Neurochemical diversity of afferent neurons that transduce sensory signals from dog ventricular myocardium

Abstract While much is known about the influence of ventricular afferent neurons on cardiovascular function in the dog, identification of the neurochemicals transmitting cardiac afferent signals to central neurons is lacking. Accordingly, we identified ventricular afferent neurons in canine dorsal r...

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Veröffentlicht in:Autonomic neuroscience 2008-08, Vol.141 (1), p.38-45
Hauptverfasser: Hoover, Donald B, Shepherd, Angela V, Southerland, E. Marie, Armour, J. Andrew, Ardell, Jeffrey L
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container_issue 1
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container_title Autonomic neuroscience
container_volume 141
creator Hoover, Donald B
Shepherd, Angela V
Southerland, E. Marie
Armour, J. Andrew
Ardell, Jeffrey L
description Abstract While much is known about the influence of ventricular afferent neurons on cardiovascular function in the dog, identification of the neurochemicals transmitting cardiac afferent signals to central neurons is lacking. Accordingly, we identified ventricular afferent neurons in canine dorsal root ganglia (DRG) and nodose ganglia by retrograde labeling after injecting horseradish peroxidase (HRP) into the anterior right and left ventricles. Primary antibodies from three host species were used in immunohistochemical experiments to simultaneously evaluate afferent somata for the presence of HRP and markers for two neurotransmitters. Only a small percentage (2%) of afferent somata were labeled with HRP. About half of the HRP-identified ventricular afferent neurons in T3 DRG also stained for substance P (SP), calcitonin gene-related peptide (CGRP), or neuronal nitric oxide synthase (nNOS), either alone or with two markers colocalized. Ventricular afferent neurons and the general population of T3 DRG neurons showed the same labeling profiles; CGRP (alone or colocalized with SP) being the most common (30–40% of ventricular afferent somata in T3 DRG). About 30% of the ventricular afferent neurons in T2 DRG displayed CGRP immunoreactivity and binding of the putative nociceptive marker IB4 . Ventricular afferent neurons of the nodose ganglia were distinct from those in the DRG by having smaller size and lacking immunoreactivity for SP, CGRP, and nNOS. These findings suggest that ventricular sensory information is transferred to the central nervous system by relatively small populations of vagal and spinal afferent neurons and that spinal afferents use a variety of neurotransmitters.
doi_str_mv 10.1016/j.autneu.2008.04.010
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Marie</creatorcontrib><creatorcontrib>Armour, J. Andrew</creatorcontrib><creatorcontrib>Ardell, Jeffrey L</creatorcontrib><title>Neurochemical diversity of afferent neurons that transduce sensory signals from dog ventricular myocardium</title><title>Autonomic neuroscience</title><addtitle>Auton Neurosci</addtitle><description>Abstract While much is known about the influence of ventricular afferent neurons on cardiovascular function in the dog, identification of the neurochemicals transmitting cardiac afferent signals to central neurons is lacking. Accordingly, we identified ventricular afferent neurons in canine dorsal root ganglia (DRG) and nodose ganglia by retrograde labeling after injecting horseradish peroxidase (HRP) into the anterior right and left ventricles. Primary antibodies from three host species were used in immunohistochemical experiments to simultaneously evaluate afferent somata for the presence of HRP and markers for two neurotransmitters. 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Electric organ</subject><subject>Signal Transduction</subject><subject>Substance P</subject><subject>Substance P - metabolism</subject><subject>Ventricular afferent neuron</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Vesicular Glutamate Transport Protein 1 - metabolism</subject><subject>Vesicular Glutamate Transport Protein 2 - metabolism</subject><issn>1566-0702</issn><issn>1872-7484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkkuP1DAQhCMEYh_wDxDyBThNaDvxIxek1QoWpBUcgLPlOJ0Zh8Re7GSk-fc4mtGycICTLfnrUrmriuIFhZICFW-H0iyzx6VkAKqEugQKj4pzqiTbyFrVj_OdC7EBCeysuEhpgAxCI54WZ1RxrjgV58XwGZcY7A4nZ81IOrfHmNx8IKEnpu8xop-JXxmfyLwzM5mj8albLJKEPoV4IMltvRkT6WOYSBe2ZJ-HorPLaCKZDsGa2LllelY86TOGz0_nZfH9w_tv1x83t19uPl1f3W4sl2retLxjljVdw4FJww2w1lhaKdE3smaopGwZF0b0mUDbMclV29vKAG1FJprqsnh31L1b2gk7u5oxo76LbjLxoINx-s8X73Z6G_aacSnz-rLAm5NADD8XTLOeXLI4jsZjWJJWqoK6aqTI5Ot_kqKpGOXN6qk-gjaGlCL293Yo6DVOPehjnHqNU0Otc5x57OXDr_weOuWXgVcnwKScX5-zsS7dcwx4pRr2YCeYF793GHWyDr3FzkW0s-6C-5-TvwXs6PzamR94wDSEJa4d0FQnpkF_Xau3Ni83DkCouvoFYeDYhA</recordid><startdate>20080818</startdate><enddate>20080818</enddate><creator>Hoover, Donald B</creator><creator>Shepherd, Angela V</creator><creator>Southerland, E. 