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...
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Veröffentlicht in: | International journal of developmental neuroscience 2011-05, Vol.29 (3), p.295-304 |
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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 |
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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 & 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</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 & histology</subject><subject>Nerve Net - pathology</subject><subject>Nerve Net - physiology</subject><subject>Nerve Net - physiopathology</subject><subject>Neurotransmission</subject><subject>Prefrontal Cortex - anatomy & histology</subject><subject>Prefrontal Cortex - growth & 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 & histology</topic><topic>Nerve Net - pathology</topic><topic>Nerve Net - physiology</topic><topic>Nerve Net - physiopathology</topic><topic>Neurotransmission</topic><topic>Prefrontal Cortex - anatomy & histology</topic><topic>Prefrontal Cortex - growth & 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> |
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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 |
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