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The Journal of Neuroscience, July 27, 2005, 25(30):7054-7061; doi:10.1523/JNEUROSCI.1529-05.2005
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Behavioral/Systems/Cognitive
Homer2 Is Necessary for EtOH-Induced Neuroplasticity
Karen K. Szumlinski,1
Kevin D. Lominac,1
Erik B. Oleson,1
Jennifer K. Walker,1
Ashley Mason,1
Marlin H. Dehoff,3
Matthias Klugman,4
Stephanie Cagle,1
Kristine Welt,1
Matthew During,5
Paul F. Worley,3
Lawrence D. Middaugh,1,2 and
Peter W. Kalivas1
1Department of Neurosciences and 2Department of Psychiatry and Behavioral Science and Charleston Alcohol Research Center, Medical University of South Carolina, Charleston, South Carolina 29425, 3Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, 4Interdisciplinary Center for Neurosciences, University of Heidelberg, 69123 Heidelberg, Germany, and 5Department of Molecular Medicine and Pathology, University of Auckland, Auckland 1003, New Zealand
Homer proteins are integral to the assembly of proteins regulating glutamate signaling and synaptic plasticity. Constitutive Homer2 gene deletion [knock-out (KO)] and rescue with adeno-associated viral (AAV) transfection of Homer2b was used to demonstrate the importance of Homer proteins in neuroplasticity produced by repeated ethanol (EtOH) administration. Homer2 KO mice avoided drinking high concentrations of EtOH and did not develop place preference or locomotor sensitization after repeated EtOH administration. The deficient behavioral plasticity to EtOH after Homer2 deletion was paralleled by a lack of augmentation in the rise in extracellular dopamine and glutamate elicited by repeated EtOH injections. The genotypic differences in EtOH-induced change in behavior and neurochemistry were essentially reversed by AAV-mediated transfection of Homer2b into accumbens cells including, differences in EtOH preference, locomotor sensitization, and EtOH-induced elevations in extracellular glutamate and dopamine. These data demonstrate a necessary and active role for accumbens Homer2 expression in regulating EtOH-induced behavioral and cellular neuroplasticity.
Key words: Homer proteins; EtOH; NMDA receptor; neuroplasticity; glutamate; dopamine
Received April 19, 2005;
revised May 24, 2005;
accepted June 12, 2005.
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