Antidepressant- and Anxiolytic-like Effects of the Phosphodiesterase-4 Inhibitor Rolipram on Behavior Depend on Cyclic AMP Response Element Binding Protein-Mediated Neurogenesis in the Hippocampus

被引:178
作者
Li, Yun-Feng [1 ,2 ]
Huang, Ying [1 ,3 ]
Amsdell, Simon L. [1 ,2 ]
Xiao, Lan [1 ,3 ]
O'Donnell, James M. [1 ,3 ]
Zhang, Han-Ting [1 ,2 ]
机构
[1] W Virginia Univ, Hlth Sci Ctr, Dept Behav Med & Psychiat, Morgantown, WV 26506 USA
[2] W Virginia Univ, Hlth Sci Ctr, Dept Physiol & Pharmacol, Morgantown, WV 26506 USA
[3] W Virginia Univ, Hlth Sci Ctr, Dept Neurobiol & Anat, Morgantown, WV 26506 USA
关键词
phosphodiesterase-4; neurogenesis; CREB; hippocampus; behavior; mice; GENERALIZED ANXIETY DISORDER; CENTRAL-NERVOUS-SYSTEM; ADULT-RAT HIPPOCAMPUS; ELEVATED PLUS-MAZE; NEURAL STEM-CELLS; RADIAL-ARM MAZE; CAMP-RESPONSE; DENTATE GYRUS; LEARNED HELPLESSNESS; MAJOR DEPRESSION;
D O I
10.1038/npp.2009.66
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Inhibition of phosphodiesterase-4 (PDE4), an enzyme that catalyzes the hydrolysis of cyclic AMP (cAMP), increases phosphorylation of the cAMP response element binding protein (pCREB) and hippocampal neurogenesis, and produces antidepressant-like effects on behavior; however, causal links among these actions have not been established. In this study, chronic administration of rolipram (0.31-1.25 mg/kg, 16-23 days) produced antidepressant- and anxiolytic-like effects on behavior in mice. It also increased cAMP and pCREB levels in the hippocampus and prefrontal cortex, but increased Sox2, a marker for mitotic progenitor cells, only in the hippocampus. Chronic rolipram treatment also increased hippocampal neurogenesis, as evidenced by increased bromodeoxyuridine (BrdU)-positive cells in the hippocampal dentate gyrus. Methylazoxymethanol (MAM), which is toxic to proliferating cells, reversed rolipram-induced increases in BrdU-positive cells and pCREB in the hippocampus and partially blocked its behavioral effects. Approximately 84% of BrdU-positive cells became newborn neurons, 93% of which co-expressed pCREB; these proportions were not altered by rolipram or MAM, either alone or in combination. Finally, 3 weeks after the end of the MAM treatment, when neurogenesis was no longer inhibited, rolipram again increased hippocampal pCREB and its antidepressant-and anxiolytic-like effects were restored. Overall, these results suggest that rolipram produces its effects on behavior in a manner that at least partially depends on its neurogenic action in the hippocampus, targeting mitotic progenitor cells rather than newborn or mature neurons; cAMP/CREB signaling in hippocampal newborn neurons is critical for neurogenesis and contributes to the behavioral effects of rolipram. Neuropsychopharmacology (2009) 34, 2404-2419; doi: 10.1038/npp.2009.66; published online 10 June 2009
引用
收藏
页码:2404 / 2419
页数:16
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