Thalamocortical and intracortical projections to the forelimb-stump SI representation of rats that sustained neonatal forelimb removal
We previously reported the abnormal expression of hindlimb receptive fields in the stump representation of the primary somatosensory cortex (SI) in rats that sustained neonatal forelimb removal when cortical γ‐aminobutyric acid (GABA) receptors were pharmacologically blocked (Lane et al. [1997] J. N...
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description | We previously reported the abnormal expression of hindlimb receptive fields in the stump representation of the primary somatosensory cortex (SI) in rats that sustained neonatal forelimb removal when cortical γ‐aminobutyric acid (GABA) receptors were pharmacologically blocked (Lane et al. [1997] J. Neurophysiol. 77:2723–2735). In this study, we attempted to identify the substrate for this functional modification. Three potential substrates were examined: 1) changes in intracortical connections within SI; 2) alterations in the projection pattern of thalamocortical afferents from the ventroposterior lateral (VPL) nucleus to SI; and 3) changes in the receptive fields of thalamocortical neurons. We used biotinylated dextran amine and Phaseolus vulgaris leucoagglutinin to examine the intracortical projections associated with the stump and hindlimb representations of SI. True Blue and Diamidino Yellow were used to study the organization of the VPL projections to SI. Finally, single‐unit recordings from VPL neurons were made to examine the functional organization of this nucleus in neonatally amputated adult rats. Tracer studies demonstrated no significant change in the intracortical connections or VPL projections associated with the stump and hindlimb SI in neonatally amputated rats. Recordings from VPL of neonatally manipulated rats revealed a small, but significant, population of cells (19.0%) within the stump representation that had dual stump and hindlimb receptive fields. Thus, the data suggest that the functional reorganization observed in SI of neonatally amputated rats may reflect functional alterations occurring in its thalamic inputs. J. Comp. Neurol. 401:187–204, 1998. © 1998 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1096-9861(19981116)401:2<187::AID-CNE3>3.0.CO;2-X |
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[1997] J. Neurophysiol. 77:2723–2735). In this study, we attempted to identify the substrate for this functional modification. Three potential substrates were examined: 1) changes in intracortical connections within SI; 2) alterations in the projection pattern of thalamocortical afferents from the ventroposterior lateral (VPL) nucleus to SI; and 3) changes in the receptive fields of thalamocortical neurons. We used biotinylated dextran amine and Phaseolus vulgaris leucoagglutinin to examine the intracortical projections associated with the stump and hindlimb representations of SI. True Blue and Diamidino Yellow were used to study the organization of the VPL projections to SI. Finally, single‐unit recordings from VPL neurons were made to examine the functional organization of this nucleus in neonatally amputated adult rats. Tracer studies demonstrated no significant change in the intracortical connections or VPL projections associated with the stump and hindlimb SI in neonatally amputated rats. Recordings from VPL of neonatally manipulated rats revealed a small, but significant, population of cells (19.0%) within the stump representation that had dual stump and hindlimb receptive fields. Thus, the data suggest that the functional reorganization observed in SI of neonatally amputated rats may reflect functional alterations occurring in its thalamic inputs. J. Comp. Neurol. 401:187–204, 1998. © 1998 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/(SICI)1096-9861(19981116)401:2<187::AID-CNE3>3.0.CO;2-X</identifier><identifier>PMID: 9822148</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Amidines ; Amputation ; Animals ; Animals, Newborn ; Biotin - analogs & derivatives ; biotinylated dextran amine ; Brachial Plexus - cytology ; Denervation ; Dextrans ; Electrophysiology ; Fluorescent Dyes ; Forelimb - innervation ; Forelimb - surgery ; Neural Pathways ; Neuronal Plasticity - physiology ; Neurons, Afferent - physiology ; Phaseolus vulgaris leucoagglutinin ; Phytohemagglutinins ; Rats - anatomy & histology ; rodent ; somatosensory and ventroposterior lateral nucleus ; Somatosensory Cortex - cytology ; Thalamus - cytology</subject><ispartof>Journal of comparative neurology (1911), 1998-11, Vol.401 (2), p.187-204</ispartof><rights>Copyright © 1998 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4353-ab1dda3c6a1ae7f4fca21b7dd1be0d453b0e64e71acb43d73fa8f15a8731d1e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291096-9861%2819981116%29401%3A2%3C187%3A%3AAID-CNE3%3E3.0.CO%3B2-X$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291096-9861%2819981116%29401%3A2%3C187%3A%3AAID-CNE3%3E3.0.CO%3B2-X$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9822148$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stojic, Andrey S.