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Reflex regulation of breathing by the paratrigeminal nucleus via multiple bulbar circuits
Sensory neurons of the jugular vagal ganglia innervate the respiratory tract and project to the poorly studied medullary paratrigeminal nucleus. In the present study, we used neuroanatomical tracing, pharmacology and physiology in guinea pig to investigate the paratrigeminal neural circuits mediatin...
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Published in: | Brain Structure and Function 2018-12, Vol.223 (9), p.4005-4022 |
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description | Sensory neurons of the jugular vagal ganglia innervate the respiratory tract and project to the poorly studied medullary paratrigeminal nucleus. In the present study, we used neuroanatomical tracing, pharmacology and physiology in guinea pig to investigate the paratrigeminal neural circuits mediating jugular ganglia-evoked respiratory reflexes. Retrogradely traced laryngeal jugular ganglia neurons were largely (> 60%) unmyelinated and expressed the neuropeptide substance P and calcitonin gene-related peptide, although a population (~ 30%) of larger diameter myelinated jugular neurons was defined by the expression of vGlut1. Within the brainstem, vagal afferent terminals were confined to the caudal two-thirds of the paratrigeminal nucleus. Electrical stimulation of the laryngeal mucosa evoked a vagally mediated respiratory slowing that was mimicked by laryngeal capsaicin application. These laryngeal reflexes were modestly reduced by neuropeptide receptor antagonist microinjections into the paratrigeminal nucleus, but abolished by ionotropic glutamate receptor antagonists.
d,l
-Homocysteic acid microinjections into the paratrigeminal nucleus mimicked the laryngeal-evoked respiratory slowing, whereas capsaicin microinjections evoked a persistent tachypnoea that was insensitive to glutamatergic inhibition but abolished by neuropeptide receptor antagonists. Extensive projections from paratrigeminal neurons were anterogradely traced throughout the pontomedullary respiratory column. Dual retrograde tracing from pontine and ventrolateral medullary termination sites, as well as immunohistochemical staining for calbindin and neurokinin 1 receptors, supported the existence of different subpopulations of paratrigeminal neurons. Collectively, these data provide anatomical and functional evidence for at least two types of post-synaptic paratrigeminal neurons involved in respiratory reflexes, highlighting an unrecognised complexity in sensory processing in this region of the brainstem. |
doi_str_mv | 10.1007/s00429-018-1732-z |
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d,l
-Homocysteic acid microinjections into the paratrigeminal nucleus mimicked the laryngeal-evoked respiratory slowing, whereas capsaicin microinjections evoked a persistent tachypnoea that was insensitive to glutamatergic inhibition but abolished by neuropeptide receptor antagonists. Extensive projections from paratrigeminal neurons were anterogradely traced throughout the pontomedullary respiratory column. Dual retrograde tracing from pontine and ventrolateral medullary termination sites, as well as immunohistochemical staining for calbindin and neurokinin 1 receptors, supported the existence of different subpopulations of paratrigeminal neurons. Collectively, these data provide anatomical and functional evidence for at least two types of post-synaptic paratrigeminal neurons involved in respiratory reflexes, highlighting an unrecognised complexity in sensory processing in this region of the brainstem.