
AbstractThe transcription factor CREB has been implicated in signalling pathways relevant for pathogenesis and therapy of depression. CREB is upregulated and activated in the hippocampus by chronic antidepressant treatment, similarly as neurogenesis. Surprisingly, a recent study using CREB‐deficient mice also demonstrates an upregulation of neurogenesis correlating with an antidepressant behavioral phenotype.1 Interestingly, CREB‐deficient mice show a rapid behavioral response to antidepressants, while wild‐type mice do not. This minireview tries to reconcile these new findings with established concepts on CREB, neurogenesis and depression. It also outlines some crucial experiments and lines of future research that could clarify some of the pending questions. BioEssays 29:957–961, 2007. © 2007 Wiley Periodicals, Inc.
Neurons, ELEMENT-BINDING PROTEIN ; ASSESSING ANTIDEPRESSANT ACTIVITY ; CAMP RESPONSE ; HIPPOCAMPAL NEUROGENESIS ; MAJOR DEPRESSION ; MESSENGER-RNA ; UP-REGULATION ; DSM-IV ; EXPRESSION ; STRESS, Depressive Disorder, Models, Neurological, Desipramine, Hippocampus, Antidepressive Agents, Mice, Mutant Strains, Up-Regulation, Mice, Hindlimb Suspension, Animals, Cyclic AMP Response Element-Binding Protein, Swimming, Forecasting, Signal Transduction
Neurons, ELEMENT-BINDING PROTEIN ; ASSESSING ANTIDEPRESSANT ACTIVITY ; CAMP RESPONSE ; HIPPOCAMPAL NEUROGENESIS ; MAJOR DEPRESSION ; MESSENGER-RNA ; UP-REGULATION ; DSM-IV ; EXPRESSION ; STRESS, Depressive Disorder, Models, Neurological, Desipramine, Hippocampus, Antidepressive Agents, Mice, Mutant Strains, Up-Regulation, Mice, Hindlimb Suspension, Animals, Cyclic AMP Response Element-Binding Protein, Swimming, Forecasting, Signal Transduction
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