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Cellular and molecular bases of neuroplasticity: brainstem effects after cochlear damage
After a cochlear lesion or auditory nerve damage, afferent connections from auditory ganglia can be highly altered. This results in a clear reduction of auditory input and an alteration of connectivity of terminals on cochlear nuclei neurons. Such a process could stimulate the reorganization of the...
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Published in: | Acta oto-laryngologica 2010-03, Vol.130 (3), p.318-325 |
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creator | Gil-Loyzaga, Pablo Carricondo, Francisco Bartolomé, Maria V. Iglesias, Mari C. Rodríguez, Fernando Poch-Broto, Joaquin |
description | After a cochlear lesion or auditory nerve damage, afferent connections from auditory ganglia can be highly altered. This results in a clear reduction of auditory input and an alteration of connectivity of terminals on cochlear nuclei neurons. Such a process could stimulate the reorganization of the neural circuits and neuroplasticity. Cochlea removal has been demonstrated to be a good model in which to analyse brainstem neuroplasticity, particularly with regard to the cochlear nuclei. After cochlea removal three main periods of degeneration and regeneration were observed. Early effects, during the first week post lesion, involved acute degeneration with nerve ending oedema and degeneration. During the second and, probably, the third post lesion weeks, degeneration was still present, even though a limited and diffuse expression of GAP-43 started. Around 1 month post lesion, degeneration at the cochlear nuclei progressively disappeared and a relevant GAP-43 expression was found. We conclude that neuroplasticity leads neurons to modify their activity and/or their synaptic tree as a consequence of animal adaptation to learning and memory. For the human being neuroplasticity is involved in language learning and comprehension, particularly the acquisition of a second language. Neuroplasticity is important for therapeutic strategies, such as hearing aids and cochlear implants. |
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This results in a clear reduction of auditory input and an alteration of connectivity of terminals on cochlear nuclei neurons. Such a process could stimulate the reorganization of the neural circuits and neuroplasticity. Cochlea removal has been demonstrated to be a good model in which to analyse brainstem neuroplasticity, particularly with regard to the cochlear nuclei. After cochlea removal three main periods of degeneration and regeneration were observed. Early effects, during the first week post lesion, involved acute degeneration with nerve ending oedema and degeneration. During the second and, probably, the third post lesion weeks, degeneration was still present, even though a limited and diffuse expression of GAP-43 started. Around 1 month post lesion, degeneration at the cochlear nuclei progressively disappeared and a relevant GAP-43 expression was found. We conclude that neuroplasticity leads neurons to modify their activity and/or their synaptic tree as a consequence of animal adaptation to learning and memory. For the human being neuroplasticity is involved in language learning and comprehension, particularly the acquisition of a second language. Neuroplasticity is important for therapeutic strategies, such as hearing aids and cochlear implants.</description><identifier>ISSN: 0001-6489</identifier><identifier>EISSN: 1651-2251</identifier><identifier>DOI: 10.3109/00016480903127468</identifier><identifier>PMID: 19593683</identifier><identifier>CODEN: AOLAAJ</identifier><language>eng</language><publisher>Stockholm: Informa UK Ltd</publisher><subject>Animals ; Auditory Pathways - pathology ; Auditory Pathways - physiopathology ; auditory system ; Biological and medical sciences ; Brain Stem - pathology ; Brain Stem - physiopathology ; brainstem ; cochlea ; Cochlear Nerve - pathology ; Cochlear Nerve - physiopathology ; cochlear nuclei ; Cochlear Nucleus - pathology ; Cochlear Nucleus - physiopathology ; Disease Models, Animal ; GAP-43 Protein - genetics ; Gene Expression - genetics ; Guinea Pigs ; Humans ; Medical sciences ; Nerve Regeneration - genetics ; Nerve Regeneration - physiology ; Neuronal Plasticity - genetics ; Neuronal Plasticity - physiology ; Neuroplasticity ; Otorhinolaryngology. Stomatology ; Synapses ; Young Adult</subject><ispartof>Acta oto-laryngologica, 2010-03, Vol.130 (3), p.318-325</ispartof><rights>2010 Informa UK Ltd. (Informa Healthcare, Taylor & Francis AS) 2010</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-20de1d491642f8b1c07b55294150ec18efc5b682a9ce03539a59d9b7b75c43433</citedby><cites>FETCH-LOGICAL-c435t-20de1d491642f8b1c07b55294150ec18efc5b682a9ce03539a59d9b7b75c43433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22474351$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19593683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gil-Loyzaga, Pablo</creatorcontrib><creatorcontrib>Carricondo, Francisco</creatorcontrib><creatorcontrib>Bartolomé, Maria V.