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Dorsolateral neostriatum contribution to incentive salience: Opioid or dopamine stimulation makes one reward cue more motivationally attractive than another

机译:背外侧新纹状体对激励显着性的贡献:阿片样物质或多巴胺刺激使一种奖励提示比另一种更具激励性

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摘要

Pavlovian cues for rewards can become attractive incentives: approached and ‘wanted’ as the rewards themselves. The motivational attractiveness of a previously learned cue is not fixed, but can be dynamically amplified during re-encounter by simultaneous activation of brain limbic circuitry. Here we report that opioid or dopamine microinjections in the dorsolateral quadrant of the neostriatum (DLS) of rats selectively amplify attraction toward a previously learned Pavlovian cue in an individualized fashion, at the expense of a competing cue. In an autoshaping (sign-tracking vs goal-tracking) paradigm, microinjection of the mu opioid receptor agonist (DAMGO) or dopamine indirect agonist (amphetamine) in DLS of sign-tracker individuals selectively enhanced their sign-tracking attraction toward the reward-predictive lever cue. By contrast, DAMGO or amphetamine in DLS of goal-trackers selectively enhanced prepotent attraction toward the reward-proximal cue of sucrose dish. Amphetamine also enhanced goal-tracking in some sign-tracker individuals (if they ever defected to the dish even once). That DLS enhancement of cue attraction was due to stronger motivation, not stronger habits was suggested by: 1) sign-trackers flexibly followed their cue to a new location when the lever was suddenly moved after DLS DAMGO microinjection, and 2) DAMGO in DLS also made sign-trackers work harder on a new instrumental nose-poke response required to earn presentations of their Pavlovian lever cue (instrumental conditioned reinforcement). Altogether, our results suggest that DLS circuitry can enhance the incentive salience of a Pavlovian reward cue, selectively making that cue a stronger motivational magnet.
机译:巴甫洛夫式的奖励线索可以成为有吸引力的激励措施:奖励本身就可以接近并“想要”。先前学习的提示的动机吸引力不是固定的,而是可以在重新遇到时通过同时激活脑边缘电路来动态放大。在这里,我们报告大鼠新纹状体(DLS)背外侧象限中的阿片样物质或多巴胺显微注射选择性地以个体化方式扩大了对先前学习的巴甫洛夫病线索的吸引力,但以竞争性线索为代价。在自动塑造(符号追踪与目标追踪)范式中,微注射阿片受体激动剂(DAMGO)或多巴胺间接激动剂(安非他明)对符号追踪者的DLS有选择性地增强了其对奖励预测的符号追踪吸引力。操纵杆提示。相比之下,目标追踪器DLS中的DAMGO或苯丙胺选择性地增强了对蔗糖碟的奖励近端提示的吸引力。苯丙胺还增强了某些体征追踪者的目标追踪能力(如果他们曾经甚至一次叛逃到菜中)。 DLS增强提示吸引力是由于动机更强,而不是更强的习惯,这是由以下方面提出的:1)当DLS DAMGO显微注射后,操纵杆突然移动时,符号跟踪器会灵活地将其提示移动到新位置,以及2)DLS中的DAMGO也使手势跟踪器在进行新的器鼻-响应时更加努力,以获取他们的巴甫洛夫杠杆提示(仪器条件增强)的演示。总之,我们的结果表明DLS电路可以增强巴甫洛夫奖赏线索的激励显着性,从而有选择地使该线索成为更强大的激励磁铁。

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