Associative regulation of Pavlovian fear conditioning: unconditional stimulus intensity, incentive shifts, and latent inhibition.

Pub Date : 1992-10-01 DOI:10.1037//0097-7403.18.4.400
S L Young, M S Fanselow
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引用次数: 99

Abstract

Conditional stimuli (CS) associated with painful unconditional stimuli (US) produce a naloxone-reversible analgesia. The analgesia serves as a negative-feedback regulation of fear conditioning that can account for the impact of US intensity and CS predictiveness on Pavlovian fear conditioning. In Experiment 1 training under naloxone produced learning curves that approached the same high asymptote despite US intensity. Shifting drug treatment during acquisition had effects that paralleled US intensity shifts. In Experiment 3 naloxone reversed Hall-Pearce (1979) negative transfer using a contextual CS, indicating that conditional analgesia acquired during the CS-weak-footshock phase retards acquisition in the CS-strong-footshock phase. Experiment 5 used a tone CS in both a latent-inhibition and a negative-transfer procedure. Only negative transfer was blocked by naloxone. Therefore, negative transfer but not latent inhibition is mediated by a reduction of US processing.

巴甫洛夫恐惧条件反射的联想调节:无条件刺激强度、激励转移和潜在抑制。
条件刺激(CS)与疼痛的无条件刺激(US)产生纳洛酮可逆镇痛。镇痛作为恐惧条件反射的负反馈调节,可以解释US强度和CS预测对巴甫洛夫恐惧条件反射的影响。在实验1中,纳洛酮训练产生的学习曲线接近相同的高渐近线,尽管美国强度。在习得过程中,药物治疗的转移与美国药物强度的转移有相似的效果。在实验3中,纳洛酮使用情境性脑电逆转Hall-Pearce(1979)负迁移,表明在CS-弱足震阶段获得的条件性镇痛阻滞了CS-强足震阶段的习得。实验5在潜在抑制和负转移过程中都使用了音调CS。只有负转移被纳洛酮阻断。因此,负迁移而非潜伏抑制是由US加工的减少介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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