</description><identifier>ISSN: 1863-2653</identifier><identifier>EISSN: 1863-2661</identifier><identifier>EISSN: 0340-2061</identifier><identifier>DOI: 10.1007/s00429-018-1732-z</identifier><identifier>PMID: 30116890</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Anatomy ; Animals ; Biomedical and Life Sciences ; Biomedicine ; Brain stem ; Calbindin ; Calcitonin ; Calcitonin gene-related peptide ; Capsaicin ; Cell Biology ; Circuits ; Data processing ; Electrical stimuli ; Female ; Glutamatergic transmission ; Glutamic acid receptors ; Guinea Pigs ; Information processing ; Male ; Medulla Oblongata - cytology ; Medulla Oblongata - physiology ; Mucosa ; Neural networks ; Neural Pathways - cytology ; Neural Pathways - physiology ; Neurokinin ; Neurokinin NK1 receptors ; Neurology ; Neuropeptides ; Neurosciences ; Original Article ; Pons - cytology ; Pons - physiology ; Reflex ; Reflexes ; Respiration ; Respiratory tract ; Sensory integration ; Sensory neurons ; Sensory Receptor Cells - physiology ; Substance P ; Vagus nerve ; Vagus Nerve - physiology</subject><ispartof>Brain Structure and Function, 2018-12, Vol.223 (9), p.4005-4022</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2018</rights><rights>Brain Structure and Function is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-77ab233fd6d2672fd574ccddbba30d2c4ab6a6d772147a441697243f83e78f983</citedby><cites>FETCH-LOGICAL-c441t-77ab233fd6d2672fd574ccddbba30d2c4ab6a6d772147a441697243f83e78f983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30116890$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Driessen, Alexandria K.</creatorcontrib><creatorcontrib>Farrell, Michael J.</creatorcontrib><creatorcontrib>Dutschmann, Mathias</creatorcontrib><creatorcontrib>Stanic, Davor</creatorcontrib><creatorcontrib>McGovern, Alice E.</creatorcontrib><creatorcontrib>Mazzone, Stuart B.</creatorcontrib><title>Reflex regulation of breathing by the paratrigeminal nucleus via multiple bulbar circuits</title><title>Brain Structure and Function</title><addtitle>Brain Struct Funct</addtitle><addtitle>Brain Struct Funct</addtitle><description>Sensory neurons of the jugular vagal ganglia innervate the respiratory tract and project to the poorly studied medullary paratrigeminal nucleus. In the present study, we used neuroanatomical tracing, pharmacology and physiology in guinea pig to investigate the paratrigeminal neural circuits mediating jugular ganglia-evoked respiratory reflexes. Retrogradely traced laryngeal jugular ganglia neurons were largely (> 60%) unmyelinated and expressed the neuropeptide substance P and calcitonin gene-related peptide, although a population (~ 30%) of larger diameter myelinated jugular neurons was defined by the expression of vGlut1. Within the brainstem, vagal afferent terminals were confined to the caudal two-thirds of the paratrigeminal nucleus. Electrical stimulation of the laryngeal mucosa evoked a vagally mediated respiratory slowing that was mimicked by laryngeal capsaicin application. These laryngeal reflexes were modestly reduced by neuropeptide receptor antagonist microinjections into the paratrigeminal nucleus, but abolished by ionotropic glutamate receptor antagonists.
d,l
-Homocysteic acid microinjections into the paratrigeminal nucleus mimicked the laryngeal-evoked respiratory slowing, whereas capsaicin microinjections evoked a persistent tachypnoea that was insensitive to glutamatergic inhibition but abolished by neuropeptide receptor antagonists. Extensive projections from paratrigeminal neurons were anterogradely traced throughout the pontomedullary respiratory column. Dual retrograde tracing from pontine and ventrolateral medullary termination sites, as well as immunohistochemical staining for calbindin and neurokinin 1 receptors, supported the existence of different subpopulations of paratrigeminal neurons. Collectively, these data provide anatomical and functional evidence for at least two types of post-synaptic paratrigeminal neurons involved in respiratory reflexes, highlighting an unrecognised complexity in sensory processing in this region of the brainstem.