4.3 Review

Roles of centromedian parafascicular nuclei of thalamus and cholinergic interneurons in the dorsal striatum in associative learning of environmental events

Journal

JOURNAL OF NEURAL TRANSMISSION
Volume 125, Issue 3, Pages 501-513

Publisher

SPRINGER WIEN
DOI: 10.1007/s00702-017-1713-z

Keywords

Thalamostriatal projection; CM-Pf; Dorsal striatum; Cholinergic interneurons; Surprise; Non-human primates

Funding

  1. Development of Biomarker Candidates for Social Behavior carried out under the Strategic Research Program for Brain Sciences from the Ministry of Education, Culture, Sports, Science and Technology of Japan [23120010, 26290009, 15K14320, 20700293, 24700425]
  2. National Institutes for Health [R01 NS025529]
  3. Grants-in-Aid for Scientific Research [15H05374, 15K14320, 16K01955, 24700425, 20700293, 15H05917, 26282221, 26290009] Funding Source: KAKEN

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The thalamus provides a massive input to the striatum, but despite accumulating evidence, the functions of this system remain unclear. It is known, however, that the centromedian (CM) and parafascicular (Pf) nuclei of the thalamus can strongly influence particular striatal neuron subtypes, notably including the cholinergic interneurons of the striatum (CINs), key regulators of striatal function. Here, we highlight the thalamostriatal system through the CM-Pf to striatal CINs. We consider how, by virtue of the direct synaptic connections of the CM and PF, their neural activity contributes to the activity of CINs and striatal projection neurons (SPNs). CM-Pf neurons are strongly activated at sudden changes in behavioral context, such as switches in action-outcome contingency or sequence of behavioral requirements, suggesting that their activity may represent change of context operationalized as associability. Striatal CINs, on the other hand, acquire and loose responses to external events associated with particular contexts. In light of this physiological evidence, we propose a hypothesis of the CM-Pf-CINs system, suggesting that it augments associative learning by generating an associability signal and promotes reinforcement learning guided by reward prediction error signals from dopamine-containing neurons. We discuss neuronal circuit and synaptic organizations based on in vivo/in vitro studies that we suppose to underlie our hypothesis. Possible implications of CM-Pf-CINs dysfunction (or degeneration) in brain diseases are also discussed by focusing on Parkinson's disease.

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