Axonal projections of pulmonary slowly adapting receptor relay neurons in the rat

We elucidated efferent projections of second‐order relay neurons (P‐cells) activated by afferents originating from slowly adapting pulmonary receptors (SARs) to determine the central pathway of the SAR‐evoked reflexes. Special attention was paid to visualizing the P‐cell projections within the nucle...

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Veröffentlicht in:Journal of comparative neurology (1911) 2002-04, Vol.446 (1), p.81-94
Hauptverfasser: Ezure, Kazuhisa, Tanaka, Ikuko, Saito, Yoshiaki, Otake, Kazuyoshi
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container_issue 1
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container_title Journal of comparative neurology (1911)
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creator Ezure, Kazuhisa
Tanaka, Ikuko
Saito, Yoshiaki
Otake, Kazuyoshi
description We elucidated efferent projections of second‐order relay neurons (P‐cells) activated by afferents originating from slowly adapting pulmonary receptors (SARs) to determine the central pathway of the SAR‐evoked reflexes. Special attention was paid to visualizing the P‐cell projections within the nucleus tractus solitarii (NTS), which may correspond to the inhibitory pathway from P‐cells to second‐order relay neurons (RAR‐cells) of rapidly adapting pulmonary receptors. P‐cells were recorded from the NTS in Nembutal‐anesthetized, paralyzed, and artificially ventilated rats. First, we used electrophysiological methods of antidromic mapping and showed that the majority of the P‐cells examined projected their axons to the caudal NTS and to the dorsolateral pons corresponding to the parabrachial complex. Second, a mixture of HRP and Neurobiotin was injected intracellularly or juxtramembranously into P‐cells. (1) Stained P‐cells (n = 7) were located laterally to the solitary tract and had dendrites extending characteristically along the lateral border of the solitary tract. (2) All P‐cells had stem axons projecting to the ipsilateral medulla. Of these, the axons from five P‐cells projected to the nucleus ambiguus and its vicinity with distributing boutons. Some of these axons further ascended in the ventrolateral medulla, and distributed boutons in the areas ventral or ventrolateral to the nucleus ambiguus. (3) All the P‐cells had axonal branches with boutons in the NTS area. In particular, axons from three P‐cells projected bilaterally to the medial NTS caudal to the obex, i.e., to the area of RAR‐cells. These results show anatomic substrates for the connections implicated in the P‐cell inhibition of RAR‐cells as well as the SAR‐induced respiratory reflexes. J. Comp. Neurol. 446:81–94, 2002. © 2002 Wiley‐Liss, Inc.
doi_str_mv 10.1002/cne.10185
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Special attention was paid to visualizing the P‐cell projections within the nucleus tractus solitarii (NTS), which may correspond to the inhibitory pathway from P‐cells to second‐order relay neurons (RAR‐cells) of rapidly adapting pulmonary receptors. P‐cells were recorded from the NTS in Nembutal‐anesthetized, paralyzed, and artificially ventilated rats. First, we used electrophysiological methods of antidromic mapping and showed that the majority of the P‐cells examined projected their axons to the caudal NTS and to the dorsolateral pons corresponding to the parabrachial complex. Second, a mixture of HRP and Neurobiotin was injected intracellularly or juxtramembranously into P‐cells. (1) Stained P‐cells (n = 7) were located laterally to the solitary tract and had dendrites extending characteristically along the lateral border of the solitary tract. (2) All P‐cells had stem axons projecting to the ipsilateral medulla. 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Comp. Neurol</addtitle><description>We elucidated efferent projections of second‐order relay neurons (P‐cells) activated by afferents originating from slowly adapting pulmonary receptors (SARs) to determine the central pathway of the SAR‐evoked reflexes. Special attention was paid to visualizing the P‐cell projections within the nucleus tractus solitarii (NTS), which may correspond to the inhibitory pathway from P‐cells to second‐order relay neurons (RAR‐cells) of rapidly adapting pulmonary receptors. P‐cells were recorded from the NTS in Nembutal‐anesthetized, paralyzed, and artificially ventilated rats. First, we used electrophysiological methods of antidromic mapping and showed that the majority of the P‐cells examined projected their axons to the caudal NTS and to the dorsolateral pons corresponding to the parabrachial complex. Second, a mixture of HRP and Neurobiotin was injected intracellularly or juxtramembranously into P‐cells. 