</creatorcontrib><creatorcontrib>Iglesias, Mari C.</creatorcontrib><creatorcontrib>Rodríguez, Fernando</creatorcontrib><creatorcontrib>Poch-Broto, Joaquin</creatorcontrib><title>Cellular and molecular bases of neuroplasticity: brainstem effects after cochlear damage</title><title>Acta oto-laryngologica</title><addtitle>Acta Otolaryngol</addtitle><description>After a cochlear lesion or auditory nerve damage, afferent connections from auditory ganglia can be highly altered. This results in a clear reduction of auditory input and an alteration of connectivity of terminals on cochlear nuclei neurons. Such a process could stimulate the reorganization of the neural circuits and neuroplasticity. Cochlea removal has been demonstrated to be a good model in which to analyse brainstem neuroplasticity, particularly with regard to the cochlear nuclei. After cochlea removal three main periods of degeneration and regeneration were observed. Early effects, during the first week post lesion, involved acute degeneration with nerve ending oedema and degeneration. During the second and, probably, the third post lesion weeks, degeneration was still present, even though a limited and diffuse expression of GAP-43 started. Around 1 month post lesion, degeneration at the cochlear nuclei progressively disappeared and a relevant GAP-43 expression was found. We conclude that neuroplasticity leads neurons to modify their activity and/or their synaptic tree as a consequence of animal adaptation to learning and memory. For the human being neuroplasticity is involved in language learning and comprehension, particularly the acquisition of a second language. Neuroplasticity is important for therapeutic strategies, such as hearing aids and cochlear implants.</description><subject>Animals</subject><subject>Auditory Pathways - pathology</subject><subject>Auditory Pathways - physiopathology</subject><subject>auditory system</subject><subject>Biological and medical sciences</subject><subject>Brain Stem - pathology</subject><subject>Brain Stem - physiopathology</subject><subject>brainstem</subject><subject>cochlea</subject><subject>Cochlear Nerve - pathology</subject><subject>Cochlear Nerve - physiopathology</subject><subject>cochlear nuclei</subject><subject>Cochlear Nucleus - pathology</subject><subject>Cochlear Nucleus - physiopathology</subject><subject>Disease Models, Animal</subject><subject>GAP-43 Protein - genetics</subject><subject>Gene Expression - genetics</subject><subject>Guinea Pigs</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Nerve Regeneration - genetics</subject><subject>Nerve Regeneration - physiology</subject><subject>Neuronal Plasticity - genetics</subject><subject>Neuronal Plasticity - physiology</subject><subject>Neuroplasticity</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Synapses</subject><subject>Young Adult</subject><issn>0001-6489</issn><issn>1651-2251</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kE-P0zAQxS0Eot3CB-CyygVxCvhPHMe7XFDFAtJKXEDiFk2cMU3lxMV2hPrtcWlghZB6Go3m957mPUJeMPpaMKrfUEpZXTVUU8G4qurmEVmzWrKSc8kek_XpXmZAr8hVjPvTqhv5lKyYllrUjViTb1t0bnYQCpj6YvQOze-tg4ix8LaYcA7-4CCmwQzpeFN0AYYpJhwLtBZNigXYhKEw3uwcZmkPI3zHZ-SJBRfx-TI35Ovd-y_bj-X95w-ftu_uS1MJmUpOe2R9pXMObpuOGao6KbmumKRoWIPWyK5uOGiDVEihQeped6pTMhtUQmzIq7PvIfgfM8bUjkM0ORRM6OfYqkrWVClVZ5KdSRN8jAFtewjDCOHYMtqe-mz_6zNrrhf3uRuxf1AsBWbg5QJANOBsgMkM8S_HeaVyTpa5t2dumKwPI_z0wfVtgqPz4Y9IXPrj9h_5DsGlnYGA7d7PYcoNX0jxC6RNoi8</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>Gil-Loyzaga, Pablo</creator><creator>Carricondo, Francisco</creator><creator>Bartolomé, Maria V.</creator><creator>Iglesias, Mari C.