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The Mediodorsal Thalamus: An Essential Partner of the Prefrontal Cortex for Cognition

Authors :
Sébastien Parnaudeau
Scott S. Bolkan
Christoph Kellendonk
Physiopathologie des Maladies du Système Nerveux Central
Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Source :
Biological Psychiatry, Biological Psychiatry, Elsevier, 2018, 83 (8), pp.648-656. ⟨10.1016/j.biopsych.2017.11.008⟩
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Deficits in cognition are a core feature of many psychiatric conditions, including schizophrenia, where the severity of such deficits is a strong predictor of long-term outcome. Impairment in cognitive domains, such as working memory and behavioral flexibility, have classically been associated with prefrontal cortex (PFC) dysfunction. However, there is increasing evidence that the PFC cannot be dissociated from its main thalamic counterpart, the mediodorsal thalamus (MD). Since the causal relationships between MD-PFC abnormalities and cognitive impairment, as well as the neuronal mechanisms underlying them, are difficult to address in humans, animal models have been employed for mechanistic insight. In this review, we discuss anatomical, behavioral, and electrophysiological findings from animal studies that provide a new understanding on how MD-PFC circuits support higher-order cognitive function. We argue that the MD may be required for amplifying and sustaining cortical representations under different behavioral conditions. These findings advance a new framework for the broader involvement of distributed thalamo-frontal circuits in cognition and point to the MD as a potential therapeutic target for improving cognitive deficits in schizophrenia and other disorders.

Details

ISSN :
00063223
Volume :
83
Database :
OpenAIRE
Journal :
Biological Psychiatry
Accession number :
edsair.doi.dedup.....0e4518cb76a93e4ec29c86e03d3a91ff
Full Text :
https://doi.org/10.1016/j.biopsych.2017.11.008