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Tanaka, Ikuko ; Saito, Yoshiaki ; Otake, Kazuyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4565-1890a28c53558a5bc2b5a90a823e059251b42629a93e20ce2f8461050e6049a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Action Potentials - physiology</topic><topic>Animals</topic><topic>Axons - physiology</topic><topic>Axons - ultrastructure</topic><topic>Bronchi - innervation</topic><topic>Bronchi - physiology</topic><topic>Cell Size - physiology</topic><topic>Dendrites - physiology</topic><topic>Dendrites - ultrastructure</topic><topic>intracellular staining</topic><topic>Mechanoreceptors - cytology</topic><topic>Mechanoreceptors - physiology</topic><topic>Nerve Net - cytology</topic><topic>Nerve Net - physiology</topic><topic>Neural Conduction - physiology</topic><topic>Neural Inhibition - physiology</topic><topic>neurobiotin</topic><topic>NTS</topic><topic>P-cell</topic><topic>Pons - cytology</topic><topic>Pons - physiology</topic><topic>Presynaptic Terminals - physiology</topic><topic>Presynaptic Terminals - ultrastructure</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reaction Time - physiology</topic><topic>respiration</topic><topic>Respiratory Center - cytology</topic><topic>Respiratory Center - physiology</topic><topic>second-order relay neurons</topic><topic>Solitary Nucleus - cytology</topic><topic>Solitary Nucleus - physiology</topic><topic>Vagus Nerve - physiology</topic><topic>Visceral Afferents - cytology</topic><topic>Visceral Afferents - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ezure, Kazuhisa</creatorcontrib><creatorcontrib>Tanaka, Ikuko</creatorcontrib><creatorcontrib>Saito, Yoshiaki</creatorcontrib><creatorcontrib>Otake, Kazuyoshi</creatorcontrib><collection>Istex</collection><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>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ezure, Kazuhisa</au><au>Tanaka, Ikuko</au><au>Saito, Yoshiaki</au><au>Otake, Kazuyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Axonal projections of pulmonary slowly adapting receptor relay neurons in the rat</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. 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First, we used electrophysiological methods of antidromic mapping and showed that the majority of the P‐cells examined projected their axons to the caudal NTS and to the dorsolateral pons corresponding to the parabrachial complex. Second, a mixture of HRP and Neurobiotin was injected intracellularly or juxtramembranously into P‐cells. (1) Stained P‐cells (n = 7) were located laterally to the solitary tract and had dendrites extending characteristically along the lateral border of the solitary tract. (2) All P‐cells had stem axons projecting to the ipsilateral medulla. Of these, the axons from five P‐cells projected to the nucleus ambiguus and its vicinity with distributing boutons. Some of these axons further ascended in the ventrolateral medulla, and distributed boutons in the areas ventral or ventrolateral to the nucleus ambiguus. (3) All the P‐cells had axonal branches with boutons in the NTS area. In particular, axons from three P‐cells projected bilaterally to the medial NTS caudal to the obex, i.e., to the area of RAR‐cells. These results show anatomic substrates for the connections implicated in the P‐cell inhibition of RAR‐cells as well as the SAR‐induced respiratory reflexes. J. Comp. Neurol. 446:81–94, 2002. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>11920722</pmid><doi>10.1002/cne.10185</doi><tpages>14</tpages></addata></record>
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subjects Action Potentials - physiology
Animals
Axons - physiology
Axons - ultrastructure
Bronchi - innervation
Bronchi - physiology
Cell Size - physiology
Dendrites - physiology
Dendrites - ultrastructure
intracellular staining
Mechanoreceptors - cytology
Mechanoreceptors - physiology
Nerve Net - cytology
Nerve Net - physiology
Neural Conduction - physiology
Neural Inhibition - physiology
neurobiotin
NTS
P-cell
Pons - cytology
Pons - physiology
Presynaptic Terminals - physiology
Presynaptic Terminals - ultrastructure
Rats
Rats, Wistar
Reaction Time - physiology
respiration
Respiratory Center - cytology
Respiratory Center - physiology
second-order relay neurons
Solitary Nucleus - cytology
Solitary Nucleus - physiology
Vagus Nerve - physiology
Visceral Afferents - cytology
Visceral Afferents - physiology
title Axonal projections of pulmonary slowly adapting receptor relay neurons in the rat
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