Synchronicity: The Role of Midbrain Dopamine in Whole-Brain Coordination

被引:17
作者
Beeler, Jeff A. [1 ,2 ]
Dreyer, Jakob Kisbye [3 ]
机构
[1] CUNY, Queens Coll, New York, NY 11367 USA
[2] CUNY, Grad Ctr, New York, NY 11367 USA
[3] Univ Copenhagen, Dept Neurosci & Pharmacol, DK-2200 Copenhagen, Denmark
基金
美国国家卫生研究院;
关键词
coherence; dopamine; phasic dopamine; striatum; synchronous dopamine activity; NUCLEUS-ACCUMBENS NEURONS; MONKEY CAUDATE NEURONS; BASAL GANGLIA; FUNCTIONAL-PROPERTIES; PREDICTION ERRORS; SUBSTANTIA-NIGRA; REWARD; MODEL; STRIATUM; VTA;
D O I
10.1523/ENEURO.0345-18.2019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页数:17
相关论文
共 140 条
[1]   INTERCELLULAR COMMUNICATION IN THE BRAIN - WIRING VERSUS VOLUME TRANSMISSION [J].
AGNATI, LF ;
ZOLI, M ;
STROMBERG, I ;
FUXE, K .
NEUROSCIENCE, 1995, 69 (03) :711-726
[2]   BASAL GANGLIA THALAMOCORTICAL CIRCUITS - THEIR ROLE IN CONTROL OF MOVEMENTS [J].
ALEXANDER, GE .
JOURNAL OF CLINICAL NEUROPHYSIOLOGY, 1994, 11 (04) :420-431
[3]   Space, time and dopamine [J].
Arbuthnott, Gordon W. ;
Wickens, Jeff .
TRENDS IN NEUROSCIENCES, 2007, 30 (02) :62-69
[4]   Information processing, dimensionality reduction and reinforcement learning in the basal ganglia [J].
Bar-Gad, I ;
Morris, G ;
Bergman, H .
PROGRESS IN NEUROBIOLOGY, 2003, 71 (06) :439-473
[5]  
Barto A. G., 1995, Models of information processing in the basal ganglia, P215, DOI [10.7551/mitpress/4708.003.0018, DOI 10.7551/MITPRESS/4708.003.0018]
[6]   To Do or Not to Do: Dopamine, Affordability and the Economics of Opportunity [J].
Beeler, Jeff A. ;
Mourra, Devry .
FRONTIERS IN INTEGRATIVE NEUROSCIENCE, 2018, 12
[7]   Circuit Architecture of VTA Dopamine Neurons Revealed by Systematic Input-Output Mapping [J].
Beier, Kevin T. ;
Steinberg, Elizabeth E. ;
DeLoach, Katherine E. ;
Xie, Stanley ;
Miyamichi, Kazunari ;
Schwarz, Lindsay ;
Gao, Xiaojing J. ;
Kremer, Eric J. ;
Malenka, Robert C. ;
Luo, Liqun .
CELL, 2015, 162 (03) :622-634
[8]   What does dopamine mean? [J].
Berke, Joshua D. .
NATURE NEUROSCIENCE, 2018, 21 (06) :787-793
[9]   The debate over dopamine's role in reward: the case for incentive salience [J].
Berridge, Kent C. .
PSYCHOPHARMACOLOGY, 2007, 191 (03) :391-431
[10]   Organization of Valence-Encoding and Projection-Defined Neurons in the Basolateral Amygdala [J].
Beyeler, Anna ;
Chang, Chia-Jung ;
Silvestre, Margaux ;
Leveque, Clementine ;
Namburi, Praneeth ;
Wildes, Craig P. ;
Tye, Kay M. .
CELL REPORTS, 2018, 22 (04) :905-918