Central sensitization and LTP: do pain and memory share similar mechanisms?
Synaptic plasticity is fundamental to many neurobiological functions, including memory and pain. Central sensitization refers to the increased synaptic efficacy established in somatosensory neurons in the dorsal horn of the spinal cord following intense peripheral noxious stimuli, tissue injury or n...
Gespeichert in:
Veröffentlicht in: | Trends in neurosciences (Regular ed.) 2003-12, Vol.26 (12), p.696-705 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 705 |
---|---|
container_issue | 12 |
container_start_page | 696 |
container_title | Trends in neurosciences (Regular ed.) |
container_volume | 26 |
creator | Ji, Ru-Rong Kohno, Tatsuro Moore, Kimberly A Woolf, Clifford J |
description | Synaptic plasticity is fundamental to many neurobiological functions, including memory and pain. Central sensitization refers to the increased synaptic efficacy established in somatosensory neurons in the dorsal horn of the spinal cord following intense peripheral noxious stimuli, tissue injury or nerve damage. This heightened synaptic transmission leads to a reduction in pain threshold, an amplification of pain responses and a spread of pain sensitivity to non-injured areas. In the cortex, LTP – a long-lasting highly localized increase in synaptic strength – is a synaptic substrate for memory and learning. Analysis of the molecular mechanisms underlying the generation and maintenance of central sensitization and LTP indicates that, although there are differences between the synaptic plasticity contributing to memory and pain, there are also striking similarities. |
doi_str_mv | 10.1016/j.tins.2003.09.017 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71379865</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0166223603003370</els_id><sourcerecordid>566296331</sourcerecordid><originalsourceid>FETCH-LOGICAL-c574t-7b1872749787fa9c77f577291be3e7639a9745fecf73efb80f70777b6f06ac183</originalsourceid><addsrcrecordid>eNqFkU1rGzEQhkVoadykfyCHsPSQ224l7cdIoRCCadMQQ3JwoTeh1Y6wzK7WkdYF59dXxoZADs1JMDzzMnofQi4YLRhlzbd1MTkfC05pWVBZUAYnZMYEiJxR8ecDmSWoyTkvm1PyOcY1pawSrPpETlnV8ErU9Yw8zNFPQfdZRB_d5F705Eafad9li-XTddaN2Ua7w2DAYQy7LK50wCy6wfU6pKFZae_iEG_OyUer-4hfju8Z-f3zx3L-K1883t3Pbxe5qaGacmjTjRwqCQKslgbA1gBcshZLhKaUWkJVWzQWSrStoBYoALSNpY02TJRn5OqQuwnj8xbjpAYXDfa99jhuowJWghRN_S7IJGepKpbAr2_A9bgNPn1C8XRsqrHaQ_wAmTDGGNCqTXCDDjvFqNoLUWu1F6L2QhSVKglJS5fH5G07YPe6cjSQgO8HAFNjfx0GFY1Db7BzAc2kutH9L_8fzEea2A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>218716641</pqid></control><display><type>article</type><title>Central sensitization and LTP: do pain and memory share similar mechanisms?</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Ji, Ru-Rong ; Kohno, Tatsuro ; Moore, Kimberly A ; Woolf, Clifford J</creator><creatorcontrib>Ji, Ru-Rong ; Kohno, Tatsuro ; Moore, Kimberly A ; Woolf, Clifford J</creatorcontrib><description>Synaptic plasticity is fundamental to many neurobiological functions, including memory and pain. Central sensitization refers to the increased synaptic efficacy established in somatosensory neurons in the dorsal horn of the spinal cord following intense peripheral noxious stimuli, tissue injury or nerve damage. This heightened synaptic transmission leads to a reduction in pain threshold, an amplification of pain responses and a spread of pain sensitivity to non-injured areas. In the cortex, LTP – a long-lasting highly localized increase in synaptic strength – is a synaptic substrate for memory and learning. Analysis of the molecular mechanisms underlying the generation and maintenance of central sensitization and LTP indicates that, although there are differences between the synaptic plasticity contributing to memory and pain, there are also striking similarities.