1976
DOI: 10.3758/bf03214426
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An opponent-process interpretation of postshock bursts in appetitive responding

Abstract: While eight food-deprived rats pressed a lever for. food during daily l-h sessions, four CS-Shock2 trials were presented. Trials were preceded by either a Shock, of .25, .50, .75 rnA or no Shock.. It was found that the rate of appetitive responding during the CS was greater on Shock,-eSShock, trials relative to CS-Shock2 trials. The data indicate that the phenomenon of postshock bursts in responding can occur in the absence of a signal for safety after shock. The results conform to the predictions of the oppon… Show more

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Cited by 8 publications
(7 citation statements)
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“…Post shock suppression diminishes as fear discrimination continues, and is mostly confined to the first two seconds immediately following shock offset. Consistent with a prior report 19 , foot shock facilitation of reward seeking emerges during later sessions. Facilitation is observed when foot shock is fully predicted on danger trials and is surprisingly delivered on uncertainty trials.…”
Section: Discussionsupporting
confidence: 89%
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“…Post shock suppression diminishes as fear discrimination continues, and is mostly confined to the first two seconds immediately following shock offset. Consistent with a prior report 19 , foot shock facilitation of reward seeking emerges during later sessions. Facilitation is observed when foot shock is fully predicted on danger trials and is surprisingly delivered on uncertainty trials.…”
Section: Discussionsupporting
confidence: 89%
“…Alternatively, the opponent process theory of acquired motivation can also provide an account of post shock increases in appetitive behaviour 19,[43][44][45] . In opponent process theory, presentation of an aversive stimulus elicits a negative hedonic 'a process' and is followed by an opponent positive 'b process'.…”
Section: Discussionmentioning
confidence: 99%
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“…We have previously reported data showing that postshock inhibition of fear did indeed increase as a function of trials (LaBarbera & Caul, 1976). However, for reasons that are not clear, this effect was not noted in the present study where subjects failed to exhibit less distress during CS z as a function of the number of CSt-shock trials during Phase 1.…”
Section: L----jcontrasting
confidence: 52%