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Neurosci Lett ; 440(3): 314-8, 2008 Aug 08.
Article in English | MEDLINE | ID: mdl-18565655

ABSTRACT

Exposure to an enriched environment (EE) enhances neurogenesis and regulates emotionality. Previous reports have revealed that the rate of neurogenesis can be influenced by various environmental, endocrine, and pharmacologic stimuli. Chronic pain is a debilitating disease state characterized by complex alterations in both peripheral and central nociceptive pathways. In the present study, we evaluated the effect of chronic pain on environmental enrichment-induced hippocampal neurogenesis. Nerve-ligated mice were housed either in a standard environment or in the EE for 4 weeks. EE increased the immunoreactivity for doublecortin (DCX), a marker for immature neuron-positive cells, in the dentate gyrus (DG). Furthermore, the number of NeuroD (a neurogenic basic helix-loop-helix factor)-positive cells, in the DG was clearly increased by EE. Under these conditions, chronic pain suppressed enriched environment-mediated induction of both DCX- and NeuroD-labeled cells. These results suggest that chronic pain has stress-like damaging modulatory effects on hippocampal neurogenesis.


Subject(s)
Cell Proliferation , Environment , Neurons/physiology , Sciatica/pathology , Sciatica/therapy , Animals , Basic Helix-Loop-Helix Transcription Factors/metabolism , Behavior, Animal , Cell Count/methods , Disease Models, Animal , Doublecortin Domain Proteins , Doublecortin Protein , Hippocampus/pathology , Hippocampus/physiopathology , Male , Mice , Mice, Inbred C57BL , Microtubule-Associated Proteins/metabolism , Nerve Tissue Proteins/metabolism , Neuropeptides/metabolism , Pain Measurement/methods , Reaction Time/physiology , Time Factors
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