Insights into the neurodevelopmental origin of schizophrenia from postmortem studies of prefrontal cortical circuitry

▶ Alterations of GABA markers relate to working memory dysfunction in schizophrenia. ▶ Developmental trajectories of working memory and inhibition in DLPFC are correlated. ▶ Normal maturational events timing reflects vulnerability to schizophrenia pathology. ▶ Disturbances in schizophrenia depend up...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of developmental neuroscience 2011-05, Vol.29 (3), p.295-304
Hauptverfasser: Beneyto, Monica, Lewis, David A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 304
container_issue 3
container_start_page 295
container_title International journal of developmental neuroscience
container_volume 29
creator Beneyto, Monica
Lewis, David A.
description ▶ Alterations of GABA markers relate to working memory dysfunction in schizophrenia. ▶ Developmental trajectories of working memory and inhibition in DLPFC are correlated. ▶ Normal maturational events timing reflects vulnerability to schizophrenia pathology. ▶ Disturbances in schizophrenia depend upon circuitry-specific susceptibility. The hypothesis that schizophrenia results from a developmental, as opposed to a degenerative, process affecting the connectivity and network plasticity of the cerebral cortex is supported by findings from morphological and molecular postmortem studies. Specifically, abnormalities in the expression of protein markers of GABA neurotransmission and the lamina- and circuit-specificity of these changes in the cortex in schizophrenia, in concert with knowledge of their developmental trajectories, offer crucial insight into the vulnerability of specific cortical networks to environmental insults during different periods of development. These findings reveal potential targets for therapeutic interventions to improve cognitive function in individuals with schizophrenia, and provide guidance for future preventive strategies to preserve cortical neurotransmission in at-risk individuals.
doi_str_mv 10.1016/j.ijdevneu.2010.08.003
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3319737</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0736574810003679</els_id><sourcerecordid>861591699</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5683-74378b8a1d897deec99241ef3a9a93320d7f96e4de60669fcf2f318e1e3278c83</originalsourceid><addsrcrecordid>eNqNkU9v1DAQxS0EokvhK1S5cdrFjhP_uSBQu5RdVeVCETfLdSYbr5I42M5Wy6evQ9oKTvRka96bn2f8EDojeEUwYR_2K7uv4NDDuMpxKmKxwpi-QAsiOF0WvPj5Ei0wp2xZ8kKcoDch7DHGZYmL1-gkx1zyIpcLNG76YHdNDJnto8tiA1liepfY0Lqhgz7qNnPe7myfuToLprG_3dB46K3Oau-6bHAhds5H6LIQx8pCmIyDh6T-6TZJtGa6WG9GG_3xLXpV6zbAu4fzFN18WX8__7q8-na5Of98tTQlE3TJC8rFrdCkEpJXAEbKvCBQUy21pDTHFa8lg6IChhmTtanzmhIBBGjOhRH0FH2cucN420Fl0jZet2rwttP-qJy26l-lt43auYOilEhOeQK8fwB492uEEFVng4G21T24MSjBOKelFPIZTlJKwuTkZLPTeBdC-qaneQhWU7hqrx7DVVO4CguVwk2NZ39v89T2mGYybGbDnW3h-Eys2l5cbzfbi_WP6_XNVMdifuzTzIKUz8GCV8FY6A1U1oOJqnL2f_PeAzui1Ns</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>861591699</pqid></control><display><type>article</type><title>Insights into the neurodevelopmental origin of schizophrenia from postmortem studies of prefrontal cortical circuitry</title><source>MEDLINE</source><source>Wiley Journals</source><creator>Beneyto, Monica ; Lewis, David A.</creator><creatorcontrib>Beneyto, Monica ; Lewis, David A.</creatorcontrib><description>▶ Alterations of GABA markers relate to working memory dysfunction in schizophrenia. ▶ Developmental trajectories of working memory and inhibition in DLPFC are correlated. ▶ Normal maturational events timing reflects vulnerability to schizophrenia pathology. ▶ Disturbances in schizophrenia depend upon circuitry-specific susceptibility. The hypothesis that schizophrenia results from a developmental, as opposed to a degenerative, process affecting the connectivity and network plasticity of the cerebral cortex is supported by findings from morphological and molecular postmortem studies. Specifically, abnormalities in the expression of protein markers of GABA neurotransmission and the lamina- and circuit-specificity of these changes in the cortex in schizophrenia, in concert with knowledge of their developmental trajectories, offer crucial insight into the vulnerability of specific cortical networks to environmental insults during different periods of development. These findings reveal potential targets for therapeutic interventions to improve cognitive function in individuals with schizophrenia, and provide guidance for future preventive strategies to preserve cortical neurotransmission in at-risk individuals.