Literature DB >> 17405450

Insights into the role of dopamine receptor systems in learning and memory.

Mufida El-Ghundi1, Brian F O'Dowd, Susan R George.   

Abstract

It is well established that learning and memory are complex processes involving and recruiting different brain modulatory neurotransmitter systems. Considerable evidence points to the involvement of dopamine in various aspects of cognition, and interest has been focused on investigating the clinical relevance of dopamine systems to age-related cognitive decline and manifestations of cognitive impairment in schizophrenia, Alzheimer's disease, Parkinson's disease and other neurodegenerative diseases. In the past decade or so, in spite of the molecular cloning of the five dopamine receptor subtypes, their specific roles in brain function remained inconclusive due to the lack of completely selective ligands that could distinguish between the members of the D1-like and D2-like dopamine receptor families. One of the most important advances in the field of dopamine research has been the generation of mutant mouse models permitting evaluation of the dopaminergic system using gene targeting technologies. These mouse models represent an important approach to explore the functional roles of closely related receptor subtypes. In this review, we present and discuss evidence on the role of dopamine receptors in different aspects of learning and memory at the cellular, molecular and behavioral levels. We compare evidence using conventional pharmacological, lesion or electrophysiological studies with results from mice with targeted deletions of different subtypes of dopamine receptor genes. We particularly focus on dopamine D1 and D2 receptors in an effort to delineate their specific roles in various aspects of cognitive function. We provide strong evidence, from our own recent work as well as others, that dopamine is part of the network that plays a very important role in cognitive function, and that although multiple dopamine receptor subtypes contribute to different aspects of learning and memory, the D1 receptor seems to play a more prominent role in mediating plasticity and specific aspects of cognitive function, including spatial learning and memory processes, reversal learning, extinction learning, and incentive learning.

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Year:  2007        PMID: 17405450     DOI: 10.1515/revneuro.2007.18.1.37

Source DB:  PubMed          Journal:  Rev Neurosci        ISSN: 0334-1763            Impact factor:   4.353


  49 in total

1.  Quantitative pharmacologic MRI: mapping the cerebral blood volume response to cocaine in dopamine transporter knockout mice.

Authors:  Teodora-Adriana Perles-Barbacaru; Daniel Procissi; Andrey V Demyanenko; F Scott Hall; George R Uhl; Russell E Jacobs
Journal:  Neuroimage       Date:  2010-12-23       Impact factor: 6.556

2.  The dopamine antagonist cis-flupenthixol blocks the expression of the conditioned positive but not the negative effects of cocaine in rats.

Authors:  Jennifer M Wenzel; Zu-In Su; Kerisa Shelton; Hiram M Dominguez; Victoria A von Furstenberg; Aaron Ettenberg
Journal:  Pharmacol Biochem Behav       Date:  2013-09-05       Impact factor: 3.533

3.  Extinction of Contextual Cocaine Memories Requires Cav1.2 within D1R-Expressing Cells and Recruits Hippocampal Cav1.2-Dependent Signaling Mechanisms.

Authors:  Caitlin E Burgdorf; Kathryn C Schierberl; Anni S Lee; Delaney K Fischer; Tracey A Van Kempen; Vladimir Mudragel; Richard L Huganir; Teresa A Milner; Michael J Glass; Anjali M Rajadhyaksha
Journal:  J Neurosci       Date:  2017-10-31       Impact factor: 6.167

4.  Effects of activation and blockade of dopamine receptors on the extinction of a passive avoidance reaction in mice with a depressive-like state.

Authors:  N I Dubrovina; D V Zinov'eva
Journal:  Neurosci Behav Physiol       Date:  2009-12-11

Review 5.  The neurobiology of social attachment: A comparative approach to behavioral, neuroanatomical, and neurochemical studies.

Authors:  Kimberly A Young; Yan Liu; Zuoxin Wang
Journal:  Comp Biochem Physiol C Toxicol Pharmacol       Date:  2008-03-02       Impact factor: 3.228

6.  Selective inactivation of adenosine A(2A) receptors in striatal neurons enhances working memory and reversal learning.

Authors:  Catherine J Wei; Philipp Singer; Joana Coelho; Detlev Boison; Joram Feldon; Benjamin K Yee; Jiang-Fan Chen
Journal:  Learn Mem       Date:  2011-06-21       Impact factor: 2.460

7.  Differential effects of dopamine receptor D1-type and D2-type antagonists and phase of the estrous cycle on social learning of food preferences, feeding, and social interactions in mice.

Authors:  Elena Choleris; Amy E Clipperton-Allen; Durene G Gray; Sebastian Diaz-Gonzalez; Robert G Welsman
Journal:  Neuropsychopharmacology       Date:  2011-04-27       Impact factor: 7.853

8.  Ramelteon Improves Post-traumatic Stress Disorder-Like Behaviors Exhibited by Fatty Acid-Binding Protein 3 Null Mice.

Authors:  Yasushi Yabuki; Ibuki Takahata; Kazuya Matsuo; Yuji Owada; Kohji Fukunaga
Journal:  Mol Neurobiol       Date:  2017-05-17       Impact factor: 5.590

9.  Ventral tegmental area disruption selectively affects CA1/CA2 but not CA3 place fields during a differential reward working memory task.

Authors:  Adria K Martig; Sheri J Y Mizumori
Journal:  Hippocampus       Date:  2011-02       Impact factor: 3.899

10.  Reciprocal modulation of function between the D1 and D2 dopamine receptors and the Na+,K+-ATPase.

Authors:  Lisa A Hazelwood; R Benjamin Free; David M Cabrera; Mette Skinbjerg; David R Sibley
Journal:  J Biol Chem       Date:  2008-11-04       Impact factor: 5.157

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