</description><subject>Anatomy</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain stem</subject><subject>Calbindin</subject><subject>Calcitonin</subject><subject>Calcitonin gene-related peptide</subject><subject>Capsaicin</subject><subject>Cell Biology</subject><subject>Circuits</subject><subject>Data processing</subject><subject>Electrical stimuli</subject><subject>Female</subject><subject>Glutamatergic transmission</subject><subject>Glutamic acid receptors</subject><subject>Guinea Pigs</subject><subject>Information processing</subject><subject>Male</subject><subject>Medulla Oblongata - cytology</subject><subject>Medulla Oblongata - physiology</subject><subject>Mucosa</subject><subject>Neural networks</subject><subject>Neural Pathways - cytology</subject><subject>Neural Pathways - physiology</subject><subject>Neurokinin</subject><subject>Neurokinin NK1 receptors</subject><subject>Neurology</subject><subject>Neuropeptides</subject><subject>Neurosciences</subject><subject>Original Article</subject><subject>Pons - cytology</subject><subject>Pons - physiology</subject><subject>Reflex</subject><subject>Reflexes</subject><subject>Respiration</subject><subject>Respiratory tract</subject><subject>Sensory integration</subject><subject>Sensory neurons</subject><subject>Sensory Receptor Cells - physiology</subject><subject>Substance P</subject><subject>Vagus nerve</subject><subject>Vagus Nerve - physiology</subject><issn>1863-2653</issn><issn>1863-2661</issn><issn>0340-2061</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LxDAURYMozjj6A9xIwI2bar4mSZcy-AWCILpwFZI0HSNpOyaNqL_eDtURBFd5kHPv4x0ADjE6xQiJs4QQI2WBsCywoKT43AJTLDktCOd4ezPP6QTspfSC0LyUuNwFE4ow5rJEU_B07-rg3mF0yxx077sWdjU00en-2bdLaD5g_-zgSkfdR790jW91gG22weUE37yGTQ69XwUHTQ5GR2h9tNn3aR_s1Dokd_D9zsDj5cXD4rq4vbu6WZzfFpYx3BdCaEMorSteES5IXc0Fs7aqjNEUVcQybbjmlRAEM6GHCC8FYbSW1AlZl5LOwMnYu4rda3apV41P1oWgW9flpAiSpZxTNhiageM_6EuX43DQSCHES4YGCo-UjV1K0dVqFX2j44fCSK29q9G7GryrtXf1OWSOvpuzaVy1SfyIHgAyAmn4apcu_q7-v_ULIMuOdw</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Driessen, Alexandria K.</creator><creator>Farrell, Michael J.</creator><creator>Dutschmann, Mathias</creator><creator>Stanic, Davor</creator><creator>McGovern, Alice E.</creator><creator>Mazzone, Stuart B.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20181201</creationdate><title>Reflex regulation of breathing by the paratrigeminal nucleus via multiple bulbar circuits</title><author>Driessen, Alexandria K. ; Farrell, Michael J. ; Dutschmann, Mathias ; Stanic, Davor ; McGovern, Alice E. ; Mazzone, Stuart B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-77ab233fd6d2672fd574ccddbba30d2c4ab6a6d772147a441697243f83e78f983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anatomy</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain stem</topic><topic>Calbindin</topic><topic>Calcitonin</topic><topic>Calcitonin gene-related peptide</topic><topic>Capsaicin</topic><topic>Cell Biology</topic><topic>Circuits</topic><topic>Data processing</topic><topic>Electrical stimuli</topic><topic>Female</topic><topic>Glutamatergic transmission</topic><topic>Glutamic acid receptors</topic><topic>Guinea Pigs</topic><topic>Information processing</topic><topic>Male</topic><topic>Medulla Oblongata - cytology</topic><topic>Medulla Oblongata - physiology</topic><topic>Mucosa</topic><topic>Neural networks</topic><topic>Neural Pathways - cytology</topic><topic>Neural Pathways - physiology</topic><topic>Neurokinin</topic><topic>Neurokinin NK1 receptors</topic><topic>Neurology</topic><topic>Neuropeptides</topic><topic>Neurosciences</topic><topic>Original Article</topic><topic>Pons - cytology</topic><topic>Pons - physiology</topic><topic>Reflex</topic><topic>Reflexes</topic><topic>Respiration</topic><topic>Respiratory tract</topic><topic>Sensory integration</topic><topic>Sensory neurons</topic><topic>Sensory Receptor Cells - physiology</topic><topic>Substance P</topic><topic>Vagus nerve</topic><topic>Vagus Nerve - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Driessen, Alexandria K.</creatorcontrib><creatorcontrib>Farrell, Michael J.