Biederman G B, Davey V A
Division of Life Sciences, University of Toronto, Scarborough, Ontario, Canada.
Behav Neurosci. 1993 Feb;107(1):215-7. doi: 10.1037//0735-7044.107.1.215.
Most drugs induce conditioned taste aversions and are therefore commonly supposed to produce nausea or sickness. Paradoxically, some drugs appear to lose induction capability when made to serve as a cue for a second drug that produces more severe sickness, perhaps through selective association with a hypothetical homeostatic or antisickness aftereffect of sickness. Using drug-drug pairings had made antisickness conditioning theory difficult to validate. We report here that rotation serves in lieu of a drug cue in rats. Rotation-drug pairings eliminate drug interactions and enable the sorts of parametric manipulations required to validate the theory. By postulating a common sickness mechanism to explain both taste aversion and aversion failure, the theory places the phenomenon within an adaptive evolutionary framework. Successful application could yield a direct countermeasure to severe nausea in clinical settings.
大多数药物会诱发条件性味觉厌恶,因此通常认为它们会引起恶心或不适。矛盾的是,一些药物在作为另一种会导致更严重不适的药物的提示物时,似乎会失去诱发能力,这可能是通过与一种假设的稳态或不适后效抗不适效应的选择性关联。使用药物-药物配对使得抗不适条件作用理论难以验证。我们在此报告,在大鼠中旋转可替代药物提示物。旋转-药物配对消除了药物相互作用,并能进行验证该理论所需的各种参数操作。通过假定一种共同的不适机制来解释味觉厌恶和厌恶失败,该理论将这一现象置于一个适应性进化框架内。成功应用可能会在临床环境中产生针对严重恶心的直接对策。