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Rhythmic Activity in a Forebrain Vocal Control Nucleus In Vitro
The learned vocalizations of songbirds constitute a rhythmic behavior that is thought to be governed by a central pattern generator and that is accompanied by highly patterned neural activity. Phasic premotor activity is observed during singing in HVC [used as a proper name following the nomenclatur...
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Published in: | The Journal of neuroscience 2005-03, Vol.25 (11), p.2811-2822 |
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description | The learned vocalizations of songbirds constitute a rhythmic behavior that is thought to be governed by a central pattern generator and that is accompanied by highly patterned neural activity. Phasic premotor activity is observed during singing in HVC [used as a proper name following the nomenclature of Reiner et al. (2004)], a telencephalic song system nucleus that is essential for song production. Moreover, HVC neurons display phasic patterns of auditory activity in response to song stimulation. To address the cellular basis of pattern generation in HVC, we investigated its rhythm-generating abilities. We report here the induction of sustained, rhythmic activity patterns in HVC when isolated in vitro. Brief, high-frequency stimulation evoked repetitive postsynaptic potentials (PSPs) and local field potentials (LFPs) from HVC neurons recorded in a brain slice preparation made from adult male zebra finches. These rhythmic events were sustained for seconds in the absence of ongoing, phasic stimulation, and they had temporal properties similar to those of syllable occurrence within zebra finch song. Paired recordings revealed synchrony between repetitive PSP and LFP occurrence, indicating that a population of cells participates in this patterned activity. The PSPs resulted from multiple, coordinated, fast-glutamatergic, synaptic inputs. Moreover, their occurrence and timing relied on inhibitory synaptic transmission. Thus, HVC itself has rhythmic abilities that could influence the timing of neural activity over relatively long time windows. These rhythmic properties may contribute to song production or perception in vivo. |
doi_str_mv | 10.1523/JNEUROSCI.5285-04.2005 |
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Phasic premotor activity is observed during singing in HVC [used as a proper name following the nomenclature of Reiner et al. (2004)], a telencephalic song system nucleus that is essential for song production. Moreover, HVC neurons display phasic patterns of auditory activity in response to song stimulation. To address the cellular basis of pattern generation in HVC, we investigated its rhythm-generating abilities. We report here the induction of sustained, rhythmic activity patterns in HVC when isolated in vitro. Brief, high-frequency stimulation evoked repetitive postsynaptic potentials (PSPs) and local field potentials (LFPs) from HVC neurons recorded in a brain slice preparation made from adult male zebra finches. These rhythmic events were sustained for seconds in the absence of ongoing, phasic stimulation, and they had temporal properties similar to those of syllable occurrence within zebra finch song. Paired recordings revealed synchrony between repetitive PSP and LFP occurrence, indicating that a population of cells participates in this patterned activity. The PSPs resulted from multiple, coordinated, fast-glutamatergic, synaptic inputs. Moreover, their occurrence and timing relied on inhibitory synaptic transmission. Thus, HVC itself has rhythmic abilities that could influence the timing of neural activity over relatively long time windows. 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Phasic premotor activity is observed during singing in HVC [used as a proper name following the nomenclature of Reiner et al. (2004)], a telencephalic song system nucleus that is essential for song production. Moreover, HVC neurons display phasic patterns of auditory activity in response to song stimulation. To address the cellular basis of pattern generation in HVC, we investigated its rhythm-generating abilities. We report here the induction of sustained, rhythmic activity patterns in HVC when isolated in vitro. Brief, high-frequency stimulation evoked repetitive postsynaptic potentials (PSPs) and local field potentials (LFPs) from HVC neurons recorded in a brain slice preparation made from adult male zebra finches. These rhythmic events were sustained for seconds in the absence of ongoing, phasic stimulation, and they had temporal properties similar to those of syllable occurrence within zebra finch song. Paired recordings revealed synchrony between repetitive PSP and LFP occurrence, indicating that a population of cells participates in this patterned activity. The PSPs resulted from multiple, coordinated, fast-glutamatergic, synaptic inputs. Moreover, their occurrence and timing relied on inhibitory synaptic transmission. Thus, HVC itself has rhythmic abilities that could influence the timing of neural activity over relatively long time windows. These rhythmic properties may contribute to song production or perception in vivo.</description><subject>6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology</subject><subject>Action Potentials - drug effects</subject><subject>Action Potentials - physiology</subject><subject>Action Potentials - radiation effects</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Behavioral/Systems/Cognitive</subject><subject>Bicuculline - analogs & derivatives</subject><subject>Bicuculline - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Dose-Response Relationship, Radiation</subject><subject>Electric Stimulation - methods</subject><subject>Excitatory Amino Acid Antagonists - pharmacology</subject><subject>Excitatory Postsynaptic Potentials - drug effects</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>Excitatory Postsynaptic Potentials - radiation effects</subject><subject>Finches</subject><subject>GABA Antagonists - pharmacology</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Models, Neurological</subject><subject>Neurons - classification</subject><subject>Neurons - drug effects</subject><subject>Neurons - physiology</subject><subject>Neurons - radiation effects</subject><subject>Patch-Clamp Techniques - methods</subject><subject>Periodicity</subject><subject>Picrotoxin - pharmacology</subject><subject>Prosencephalon - cytology</subject><subject>Reaction Time - drug effects</subject><subject>Reaction Time - physiology</subject><subject>Reaction Time - radiation effects</subject><subject>Synaptic Transmission</subject><subject>Taeniopygia guttata</subject><subject>Vocalization, Animal - physiology</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpVkF1P2zAUhq1paBTYX0C52q5SbMfOcW82oapAEQKJj91ajmMTT07N7ISq_x5XrRhc2fL7nNdHD0KnBE8Jp9XZ9e3i6f7uYb6ccip4idmUYsy_oElOZyVlmHxFE0wBlzUDdoiOUvqLMQZM4Bs6JByAVoxM0O_7bjN0vdPFuR7cqxs2hVsVqrgI0TRR5fufoJUv5mE1xOCL21F7M6ZimQOXX07QgVU-me_78xg9XSwe51flzd3lcn5-U2pGYSiNAGFZBXUDLdZVqzRtLW-E1oIzULaZNUJhaluBWzMDbcG2dSMsVLRlvOHVMfq1630Zm9602uR1lJcv0fUqbmRQTn5OVq6Tz-FV1kA5YTgX_NgXxPBvNGmQvUvaeK9WJoxJEuDAZ7TOYL0DdQwpRWPfPyFYbt3Ld_dy615iJrfu8-DpxxX_j-1lZ-DnDujcc7d20cjUK-8zTuR6vaZcEiKpIKR6Axaij-8</recordid><startdate>20050316</startdate><enddate>20050316</enddate><creator>Solis, Michele M</creator><creator>Perkel, David J</creator><general>Soc Neuroscience</general><general>Society for Neuroscience</general><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>5PM</scope></search><sort><creationdate>20050316</creationdate><title>Rhythmic Activity in a Forebrain Vocal Control Nucleus In Vitro</title><author>Solis, Michele M ; Perkel, David J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-e878f4376b7d0c3dac2df5b8cc8547afb9b8a02fd80de97cf7fd6b8f732d45b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology</topic><topic>Action Potentials - drug effects</topic><topic>Action Potentials - physiology</topic><topic>Action Potentials - radiation effects</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Behavioral/Systems/Cognitive</topic><topic>Bicuculline - analogs & derivatives</topic><topic>Bicuculline - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Dose-Response Relationship, Radiation</topic><topic>Electric Stimulation - methods</topic><topic>Excitatory Amino Acid Antagonists - pharmacology</topic><topic>Excitatory Postsynaptic Potentials - drug effects</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>Excitatory Postsynaptic Potentials - radiation effects</topic><topic>Finches</topic><topic>GABA Antagonists - pharmacology</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Models, Neurological</topic><topic>Neurons - classification</topic><topic>Neurons - drug effects</topic><topic>Neurons - physiology</topic><topic>Neurons - radiation effects</topic><topic>Patch-Clamp Techniques - methods</topic><topic>Periodicity</topic><topic>Picrotoxin - pharmacology</topic><topic>Prosencephalon - cytology</topic><topic>Reaction Time - drug effects</topic><topic>Reaction Time - physiology</topic><topic>Reaction Time - radiation effects</topic><topic>Synaptic Transmission</topic><topic>Taeniopygia guttata</topic><topic>Vocalization, Animal - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Solis, Michele M</creatorcontrib><creatorcontrib>Perkel, David J</creatorcontrib><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>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Solis, Michele M</au><au>Perkel, David J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rhythmic Activity in a Forebrain Vocal Control Nucleus In Vitro</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2005-03-16</date><risdate>2005</risdate><volume>25</volume><issue>11</issue><spage>2811</spage><epage>2822</epage><pages>2811-2822</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>The learned vocalizations of songbirds constitute a rhythmic behavior that is thought to be governed by a central pattern generator and that is accompanied by highly patterned neural activity. Phasic premotor activity is observed during singing in HVC [used as a proper name following the nomenclature of Reiner et al. (2004)], a telencephalic song system nucleus that is essential for song production. Moreover, HVC neurons display phasic patterns of auditory activity in response to song stimulation. To address the cellular basis of pattern generation in HVC, we investigated its rhythm-generating abilities. We report here the induction of sustained, rhythmic activity patterns in HVC when isolated in vitro. Brief, high-frequency stimulation evoked repetitive postsynaptic potentials (PSPs) and local field potentials (LFPs) from HVC neurons recorded in a brain slice preparation made from adult male zebra finches. These rhythmic events were sustained for seconds in the absence of ongoing, phasic stimulation, and they had temporal properties similar to those of syllable occurrence within zebra finch song. Paired recordings revealed synchrony between repetitive PSP and LFP occurrence, indicating that a population of cells participates in this patterned activity. The PSPs resulted from multiple, coordinated, fast-glutamatergic, synaptic inputs. Moreover, their occurrence and timing relied on inhibitory synaptic transmission. Thus, HVC itself has rhythmic abilities that could influence the timing of neural activity over relatively long time windows. These rhythmic properties may contribute to song production or perception in vivo.</abstract><cop>United States</cop><pub>Soc Neuroscience</pub><pmid>15772341</pmid><doi>10.1523/JNEUROSCI.5285-04.2005</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology Action Potentials - drug effects Action Potentials - physiology Action Potentials - radiation effects Analysis of Variance Animals Behavioral/Systems/Cognitive Bicuculline - analogs & derivatives Bicuculline - pharmacology Dose-Response Relationship, Drug Dose-Response Relationship, Radiation Electric Stimulation - methods Excitatory Amino Acid Antagonists - pharmacology Excitatory Postsynaptic Potentials - drug effects Excitatory Postsynaptic Potentials - physiology Excitatory Postsynaptic Potentials - radiation effects Finches GABA Antagonists - pharmacology In Vitro Techniques Male Models, Neurological Neurons - classification Neurons - drug effects Neurons - physiology Neurons - radiation effects Patch-Clamp Techniques - methods Periodicity Picrotoxin - pharmacology Prosencephalon - cytology Reaction Time - drug effects Reaction Time - physiology Reaction Time - radiation effects Synaptic Transmission Taeniopygia guttata Vocalization, Animal - physiology |
title | Rhythmic Activity in a Forebrain Vocal Control Nucleus In Vitro |
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