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Contribution of the lateral lemniscus to the control of swallowing in decerebrate cats
•Role of lemniscal area in the swallowing control was examined in decerebrate cats.•Stimulation of LLD facilitated but that of LLV and PBN–KFN inhibited swallowing.•Injections of glutamatergic and GABAergic agents into the LLD modulated swallowing.•LLD, a relay nucleus of auditory sensation, may con...
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Published in: | Neuroscience 2013-12, Vol.254, p.260-274 |
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description | •Role of lemniscal area in the swallowing control was examined in decerebrate cats.•Stimulation of LLD facilitated but that of LLV and PBN–KFN inhibited swallowing.•Injections of glutamatergic and GABAergic agents into the LLD modulated swallowing.•LLD, a relay nucleus of auditory sensation, may contribute to swallowing control.•Lemniscal area may have functional topography in the control of swallowing.
Lateral lemniscus, a relay nucleus of auditory sensation, is involved in the control of phonatory movements such as human speech and vocalization of animals. The present study was designed to test whether neurons in the lateral lemniscus contributed to the control of swallowing, one of non-phonic oro-pharyngolaryngeal movements. In acutely decerebrated cats (n=15), swallowing was induced by electrical stimulation (20–80μA at 10Hz for 20s with rectangular pulses of 0.2ms duration) delivered to the superior laryngeal nerve (SLN). Repetitive electrical stimulation (30–50μA at 50Hz for 10–20s) applied to the dorsal nucleus of the lateral lemniscus (LLD) increased the number and reduced the latency to the onset of the SLN-induced swallowing. On the other hand, stimulation of the ventral nucleus of the lateral lemniscus and the paralemniscal area, corresponding to the ventrolateral part of the parabrachial nucleus and the Kölliker–Fuse nucleus, often suppressed the SLN-induced swallowing. Microinjection of NMDA (0.1–0.15μl, 5.0–10mM) into the LLD through a stereotaxically placed glass micropipette facilitated the SLN-induced swallowing, i.e., the number was increased and the latency of swallowing was reduced. We also injected muscimol (a gamma amino-butyric acid (GABA)A receptor agonist), bicuculline (a GABAA receptor antagonist) and baclofen (a GABAB receptor agonist) into the LLD (0.1–0.15μl and 5.0mM for each substance). It was observed that an injection of muscimol suppressed the SLN-induced swallowing. However, an injection of bicuculline facilitated the swallowing. An injection of baclofen did not alter the swallowing. These results suggest the presence of functional topography in the lateral lemniscus and the paralemniscal area in relation to the control of swallowing. The facilitatory LLD-effects on swallowing are modulated by glutamatergic and GABAergic receptors on neurons in the LLD. |
doi_str_mv | 10.1016/j.neuroscience.2013.09.036 |
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Lateral lemniscus, a relay nucleus of auditory sensation, is involved in the control of phonatory movements such as human speech and vocalization of animals. The present study was designed to test whether neurons in the lateral lemniscus contributed to the control of swallowing, one of non-phonic oro-pharyngolaryngeal movements. In acutely decerebrated cats (n=15), swallowing was induced by electrical stimulation (20–80μA at 10Hz for 20s with rectangular pulses of 0.2ms duration) delivered to the superior laryngeal nerve (SLN). Repetitive electrical stimulation (30–50μA at 50Hz for 10–20s) applied to the dorsal nucleus of the lateral lemniscus (LLD) increased the number and reduced the latency to the onset of the SLN-induced swallowing. On the other hand, stimulation of the ventral nucleus of the lateral lemniscus and the paralemniscal area, corresponding to the ventrolateral part of the parabrachial nucleus and the Kölliker–Fuse nucleus, often suppressed the SLN-induced swallowing. Microinjection of NMDA (0.1–0.15μl, 5.0–10mM) into the LLD through a stereotaxically placed glass micropipette facilitated the SLN-induced swallowing, i.e., the number was increased and the latency of swallowing was reduced. We also injected muscimol (a gamma amino-butyric acid (GABA)A receptor agonist), bicuculline (a GABAA receptor antagonist) and baclofen (a GABAB receptor agonist) into the LLD (0.1–0.15μl and 5.0mM for each substance). It was observed that an injection of muscimol suppressed the SLN-induced swallowing. However, an injection of bicuculline facilitated the swallowing. An injection of baclofen did not alter the swallowing. These results suggest the presence of functional topography in the lateral lemniscus and the paralemniscal area in relation to the control of swallowing. The facilitatory LLD-effects on swallowing are modulated by glutamatergic and GABAergic receptors on neurons in the LLD.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/j.neuroscience.2013.09.036</identifier><identifier>PMID: 24080429</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Animals ; audiomotor control ; Auditory Pathways - drug effects ; Auditory Pathways - physiology ; Bicuculline - pharmacology ; Biological and medical sciences ; brainstem ; Cats ; central pattern generator ; Decerebrate State - physiopathology ; Deglutition - drug effects ; Deglutition - physiology ; Electric Stimulation - methods ; Electromyography - methods ; Female ; Fundamental and applied biological sciences. Psychology ; GABAergic projection ; Male ; Muscimol - pharmacology ; Neurology ; oro-pharyngolaryngeal movement ; respiratory movements ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 2013-12, Vol.254, p.260-274</ispartof><rights>IBRO</rights><rights>2013 IBRO</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2013 IBRO. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c645t-1f7c90eb21234bf253a73a3f73c79773b32fb70487241b521fcf84d3b4d46a913</citedby><cites>FETCH-LOGICAL-c645t-1f7c90eb21234bf253a73a3f73c79773b32fb70487241b521fcf84d3b4d46a913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28010187$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24080429$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ota, R</creatorcontrib><creatorcontrib>Takakusaki, K</creatorcontrib><creatorcontrib>Katada, A</creatorcontrib><creatorcontrib>Harada, H</creatorcontrib><creatorcontrib>Nonaka, S</creatorcontrib><creatorcontrib>Harabuchi, Y</creatorcontrib><title>Contribution of the lateral lemniscus to the control of swallowing in decerebrate cats</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>•Role of lemniscal area in the swallowing control was examined in decerebrate cats.•Stimulation of LLD facilitated but that of LLV and PBN–KFN inhibited swallowing.•Injections of glutamatergic and GABAergic agents into the LLD modulated swallowing.•LLD, a relay nucleus of auditory sensation, may contribute to swallowing control.•Lemniscal area may have functional topography in the control of swallowing.
