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Enhanced incentive motivation in obesity-prone rats is mediated by NAc core CP-AMPARs

机译:NAc核心CP-AMPAR介导肥胖易发大鼠的增强动机

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摘要

Studies in humans suggest that stronger incentive motivational responses to Pavlovian food cues may drive over-consumption leading to and maintaining obesity, particularly in susceptible individuals. However, whether this enhanced incentive motivation emerges as a consequence of obesity or rather precedes obesity is unknown. Moreover, while human imaging studies have provided important information about differences in striatal responsiveness between susceptible and non-susceptible individuals, the neural mechanisms mediating these behavioral differences are unknown. The Nucleus Accumbens (NAc) mediates cue-triggered reward seeking and activity in the NAc is enhanced in obesity-susceptible populations. Therefore here, we used selectively-bred obesity-prone and obesity-resistant rats to examine intrinsic differences in incentive motivation, and the role of NAc AMPARs in the expression of these behaviors prior to obesity. We found that obesity-prone rats exhibit robust cue-triggered food-seeking (Pavlovian-to-instrumental transfer, PIT). Using intra-NAc infusion of AMPAR antagonists, we show that this behavior is selectively mediated by CP-AMPARs in the NAc core. Additionally, biochemical data suggest that this is due in part to experience-induced increases in CP-AMPAR surface expression in the NAc of obesity-prone rats. In contrast, in obesity-resistant rats PIT was weak and unreliable and training did not increase NAc AMPAR surface expression. Collectively, these data show that food cues acquire greater incentive motivational control in obesity-susceptible populations prior to the development of obesity. This provides support to the idea that enhanced intrinsic incentive motivation may be a contributing factor, rather than a consequence of obesity. In addition, these data demonstrate a novel role for experience-induced up-regulation of NAc CP-AMPARs in PIT, pointing to potential mechanistic parallels between the processes leading to addiction and to obesity.
机译:对人体的研究表明,对巴甫洛夫饮食线索的更强激励动机反应可能会导致过度消费,导致并维持肥胖,特别是在易感人群中。然而,这种增强的激励动机是由于肥胖而出现还是先于肥胖而未知。此外,尽管人体成像研究已经提供了有关易感个体与非易感个体之间纹状体反应性差异的重要信息,但介导这些行为差异的神经机制尚不清楚。伏隔核(NAc)介导线索触发的奖励寻求,并且在肥胖易感人群中NAc中的活性增强。因此,在这里,我们使用选择性饲养的易发肥胖和抗肥胖的大鼠研究了诱因动机的内在差异,以及NAc AMPAR在肥胖之前这些行为表达中的作用。我们发现,容易肥胖的大鼠表现出强大的提示触发的食物寻找(巴甫洛夫式到器械式转换,PIT)。使用AMPAR拮抗剂的NAc内输注,我们表明这种行为是由NAc核心中的CP-AMPAR选择性介导的。此外,生化数据表明,这部分归因于肥胖易发大鼠NAc中经验诱导的CP-AMPAR表面表达增加。相反,在抗肥胖的大鼠中PIT较弱且不可靠,并且训练并未增加NAc AMPAR表面表达。总的来说,这些数据表明,在肥胖症发展之前,对肥胖易感人群的食物提示获得了更大的激励动机控制。这为以下观点提供了支持:增强的内在动机可能是促成因素,而不是肥胖的结果。此外,这些数据证明了PIT中NAc CP-AMPAR的经验诱导上调具有新的作用,指出了导致成瘾和肥胖的过程之间可能存在的机械相似性。

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