for the Experimental Analysis of Behavior
KW - concurrent fixed‐ratio schedules
KW - lip‐contact response
KW - oral drug self‐administration
KW - phencyclidine
KW - reinforcing efficacy
KW - rhesus monkeys
KW - saccharin
KW - suppression of drug‐reinforced behavior
UR - http://www.scopus.com/inward/record.url?scp=0021947749&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0021947749&partnerID=8YFLogxK
U2 - 10.1901/jeab.1985.43-131
DO - 10.1901/jeab.1985.43-131
M3 - Article
C2 - 3981084
AN - SCOPUS:0021947749
SN - 0022-5002
VL - 43
SP - 131
EP - 144
JO - Journal of the Experimental Analysis of Behavior
JF - Journal of the Experimental Analysis of Behavior
IS - 1
ER -