Releasing dentate nucleus cells from Purkinje cell inhibition generates output from the cerebrocerebellum
The cerebellum generates its vast amount of output to the cerebral cortex through the dentate nucleus (DN) that is essential for precise limb movements in primates. Nuclear cells in DN generate burst activity prior to limb movement, and inactivation of DN results in cerebellar ataxia. The question i...
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description | The cerebellum generates its vast amount of output to the cerebral cortex through the dentate nucleus (DN) that is essential for precise limb movements in primates. Nuclear cells in DN generate burst activity prior to limb movement, and inactivation of DN results in cerebellar ataxia. The question is how DN cells become active under intensive inhibitory drive from Purkinje cells (PCs). There are two excitatory inputs to DN, mossy fiber and climbing fiber collaterals, but neither of them appears to have sufficient strength for generation of burst activity in DN. Therefore, we can assume two possible mechanisms: post-inhibitory rebound excitation and disinhibition. If rebound excitation works, phasic excitation of PCs and a concomitant inhibition of DN cells should precede the excitation of DN cells. On the other hand, if disinhibition plays a primary role, phasic suppression of PCs and activation of DN cells should be observed at the same timing. To examine these two hypotheses, we compared the activity patterns of PCs in the cerebrocerebellum and DN cells during step-tracking wrist movements in three Japanese monkeys. As a result, we found that the majority of wrist-movement-related PCs were suppressed prior to movement onset and the majority of wrist-movement-related DN cells showed concurrent burst activity without prior suppression. In a minority of PCs and DN cells, movement-related increases and decreases in activity, respectively, developed later. These activity patterns suggest that the initial burst activity in DN cells is generated by reduced inhibition from PCs, i.e., by disinhibition. Our results indicate that suppression of PCs, which has been considered secondary to facilitation, plays the primary role in generating outputs from DN. Our findings provide a new perspective on the mechanisms used by PCs to influence limb motor control and on the plastic changes that underlie motor learning in the cerebrocerebellum. |
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Nuclear cells in DN generate burst activity prior to limb movement, and inactivation of DN results in cerebellar ataxia. The question is how DN cells become active under intensive inhibitory drive from Purkinje cells (PCs). There are two excitatory inputs to DN, mossy fiber and climbing fiber collaterals, but neither of them appears to have sufficient strength for generation of burst activity in DN. Therefore, we can assume two possible mechanisms: post-inhibitory rebound excitation and disinhibition. If rebound excitation works, phasic excitation of PCs and a concomitant inhibition of DN cells should precede the excitation of DN cells. On the other hand, if disinhibition plays a primary role, phasic suppression of PCs and activation of DN cells should be observed at the same timing. To examine these two hypotheses, we compared the activity patterns of PCs in the cerebrocerebellum and DN cells during step-tracking wrist movements in three Japanese monkeys. As a result, we found that the majority of wrist-movement-related PCs were suppressed prior to movement onset and the majority of wrist-movement-related DN cells showed concurrent burst activity without prior suppression. In a minority of PCs and DN cells, movement-related increases and decreases in activity, respectively, developed later. These activity patterns suggest that the initial burst activity in DN cells is generated by reduced inhibition from PCs, i.e., by disinhibition. Our results indicate that suppression of PCs, which has been considered secondary to facilitation, plays the primary role in generating outputs from DN. Our findings provide a new perspective on the mechanisms used by PCs to influence limb motor control and on the plastic changes that underlie motor learning in the cerebrocerebellum.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0108774</identifier><identifier>PMID: 25279763</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Action Potentials - physiology ; Activity patterns ; Animals ; Ataxia ; Biology and Life Sciences ; Bursting strength ; Cerebellar ataxia ; Cerebellar Cortex - physiology ; Cerebellar Nuclei - physiology ; Cerebellum ; Cerebellum - physiology ; Cerebral cortex ; Deactivation ; Dentate nucleus ; Excitation ; Inactivation ; Inhibition ; Laboratory animals ; Macaca ; Monkeys ; Motor skill learning ; Motor task performance ; Movement - physiology ; Neural Inhibition - physiology ; Neurosciences ; NMR ; Nuclear magnetic resonance ; Nuclei ; Nuclei (cytology) ; Physiology ; Plasticity ; Primates ; Purkinje cells ; Purkinje Cells - physiology ; Science ; Wrist</subject><ispartof>PloS one, 2014-10, Vol.9 (10), p.e108774-e108774</ispartof><rights>2014 Ishikawa et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 Ishikawa et al 2014 Ishikawa et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-eeb702ed2e9f6f3a3f40a5fbca75c48273e5506e79fb5abd5e474944c33a953a3</citedby><cites>FETCH-LOGICAL-c526t-eeb702ed2e9f6f3a3f40a5fbca75c48273e5506e79fb5abd5e474944c33a953a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184834/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184834/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25279763$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Aumann, Tim Douglas</contributor><creatorcontrib>Ishikawa, Takahiro</creatorcontrib><creatorcontrib>Tomatsu, Saeka</creatorcontrib><creatorcontrib>Tsunoda, Yoshiaki</creatorcontrib><creatorcontrib>Lee, Jongho</creatorcontrib><creatorcontrib>Hoffman, Donna S</creatorcontrib><creatorcontrib>Kakei, Shinji</creatorcontrib><title>Releasing dentate nucleus cells from Purkinje cell inhibition generates output from the cerebrocerebellum</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The cerebellum generates its vast amount of output to the cerebral cortex