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Impacts of inter-trial interval duration on a computational model of sign-tracking vs. goal-tracking behaviour

机译:试用间隔持续时间对签名跟踪计算模型的影响与目标跟踪行为的计算模型

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摘要

In the context of Pavlovian conditioning, two types of behaviour may emerge within the population (Flagel et al. Nature, 469(7328): 53-57, 2011). Animals may choose to engage either with the conditioned stimulus (CS), a behaviour known as sign-tracking (ST) which is sensitive to dopamine inhibition for its acquisition, or with the food cup in which the reward or unconditioned stimulus (US) will eventually be delivered, a behaviour known as goal-tracking (GT) which is dependent on dopamine for its expression only. Previous work by Lesaint et al. (PLoS Comput Biol, 10(2), 2014) offered a computational explanation for these phenomena and led to the prediction that varying the duration of the inter-trial interval (ITI) would change the relative ST-GT proportion in the population as well as phasic dopamine responses. A recent study verified this prediction, but also found a rich variance of ST and GT behaviours within the trial which goes beyond the original computational model. In this paper, we provide a computational perspective on these novel results.
机译:在Pavlovian调理的背景下,人口中可能出现两种类型的行为(Plagel等人。大自然,469(7328):53-57,2011)。动物可以选择与调节刺激(CS)一起接合,称为签署跟踪(ST)的行为,这些行为对其采集的多巴胺抑制敏感,或者与奖励或无条件刺激(美国)威胁的食物杯最终被交付,一种称为目标跟踪(GT)的行为,其依赖于多巴胺仅为其表达式。以前的工作由LeSaint等。 (PLO计算BIOL,10(2),2014)为这些现象提供了计算说明,并导致了改变试验间隔的持续时间(ITI)的预测也会改变人口中的相对ST-GT比例作为相序的多巴胺反应。最近的一项研究验证了这一预测,还发现了在试验中的ST和GT行为的丰富方案,其超出了原始计算模型。在本文中,我们提供了对这些新的结果的计算视角。

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