Chronic Unpredictable Stress Decreases Cell Proliferation in the Cerebral Cortex of the Adult Rat
One of the most consistent morphologic findings in postmortem studies of brain tissue from depressed patients is a decrease in the number of glia in the prefrontal cortex. However, little is known about the mechanisms that contribute to this decrease in cell number. To address this question, we subj...
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Published in | Biological psychiatry (1969) Vol. 62; no. 5; pp. 496 - 504 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.09.2007
Elsevier Science |
Subjects | |
Online Access | Get full text |
ISSN | 0006-3223 1873-2402 |
DOI | 10.1016/j.biopsych.2007.02.006 |
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Abstract | One of the most consistent morphologic findings in postmortem studies of brain tissue from depressed patients is a decrease in the number of glia in the prefrontal cortex. However, little is known about the mechanisms that contribute to this decrease in cell number.
To address this question, we subjected adult rats to chronic stress, a vulnerability factor for depression, and measured cell proliferation as a potential cellular mechanism that could underlie glial reduction in depression.
We found that exposure to chronic unpredictable stress (CUS) for 15 days significantly decreased cell proliferation in neocortex by approximately 35%. This effect was dependent on the duration, intensity and type of stress, and was region-specific. Analysis of cell phenotype demonstrated that there was a decrease in the number of oligodendrocytes and endothelial cells. Finally, using a CUS paradigm that allows for analysis of anhedonia, we found that chronic antidepressant administration reversed the decrease in cortical cell proliferation, as well as the deficit in sucrose preference.
These findings are consistent with the possibility that decreased cell proliferation could contribute to reductions in glia in prefrontal cortex of depressed subjects and further elucidate the cellular actions of stress and antidepressants. |
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AbstractList | One of the most consistent morphologic findings in postmortem studies of brain tissue from depressed patients is a decrease in the number of glia in the prefrontal cortex. However, little is known about the mechanisms that contribute to this decrease in cell number.
To address this question, we subjected adult rats to chronic stress, a vulnerability factor for depression, and measured cell proliferation as a potential cellular mechanism that could underlie glial reduction in depression.
We found that exposure to chronic unpredictable stress (CUS) for 15 days significantly decreased cell proliferation in neocortex by approximately 35%. This effect was dependent on the duration, intensity and type of stress, and was region-specific. Analysis of cell phenotype demonstrated that there was a decrease in the number of oligodendrocytes and endothelial cells. Finally, using a CUS paradigm that allows for analysis of anhedonia, we found that chronic antidepressant administration reversed the decrease in cortical cell proliferation, as well as the deficit in sucrose preference.
These findings are consistent with the possibility that decreased cell proliferation could contribute to reductions in glia in prefrontal cortex of depressed subjects and further elucidate the cellular actions of stress and antidepressants. Background One of the most consistent morphologic findings in postmortem studies of brain tissue from depressed patients is a decrease in the number of glia in the prefrontal cortex. However, little is known about the mechanisms that contribute to this decrease in cell number. Methods To address this question, we subjected adult rats to chronic stress, a vulnerability factor for depression, and measured cell proliferation as a potential cellular mechanism that could underlie glial reduction in depression. Results We found that exposure to chronic unpredictable stress (CUS) for 15 days significantly decreased cell proliferation in neocortex by approximately 35%. This effect was dependent on the duration, intensity and type of stress, and was region-specific. Analysis of cell phenotype demonstrated that there was a decrease in the number of oligodendrocytes and endothelial cells. Finally, using a CUS paradigm that allows for analysis of anhedonia, we found that chronic antidepressant administration reversed the decrease in cortical cell proliferation, as well as the deficit in sucrose preference. Conclusion These findings are consistent with the possibility that decreased cell proliferation could contribute to reductions in glia in prefrontal cortex of depressed subjects and further elucidate the cellular actions of stress and antidepressants. One of the most consistent morphologic findings in postmortem studies of brain tissue from depressed patients is a decrease in the number of glia in the prefrontal cortex. However, little is known about the mechanisms that contribute to this decrease in cell number.BACKGROUNDOne of the most consistent morphologic findings