Selective vulnerability of the developing brain to lead
Environmental lead exposure in young children who ingest household paint dust or other sources impairs their potential intelligence in a linear, dose-dependent fashion in contrast to its far more subtle effects on other neurologic functions. Basic investigations have identified three interrelated st...
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Veröffentlicht in: | Current opinion in neurology 1998-12, Vol.11 (6), p.689-693 |
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description | Environmental lead exposure in young children who ingest household paint dust or other sources impairs their potential intelligence in a linear, dose-dependent fashion in contrast to its far more subtle effects on other neurologic functions. Basic investigations have identified three interrelated steps in synaptic neurotransmission at which low levels of lead can disrupt signal processing. Lead enhances background transmitter release, but impairs stimulated release, inhibits function at the N-methyl-D-aspartate-type glutamate receptor and stimulates background levels of the intracellular messenger protein kinase C. Taken together these effects have the effect of diminishing the synaptic signal to noise ratio. The ability of lead to enhance 'synaptic noise' during a critical early period of postnatal development may permanently disrupt the architecture of cortical processing units by depriving them of high resolution environmental signals needed to refine synaptic connections. |
doi_str_mv | 10.1097/00019052-199812000-00013 |
format | Article |
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Basic investigations have identified three interrelated steps in synaptic neurotransmission at which low levels of lead can disrupt signal processing. Lead enhances background transmitter release, but impairs stimulated release, inhibits function at the N-methyl-D-aspartate-type glutamate receptor and stimulates background levels of the intracellular messenger protein kinase C. Taken together these effects have the effect of diminishing the synaptic signal to noise ratio. The ability of lead to enhance 'synaptic noise' during a critical early period of postnatal development may permanently disrupt the architecture of cortical processing units by depriving them of high resolution environmental signals needed to refine synaptic connections.</description><identifier>ISSN: 1350-7540</identifier><identifier>DOI: 10.1097/00019052-199812000-00013</identifier><identifier>PMID: 9870138</identifier><language>eng</language><publisher>England</publisher><subject>Adolescent ; Adult ; Animals ; Brain Damage, Chronic - chemically induced ; Brain Damage, Chronic - diagnosis ; Brain Damage, Chronic - physiopathology ; Cerebral Cortex - drug effects ; Cerebral Cortex - physiopathology ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Infant, Newborn ; Intelligence - drug effects ; Intelligence - physiology ; Lead - adverse effects ; Lead Poisoning - diagnosis ; Lead Poisoning - physiopathology ; Male ; Pregnancy ; Synaptic Transmission - drug effects ; Synaptic Transmission - physiology</subject><ispartof>Current opinion in neurology, 1998-12, Vol.11 (6), p.689-693</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c310t-5912806bb1b05b6431adaf0dbf4356ef24d55ecb8e4c4ea44666a285876c961b3</citedby><cites>FETCH-LOGICAL-c310t-5912806bb1b05b6431adaf0dbf4356ef24d55ecb8e4c4ea44666a285876c961b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9870138$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Johnston, M V</creatorcontrib><creatorcontrib>Goldstein, G W</creatorcontrib><title>Selective vulnerability of the developing brain to lead</title><title>Current opinion in neurology</title><addtitle>Curr Opin Neurol</addtitle><description>Environmental lead exposure in young children who ingest household paint dust or other sources impairs their potential intelligence in a linear, dose-dependent fashion in contrast to its far more subtle effects on other neurologic functions. Basic investigations have identified three interrelated steps in synaptic neurotransmission at which low levels of lead can disrupt signal processing. Lead enhances background transmitter release, but impairs stimulated release, inhibits function at the N-methyl-D-aspartate-type glutamate receptor and stimulates background levels of the intracellular messenger protein kinase C. Taken together these effects have the effect of diminishing the synaptic signal to noise ratio. The ability of lead to enhance 'synaptic noise' during a critical early period of postnatal development may permanently disrupt the architecture of cortical processing units by depriving them of high resolution environmental signals needed to refine synaptic connections.