|   | 
Details
   web
Records
Author Czeh, B.; Muller-Keuker, J.I.H.; Rygula, R.; Abumaria, N.; Hiemke, C.; Domenici, E.; Fuchs, E.
Title (up) Chronic Social Stress Inhibits Cell Proliferation in the Adult Medial Prefrontal Cortex: Hemispheric Asymmetry and Reversal by Fluoxetine Treatment Type Journal Article
Year 2006 Publication Abbreviated Journal Neuropsychopharmacology
Volume 32 Issue 7 Pages 1490-1503
Keywords neurogenesis, stereology, cell number, glia, NG2, hippocampus
Abstract Profound neuroplastic changes have been demonstrated in various limbic structures after chronic stress exposure and antidepressant treatment in animal models of mood disorders. Here, we examined in rats the effect of chronic social stress and concomitant antidepressant treatment on cell proliferation in the medial prefrontal cortex (mPFC). We also examined possible hemispheric differences. Animals were subjected to 5 weeks of daily social defeat by an aggressive conspecific and received concomitant, daily, oral fluoxetine (10 mg/kg) during the last 4 weeks. Bromodeoxyuridine (BrdU) labeling and quantitative stereological techniques were used to evaluate the treatment effects on proliferation and survival of newborn cells in limbic structures such as the mPFC and the hippocampal dentate gyrus, in comparison with nonlimbic structures such as the primary motor cortex and the subventricular zone. Phenotypic analysis showed that neurogenesis dominated the dentate gyrus, whereas in the mPFC most newborn cells were glia, with smaller numbers of endothelial cells. Chronic stress significantly suppressed cytogenesis in the mPFC and neurogenesis in the dentate gyrus, but had minor effect in nonlimbic structures. Fluoxetine treatment counteracted the inhibitory effect of stress. Hemispheric comparison revealed that the rate of cytogenesis was significantly higher in the left mPFC of control animals, whereas stress inverted this asymmetry, yielding a significantly higher incidence of newborn cells in the right mPFC. Fluoxetine treatment abolished hemispheric asymmetry in both control and stressed animals. These pronounced changes in gliogenesis after chronic stress exposure may relate to the abnormalities of glial cell numbers reported in the frontolimbic areas of depressed patients.
Address
Corporate Author Thesis
Publisher Place of Publication Editor
Language Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0893-133x ISBN Medium
Area Expedition Conference
Notes Approved no
Call Number Equine Behaviour @ team @ Serial 5785
Permanent link to this record
 

 
Author Bosch, O.J.; Nair, H.P.; Ahern, T.H.; Neumann, I.D.; Young, L.J.
Title (up) The CRF System Mediates Increased Passive Stress-Coping Behavior Following the Loss of a Bonded Partner in a Monogamous Rodent Type Journal Article
Year 2008 Publication Abbreviated Journal Neuropsychopharmacology
Volume 34 Issue 6 Pages 1406-1415
Keywords prairie vole; passive stress-coping; forced swim test; tail suspension test; elevated plus-maze; hypothalamo–pituitary–adrenal axis
Abstract Social relationships significantly influence physiology and behavior, including the hypothalamo–pituitary–adrenal axis, anxiety, and mental

health. Disruption of social bonds through separation or death often results in profound grieving, depression, and physical illness. As the

monogamous prairie vole forms enduring, selective pair bonds with the mating partner, they provide an animal model to study the

physiological consequences of pair bonding and, thus, the loss of the bonded partner. Male prairie voles were paired with a novel female

or male sibling. After 5 days, half of the males of each group were separated from the partner. Elevated plus-maze, forced swim, and tail

suspension tests were used to assess anxiety-like and passive stress-coping behaviors indicative of depressive-like behavior. Following 4

days of separation from the female but not the male partner, experimental males displayed increased passive stress-coping. This effect

was abolished by long-term intracerebroventricular infusion of a nonselective corticotropin-releasing factor (CRF) receptor antagonist

without disrupting the bond itself. Both CRF type 1 and 2 receptors were involved in the emergence of passive stress-coping behavior.

Furthermore, pairing with a female was associated with elevated CRF mRNA in the bed nucleus of the stria terminalis, and partner loss

elicited a pronounced increase in circulating corticosteroid and adrenal weight. We speculate that the CRF system may mediate an

aversive affect following separation from the female partner, which may facilitate proximity seeking between the pair-bonded individuals.

Hence, the prairie vole model may provide insights into brain mechanisms involved in the psychopathological consequences of partner

loss.
Address
Corporate Author Thesis
Publisher American College of Neuropsychopharmacology Place of Publication Editor
Language Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0893-133x ISBN Medium
Area Expedition Conference
Notes Approved no
Call Number Equine Behaviour @ team @ Serial 5731
Permanent link to this record