Sources of GABAergic input to the inferior colliculus of the rat
We have studied the GABAergic projections to the inferior colliculus (IC) of the rat by combining the retrograde transport of horseradish peroxidase (HRP) and immunohistochemistry for γ‐amino butyric acid (GABA). Medium‐sized (0.06–0.14 μl) HRP injections were made in the ventral part of the central...
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Veröffentlicht in: | Journal of comparative neurology (1911) 1996-08, Vol.372 (2), p.309-326 |
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description | We have studied the GABAergic projections to the inferior colliculus (IC) of the rat by combining the retrograde transport of horseradish peroxidase (HRP) and immunohistochemistry for γ‐amino butyric acid (GABA). Medium‐sized (0.06–0.14 μl) HRP injections were made in the ventral part of the central nucleus (CNIC), in the dorsal part of the CNIC, in the dorsal cortex (DCIC), and in the external cortex (ECIC) of the IC. Single HRP‐labeled and double (HRP‐GABA)‐labeled neurons were systematically counted in all brainstem auditory nuclei.
Our results revealed that the IC receives GABAergic afferent connections from ipsi‐ and contralateral brainstem auditory nuclei. Most of the contralateral GABAergic input originates in the IC and the dorsal nucleus of the lateral lemniscus (DNLL). The dorsal region of the IC (DCIC and dorsal part of the CNIC) receives connections mostly from its homonimous contralateral region, and the ventral region from the contralateral DNLL. The commissural GABAergic projections originate in a morphologically heterogeneous neuronal population that includes small to medium‐sized round and fusiform neurons as well as large and giant neurons. Quantitatively, the ipsilateral ventral nucleus of the lateral lemniscus is the most important source of GABAergic input to the CNIC. In the superior olivary complex, a smaller number of neurons, which lie mainly in the periolivary nuclei, display double labeling. In the contralateral cochlear nuclei, only a few of the retrogradely labeled neurons were GABA immunoreactive.
These findings give us more information about the role of GABA in the auditory system, indicating that inhibitory inputs from different ipsi‐ and contralateral, mono‐ and binaural auditory brainstem centers converge in the IC. © 1996 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1096-9861(19960819)372:2<309::AID-CNE11>3.0.CO;2-E |
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Our results revealed that the IC receives GABAergic afferent connections from ipsi‐ and contralateral brainstem auditory nuclei. Most of the contralateral GABAergic input originates in the IC and the dorsal nucleus of the lateral lemniscus (DNLL). The dorsal region of the IC (DCIC and dorsal part of the CNIC) receives connections mostly from its homonimous contralateral region, and the ventral region from the contralateral DNLL. The commissural GABAergic projections originate in a morphologically heterogeneous neuronal population that includes small to medium‐sized round and fusiform neurons as well as large and giant neurons. Quantitatively, the ipsilateral ventral nucleus of the lateral lemniscus is the most important source of GABAergic input to the CNIC. In the superior olivary complex, a smaller number of neurons, which lie mainly in the periolivary nuclei, display double labeling. In the contralateral cochlear nuclei, only a few of the retrogradely labeled neurons were GABA immunoreactive.