through the dentate nucleus (DN) that is essential for precise limb movements in primates. Nuclear cells in DN generate burst activity prior to limb movement, and inactivation of DN results in cerebellar ataxia. The question is how DN cells become active under intensive inhibitory drive from Purkinje cells (PCs). There are two excitatory inputs to DN, mossy fiber and climbing fiber collaterals, but neither of them appears to have sufficient strength for generation of burst activity in DN. Therefore, we can assume two possible mechanisms: post-inhibitory rebound excitation and disinhibition. If rebound excitation works, phasic excitation of PCs and a concomitant inhibition of DN cells should precede the excitation of DN cells. On the other hand, if disinhibition plays a primary role, phasic suppression of PCs and activation of DN cells should be observed at the same timing. To examine these two hypotheses, we compared the activity patterns of PCs in the cerebrocerebellum and DN cells during step-tracking wrist movements in three Japanese monkeys. As a result, we found that the majority of wrist-movement-related PCs were suppressed prior to movement onset and the majority of wrist-movement-related DN cells showed concurrent burst activity without prior suppression. In a minority of PCs and DN cells, movement-related increases and decreases in activity, respectively, developed later. These activity patterns suggest that the initial burst activity in DN cells is generated by reduced inhibition from PCs, i.e., by disinhibition. Our results indicate that suppression of PCs, which has been considered secondary to facilitation, plays the primary role in generating outputs from DN. Our findings provide a new perspective on the mechanisms used by PCs to influence limb motor control and on the plastic changes that underlie motor learning in the cerebrocerebellum.</description><subject>Action Potentials - physiology</subject><subject>Activity patterns</subject><subject>Animals</subject><subject>Ataxia</subject><subject>Biology and Life Sciences</subject><subject>Bursting strength</subject><subject>Cerebellar ataxia</subject><subject>Cerebellar Cortex - physiology</subject><subject>Cerebellar Nuclei - physiology</subject><subject>Cerebellum</subject><subject>Cerebellum - physiology</subject><subject>Cerebral cortex</subject><subject>Deactivation</subject><subject>Dentate nucleus</subject><subject>Excitation</subject><subject>Inactivation</subject><subject>Inhibition</subject><subject>Laboratory animals</subject><subject>Macaca</subject><subject>Monkeys</subject><subject>Motor skill learning</subject><subject>Motor task performance</subject><subject>Movement - physiology</subject><subject>Neural Inhibition - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ishikawa, Takahiro</au><au>Tomatsu, Saeka</au><au>Tsunoda, Yoshiaki</au><au>Lee, Jongho</au><au>Hoffman, Donna S</au><au>Kakei, Shinji</au><au>Aumann, Tim Douglas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Releasing dentate nucleus cells from Purkinje cell inhibition generates output from the cerebrocerebellum</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-10-03</date><risdate>2014</risdate><volume>9</volume><issue>10</issue><spage>e108774</spage><epage>e108774</epage><pages>e108774-e108774</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The cerebellum generates its vast amount of output to the cerebral cortex through the dentate nucleus (DN) that is essential for precise limb movements in primates. Nuclear cells in DN generate burst activity prior to limb movement, and inactivation of DN results in cerebellar ataxia. The question is how DN cells become active under intensive inhibitory drive from Purkinje cells (PCs). There are two excitatory inputs to DN, mossy fiber and climbing fiber collaterals, but neither of them appears to have sufficient strength for generation of burst activity in DN. Therefore, we can assume two possible mechanisms: post-inhibitory rebound excitation and disinhibition. If rebound excitation works, phasic excitation of PCs and a concomitant inhibition of DN cells should precede the excitation of DN cells. On the other hand, if disinhibition plays a primary role, phasic suppression of PCs and activation of DN cells should be observed at the same timing. To examine these two hypotheses, we compared the activity patterns of PCs in the cerebrocerebellum and DN cells during step-tracking wrist movements in three Japanese monkeys. As a result, we found that the majority of wrist-movement-related PCs were suppressed prior to movement onset and the majority of wrist-movement-related DN cells showed concurrent burst activity without prior suppression. In a minority of PCs and DN cells, movement-related increases and decreases in activity, respectively, developed later. These activity patterns suggest that the initial burst activity in DN cells is generated by reduced inhibition from PCs, i.e., by disinhibition. Our results indicate that suppression of PCs, which has been considered secondary to facilitation, plays the primary role in generating outputs from DN. Our findings provide a new perspective on the mechanisms used by PCs to influence limb motor control and on the plastic changes that underlie motor learning in the cerebrocerebellum.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25279763</pmid><doi>10.1371/journal.pone.0108774</doi><oa>free_for_read</oa></addata></record> |
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subjects | Action Potentials - physiology Activity patterns Animals Ataxia Biology and Life Sciences Bursting strength Cerebellar ataxia Cerebellar Cortex - physiology Cerebellar Nuclei - physiology Cerebellum Cerebellum - physiology Cerebral cortex Deactivation Dentate nucleus Excitation Inactivation Inhibition Laboratory animals Macaca Monkeys Motor skill learning Motor task performance Movement - physiology Neural Inhibition - physiology Neurosciences NMR Nuclear magnetic resonance Nuclei Nuclei (cytology) Physiology Plasticity Primates Purkinje cells Purkinje Cells - physiology Science Wrist |
title | Releasing dentate nucleus cells from Purkinje cell inhibition generates output from the cerebrocerebellum |
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