</creator><creator>Rodríguez, Fernando</creator><creator>Poch-Broto, Joaquin</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Informa</general><scope>IQODW</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></search><sort><creationdate>20100301</creationdate><title>Cellular and molecular bases of neuroplasticity: brainstem effects after cochlear damage</title><author>Gil-Loyzaga, Pablo ; Carricondo, Francisco ; Bartolomé, Maria V. ; Iglesias, Mari C. ; Rodríguez, Fernando ; Poch-Broto, Joaquin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-20de1d491642f8b1c07b55294150ec18efc5b682a9ce03539a59d9b7b75c43433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Auditory Pathways - pathology</topic><topic>Auditory Pathways - physiopathology</topic><topic>auditory system</topic><topic>Biological and medical sciences</topic><topic>Brain Stem - pathology</topic><topic>Brain Stem - physiopathology</topic><topic>brainstem</topic><topic>cochlea</topic><topic>Cochlear Nerve - pathology</topic><topic>Cochlear Nerve - physiopathology</topic><topic>cochlear nuclei</topic><topic>Cochlear Nucleus - pathology</topic><topic>Cochlear Nucleus - physiopathology</topic><topic>Disease Models, Animal</topic><topic>GAP-43 Protein - genetics</topic><topic>Gene Expression - genetics</topic><topic>Guinea Pigs</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Nerve Regeneration - genetics</topic><topic>Nerve Regeneration - physiology</topic><topic>Neuronal Plasticity - genetics</topic><topic>Neuronal Plasticity - physiology</topic><topic>Neuroplasticity</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Synapses</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gil-Loyzaga, Pablo</creatorcontrib><creatorcontrib>Carricondo, Francisco</creatorcontrib><creatorcontrib>Bartolomé, Maria V.</creatorcontrib><creatorcontrib>Iglesias, Mari C.</creatorcontrib><creatorcontrib>Rodríguez, Fernando</creatorcontrib><creatorcontrib>Poch-Broto, Joaquin</creatorcontrib><collection>Pascal-Francis</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><jtitle>Acta oto-laryngologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gil-Loyzaga, Pablo</au><au>Carricondo, Francisco</au><au>Bartolomé, Maria V.</au><au>Iglesias, Mari C.</au><au>Rodríguez, Fernando</au><au>Poch-Broto, Joaquin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular and molecular bases of neuroplasticity: brainstem effects after cochlear damage</atitle><jtitle>Acta oto-laryngologica</jtitle><addtitle>Acta Otolaryngol</addtitle><date>2010-03-01</date><risdate>2010</risdate><volume>130</volume><issue>3</issue><spage>318</spage><epage>325</epage><pages>318-325</pages><issn>0001-6489</issn><eissn>1651-2251</eissn><coden>AOLAAJ</coden><abstract>After a cochlear lesion or auditory nerve damage, afferent connections from auditory ganglia can be highly altered. This results in a clear reduction of auditory input and an alteration of connectivity of terminals on cochlear nuclei neurons. Such a process could stimulate the reorganization of the neural circuits and neuroplasticity. Cochlea removal has been demonstrated to be a good model in which to analyse brainstem neuroplasticity, particularly with regard to the cochlear nuclei. After cochlea removal three main periods of degeneration and regeneration were observed. Early effects, during the first week post lesion, involved acute degeneration with nerve ending oedema and degeneration. During the second and, probably, the third post lesion weeks, degeneration was still present, even though a limited and diffuse expression of GAP-43 started. Around 1 month post lesion, degeneration at the cochlear nuclei progressively disappeared and a relevant GAP-43 expression was found. We conclude that neuroplasticity leads neurons to modify their activity and/or their synaptic tree as a consequence of animal adaptation to learning and memory. For the human being neuroplasticity is involved in language learning and comprehension, particularly the acquisition of a second language. Neuroplasticity is important for therapeutic strategies, such as hearing aids and cochlear implants.</abstract><cop>Stockholm</cop><pub>Informa UK Ltd</pub><pmid>19593683</pmid><doi>10.3109/00016480903127468</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Auditory Pathways - pathology Auditory Pathways - physiopathology auditory system Biological and medical sciences Brain Stem - pathology Brain Stem - physiopathology brainstem cochlea Cochlear Nerve - pathology Cochlear Nerve - physiopathology cochlear nuclei Cochlear Nucleus - pathology Cochlear Nucleus - physiopathology Disease Models, Animal GAP-43 Protein - genetics Gene Expression - genetics Guinea Pigs Humans Medical sciences Nerve Regeneration - genetics Nerve Regeneration - physiology Neuronal Plasticity - genetics Neuronal Plasticity - physiology Neuroplasticity Otorhinolaryngology. Stomatology Synapses Young Adult |
title | Cellular and molecular bases of neuroplasticity: brainstem effects after cochlear damage |
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