These findings give us more information about the role of GABA in the auditory system, indicating that inhibitory inputs from different ipsi‐ and contralateral, mono‐ and binaural auditory brainstem centers converge in the IC. © 1996 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/(SICI)1096-9861(19960819)372:2<309::AID-CNE11>3.0.CO;2-E</identifier><identifier>PMID: 8863133</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>acoustic midbrain ; afferent connections ; Animals ; binaural processing ; GABA ; gamma-Aminobutyric Acid - metabolism ; Immunohistochemistry ; Inferior Colliculi - metabolism ; Neural Pathways - metabolism ; Rats ; Rats, Sprague-Dawley</subject><ispartof>Journal of comparative neurology (1911), 1996-08, Vol.372 (2), p.309-326</ispartof><rights>Copyright © 1996 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5041-f3a9050690bb7cae3bffa942fd0feaf028842d89fb51b9176feb33b9a30fbd313</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%2819960819%29372%3A2%3C309%3A%3AAID-CNE11%3E3.0.CO%3B2-E$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291096-9861%2819960819%29372%3A2%3C309%3A%3AAID-CNE11%3E3.0.CO%3B2-E$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8863133$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>González-Hernández, Tomás</creatorcontrib><creatorcontrib>Mantolán-Sarmiento, Beatriz</creatorcontrib><creatorcontrib>González-González, Belén</creatorcontrib><creatorcontrib>Pérez-González, Herminia</creatorcontrib><title>Sources of GABAergic input to the inferior colliculus of the rat</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>We have studied the GABAergic projections to the inferior colliculus (IC) of the rat by combining the retrograde transport of horseradish peroxidase (HRP) and immunohistochemistry for γ‐amino butyric acid (GABA). Medium‐sized (0.06–0.14 μl) HRP injections were made in the ventral part of the central nucleus (CNIC), in the dorsal part of the CNIC, in the dorsal cortex (DCIC), and in the external cortex (ECIC) of the IC. Single HRP‐labeled and double (HRP‐GABA)‐labeled neurons were systematically counted in all brainstem auditory nuclei.
Our results revealed that the IC receives GABAergic afferent connections from ipsi‐ and contralateral brainstem auditory nuclei. Most of the contralateral GABAergic input originates in the IC and the dorsal nucleus of the lateral lemniscus (DNLL). The dorsal region of the IC (DCIC and dorsal part of the CNIC) receives connections mostly from its homonimous contralateral region, and the ventral region from the contralateral DNLL. The commissural GABAergic projections originate in a morphologically heterogeneous neuronal population that includes small to medium‐sized round and fusiform neurons as well as large and giant neurons. Quantitatively, the ipsilateral ventral nucleus of the lateral lemniscus is the most important source of GABAergic input to the CNIC. In the superior olivary complex, a smaller number of neurons, which lie mainly in the periolivary nuclei, display double labeling. In the contralateral cochlear nuclei, only a few of the retrogradely labeled neurons were GABA immunoreactive.
These findings give us more information about the role of GABA in the auditory system, indicating that inhibitory inputs from different ipsi‐ and contralateral, mono‐ and binaural auditory brainstem centers converge in the IC. © 1996 Wiley‐Liss, Inc.</description><subject>acoustic midbrain</subject><subject>afferent connections</subject><subject>Animals</subject><subject>binaural processing</subject><subject>GABA</subject><subject>gamma-Aminobutyric Acid - metabolism</subject><subject>Immunohistochemistry</subject><subject>Inferior Colliculi - metabolism</subject><subject>Neural Pathways - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU-P0zAQxS0EWsrCR0DKCe0eUsZ2E9sFoS2hlKKlFVr-nkZ2ai-BdFPsRLDfHmdTegFpT5Zn3vzeaB4hZxTGFIA9PblYFstTCipPlczpCVUqB0nVKRdsyp5zUNPpbPkqLVZzSl_wMYyL9TOWzu-Q0WHoLhlFFE3jqLhPHoTwHQCU4vKIHEmZc8r5iJxdNJ0vbUgalyxmL2fWX1ZlUl3tujZpm6T9ZuPHWV81Pimbuq7Kru5u1H3L6_Yhued0Heyj_XtMPr6efyjepOfrxbKYnadlBhOaOq4VZJArMEaU2nLjnFYT5jbgrHbApJywjVTOZNQoKnJnDedGaQ7ObOKux-TJwN355mdnQ4vbKpS2rvWVbbqAIs5TwcStQppJKTlTUfhlEJa-CcFbhztfbbW_RgrYp4DYp4D9QbE_KP5NAWMKyDCmgBhTwJsUkCNgsY71eUQ_3u_Qma3dHMD7s8f-16H_q6rt9T--t9v-z3UoRHY6sKvQ2t8HtvY_MBdcZPh5tcBPb7P3q3eZQMb_AOrwsTQ</recordid><startdate>19960819</startdate><enddate>19960819</enddate><creator>González-Hernández, Tomás</creator><creator>Mantolán-Sarmiento, Beatriz</creator><creator>González-González, Belén</creator><creator>Pérez-González, Herminia</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>19960819</creationdate><title>Sources