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Vol. 281, Issue 3, 1357-1367, 1997
Department of Pharmacology and Toxicology, University of Arkansas
for Medical Sciences, Little Rock, Arkansas
The effects of methamphetamine, phencyclidine and
9-tetrahydrocannabinol on responding under temporal
response differentiation schedules were studied under three different
time requirements. Under the schedules studied, Sprague-Dawley rats
were required to make a continuous response for at least a minimum time
duration, but not more than a maximum. Base-line performance under a
temporal differentiation schedule usually produces a normal frequency
distribution of response durations with the peak at or near the minimum
duration required for delivery of the reinforcer. These frequencies
were summed to calculate cumulative frequencies that were plotted as sigmoidal curves. Under the temporal differentiation 1-1.3 sec schedule, methamphetamine increased the frequency of short response durations at low doses, whereas high doses produced both long and short
response durations, flattening the relative frequency distribution.
Under the temporal differentiation 4-5.2 sec and 10-13 sec schedules,
methamphetamine produced only short response durations, which shifted
the relative frequency and cumulative frequency distribution of
response durations leftward.
9-Tetrahydrocannabinol had
little effect under the temporal differentiation 1-1.3 sec and 4-5.2
sec schedules, but it greatly increased the relative frequency of short
response durations under the 10-13 sec schedule. Phencyclidine
produced a similar effect under all temporal differentiation schedules,
increasing the relative frequency of short response durations. Thus the
effect of drugs on timing behavior under these temporal differentiation
schedules not only depended on the drug, but also depended on the dose
and the time parameters of the schedule. These data suggest that drugs
produce multiple effects on timing behaviors that depend on complex
interactions among several factors.
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G. Y. H. Mcclure and D. E. Mcmillan J. Pharmacol. Exp. Ther., June 1, 1997; 281(3): 1368 - 1380. [Abstract] [Full Text] |
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