Modulation of Anxiety-Like Behavior and Morphine Dependence in CREB-Deficient Mice

• DOI: 10.1038/sj.npp.1300416
• Publication Date: 2004-03-18T10:51:55Z
• Authors: Olga Valverde; Theo Mantamadiotis; María Torrecilla; Luisa Ugedo; Joseba Pineda; Susanne Bleckmann; Peter Gass; Oliver Kretz; Jennifer M Mitchell; Günther Schütz; Rafael Maldonado
• Keywords: Mice, Knockout; 0301 basic medicine; Analysis of Variance; Time Factors; Behavior, Animal; Spatial Behavior; Anxiety; Motor Activity; Immunohistochemistry; 3. Good health; Mice; 03 medical and health sciences; Exploratory Behavior; Reaction Time; Animals; Conditioning, Operant; Protein Isoforms; Locus Coeruleus; Cyclic AMP Response Element-Binding Protein; Maze Learning; Morphine Dependence

The transcription factor cAMP-responsive element binding protein (CREB) has been shown to regulate different physiological responses including drug addiction and emotional behavior. Molecular changes including adaptive modifications of the transcription factor CREB are produced during drug dependence in many regions of the brain, including the locus coeruleus (LC), but the molecular mechanisms involving CREB within these regions have remained controversial. To further investigate the involvement of CREB in emotional behavior, drug reward and opioid physical dependence, we used two independently generated CREB-deficient mice. We employed the Cre/loxP system to generate mice with a conditional CREB mutation restricted to the nervous system, where all CREB isoforms are lacking in the brain (Crebl(NesCre)). A genetically defined cohort of the previously described hypomorphic Crebl(alphadelta) mice, in which the two major transcriptionally active isoforms (alpha and delta) are disrupted throughout the organism, were also used. First, we investigated the responses to stress of the CREB-deficient mice in several paradigms, and we found an increased anxiogenic-like response in the both Creb1 mutant mice in different behavioral models. We investigated the rewarding properties of drugs of abuse (cocaine and morphine) and natural reward (food) using the conditioned place-preference paradigm. No modification of motivational responses of morphine, cocaine, or food was observed in mutant mice. Finally, we evaluated opioid dependence by measuring the behavioral expression of morphine withdrawal and electrophysiological recordings of LC neurons. We showed an important attenuation of the behavioral expression of abstinence and a decrease in the hyperactivity of LC neurons in both Creb1 mutant mice. Our results emphasize the selective role played by neuronal CREB in emotional-like behavior and the somatic expression morphine withdrawal, without participating in the rewarding properties induced by morphine and cocaine.