Queens College and the Graduate Center, City University New York, New York 11367, NY
Department of Neuroscience and Pharmacology, University of Copenhagen, Copenhagen 2200, Denmark.
eNeuro. 2019 May 3;6(2). doi: 10.1523/ENEURO.0345-18.2019. Print 2019 Mar/Apr.
Midbrain dopamine seems to play an outsized role in motivated behavior and learning. Widely associated with mediating reward-related behavior, decision making, and learning, dopamine continues to generate controversies in the field. While many studies and theories focus on what dopamine cells encode, the question of how the midbrain derives the information it encodes is poorly understood and comparatively less addressed. Recent anatomical studies suggest greater diversity and complexity of afferent inputs than previously appreciated, requiring rethinking of prior models. Here, we elaborate a hypothesis that construes midbrain dopamine as implementing a Bayesian selector in which individual dopamine cells sample afferent activity across distributed brain substrates, comprising evidence to be evaluated on the extent to which stimuli in the on-going sensorimotor stream organizes distributed, parallel processing, reflecting implicit value. To effectively generate a temporally resolved phasic signal, a population of dopamine cells must exhibit synchronous activity. We argue that synchronous activity across a population of dopamine cells signals consensus across distributed afferent substrates, invigorating responding to recognized opportunities and facilitating further learning. In framing our hypothesis, we shift from the question of how value is computed to the broader question of how the brain achieves coordination across distributed, parallel processing. We posit the midbrain is part of an "axis of agency" in which the prefrontal cortex (PFC), basal ganglia (BGS), and midbrain form an axis mediating control, coordination, and consensus, respectively.
中脑多巴胺似乎在动机行为和学习中起着重要作用。它与介导与奖励相关的行为、决策和学习广泛相关,在该领域继续引发争议。虽然许多研究和理论都集中在多巴胺细胞编码什么,但中脑如何获取其编码的信息的问题理解甚少,相对较少涉及。最近的解剖学研究表明,传入输入的多样性和复杂性超出了先前的认识,需要重新思考先前的模型。在这里,我们提出了一个假设,即中脑多巴胺作为一种贝叶斯选择器来实施,其中单个多巴胺细胞在分布式大脑基质中对传入活动进行采样,包括基于刺激在进行中的感觉运动流中的组织程度来评估证据的价值分布式、并行处理,反映隐性价值。为了有效地生成时间分辨的相位信号,一群多巴胺细胞必须表现出同步活动。我们认为,一群多巴胺细胞的同步活动标志着分布在不同传入基质中的共识,激发对公认机会的反应,并促进进一步学习。在构建我们的假设时,我们从价值如何被计算的问题转移到大脑如何在分布式、并行处理中实现协调的更广泛问题。我们假设中脑是“代理轴”的一部分,其中前额叶皮层(PFC)、基底神经节(BGS)和中脑分别形成介导控制、协调和共识的轴。