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 inBiological psychiatry (1969) Vol. 62; no. 5; pp. 496 - 504
Main Authors Banasr, Mounira, Valentine, Gerald W., Li, Xiao-Yuan, Gourley, Shannon L., Taylor, Jane R., Duman, Ronald S.
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.09.2007
Elsevier Science
Subjects
Online AccessGet full text
ISSN0006-3223
1873-2402
DOI10.1016/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.
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
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  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.
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  givenname: Ronald S.
  surname: Duman
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  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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Issue 5
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
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0006322307000996
https://www.clinicalkey.es/playcontent/1-s2.0-S0006322307000996
https://dx.doi.org/10.1016/j.biopsych.2007.02.006
https://www.ncbi.nlm.nih.gov/pubmed/17585885
https://www.proquest.com/docview/68203768
Volume 62
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