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| Research article summary (published 29 Nov 2008): |
Corticosterone regulates pERK1/2 map kinase in a chronic depression model.
Full Abstract
Neurotransmitter- or neurotrophin-regulated intracellular signaling in the hippocampus is hypothesized to contribute to depression and antidepressant (ADT) efficacy. Extracellular signal-regulated kinase 1/2 (ERK1/2) is downstream of several receptor types and regulates transcriptional activity of many targets; ERK1/2 may thereby influence mood and affect. Using a novel, ADT-sensitive depression model in mice, we show that prior corticosterone exposure decreases motivated behavior, sucrose consumption, and pERK1/2 in the dentate gyrus, but not in CA1/CA3. Notably, prefrontal cortical targets were also regulated. Our data suggest ADTs restore hippocampal pERK1/2 after stress-related insult, and potentially reveal a novel role for prefrontal neurotrophins in depressive-like symptomology.
Author information
Author/s: Gourley, Shannon L (SL); Wu, Florence J (FJ); Taylor, Jane R (JR);
Affiliation: Interdepartmental Neuroscience Program, Yale University, New Haven, Connecticut, USA.
Grants: MH025642 (Agency:NIMH NIH HHS)
Journal and publication information
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal: Annals of the New York Academy of Sciences (Ann N Y Acad Sci), published in United States. (Language: eng)
Reference: 2008-Dec; vol 1148 (issue ) : pp 509-14
Dates: Created 2009/01/05; Completed 2009/01/23;
PMID: 19120149, status: MEDLINE (last retrieval date: 2/18/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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