</creatorcontrib><creatorcontrib>Dutschmann, Mathias</creatorcontrib><creatorcontrib>Stanic, Davor</creatorcontrib><creatorcontrib>McGovern, Alice E.</creatorcontrib><creatorcontrib>Mazzone, Stuart B.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Psychology Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Brain Structure and Function</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Driessen, Alexandria K.</au><au>Farrell, Michael J.</au><au>Dutschmann, Mathias</au><au>Stanic, Davor</au><au>McGovern, Alice E.</au><au>Mazzone, Stuart B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reflex regulation of breathing by the paratrigeminal nucleus via multiple bulbar circuits</atitle><jtitle>Brain Structure and Function</jtitle><stitle>Brain Struct Funct</stitle><addtitle>Brain Struct Funct</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>223</volume><issue>9</issue><spage>4005</spage><epage>4022</epage><pages>4005-4022</pages><issn>1863-2653</issn><eissn>1863-2661</eissn><eissn>0340-2061</eissn><abstract>Sensory neurons of the jugular vagal ganglia innervate the respiratory tract and project to the poorly studied medullary paratrigeminal nucleus. In the present study, we used neuroanatomical tracing, pharmacology and physiology in guinea pig to investigate the paratrigeminal neural circuits mediating jugular ganglia-evoked respiratory reflexes. Retrogradely traced laryngeal jugular ganglia neurons were largely (> 60%) unmyelinated and expressed the neuropeptide substance P and calcitonin gene-related peptide, although a population (~ 30%) of larger diameter myelinated jugular neurons was defined by the expression of vGlut1. Within the brainstem, vagal afferent terminals were confined to the caudal two-thirds of the paratrigeminal nucleus. Electrical stimulation of the laryngeal mucosa evoked a vagally mediated respiratory slowing that was mimicked by laryngeal capsaicin application. These laryngeal reflexes were modestly reduced by neuropeptide receptor antagonist microinjections into the paratrigeminal nucleus, but abolished by ionotropic glutamate receptor antagonists.
d,l
-Homocysteic acid microinjections into the paratrigeminal nucleus mimicked the laryngeal-evoked respiratory slowing, whereas capsaicin microinjections evoked a persistent tachypnoea that was insensitive to glutamatergic inhibition but abolished by neuropeptide receptor antagonists. Extensive projections from paratrigeminal neurons were anterogradely traced throughout the pontomedullary respiratory column. Dual retrograde tracing from pontine and ventrolateral medullary termination sites, as well as immunohistochemical staining for calbindin and neurokinin 1 receptors, supported the existence of different subpopulations of paratrigeminal neurons. Collectively, these data provide anatomical and functional evidence for at least two types of post-synaptic paratrigeminal neurons involved in respiratory reflexes, highlighting an unrecognised complexity in sensory processing in this region of the brainstem.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>30116890</pmid><doi>10.1007/s00429-018-1732-z</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anatomy Animals Biomedical and Life Sciences Biomedicine Brain stem Calbindin Calcitonin Calcitonin gene-related peptide Capsaicin Cell Biology Circuits Data processing Electrical stimuli Female Glutamatergic transmission Glutamic acid receptors Guinea Pigs Information processing Male Medulla Oblongata - cytology Medulla Oblongata - physiology Mucosa Neural networks Neural Pathways - cytology Neural Pathways - physiology Neurokinin Neurokinin NK1 receptors Neurology Neuropeptides Neurosciences Original Article Pons - cytology Pons - physiology Reflex Reflexes Respiration Respiratory tract Sensory integration Sensory neurons Sensory Receptor Cells - physiology Substance P Vagus nerve Vagus Nerve - physiology |
title | Reflex regulation of breathing by the paratrigeminal nucleus via multiple bulbar circuits |
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