Subcortical nuclei of the human ascending arousal system encode anticipated reward but do not predict subsequent memory.

IF 2.9 2区 医学 Q2 NEUROSCIENCES
Beth Lloyd, Steven Miletić, Pierre-Louis Bazin, Scott Isherwood, Desmond H Y Tse, Asta K Håberg, Birte Forstmann, Sander Nieuwenhuis
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引用次数: 0

Abstract

Subcortical nuclei of the ascending arousal system (AAS) play an important role in regulating brain and cognition. However, functional MRI (fMRI) of these nuclei in humans involves unique challenges due to their size and location deep within the brain. Here, we used ultra-high-field MRI and other methodological advances to investigate the activity of 6 subcortical nuclei during reward anticipation and memory encoding: the locus coeruleus (LC), basal forebrain, median and dorsal raphe nuclei, substantia nigra, and ventral tegmental area. Participants performed a monetary incentive delay task, which successfully induced a state of reward anticipation, and a 24-h delayed surprise memory test. Region-of-interest analyses revealed that activity in all subcortical nuclei increased in anticipation of potential rewards as opposed to neutral outcomes. In contrast, activity in none of the nuclei predicted memory performance 24 h later. These findings provide new insights into the cognitive functions that are supported by the human AAS.

人类上升唤醒系统的皮层下核编码预期的奖励,但不预测随后的记忆。
上升觉醒系统皮层下核在调节大脑和认知方面起着重要作用。然而,由于这些核在大脑深处的大小和位置,对人类核的功能性MRI (fMRI)具有独特的挑战。本研究利用超高场核磁共振等方法研究了奖赏预期和记忆编码过程中6个皮质下核的活动:蓝斑核(LC)、基底前脑、中缝核和中缝背核、黑质和腹侧被盖区。参与者完成了一项金钱激励延迟任务,该任务成功地诱导了奖励预期状态,并进行了24小时延迟惊喜记忆测试。兴趣区域分析显示,与中性结果相反,所有皮质下核的活动在预期潜在奖励时增加。相比之下,没有一个核的活动预测24小时后的记忆表现。这些发现为人类AAS支持的认知功能提供了新的见解。
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来源期刊
Cerebral cortex
Cerebral cortex 医学-神经科学
CiteScore
6.30
自引率
8.10%
发文量
510
审稿时长
2 months
期刊介绍: Cerebral Cortex publishes papers on the development, organization, plasticity, and function of the cerebral cortex, including the hippocampus. Studies with clear relevance to the cerebral cortex, such as the thalamocortical relationship or cortico-subcortical interactions, are also included. The journal is multidisciplinary and covers the large variety of modern neurobiological and neuropsychological techniques, including anatomy, biochemistry, molecular neurobiology, electrophysiology, behavior, artificial intelligence, and theoretical modeling. In addition to research articles, special features such as brief reviews, book reviews, and commentaries are included.
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