</description><identifier>ISSN: 0166-2236</identifier><identifier>EISSN: 1878-108X</identifier><identifier>DOI: 10.1016/j.tins.2003.09.017</identifier><identifier>PMID: 14624855</identifier><identifier>CODEN: TNSCDR</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Humans ; Long-Term Potentiation - physiology ; Memory - physiology ; Nervous system ; Neurology ; Neurons ; Pain - physiopathology ; Sensation - physiology ; Spinal cord injuries</subject><ispartof>Trends in neurosciences (Regular ed.), 2003-12, Vol.26 (12), p.696-705</ispartof><rights>2003 Elsevier Ltd</rights><rights>Copyright Elsevier Sequoia S.A. Dec 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c574t-7b1872749787fa9c77f577291be3e7639a9745fecf73efb80f70777b6f06ac183</citedby><cites>FETCH-LOGICAL-c574t-7b1872749787fa9c77f577291be3e7639a9745fecf73efb80f70777b6f06ac183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.tins.2003.09.017$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14624855$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ji, Ru-Rong</creatorcontrib><creatorcontrib>Kohno, Tatsuro</creatorcontrib><creatorcontrib>Moore, Kimberly A</creatorcontrib><creatorcontrib>Woolf, Clifford J</creatorcontrib><title>Central sensitization and LTP: do pain and memory share similar mechanisms?</title><title>Trends in neurosciences (Regular ed.)</title><addtitle>Trends Neurosci</addtitle><description>Synaptic plasticity is fundamental to many neurobiological functions, including memory and pain. Central sensitization refers to the increased synaptic efficacy established in somatosensory neurons in the dorsal horn of the spinal cord following intense peripheral noxious stimuli, tissue injury or nerve damage. This heightened synaptic transmission leads to a reduction in pain threshold, an amplification of pain responses and a spread of pain sensitivity to non-injured areas. In the cortex, LTP – a long-lasting highly localized increase in synaptic strength – is a synaptic substrate for memory and learning. Analysis of the molecular mechanisms underlying the generation and maintenance of central sensitization and LTP indicates that, although there are differences between the synaptic plasticity contributing to memory and pain, there are also striking similarities.</description><subject>Animals</subject><subject>Humans</subject><subject>Long-Term Potentiation - physiology</subject><subject>Memory - physiology</subject><subject>Nervous system</subject><subject>Neurology</subject><subject>Neurons</subject><subject>Pain - physiopathology</subject><subject>Sensation - physiology</subject><subject>Spinal cord injuries</subject><issn>0166-2236</issn><issn>1878-108X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1rGzEQhkVoadykfyCHsPSQ224l7cdIoRCCadMQQ3JwoTeh1Y6wzK7WkdYF59dXxoZADs1JMDzzMnofQi4YLRhlzbd1MTkfC05pWVBZUAYnZMYEiJxR8ecDmSWoyTkvm1PyOcY1pawSrPpETlnV8ErU9Yw8zNFPQfdZRB_d5F705Eafad9li-XTddaN2Ua7w2DAYQy7LK50wCy6wfU6pKFZae_iEG_OyUer-4hfju8Z-f3zx3L-K1883t3Pbxe5qaGacmjTjRwqCQKslgbA1gBcshZLhKaUWkJVWzQWSrStoBYoALSNpY02TJRn5OqQuwnj8xbjpAYXDfa99jhuowJWghRN_S7IJGepKpbAr2_A9bgNPn1C8XRsqrHaQ_wAmTDGGNCqTXCDDjvFqNoLUWu1F6L2QhSVKglJS5fH5G07YPe6cjSQgO8HAFNjfx0GFY1Db7BzAc2kutH9L_8fzEea2A</recordid><startdate>20031201</startdate><enddate>20031201</enddate><creator>Ji, Ru-Rong</creator><creator>Kohno, Tatsuro</creator><creator>Moore, Kimberly A</creator><creator>Woolf, Clifford J</creator><general>Elsevier Ltd</general><general>Elsevier Sequoia S.A</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20031201</creationdate><title>Central sensitization and LTP: do pain and memory share similar mechanisms?