Diversity and Homogeneity in Responses of Midbrain Dopamine Neurons

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Dopamine neurons of the ventral midbrain have been found to signal a reward prediction error that can mediate positive reinforcement. Despite the demonstration of modest diversity at the cellular and molecular levels, there has been little analysis of response diversity in behaving animals. Here we examine response diversity in rhesus macaques to appetitive, aversive, and neutral stimuli having relative motivational values that were measured and controlled through a choice task. First, consistent with previous studies, we observed a continuum of response variability and an apparent absence of distinct clusters in scatter plots, suggesting a lack of statistically discrete subpopulations of neurons. Second, we found that a group of "sensitive" neurons tend to be more strongly suppressed by a variety of stimuli and to be more strongly activated by juice. Third, neurons in the "ventral tier" of substantia nigra were found to have greater suppression, and a subset of these had higher baseline firing rates and late "rebound" activation after suppression. These neurons could belong to a previously identified subgroup of dopamine neurons that express high levels of H-type cation channels but lack calbindin. Fourth, neurons further rostral exhibited greater suppression. Fifth, although we observed weak activation of some neurons by aversive stimuli, this was not associated with their aversiveness. In conclusion, we find a diversity of response properties, distributed along a continuum, within what may be a single functional population of neurons signaling reward prediction error.
Publisher
SOC NEUROSCIENCE
Issue Date
2013-03
Language
English
Article Type
Article
Keywords

VENTRAL TEGMENTAL AREA; REWARD; INHIBITION; ACTIVATION; PREDICTION; DURATION; RECEPTOR; STIMULI; PRIMATE; SIGNALS

Citation

JOURNAL OF NEUROSCIENCE, v.33, no.11, pp.4693 - 4709

ISSN
0270-6474
DOI
10.1523/JNEUROSCI.3886-12.2013
URI
http://hdl.handle.net/10203/174849
Appears in Collection
BiS-Journal Papers(저널논문)
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