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Role of vascular endothelial growth factor in adult hippocampal neurogenesis: implications for the pathophysiology and treatment of depression
Authors:Fournier Neil M  Duman Ronald S
Affiliation:Laboratory of Molecular Psychiatry, Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06508, United States
Abstract:It is now well established that the adult brain has the capacity to generate new neurons throughout life. Although the functional significance of adult neurogenesis still remains to be established, increasing evidence has implicated compromised hippocampal neurogenesis as a possible contributor in the development of major depressive disorder. Antidepressants increase hippocampal neurogenesis and there is evidence in rodent models that the therapeutic efficacy of these agents is attributable, in part, to this neurogenic effect. As such, considerable interest has been directed at identifying molecular signals, including neurotrophic factors and related signaling pathways that are associated with antidepressant action and could operate as key modulators in the regulation of neurogenesis in the adult hippocampus. One interesting candidate is vascular endothelial growth factor (VEGF), which is known to possess strong neurogenic effects. In this review, we will discuss the involvement of VEGF signaling in the etiology and treatment of depression.
Keywords:ANP, transient amplifying neuronal progenitor cell   BDNF, brain-derived neurotrophic factor   BrdU, bromodeoxyuridine   ECS, electroconvulsive seizure   FGF-2, fibroblast growth factor   IGF-1, insulin-like growth factor   MDD, major depressive disorder   NSF, novelty suppressed feeding   QNP, quiescent neuronal precursor cell   SGZ, subgranular zone   SVZ, subventricular zone   VEGF, vascular endothelial growth factor
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