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Animals</subject><subject>Brain Damage, Chronic - chemically induced</subject><subject>Brain Damage, Chronic - diagnosis</subject><subject>Brain Damage, Chronic - physiopathology</subject><subject>Cerebral Cortex - drug effects</subject><subject>Cerebral Cortex - physiopathology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Intelligence - drug effects</subject><subject>Intelligence - physiology</subject><subject>Lead - adverse effects</subject><subject>Lead Poisoning - diagnosis</subject><subject>Lead Poisoning - physiopathology</subject><subject>Male</subject><subject>Pregnancy</subject><subject>Synaptic Transmission - drug effects</subject><subject>Synaptic Transmission - physiology</subject><issn>1350-7540</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9j8tOwzAQAH0AlVL4BCT_gGH9jH1EFY9KlTgA58hO1hDkJpWTRurfk9LS02pHOysNIZTDPQdXPAAAd6AF485ZLqaVHZC8IHMuNbBCK7gi133_M2EnTDEjM2eL6cLOSfGOCauhGZGOu9Ri9qFJzbCnXaTDN9IaR0zdtmm_aMi-aenQ0YS-viGX0aceb09zQT6fnz6Wr2z99rJaPq5ZJTkMTDsuLJgQeAAdjJLc1z5CHaKS2mAUqtYaq2BRVQq9UsYYL6y2hamc4UEuiD3-rXLX9xljuc3Nxud9yaE85Jf_-eU5_w_JSb07qttd2GB9Fk_t8heNv1cR</recordid><startdate>19981201</startdate><enddate>19981201</enddate><creator>Johnston, M V</creator><creator>Goldstein, G W</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19981201</creationdate><title>Selective vulnerability of the developing brain to lead</title><author>Johnston, M V ; Goldstein, G W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c310t-5912806bb1b05b6431adaf0dbf4356ef24d55ecb8e4c4ea44666a285876c961b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Animals</topic><topic>Brain Damage, Chronic - chemically induced</topic><topic>Brain Damage, Chronic - diagnosis</topic><topic>Brain Damage, Chronic - physiopathology</topic><topic>Cerebral Cortex - drug effects</topic><topic>Cerebral Cortex - physiopathology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Intelligence - drug effects</topic><topic>Intelligence - physiology</topic><topic>Lead - adverse effects</topic><topic>Lead Poisoning - diagnosis</topic><topic>Lead Poisoning - physiopathology</topic><topic>Male</topic><topic>Pregnancy</topic><topic>Synaptic Transmission - drug effects</topic><topic>Synaptic Transmission - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Johnston, M V</creatorcontrib><creatorcontrib>Goldstein, G W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Current opinion in neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Johnston, M V</au><au>Goldstein, G W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective vulnerability of the developing brain to lead</atitle><jtitle>Current opinion in neurology</jtitle><addtitle>Curr Opin Neurol</addtitle><date>1998-12-01</date><risdate>1998</risdate><volume>11</volume><issue>6</issue><spage>689</spage><epage>693</epage><pages>689-693</pages><issn>1350-7540</issn><abstract>Environmental lead exposure in young children who ingest household paint dust or other sources impairs their potential intelligence in a linear, dose-dependent fashion in contrast to its far more subtle effects on other neurologic functions. Basic investigations have identified three interrelated steps in synaptic neurotransmission at which low levels of lead can disrupt signal processing. Lead enhances background transmitter release, but impairs stimulated release, inhibits function at the N-methyl-D-aspartate-type glutamate receptor and stimulates background levels of the intracellular messenger protein kinase C. Taken together these effects have the effect of diminishing the synaptic signal to noise ratio. The ability of lead to enhance 'synaptic noise' during a critical early period of postnatal development may permanently disrupt the architecture of cortical processing units by depriving them of high resolution environmental signals needed to refine synaptic connections.</abstract><cop>England</cop><pmid>9870138</pmid><doi>10.1097/00019052-199812000-00013</doi><tpages>5</tpages></addata></record> |
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source | Journals@Ovid Ovid Autoload; MEDLINE |
subjects | Adolescent Adult Animals Brain Damage, Chronic - chemically induced Brain Damage, Chronic - diagnosis Brain Damage, Chronic - physiopathology Cerebral Cortex - drug effects Cerebral Cortex - physiopathology Child Child, Preschool Female Humans Infant Infant, Newborn Intelligence - drug effects Intelligence - physiology Lead - adverse effects Lead Poisoning - diagnosis Lead Poisoning - physiopathology Male Pregnancy Synaptic Transmission - drug effects Synaptic Transmission - physiology |
title | Selective vulnerability of the developing brain to lead |
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