</description><identifier>ISSN: 0736-5748</identifier><identifier>ISSN: 1873-474X</identifier><identifier>EISSN: 1873-474X</identifier><identifier>DOI: 10.1016/j.ijdevneu.2010.08.003</identifier><identifier>PMID: 20797429</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Autopsy ; Biomarkers - metabolism ; Development ; GABA ; gamma-Aminobutyric Acid - metabolism ; Glutamate ; Humans ; Nerve Net - anatomy &amp; histology ; Nerve Net - pathology ; Nerve Net - physiology ; Nerve Net - physiopathology ; Neurotransmission ; Prefrontal Cortex - anatomy &amp; histology ; Prefrontal Cortex - growth &amp; development ; Prefrontal Cortex - physiopathology ; Protein Subunits - metabolism ; Receptors, GABA-A - metabolism ; Schizophrenia - pathology ; Schizophrenia - physiopathology</subject><ispartof>International journal of developmental neuroscience, 2011-05, Vol.29 (3), p.295-304</ispartof><rights>2010 ISDN</rights><rights>2011 ISDN</rights><rights>Copyright © 2010 ISDN. Published by Elsevier Ltd. All rights reserved.</rights><rights>2010 ISDN. Published by Elsevier Ltd. All rights reserved. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5683-74378b8a1d897deec99241ef3a9a93320d7f96e4de60669fcf2f318e1e3278c83</citedby><cites>FETCH-LOGICAL-c5683-74378b8a1d897deec99241ef3a9a93320d7f96e4de60669fcf2f318e1e3278c83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1016%2Fj.ijdevneu.2010.08.003$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1016%2Fj.ijdevneu.2010.08.003$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20797429$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beneyto, Monica</creatorcontrib><creatorcontrib>Lewis, David A.</creatorcontrib><title>Insights into the neurodevelopmental origin of schizophrenia from postmortem studies of prefrontal cortical circuitry</title><title>International journal of developmental neuroscience</title><addtitle>Int J Dev Neurosci</addtitle><description>▶ Alterations of GABA markers relate to working memory dysfunction in schizophrenia. ▶ Developmental trajectories of working memory and inhibition in DLPFC are correlated. ▶ Normal maturational events timing reflects vulnerability to schizophrenia pathology. ▶ Disturbances in schizophrenia depend upon circuitry-specific susceptibility. The hypothesis that schizophrenia results from a developmental, as opposed to a degenerative, process affecting the connectivity and network plasticity of the cerebral cortex is supported by findings from morphological and molecular postmortem studies. Specifically, abnormalities in the expression of protein markers of GABA neurotransmission and the lamina- and circuit-specificity of these changes in the cortex in schizophrenia, in concert with knowledge of their developmental trajectories, offer crucial insight into the vulnerability of specific cortical networks to environmental insults during different periods of development. These findings reveal potential targets for therapeutic interventions to improve cognitive function in individuals with schizophrenia, and provide guidance for future preventive strategies to preserve cortical neurotransmission in at-risk individuals.</description><subject>Autopsy</subject><subject>Biomarkers - metabolism</subject><subject>Development</subject><subject>GABA</subject><subject>gamma-Aminobutyric Acid - metabolism</subject><subject>Glutamate</subject><subject>Humans</subject><subject>Nerve Net - anatomy &amp; histology</subject><subject>Nerve Net - pathology</subject><subject>Nerve Net - physiology</subject><subject>Nerve Net - physiopathology</subject><subject>Neurotransmission</subject><subject>Prefrontal Cortex - anatomy &amp; histology</subject><subject>Prefrontal Cortex - growth &amp; development</subject><subject>Prefrontal Cortex - physiopathology</subject><subject>Protein Subunits - metabolism</subject><subject>Receptors, GABA-A - metabolism</subject><subject>Schizophrenia - pathology</subject><subject>Schizophrenia - physiopathology</subject><issn>0736-5748</issn><issn>1873-474X</issn><issn>1873-474X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9v1DAQxS0EokvhK1S5cdrFjhP_uSBQu5RdVeVCETfLdSYbr5I42M5Wy6evQ9oKTvRka96bn2f8EDojeEUwYR_2K7uv4NDDuMpxKmKxwpi-QAsiOF0WvPj5Ei0wp2xZ8kKcoDch7DHGZYmL1-gkx1zyIpcLNG76YHdNDJnto8tiA1liepfY0Lqhgz7qNnPe7myfuToLprG_3dB46K3Oau-6bHAhds5H6LIQx8pCmIyDh6T-6TZJtGa6WG9GG_3xLXpV6zbAu4fzFN18WX8__7q8-na5Of98tTQlE3TJC8rFrdCkEpJXAEbKvCBQUy21pDTHFa8lg6IChhmTtanzmhIBBGjOhRH0FH2cucN420Fl0jZet2rwttP-qJy26l-lt43auYOilEhOeQK8fwB492uEEFVng4G21T24MSjBOKelFPIZTlJKwuTkZLPTeBdC-qaneQhWU7hqrx7DVVO4CguVwk2NZ39v89T2mGYybGbDnW3h-Eys2l5cbzfbi_WP6_XNVMdifuzTzIKUz8GCV8FY6A1U1oOJqnL2f_PeAzui1Ns</recordid><startdate>201105</startdate><enddate>201105</enddate><creator>Beneyto, Monica</creator><creator>Lewis, David A.