of GABAergic input to the inferior colliculus of the rat</title><author>González-Hernández, Tomás ; Mantolán-Sarmiento, Beatriz ; González-González, Belén ; Pérez-González, Herminia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5041-f3a9050690bb7cae3bffa942fd0feaf028842d89fb51b9176feb33b9a30fbd313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>acoustic midbrain</topic><topic>afferent connections</topic><topic>Animals</topic><topic>binaural processing</topic><topic>GABA</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>Immunohistochemistry</topic><topic>Inferior Colliculi - metabolism</topic><topic>Neural Pathways - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>González-Hernández, Tomás</creatorcontrib><creatorcontrib>Mantolán-Sarmiento, Beatriz</creatorcontrib><creatorcontrib>González-González, Belén</creatorcontrib><creatorcontrib>Pérez-González, Herminia</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>González-Hernández, Tomás</au><au>Mantolán-Sarmiento, Beatriz</au><au>González-González, Belén</au><au>Pérez-González, Herminia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sources of GABAergic input to the inferior colliculus of the rat</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>1996-08-19</date><risdate>1996</risdate><volume>372</volume><issue>2</issue><spage>309</spage><epage>326</epage><pages>309-326</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>We have studied the GABAergic projections to the inferior colliculus (IC) of the rat by combining the retrograde transport of horseradish peroxidase (HRP) and immunohistochemistry for γ‐amino butyric acid (GABA). Medium‐sized (0.06–0.14 μl) HRP injections were made in the ventral part of the central nucleus (CNIC), in the dorsal part of the CNIC, in the dorsal cortex (DCIC), and in the external cortex (ECIC) of the IC. Single HRP‐labeled and double (HRP‐GABA)‐labeled neurons were systematically counted in all brainstem auditory nuclei.
Our results revealed that the IC receives GABAergic afferent connections from ipsi‐ and contralateral brainstem auditory nuclei. Most of the contralateral GABAergic input originates in the IC and the dorsal nucleus of the lateral lemniscus (DNLL). The dorsal region of the IC (DCIC and dorsal part of the CNIC) receives connections mostly from its homonimous contralateral region, and the ventral region from the contralateral DNLL. The commissural GABAergic projections originate in a morphologically heterogeneous neuronal population that includes small to medium‐sized round and fusiform neurons as well as large and giant neurons. Quantitatively, the ipsilateral ventral nucleus of the lateral lemniscus is the most important source of GABAergic input to the CNIC. In the superior olivary complex, a smaller number of neurons, which lie mainly in the periolivary nuclei, display double labeling. In the contralateral cochlear nuclei, only a few of the retrogradely labeled neurons were GABA immunoreactive.
These findings give us more information about the role of GABA in the auditory system, indicating that inhibitory inputs from different ipsi‐ and contralateral, mono‐ and binaural auditory brainstem centers converge in the IC. © 1996 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>8863133</pmid><doi>10.1002/(SICI)1096-9861(19960819)372:2<309::AID-CNE11>3.0.CO;2-E</doi><tpages>18</tpages></addata></record> |
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subjects | acoustic midbrain afferent connections Animals binaural processing GABA gamma-Aminobutyric Acid - metabolism Immunohistochemistry Inferior Colliculi - metabolism Neural Pathways - metabolism Rats Rats, Sprague-Dawley |
title | Sources of GABAergic input to the inferior colliculus of the rat |
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