in postmortem studies of brain tissue from depressed patients is a decrease in the number of glia in the prefrontal cortex. However, little is known about the mechanisms that contribute to this decrease in cell number.To address this question, we subjected adult rats to chronic stress, a vulnerability factor for depression, and measured cell proliferation as a potential cellular mechanism that could underlie glial reduction in depression.METHODSTo address this question, we subjected adult rats to chronic stress, a vulnerability factor for depression, and measured cell proliferation as a potential cellular mechanism that could underlie glial reduction in depression.We found that exposure to chronic unpredictable stress (CUS) for 15 days significantly decreased cell proliferation in neocortex by approximately 35%. This effect was dependent on the duration, intensity and type of stress, and was region-specific. Analysis of cell phenotype demonstrated that there was a decrease in the number of oligodendrocytes and endothelial cells. Finally, using a CUS paradigm that allows for analysis of anhedonia, we found that chronic antidepressant administration reversed the decrease in cortical cell proliferation, as well as the deficit in sucrose preference.RESULTSWe found that exposure to chronic unpredictable stress (CUS) for 15 days significantly decreased cell proliferation in neocortex by approximately 35%. This effect was dependent on the duration, intensity and type of stress, and was region-specific. Analysis of cell phenotype demonstrated that there was a decrease in the number of oligodendrocytes and endothelial cells. Finally, using a CUS paradigm that allows for analysis of anhedonia, we found that chronic antidepressant administration reversed the decrease in cortical cell proliferation, as well as the deficit in sucrose preference.These findings are consistent with the possibility that decreased cell proliferation could contribute to reductions in glia in prefrontal cortex of depressed subjects and further elucidate the cellular actions of stress and antidepressants.CONCLUSIONThese findings are consistent with the possibility that decreased cell proliferation could contribute to reductions in glia in prefrontal cortex of depressed subjects and further elucidate the cellular actions of stress and antidepressants. |
Author | Duman, Ronald S. Gourley, Shannon L. Taylor, Jane R. Valentine, Gerald W. Li, Xiao-Yuan Banasr, Mounira |
Author_xml | – sequence: 1 givenname: Mounira surname: Banasr fullname: Banasr, Mounira – sequence: 2 givenname: Gerald W. surname: Valentine fullname: Valentine, Gerald W. – sequence: 3 givenname: Xiao-Yuan surname: Li fullname: Li, Xiao-Yuan – sequence: 4 givenname: Shannon L. surname: Gourley fullname: Gourley, Shannon L. – sequence: 5 givenname: Jane R. surname: Taylor fullname: Taylor, Jane R. – sequence: 6 givenname: Ronald S. surname: Duman fullname: Duman, Ronald S. email: ronald.duman@yale.edu |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19018750$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/17585885$$D View this record in MEDLINE/PubMed |
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Keywords | Antidepressant endothelial cells NG2-glia chronic stress depression cell proliferation Mood disorder Cell proliferation Endothelial cell Cerebral cortex Rat Psychotropic Neuroglia Rodentia Central nervous system Depression Stress Encephalon Vertebrata Chemotherapy Chronic Mammalia Treatment Adult animal Antidepressant agent |
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Snippet | One of the most consistent morphologic findings in postmortem studies of brain tissue from depressed patients is a decrease in the number of glia in the... Background One of the most consistent morphologic findings in postmortem studies of brain tissue from depressed patients is a decrease in the number of glia in... |
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SubjectTerms | Adult and adolescent clinical studies Analysis of Variance Animals Antidepressant Antidepressive Agents, Second-Generation - pharmacology Antidepressive Agents, Second-Generation - therapeutic use Behavior, Animal Biological and medical sciences Bromodeoxyuridine - metabolism cell proliferation Cell Proliferation - drug effects Cerebral Cortex - drug effects Cerebral Cortex - pathology chronic stress Conditioning, Operant - drug effects Conditioning, Operant - physiology Corticosterone - pharmacology Depression Disease Models, Animal endothelial cells Fluoxetine - pharmacology Fluoxetine - therapeutic use Ki-67 Antigen - metabolism Male Medical sciences Mood disorders Neuroglia - metabolism Neuroglia - pathology Neurons - metabolism Neurons - pathology Neuropharmacology NG2-glia Pharmacology. Drug treatments Psychiatry Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychopharmacology Rats Rats, Sprague-Dawley Stress, Psychological - drug therapy Stress, Psychological - pathology Stress, Psychological - physiopathology |
Title | Chronic Unpredictable Stress Decreases Cell Proliferation in the Cerebral Cortex of the Adult Rat |
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