Estrogen Promotes Stress Sensitivity in a Prefrontal Cortex–Amygdala Pathway
We have recently reported in male rats that medial prefrontal cortex (mPFC) neurons that project to the basolateral nucleus of the amygdala (BLA) are resilient to stress-induced dendritic remodeling. The present study investigated whether this also occurs in female rats. This pathway was identified...
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creator | Shansky, Rebecca M. Hamo, Carine Hof, Patrick R. Lou, Wendy McEwen, Bruce S. Morrison, John H. |
description | We have recently reported in male rats that medial prefrontal cortex (mPFC) neurons that project to the basolateral nucleus of the amygdala (BLA) are resilient to stress-induced dendritic remodeling. The present study investigated whether this also occurs in female rats. This pathway was identified using the retrograde tracer Fast Blue injected into the BLA of ovariectomized female rats with estrogen replacement (OVX + E) and without (OVX + veh). Animals were exposed for 10 days either to 2-h immobilization stress or to home cage rest, after which layer III mPFC neurons that were either retrogradely labeled by Fast Blue or unlabeled were filled with Lucifer Yellow and analyzed for apical dendritic length and spine density. No dendritic remodeling occurred in unlabeled neurons from OVX + veh or OVX + E animals. In BLA-projecting neurons, however, stress had no effect on length in OVX + veh animals, but stressed OVX + E females showed greater dendritic length than controls at intermediate branches. Stress also caused an increase in spine density in all neurons in OVX + veh animals and a spine density increase in BLA-projecting neurons in OVX + E females. Estrogen also increased spine density on BLA-projecting neurons in unstressed animals. These data demonstrate both independent effects of estrogen on pyramidal cell morphology and effects that are interactive with stress, with the BLA-projecting neurons being sensitive to both kinds of effects. |
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The present study investigated whether this also occurs in female rats. This pathway was identified using the retrograde tracer Fast Blue injected into the BLA of ovariectomized female rats with estrogen replacement (OVX + E) and without (OVX + veh). Animals were exposed for 10 days either to 2-h immobilization stress or to home cage rest, after which layer III mPFC neurons that were either retrogradely labeled by Fast Blue or unlabeled were filled with Lucifer Yellow and analyzed for apical dendritic length and spine density. No dendritic remodeling occurred in unlabeled neurons from OVX + veh or OVX + E animals. In BLA-projecting neurons, however, stress had no effect on length in OVX + veh animals, but stressed OVX + E females showed greater dendritic length than controls at intermediate branches. Stress also caused an increase in spine density in all neurons in OVX + veh animals and a spine density increase in BLA-projecting neurons in OVX + E females. Estrogen also increased spine density on BLA-projecting neurons in unstressed animals. These data demonstrate both independent effects of estrogen on pyramidal cell morphology and effects that are interactive with stress, with the BLA-projecting neurons being sensitive to both kinds of effects.</description><identifier>ISSN: 1047-3211</identifier><identifier>EISSN: 1460-2199</identifier><identifier>DOI: 10.1093/cercor/bhq003</identifier><identifier>PMID: 20139149</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Amygdala - cytology ; Amygdala - drug effects ; Amygdala - physiopathology ; Animals ; connectivity ; dendritic arborization ; Disease Models, Animal ; Estrogens - pharmacology ; Estrogens - physiology ; Female ; medial prefrontal cortex ; Neural Pathways - cytology ; Neural Pathways - drug effects ; Neural Pathways - physiopathology ; neural plasticity ; Prefrontal Cortex - cytology ; Prefrontal Cortex - drug effects ; Prefrontal Cortex - physiopathology ; Rats ; Rats, Sprague-Dawley ; sex difference ; Stress, Psychological - metabolism ; Stress, Psychological - physiopathology</subject><ispartof>Cerebral cortex (New York, N.Y. 1991), 2010-11, Vol.20 (11), p.2560-2567</ispartof><rights>The Author 2010. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c500t-f3c4f8fddf5fd105288f424afc6622f5f9b8c2c618d68c3ec3d935aa8b40f8d23</citedby><cites>FETCH-LOGICAL-c500t-f3c4f8fddf5fd105288f424afc6622f5f9b8c2c618d68c3ec3d935aa8b40f8d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20139149$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shansky, Rebecca M.</creatorcontrib><creatorcontrib>Hamo, Carine</creatorcontrib><creatorcontrib>Hof, Patrick R.</creatorcontrib><creatorcontrib>Lou, Wendy</creatorcontrib><creatorcontrib>McEwen, Bruce S.</creatorcontrib><creatorcontrib>Morrison, John H.</creatorcontrib><title>Estrogen Promotes Stress Sensitivity in a Prefrontal Cortex–Amygdala Pathway</title><title>Cerebral cortex (New York, N.Y. 1991)</title><addtitle>Cereb Cortex</addtitle><description>We have recently reported in male rats that medial prefrontal cortex (mPFC) neurons that project to the basolateral nucleus of the amygdala (BLA) are resilient to stress-induced dendritic remodeling. The present study investigated whether this also occurs in female rats. This pathway was identified using the retrograde tracer Fast Blue injected into the BLA of ovariectomized female rats with estrogen replacement (OVX + E) and without (OVX + veh). Animals were exposed for 10 days either to 2-h immobilization stress or to home cage rest, after which layer III mPFC neurons that were either retrogradely labeled by Fast Blue or unlabeled were filled with Lucifer Yellow and analyzed for apical dendritic length and spine density. No dendritic remodeling occurred in unlabeled neurons from OVX + veh or OVX + E animals. In BLA-projecting neurons, however, stress had no effect on length in OVX + veh animals, but stressed OVX + E females showed greater dendritic length than controls at intermediate branches. Stress also caused an increase in spine density in all neurons in OVX + veh animals and a spine density increase in BLA-projecting neurons in OVX + E females. Estrogen also increased spine density on BLA-projecting neurons in unstressed animals. These data demonstrate both independent effects of estrogen on pyramidal cell morphology and effects that are interactive with stress, with the BLA-projecting neurons being sensitive to both kinds of effects.</description><subject>Amygdala - cytology</subject><subject>Amygdala - drug effects</subject><subject>Amygdala - physiopathology</subject><subject>Animals</subject><subject>connectivity</subject><subject>dendritic arborization</subject><subject>Disease Models, Animal</subject><subject>Estrogens - pharmacology</subject><subject>Estrogens - physiology</subject><subject>Female</subject><subject>medial prefrontal cortex</subject><subject>Neural Pathways - cytology</subject><subject>Neural Pathways - drug effects</subject><subject>Neural Pathways - physiopathology</subject><subject>neural plasticity</subject><subject>Prefrontal Cortex - cytology</subject><subject>Prefrontal Cortex - drug effects</subject><subject>Prefrontal Cortex - physiopathology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>sex difference</subject><subject>Stress, Psychological - metabolism</subject><subject>Stress, Psychological - physiopathology</subject><issn>1047-3211</issn><issn>1460-2199</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1uEzEUhS1URH9g2S2aXVfT-ndsb5DaqG0qIqBqQagby_HYiWFmnNpO2-x4B96QJ8EoJdBVV_fqnk9H994DwD6ChwhKcmRsNCEeTee3EJIXYAfRBtYYSblVekh5TTBC22A3pW8QIo4ZfgW2MUREIip3wIfTlGOY2aH6FEMfsk3VVY42lWKH5LO_83lV-aHSBbAuhiHrrhqFmO3Drx8_j_vVrNVdEXWe3-vVa_DS6S7ZN491D3w-O70ejevJx_OL0fGkNgzCXDtiqBOubR1zLYIMC-EoptqZpsG4DOVUGGwaJNpGGGINaSVhWosphU60mOyBd2vfxXLa29bYIUfdqUX0vY4rFbRXT5XBz9Us3CksGRKUFIODR4MYbpc2ZdX7ZGzX6cGGZVKCNZxjQuSzJGecNohwVMh6TZoYUirf2uyDoPoTllqHpdZhFf7t_0ds6L_p_DP0qbx7o-v4XTWccKbGX2_Ul5PJ9fvL8aWakN9DBaT6</recordid><startdate>20101101</startdate><enddate>20101101</enddate><creator>Shansky, Rebecca M.</creator><creator>Hamo, Carine</creator><creator>Hof, Patrick R.</creator><creator>Lou, Wendy</creator><creator>McEwen, Bruce S.</creator><creator>Morrison, John H.