Lateral lemniscus, a relay nucleus of auditory sensation, is involved in the control of phonatory movements such as human speech and vocalization of animals. The present study was designed to test whether neurons in the lateral lemniscus contributed to the control of swallowing, one of non-phonic oro-pharyngolaryngeal movements. In acutely decerebrated cats (n=15), swallowing was induced by electrical stimulation (20–80μA at 10Hz for 20s with rectangular pulses of 0.2ms duration) delivered to the superior laryngeal nerve (SLN). Repetitive electrical stimulation (30–50μA at 50Hz for 10–20s) applied to the dorsal nucleus of the lateral lemniscus (LLD) increased the number and reduced the latency to the onset of the SLN-induced swallowing. On the other hand, stimulation of the ventral nucleus of the lateral lemniscus and the paralemniscal area, corresponding to the ventrolateral part of the parabrachial nucleus and the Kölliker–Fuse nucleus, often suppressed the SLN-induced swallowing. Microinjection of NMDA (0.1–0.15μl, 5.0–10mM) into the LLD through a stereotaxically placed glass micropipette facilitated the SLN-induced swallowing, i.e., the number was increased and the latency of swallowing was reduced. We also injected muscimol (a gamma amino-butyric acid (GABA)A receptor agonist), bicuculline (a GABAA receptor antagonist) and baclofen (a GABAB receptor agonist) into the LLD (0.1–0.15μl and 5.0mM for each substance). It was observed that an injection of muscimol suppressed the SLN-induced swallowing. However, an injection of bicuculline facilitated the swallowing. An injection of baclofen did not alter the swallowing. These results suggest the presence of functional topography in the lateral lemniscus and the paralemniscal area in relation to the control of swallowing. The facilitatory LLD-effects on swallowing are modulated by glutamatergic and GABAergic receptors on neurons in the LLD.</description><subject>Animals</subject><subject>audiomotor control</subject><subject>Auditory Pathways - drug effects</subject><subject>Auditory Pathways - physiology</subject><subject>Bicuculline - pharmacology</subject><subject>Biological and medical sciences</subject><subject>brainstem</subject><subject>Cats</subject><subject>central pattern generator</subject><subject>Decerebrate State - physiopathology</subject><subject>Deglutition - drug effects</subject><subject>Deglutition - physiology</subject><subject>Electric Stimulation - methods</subject><subject>Electromyography - methods</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GABAergic projection</subject><subject>Male</subject><subject>Muscimol - pharmacology</subject><subject>Neurology</subject><subject>oro-pharyngolaryngeal movement</subject><subject>respiratory movements</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNkkmP1DAQhS0EYnoa_gKKkJC4JJSXxAkHJNQMizQSB5ar5ThlcOO2BzthNP8eh24WcQFffPBXfk_vFSEPKTQUaPdk3wRcUszGYTDYMKC8gaEB3t0iG9pLXstWiNtkAxy6WrSMnZHznPdQTiv4XXLGBPQg2LAhH3cxzMmNy-xiqKKt5s9YeT1j0r7yeAgumyVXc_zxYFY4-pXL19r7eO3Cp8qFakKDCcdUBiuj53yP3LHaZ7x_urfkw8uL97vX9eXbV292zy9r04l2rqmVZgAcGWVcjJa1XEuuuZXcyEFKPnJmRwmil0zQsWXUGtuLiY9iEp0eKN-Sx8d_r1L8umCe1aEYRu91wLhkRTvellyA8X-joh1oS4H1BX16RE1JOSe06iq5g043ioJaK1B79WcFaq1AwaCKVBl-cNJZxgNOv0Z_Zl6ARydAZ6O9TToYl39zPRSJ0uKWvDhyWAL85jCpk9zkEppZTdH9n59nf31jvAuuKH_BG8z7uKRQKlJUZaZAvVuXZt0ZyqEYLj6-A7izv8g</recordid><startdate>20131219</startdate><enddate>20131219</enddate><creator>Ota, R</creator><creator>Takakusaki, K</creator><creator>Katada, A</creator><creator>Harada, H</creator><creator>Nonaka, S</creator><creator>Harabuchi, Y</creator><general>Elsevier Ltd</general><general>Elsevier</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>7X8</scope><scope>7TK</scope></search><sort><creationdate>20131219</creationdate><title>Contribution of the lateral lemniscus to the control of swallowing in decerebrate cats</title><author>Ota, R ; Takakusaki, K ; Katada, A ; Harada, H ; Nonaka, S ; Harabuchi, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c645t-1f7c90eb21234bf253a73a3f73c79773b32fb70487241b521fcf84d3b4d46a913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>audiomotor control</topic><topic>Auditory Pathways - drug effects</topic><topic>Auditory Pathways - physiology</topic><topic>Bicuculline - pharmacology</topic><topic>Biological and medical sciences</topic><topic>brainstem</topic><topic>Cats</topic><topic>central pattern generator</topic><topic>Decerebrate State - physiopathology</topic><topic>Deglutition - drug effects</topic><topic>Deglutition - physiology</topic><topic>Electric Stimulation - methods</topic><topic>Electromyography - methods</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GABAergic projection</topic><topic>Male</topic><topic>Muscimol - pharmacology</topic><topic>Neurology</topic><topic>oro-pharyngolaryngeal movement</topic><topic>respiratory movements</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ota, R</creatorcontrib><creatorcontrib>Takakusaki, K</creatorcontrib><creatorcontrib>Katada, A</creatorcontrib><creatorcontrib>Harada, H</creatorcontrib><creatorcontrib>Nonaka, S</creatorcontrib><creatorcontrib>Harabuchi, Y</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>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ota, R</au><au>Takakusaki, K</au><au>Katada, A</au><au>Harada, H</au><au>Nonaka, S</au><au>Harabuchi, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Contribution of the lateral lemniscus to the control of swallowing in decerebrate cats</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2013-12-19</date><risdate>2013</risdate><volume>254</volume><spage>260</spage><epage>274</epage><pages>260-274</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>•Role of lemniscal area in the swallowing control was examined in decerebrate cats.•Stimulation of LLD facilitated but that of LLV and PBN–KFN inhibited swallowing.•Injections of glutamatergic and GABAergic agents into the LLD modulated swallowing.•LLD, a relay nucleus of auditory sensation, may contribute to swallowing control.•Lemniscal area may have functional topography in the control of swallowing.
Lateral lemniscus, a relay nucleus of auditory sensation, is involved in the control of phonatory movements such as human speech and vocalization of animals. The present study was designed to test whether neurons in the lateral lemniscus contributed to the control of swallowing, one of non-phonic oro-pharyngolaryngeal movements. In acutely decerebrated cats (n=15), swallowing was induced by electrical stimulation (20–80μA at 10Hz for 20s with rectangular pulses of 0.2ms duration) delivered to the superior laryngeal nerve (SLN). Repetitive electrical stimulation (30–50μA at 50Hz for 10–20s) applied to the dorsal nucleus of the lateral lemniscus (LLD) increased the number and reduced the latency to the onset of the SLN-induced swallowing. On the other hand, stimulation of the ventral nucleus of the lateral lemniscus and the paralemniscal area, corresponding to the ventrolateral part of the parabrachial nucleus and the Kölliker–Fuse nucleus, often suppressed the SLN-induced swallowing. Microinjection of NMDA (0.1–0.15μl, 5.0–10mM) into the LLD through a stereotaxically placed glass micropipette facilitated the SLN-induced swallowing, i.e., the number was increased and the latency of swallowing was reduced. We also injected muscimol (a gamma amino-butyric acid (GABA)A receptor agonist), bicuculline (a GABAA receptor antagonist) and baclofen (a GABAB receptor agonist) into the LLD (0.1–0.15μl and 5.0mM for each substance). It was observed that an injection of muscimol suppressed the SLN-induced swallowing. However, an injection of bicuculline facilitated the swallowing. An injection of baclofen did not alter the swallowing. These results suggest the presence of functional topography in the lateral lemniscus and the paralemniscal area in relation to the control of swallowing. The facilitatory LLD-effects on swallowing are modulated by glutamatergic and GABAergic receptors on neurons in the LLD.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>24080429</pmid><doi>10.1016/j.neuroscience.2013.09.036</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals audiomotor control Auditory Pathways - drug effects Auditory Pathways - physiology Bicuculline - pharmacology Biological and medical sciences brainstem Cats central pattern generator Decerebrate State - physiopathology Deglutition - drug effects Deglutition - physiology Electric Stimulation - methods Electromyography - methods Female Fundamental and applied biological sciences. Psychology GABAergic projection Male Muscimol - pharmacology Neurology oro-pharyngolaryngeal movement respiratory movements Vertebrates: nervous system and sense organs |
title | Contribution of the lateral lemniscus to the control of swallowing in decerebrate cats |
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