</title><author>Ji, Ru-Rong ; Kohno, Tatsuro ; Moore, Kimberly A ; Woolf, Clifford J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-7b1872749787fa9c77f577291be3e7639a9745fecf73efb80f70777b6f06ac183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Humans</topic><topic>Long-Term Potentiation - physiology</topic><topic>Memory - physiology</topic><topic>Nervous system</topic><topic>Neurology</topic><topic>Neurons</topic><topic>Pain - physiopathology</topic><topic>Sensation - physiology</topic><topic>Spinal cord injuries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ji, Ru-Rong</creatorcontrib><creatorcontrib>Kohno, Tatsuro</creatorcontrib><creatorcontrib>Moore, Kimberly A</creatorcontrib><creatorcontrib>Woolf, Clifford J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Trends in neurosciences (Regular ed.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ji, Ru-Rong</au><au>Kohno, Tatsuro</au><au>Moore, Kimberly A</au><au>Woolf, Clifford J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Central sensitization and LTP: do pain and memory share similar mechanisms?</atitle><jtitle>Trends in neurosciences (Regular ed.)</jtitle><addtitle>Trends Neurosci</addtitle><date>2003-12-01</date><risdate>2003</risdate><volume>26</volume><issue>12</issue><spage>696</spage><epage>705</epage><pages>696-705</pages><issn>0166-2236</issn><eissn>1878-108X</eissn><coden>TNSCDR</coden><abstract>Synaptic plasticity is fundamental to many neurobiological functions, including memory and pain. Central sensitization refers to the increased synaptic efficacy established in somatosensory neurons in the dorsal horn of the spinal cord following intense peripheral noxious stimuli, tissue injury or nerve damage. This heightened synaptic transmission leads to a reduction in pain threshold, an amplification of pain responses and a spread of pain sensitivity to non-injured areas. In the cortex, LTP – a long-lasting highly localized increase in synaptic strength – is a synaptic substrate for memory and learning. Analysis of the molecular mechanisms underlying the generation and maintenance of central sensitization and LTP indicates that, although there are differences between the synaptic plasticity contributing to memory and pain, there are also striking similarities.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>14624855</pmid><doi>10.1016/j.tins.2003.09.017</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0166-2236 |
ispartof | Trends in neurosciences (Regular ed.), 2003-12, Vol.26 (12), p.696-705 |
issn | 0166-2236 1878-108X |
language | eng |
recordid | cdi_proquest_miscellaneous_71379865 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Animals Humans Long-Term Potentiation - physiology Memory - physiology Nervous system Neurology Neurons Pain - physiopathology Sensation - physiology Spinal cord injuries |
title | Central sensitization and LTP: do pain and memory share similar mechanisms? |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T20%3A09%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Central%20sensitization%20and%20LTP:%20do%20pain%20and%20memory%20share%20similar%20mechanisms?&rft.jtitle=Trends%20in%20neurosciences%20(Regular%20ed.)&rft.au=Ji,%20Ru-Rong&rft.date=2003-12-01&rft.volume=26&rft.issue=12&rft.spage=696&rft.epage=705&rft.pages=696-705&rft.issn=0166-2236&rft.eissn=1878-108X&rft.coden=TNSCDR&rft_id=info:doi/10.1016/j.tins.2003.09.017&rft_dat=%3Cproquest_cross%3E566296331%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=218716641&rft_id=info:pmid/14624855&rft_els_id=S0166223603003370&rfr_iscdi=true |