</creatorcontrib><creatorcontrib>Lane, Richard D.</creatorcontrib><creatorcontrib>Killackey, Herbert P.</creatorcontrib><creatorcontrib>Qadri, Babar A.</creatorcontrib><creatorcontrib>Rhoades, Robert W.</creatorcontrib><title>Thalamocortical and intracortical projections to the forelimb-stump SI representation of rats that sustained neonatal forelimb removal</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>We previously reported the abnormal expression of hindlimb receptive fields in the stump representation of the primary somatosensory cortex (SI) in rats that sustained neonatal forelimb removal when cortical γ‐aminobutyric acid (GABA) receptors were pharmacologically blocked (Lane et al. [1997] J. Neurophysiol. 77:2723–2735). In this study, we attempted to identify the substrate for this functional modification. Three potential substrates were examined: 1) changes in intracortical connections within SI; 2) alterations in the projection pattern of thalamocortical afferents from the ventroposterior lateral (VPL) nucleus to SI; and 3) changes in the receptive fields of thalamocortical neurons. We used biotinylated dextran amine and Phaseolus vulgaris leucoagglutinin to examine the intracortical projections associated with the stump and hindlimb representations of SI. True Blue and Diamidino Yellow were used to study the organization of the VPL projections to SI. Finally, single‐unit recordings from VPL neurons were made to examine the functional organization of this nucleus in neonatally amputated adult rats. Tracer studies demonstrated no significant change in the intracortical connections or VPL projections associated with the stump and hindlimb SI in neonatally amputated rats. Recordings from VPL of neonatally manipulated rats revealed a small, but significant, population of cells (19.0%) within the stump representation that had dual stump and hindlimb receptive fields. Thus, the data suggest that the functional reorganization observed in SI of neonatally amputated rats may reflect functional alterations occurring in its thalamic inputs. J. Comp. Neurol. 401:187–204, 1998. © 1998 Wiley‐Liss, Inc.</description><subject>Amidines</subject><subject>Amputation</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biotin - analogs & derivatives</subject><subject>biotinylated dextran amine</subject><subject>Brachial Plexus - cytology</subject><subject>Denervation</subject><subject>Dextrans</subject><subject>Electrophysiology</subject><subject>Fluorescent Dyes</subject><subject>Forelimb - innervation</subject><subject>Forelimb - surgery</subject><subject>Neural Pathways</subject><subject>Neuronal Plasticity - physiology</subject><subject>Neurons, Afferent - physiology</subject><subject>Phaseolus vulgaris leucoagglutinin</subject><subject>Phytohemagglutinins</subject><subject>Rats - anatomy & histology</subject><subject>rodent</subject><subject>somatosensory and ventroposterior lateral nucleus</subject><subject>Somatosensory Cortex - cytology</subject><subject>Thalamus - cytology</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV1v0zAUhiMEGmPwE5B8hbaLFJ84ieOCQFNYR8W0XnRoEzdHJ4mjZuSj2C6wP8DvxqFduQBpV5at9zzvsZ4geA98ApxHr4-X83x-AlylocpSOAalMgBIT2IO0-gtZHI6PZ1_CPPLM_FOTPgkX7yJwptHweF-5nFw6EkQKpXKp8Eza28550qJ7CA4UFkUQZwdBr-uVtRSN5SDcU1JLaO-Yk3vDO1f1ma41aVrht4yNzC30qwejG6brgit23Rrtpwzo9dGW907GoNsqJkh5_MrcsxurKOm1xXr9dCT88x7gJ_rhu_UPg-e1NRa_WJ3HgWfZ2dX-cfwYnE-z08vwjIWiQipgKoiUaYEpGUd1yVFUMiqgkLzKk5EwXUaawlUFrGopKgpqyGhTAqoQCfiKHi15fpPfdto67BrbKnblvxqG4uS85QnoB4MggQFUZb54PU2WJrBWqNrXJumI3OHwHFUiTiqxFELjlrwXiV6lRihV4noVeKoEgVyzBf--caTX-5W2BSdrvbcnbu_zT-aVt_9U_tw639K_9w9OdySG-v0zz2ZzFdMpZAJXl-eYzz78mmZzHyR-A1mZ81P</recordid><startdate>19981116</startdate><enddate>19981116</enddate><creator>Stojic, Andrey S.</creator><creator>Lane, Richard D.</creator><creator>Killackey, Herbert P.</creator><creator>Qadri, Babar A.</creator><creator>Rhoades, Robert W.