</creator><general>Elsevier Ltd</general><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>7TK</scope><scope>5PM</scope></search><sort><creationdate>201105</creationdate><title>Insights into the neurodevelopmental origin of schizophrenia from postmortem studies of prefrontal cortical circuitry</title><author>Beneyto, Monica ; Lewis, David A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5683-74378b8a1d897deec99241ef3a9a93320d7f96e4de60669fcf2f318e1e3278c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Autopsy</topic><topic>Biomarkers - metabolism</topic><topic>Development</topic><topic>GABA</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>Glutamate</topic><topic>Humans</topic><topic>Nerve Net - anatomy &amp; histology</topic><topic>Nerve Net - pathology</topic><topic>Nerve Net - physiology</topic><topic>Nerve Net - physiopathology</topic><topic>Neurotransmission</topic><topic>Prefrontal Cortex - anatomy &amp; histology</topic><topic>Prefrontal Cortex - growth &amp; development</topic><topic>Prefrontal Cortex - physiopathology</topic><topic>Protein Subunits - metabolism</topic><topic>Receptors, GABA-A - metabolism</topic><topic>Schizophrenia - pathology</topic><topic>Schizophrenia - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beneyto, Monica</creatorcontrib><creatorcontrib>Lewis, David A.</creatorcontrib><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>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of developmental neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beneyto, Monica</au><au>Lewis, David A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insights into the neurodevelopmental origin of schizophrenia from postmortem studies of prefrontal cortical circuitry</atitle><jtitle>International journal of developmental neuroscience</jtitle><addtitle>Int J Dev Neurosci</addtitle><date>2011-05</date><risdate>2011</risdate><volume>29</volume><issue>3</issue><spage>295</spage><epage>304</epage><pages>295-304</pages><issn>0736-5748</issn><issn>1873-474X</issn><eissn>1873-474X</eissn><abstract>▶ Alterations of GABA markers relate to working memory dysfunction in schizophrenia. ▶ Developmental trajectories of working memory and inhibition in DLPFC are correlated. ▶ Normal maturational events timing reflects vulnerability to schizophrenia pathology. ▶ Disturbances in schizophrenia depend upon circuitry-specific susceptibility. The hypothesis that schizophrenia results from a developmental, as opposed to a degenerative, process affecting the connectivity and network plasticity of the cerebral cortex is supported by findings from morphological and molecular postmortem studies. Specifically, abnormalities in the expression of protein markers of GABA neurotransmission and the lamina- and circuit-specificity of these changes in the cortex in schizophrenia, in concert with knowledge of their developmental trajectories, offer crucial insight into the vulnerability of specific cortical networks to environmental insults during different periods of development. These findings reveal potential targets for therapeutic interventions to improve cognitive function in individuals with schizophrenia, and provide guidance for future preventive strategies to preserve cortical neurotransmission in at-risk individuals.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>20797429</pmid><doi>10.1016/j.ijdevneu.2010.08.003</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0736-5748
ispartof International journal of developmental neuroscience, 2011-05, Vol.29 (3), p.295-304
issn 0736-5748
1873-474X
1873-474X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3319737
source MEDLINE; Wiley Journals
subjects Autopsy
Biomarkers - metabolism
Development
GABA
gamma-Aminobutyric Acid - metabolism
Glutamate
Humans
Nerve Net - anatomy & histology
Nerve Net - pathology
Nerve Net - physiology
Nerve Net - physiopathology
Neurotransmission
Prefrontal Cortex - anatomy & histology
Prefrontal Cortex - growth & development
Prefrontal Cortex - physiopathology
Protein Subunits - metabolism
Receptors, GABA-A - metabolism
Schizophrenia - pathology
Schizophrenia - physiopathology
title Insights into the neurodevelopmental origin of schizophrenia from postmortem studies of prefrontal cortical circuitry
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T11%3A25%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Insights%20into%20the%20neurodevelopmental%20origin%20of%20schizophrenia%20from%20postmortem%20studies%20of%20prefrontal%20cortical%20circuitry&rft.jtitle=International%20journal%20of%20developmental%20neuroscience&rft.au=Beneyto,%20Monica&rft.date=2011-05&rft.volume=29&rft.issue=3&rft.spage=295&rft.epage=304&rft.pages=295-304&rft.issn=0736-5748&rft.eissn=1873-474X&rft_id=info:doi/10.1016/j.ijdevneu.2010.08.003&rft_dat=%3Cproquest_pubme%3E861591699%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=861591699&rft_id=info:pmid/20797429&rft_els_id=S0736574810003679&rfr_iscdi=true