ABA chronic dosing of D-amphetamine produces differential drug effects in two variants of a temporal discrimination procedure in pigeons

2009 ◽  
Vol 20 (8) ◽  
pp. 705-719 ◽  
Author(s):  
Erin A. McClure ◽  
Kathryn A. Saulsgiver ◽  
Clive D.L. Wynne
2020 ◽  
Author(s):  
Başak Akdoğan ◽  
Amita Wanar ◽  
Benjamin Kyle Gersten ◽  
Charles Randy Gallistel ◽  
Peter Balsam

Temporal information-processing is critical for adaptive behavior and goal-directed action. It is thus crucial to understand how the temporal distance between behaviorally relevant events is encoded to guide behavior. However, research on temporal representations has yielded mixed findings as to whether organisms utilize relative versus absolute judgments of time intervals. To address this fundamental question about the timing mechanism, we tested mice in a duration discrimination procedure in which they learned to correctly categorize tones of different durations as short or long. After being trained on a pair of target intervals the mice transferred to conditions in which cue durations and corresponding response locations were systematically manipulated. Specifically, responses and/or durations of cues were switched in different experimental phases so that either the relative or absolute mapping remained constant. The findings indicate that the transfer occurred most readily when relative relationships of durations and response locations were preserved. In contrast, when the animals had to re-map these relative relations, their temporal discrimination ability was impaired, and they required extensive training to re-establish temporal control. However, preserving the response location of one of the cue durations in such conditions was found to help with initial transfer. These results demonstrate that mice can represent experienced durations both as having a certain magnitude (absolute representation) and as being shorter or longer of the two durations (an ordinal relation to other cue durations), with relational control having a greater influence in temporal discriminations.


2008 ◽  
Vol 77 (3) ◽  
pp. 357-363 ◽  
Author(s):  
Elliot A. Ludvig ◽  
Fuat Balci ◽  
Kristy M. Longpre

2006 ◽  
Vol 71 (2-3) ◽  
pp. 135-143 ◽  
Author(s):  
L.M. Lieving ◽  
S.D. Lane ◽  
D.R. Cherek ◽  
O.V. Tcheremissine

2009 ◽  
Vol 20 (7) ◽  
pp. 668-672 ◽  
Author(s):  
Erin A. McClure ◽  
Kathryn A. Saulsgiver ◽  
Clive D.L. Wynne

2009 ◽  
Vol 23 (3) ◽  
pp. 104-112 ◽  
Author(s):  
Stefan Duschek ◽  
Heike Heiss ◽  
Boriana Buechner ◽  
Rainer Schandry

Recent studies have revealed evidence for increased pain sensitivity in individuals with chronically low blood pressure. The present trial explored whether pain sensitivity can be reduced by pharmacological elevation of blood pressure. Effects of the sympathomimetic midodrine on threshold and tolerance to heat pain were examined in 52 hypotensive persons (mean blood pressure 96/61 mmHg) based on a randomized, placebo-controlled, double-blind design. Heat stimuli were applied to the forearm via a contact thermode. Confounding of drug effects on pain perception with changes in skin temperature, temperature sensitivity, and mood were statistically controlled for. Compared to placebo, higher pain threshold and tolerance, increased blood pressure, as well as reduced heart rate were observed under the sympathomimetic condition. Increases in systolic blood pressure between points of measurement correlated positively with increases in pain threshold and tolerance, and decreases in heart rate were associated with increases in pain threshold. The findings underline the causal role of hypotension in the augmented pain sensitivity related to this condition. Pain reduction as a function of heart rate decrease suggests involvement of a baroreceptor-related mechanism in the pain attrition. The increased proneness of persons with chronic hypotension toward clinical pain is discussed.


1993 ◽  
Vol 38 (2) ◽  
pp. 158-158
Author(s):  
George V. Rebec

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