</creator><general>John Wiley & Sons, Inc</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>19981116</creationdate><title>Thalamocortical and intracortical projections to the forelimb-stump SI representation of rats that sustained neonatal forelimb removal</title><author>Stojic, Andrey S. ; Lane, Richard D. ; Killackey, Herbert P. ; Qadri, Babar A. ; Rhoades, Robert W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4353-ab1dda3c6a1ae7f4fca21b7dd1be0d453b0e64e71acb43d73fa8f15a8731d1e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Amidines</topic><topic>Amputation</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biotin - analogs & derivatives</topic><topic>biotinylated dextran amine</topic><topic>Brachial Plexus - cytology</topic><topic>Denervation</topic><topic>Dextrans</topic><topic>Electrophysiology</topic><topic>Fluorescent Dyes</topic><topic>Forelimb - innervation</topic><topic>Forelimb - surgery</topic><topic>Neural Pathways</topic><topic>Neuronal Plasticity - physiology</topic><topic>Neurons, Afferent - physiology</topic><topic>Phaseolus vulgaris leucoagglutinin</topic><topic>Phytohemagglutinins</topic><topic>Rats - anatomy & histology</topic><topic>rodent</topic><topic>somatosensory and ventroposterior lateral nucleus</topic><topic>Somatosensory Cortex - cytology</topic><topic>Thalamus - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stojic, Andrey S.</creatorcontrib><creatorcontrib>Lane, Richard D.</creatorcontrib><creatorcontrib>Killackey, Herbert P.</creatorcontrib><creatorcontrib>Qadri, Babar A.</creatorcontrib><creatorcontrib>Rhoades, Robert W.</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stojic, Andrey S.</au><au>Lane, Richard D.</au><au>Killackey, Herbert P.</au><au>Qadri, Babar A.</au><au>Rhoades, Robert W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thalamocortical and intracortical projections to the forelimb-stump SI representation of rats that sustained neonatal forelimb removal</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>1998-11-16</date><risdate>1998</risdate><volume>401</volume><issue>2</issue><spage>187</spage><epage>204</epage><pages>187-204</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>We previously reported the abnormal expression of hindlimb receptive fields in the stump representation of the primary somatosensory cortex (SI) in rats that sustained neonatal forelimb removal when cortical γ‐aminobutyric acid (GABA) receptors were pharmacologically blocked (Lane et al. [1997] J. Neurophysiol. 77:2723–2735). In this study, we attempted to identify the substrate for this functional modification. Three potential substrates were examined: 1) changes in intracortical connections within SI; 2) alterations in the projection pattern of thalamocortical afferents from the ventroposterior lateral (VPL) nucleus to SI; and 3) changes in the receptive fields of thalamocortical neurons. We used biotinylated dextran amine and Phaseolus vulgaris leucoagglutinin to examine the intracortical projections associated with the stump and hindlimb representations of SI. True Blue and Diamidino Yellow were used to study the organization of the VPL projections to SI. Finally, single‐unit recordings from VPL neurons were made to examine the functional organization of this nucleus in neonatally amputated adult rats. Tracer studies demonstrated no significant change in the intracortical connections or VPL projections associated with the stump and hindlimb SI in neonatally amputated rats. Recordings from VPL of neonatally manipulated rats revealed a small, but significant, population of cells (19.0%) within the stump representation that had dual stump and hindlimb receptive fields. Thus, the data suggest that the functional reorganization observed in SI of neonatally amputated rats may reflect functional alterations occurring in its thalamic inputs. J. Comp. Neurol. 401:187–204, 1998. © 1998 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>9822148</pmid><doi>10.1002/(SICI)1096-9861(19981116)401:2<187::AID-CNE3>3.0.CO;2-X</doi><tpages>18</tpages></addata></record> |
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subjects | Amidines Amputation Animals Animals, Newborn Biotin - analogs & derivatives biotinylated dextran amine Brachial Plexus - cytology Denervation Dextrans Electrophysiology Fluorescent Dyes Forelimb - innervation Forelimb - surgery Neural Pathways Neuronal Plasticity - physiology Neurons, Afferent - physiology Phaseolus vulgaris leucoagglutinin Phytohemagglutinins Rats - anatomy & histology rodent somatosensory and ventroposterior lateral nucleus Somatosensory Cortex - cytology Thalamus - cytology |
title | Thalamocortical and intracortical projections to the forelimb-stump SI representation of rats that sustained neonatal forelimb removal |
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