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Andrew ; Ardell, Jeffrey L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c578t-b5d2c29d95027a5a02bac1386f9742e877b256a6fd95ecd2758bfc3a01b697493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Advanced Basic Science</topic><topic>Afferent Pathways - metabolism</topic><topic>Afferent Pathways - physiology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Calcitonin gene-related peptide</topic><topic>Calcitonin Gene-Related Peptide - metabolism</topic><topic>Cell Count</topic><topic>Dogs</topic><topic>Dorsal root ganglion</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. 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Electric organ</topic><topic>Signal Transduction</topic><topic>Substance P</topic><topic>Substance P - metabolism</topic><topic>Ventricular afferent neuron</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Vesicular Glutamate Transport Protein 1 - metabolism</topic><topic>Vesicular Glutamate Transport Protein 2 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoover, Donald B</creatorcontrib><creatorcontrib>Shepherd, Angela V</creatorcontrib><creatorcontrib>Southerland, E. Marie</creatorcontrib><creatorcontrib>Armour, J. 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Andrew</au><au>Ardell, Jeffrey L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurochemical diversity of afferent neurons that transduce sensory signals from dog ventricular myocardium</atitle><jtitle>Autonomic neuroscience</jtitle><addtitle>Auton Neurosci</addtitle><date>2008-08-18</date><risdate>2008</risdate><volume>141</volume><issue>1</issue><spage>38</spage><epage>45</epage><pages>38-45</pages><issn>1566-0702</issn><eissn>1872-7484</eissn><abstract>Abstract While much is known about the influence of ventricular afferent neurons on cardiovascular function in the dog, identification of the neurochemicals transmitting cardiac afferent signals to central neurons is lacking. Accordingly, we identified ventricular afferent neurons in canine dorsal root ganglia (DRG) and nodose ganglia by retrograde labeling after injecting horseradish peroxidase (HRP) into the anterior right and left ventricles. Primary antibodies from three host species were used in immunohistochemical experiments to simultaneously evaluate afferent somata for the presence of HRP and markers for two neurotransmitters. Only a small percentage (2%) of afferent somata were labeled with HRP. About half of the HRP-identified ventricular afferent neurons in T3 DRG also stained for substance P (SP), calcitonin gene-related peptide (CGRP), or neuronal nitric oxide synthase (nNOS), either alone or with two markers colocalized. Ventricular afferent neurons and the general population of T3 DRG neurons showed the same labeling profiles; CGRP (alone or colocalized with SP) being the most common (30–40% of ventricular afferent somata in T3 DRG). About 30% of the ventricular afferent neurons in T2 DRG displayed CGRP immunoreactivity and binding of the putative nociceptive marker IB4 . Ventricular afferent neurons of the nodose ganglia were distinct from those in the DRG by having smaller size and lacking immunoreactivity for SP, CGRP, and nNOS. These findings suggest that ventricular sensory information is transferred to the central nervous system by relatively small populations of vagal and spinal afferent neurons and that spinal afferents use a variety of neurotransmitters.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>18558516</pmid><doi>10.1016/j.autneu.2008.04.010</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Advanced Basic Science
Afferent Pathways - metabolism
Afferent Pathways - physiology
Animals
Biological and medical sciences
Calcitonin gene-related peptide
Calcitonin Gene-Related Peptide - metabolism
Cell Count
Dogs
Dorsal root ganglion
Female
Fundamental and applied biological sciences. Psychology
Ganglia, Spinal - cytology
Ganglia, Spinal - metabolism
Heart Ventricles - cytology
Heart Ventricles - metabolism
Immunohistochemistry
Lectins - metabolism
Male
Medical Education
Microscopy, Confocal
Myocardium - cytology
Myocardium - metabolism
Neuronal nitric oxide synthase
Neurons, Afferent - cytology
Neurons, Afferent - metabolism
Nitric Oxide Synthase Type I - metabolism
Nociceptors - metabolism
Nodose ganglion
Nodose Ganglion - cytology
Nodose Ganglion - metabolism
Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ
Signal Transduction
Substance P
Substance P - metabolism
Ventricular afferent neuron
Vertebrates: nervous system and sense organs
Vesicular Glutamate Transport Protein 1 - metabolism
Vesicular Glutamate Transport Protein 2 - metabolism
title Neurochemical diversity of afferent neurons that transduce sensory signals from dog ventricular myocardium
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