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QG</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20101101</creationdate><title>Estrogen Promotes Stress Sensitivity in a Prefrontal Cortex–Amygdala Pathway</title><author>Shansky, Rebecca M. ; Hamo, Carine ; Hof, Patrick R. ; Lou, Wendy ; McEwen, Bruce S. ; Morrison, John H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-f3c4f8fddf5fd105288f424afc6622f5f9b8c2c618d68c3ec3d935aa8b40f8d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Amygdala - cytology</topic><topic>Amygdala - drug effects</topic><topic>Amygdala - physiopathology</topic><topic>Animals</topic><topic>connectivity</topic><topic>dendritic arborization</topic><topic>Disease Models, Animal</topic><topic>Estrogens - pharmacology</topic><topic>Estrogens - physiology</topic><topic>Female</topic><topic>medial prefrontal cortex</topic><topic>Neural Pathways - cytology</topic><topic>Neural Pathways - drug effects</topic><topic>Neural Pathways - physiopathology</topic><topic>neural plasticity</topic><topic>Prefrontal Cortex - cytology</topic><topic>Prefrontal Cortex - drug effects</topic><topic>Prefrontal Cortex - physiopathology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>sex difference</topic><topic>Stress, Psychological - metabolism</topic><topic>Stress, Psychological - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shansky, Rebecca M.</creatorcontrib><creatorcontrib>Hamo, Carine</creatorcontrib><creatorcontrib>Hof, Patrick R.</creatorcontrib><creatorcontrib>Lou, Wendy</creatorcontrib><creatorcontrib>McEwen, Bruce S.</creatorcontrib><creatorcontrib>Morrison, John H.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cerebral cortex (New York, N.Y. 1991)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shansky, Rebecca M.</au><au>Hamo, Carine</au><au>Hof, Patrick R.</au><au>Lou, Wendy</au><au>McEwen, Bruce S.</au><au>Morrison, John H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Estrogen Promotes Stress Sensitivity in a Prefrontal Cortex–Amygdala Pathway</atitle><jtitle>Cerebral cortex (New York, N.Y. 1991)</jtitle><addtitle>Cereb Cortex</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>20</volume><issue>11</issue><spage>2560</spage><epage>2567</epage><pages>2560-2567</pages><issn>1047-3211</issn><eissn>1460-2199</eissn><abstract>We have recently reported in male rats that medial prefrontal cortex (mPFC) neurons that project to the basolateral nucleus of the amygdala (BLA) are resilient to stress-induced dendritic remodeling. The present study investigated whether this also occurs in female rats. This pathway was identified using the retrograde tracer Fast Blue injected into the BLA of ovariectomized female rats with estrogen replacement (OVX + E) and without (OVX + veh). Animals were exposed for 10 days either to 2-h immobilization stress or to home cage rest, after which layer III mPFC neurons that were either retrogradely labeled by Fast Blue or unlabeled were filled with Lucifer Yellow and analyzed for apical dendritic length and spine density. No dendritic remodeling occurred in unlabeled neurons from OVX + veh or OVX + E animals. In BLA-projecting neurons, however, stress had no effect on length in OVX + veh animals, but stressed OVX + E females showed greater dendritic length than controls at intermediate branches. Stress also caused an increase in spine density in all neurons in OVX + veh animals and a spine density increase in BLA-projecting neurons in OVX + E females. 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subjects | Amygdala - cytology Amygdala - drug effects Amygdala - physiopathology Animals connectivity dendritic arborization Disease Models, Animal Estrogens - pharmacology Estrogens - physiology Female medial prefrontal cortex Neural Pathways - cytology Neural Pathways - drug effects Neural Pathways - physiopathology neural plasticity Prefrontal Cortex - cytology Prefrontal Cortex - drug effects Prefrontal Cortex - physiopathology Rats Rats, Sprague-Dawley sex difference Stress, Psychological - metabolism Stress, Psychological - physiopathology |
title | Estrogen Promotes Stress Sensitivity in a Prefrontal Cortex–Amygdala Pathway |
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