Associative learning and CA3-CA1 synaptic plasticity are impaired in D 1R null, Drd1a-/- mice and in hippocampal siRNA silenced Drd1a mice

Oskar Ortiz, José María Delgado-García, Isabel Espadas, Amine Bahí, Ramón Trullas, Jean Luc Dreyer, Agnès Gruart, Rosario Moratalla

Research output: Contribution to journalArticlepeer-review

125 Citations (Scopus)

Abstract

Associative learning depends on multiple cortical and subcortical structures, including striatum, hippocampus, and amygdala. Both glutamatergic and dopaminergic neurotransmitter systems have been implicated in learning and memory consolidation. While the role of glutamate is well established, the role of dopamine and its receptors in these processes is less clear. In this study, we used two models of dopamine D1 receptor (D1R, Drd1a) loss, D1R knock-out mice (Drd1a-/-) and mice with intrahippocampal injections of Drd1a-siRNA (small interfering RNA), to study the role of D1R in different models of learning, hippocampal long-term potentiation (LTP) and associated gene expression. D1R loss markedly reduced spatial learning, fear learning, and classical conditioning of the eyelid response, as well as the associated activity-dependent synaptic plasticity in the hippocampal CA1-CA3 synapse. These results provide the first experimental demonstration that D1R is required for trace eyeblink conditioning and associated changes in synaptic strength in hippocampus of behaving mice. Drd1a-siRNA mice were indistinguishable from Drd1a-/- mice in all experiments, indicating that hippocampal knockdown was as effective as global inactivation and that the observed effects are caused by loss of D1R and not by indirect developmental effects of Drd1a-/-. Finally, in vivo LTP and LTP-induced expression of Egr1 in the hippocampus were significantly reduced in Drd1a-/- and Drd1a-siRNA, indicating an important role for D1R in these processes. Our data reveal a functional relationship between acquisition of associative learning, increase in synaptic strength at the CA3-CA1 synapse, and Egr1 induction in the hippocampus by demonstrating that all three are dramatically impaired when D1R is eliminated or reduced.

Original languageEnglish
Pages (from-to)12288-12300
Number of pages13
JournalJournal of Neuroscience
Volume30
Issue number37
DOIs
Publication statusPublished - Sept 15 2010
Externally publishedYes

ASJC Scopus subject areas

  • General Medicine

Fingerprint

Dive into the research topics of 'Associative learning and CA3-CA1 synaptic plasticity are impaired in D 1R null, Drd1a-/- mice and in hippocampal siRNA silenced Drd1a mice'. Together they form a unique fingerprint.

Cite this