Histaminergic neurons in the central and peripheral nervous system of gastropods (Helix, Lymnaea): An immunocytochemical, biochemical, and electrophysiological approach
Distribution, chemical‐neuroanatomy, concentration, and uptake‐release properties of histamine (HA)‐containing neurons and the possible physiological effects of HA in the central and peripheral nervous system of the pulmonate snails, Helix pomatia and Lymnaea stagnalis, are described. In the CNS of...
Gespeichert in:
Veröffentlicht in: | Journal of comparative neurology (1911) 2004-07, Vol.475 (3), p.391-405 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 405 |
---|---|
container_issue | 3 |
container_start_page | 391 |
container_title | Journal of comparative neurology (1911) |
container_volume | 475 |
creator | Hegedűs, Endre Kaslin, Jan Hiripi, László Kiss, Tibor Panula, Pertti Elekes, Károly |
description | Distribution, chemical‐neuroanatomy, concentration, and uptake‐release properties of histamine (HA)‐containing neurons and the possible physiological effects of HA in the central and peripheral nervous system of the pulmonate snails, Helix pomatia and Lymnaea stagnalis, are described. In the CNS of both species, the distribution pattern of HA‐immunoreactive (HA‐IR) neurons was similar. In both species the majority were located in the buccal, cerebral, and pedal ganglia. In Helix, ∼400 HA‐IR neurons were seen, whereas in Lymnaea ∼130 labeled cells were visualized. The neuropils, connectives, commissures, several peripheral nerves, and a part of the peripheral tissues (lip and foot of both species and the upper tentacles of Helix) were innervated by HA‐IR elements. Numerous sensory cells were found in the tentacles, lip, and statocysts. The HA concentration values assayed by HPLC ranged from 4.8 to 47.4 pmol/mg in the different central ganglia of Helix, and from 4.3 to 18.6 pmol/mg in Lymnaea CNS, whereas the peripheral tissues contained 0.33–1 pmol/mg HA in Helix and 0.26–0.46 pmol/mg in Lymnaea. In the Lymnaea CNS, a high‐affinity (37.6 μM), single component 3H‐HA uptake system was demonstrated. 3H‐HA release evoked by either electrical stimulation or 100 mM K+ could be prevented in Ca2+‐free physiological solution. Voltage‐clamp experiments indicated specific changes caused by HA in the membrane conductance of identified central neurons of Helix and Lymnaea. Exogenously applied 10‐5 M HA resulted in the acceleration of locomotion (gliding by foot cilia) of Lymnaea. The findings suggest an important signaling role of HA, described here for the first time, in the nervous system of higher‐order, pulmonate, gastropods, involving efferent, integrative, and sensory functions. The data can also be applied as a background for further specification of HA in the regulation of different behaviors in these species. J. Comp. Neurol. 475:391–405, 2004. © 2004 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/cne.20171 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_66661863</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>66661863</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4251-d0769da46ab9dfea7f7e597b55c213645bd5f2beb1edf576afea86999a5ac3a73</originalsourceid><addsrcrecordid>eNp1kc9u1DAQhy0EotvCgRdAPiEqNa2drO2YW7Vqu6irwqGIo-U4k11DYqd2As0b8Zg47PLngi_WaL75RqMfQq8oOaeE5BfGwXlOqKBP0IISyTNZcvoULVKPZlJycYSOY_xCCJGyKJ-jI8rynEpWLNCPtY2D7qyDsLUGOxiDdxFbh4cdYANuCLrF2tW4h2D7Hcxlgr_5MeI4xQE67Bu81XEIvvd1xG_X0NrHM7yZOqdBn77Dlw7brhudN9PgzQ46a3R7hiv7TzFvgBbMbNlN0frWb-cO1n0fvDa7F-hZo9sILw__Cfp0fXW_WmebDzfvV5ebzCxzRrOaCC5rveS6knUDWjQCmBQVYyanBV-yqmZNXkFFoW6Y4DoxJZdSaqZNoUVxgt7svWntwwhxUJ2NBtpWO0g3K54eLXmRwNM9aIKPMUCj-mA7HSZFiZpjUSkW9SuWxL4-SMeqg_ovecghARd74LttYfq_Sa3urn4rs_1Eyg8e_0zo8FVxUQimPt_dqM09uS1vP5ZKFD8BS7iq9Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>66661863</pqid></control><display><type>article</type><title>Histaminergic neurons in the central and peripheral nervous system of gastropods (Helix, Lymnaea): An immunocytochemical, biochemical, and electrophysiological approach</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Hegedűs, Endre ; Kaslin, Jan ; Hiripi, László ; Kiss, Tibor ; Panula, Pertti ; Elekes, Károly</creator><creatorcontrib>Hegedűs, Endre ; Kaslin, Jan ; Hiripi, László ; Kiss, Tibor ; Panula, Pertti ; Elekes, Károly</creatorcontrib><description>Distribution, chemical‐neuroanatomy, concentration, and uptake‐release properties of histamine (HA)‐containing neurons and the possible physiological effects of HA in the central and peripheral nervous system of the pulmonate snails, Helix pomatia and Lymnaea stagnalis, are described. In the CNS of both species, the distribution pattern of HA‐immunoreactive (HA‐IR) neurons was similar. In both species the majority were located in the buccal, cerebral, and pedal ganglia. In Helix, ∼400 HA‐IR neurons were seen, whereas in Lymnaea ∼130 labeled cells were visualized. The neuropils, connectives, commissures, several peripheral nerves, and a part of the peripheral tissues (lip and foot of both species and the upper tentacles of Helix) were innervated by HA‐IR elements. Numerous sensory cells were found in the tentacles, lip, and statocysts. The HA concentration values assayed by HPLC ranged from 4.8 to 47.4 pmol/mg in the different central ganglia of Helix, and from 4.3 to 18.6 pmol/mg in Lymnaea CNS, whereas the peripheral tissues contained 0.33–1 pmol/mg HA in Helix and 0.26–0.46 pmol/mg in Lymnaea. In the Lymnaea CNS, a high‐affinity (37.6 μM), single component 3H‐HA uptake system was demonstrated. 3H‐HA release evoked by either electrical stimulation or 100 mM K+ could be prevented in Ca2+‐free physiological solution. Voltage‐clamp experiments indicated specific changes caused by HA in the membrane conductance of identified central neurons of Helix and Lymnaea. Exogenously applied 10‐5 M HA resulted in the acceleration of locomotion (gliding by foot cilia) of Lymnaea. The findings suggest an important signaling role of HA, described here for the first time, in the nervous system of higher‐order, pulmonate, gastropods, involving efferent, integrative, and sensory functions. The data can also be applied as a background for further specification of HA in the regulation of different behaviors in these species. J. Comp. Neurol. 475:391–405, 2004. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.20171</identifier><identifier>PMID: 15221953</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Behavior, Animal ; biochemistry ; Biochemistry - methods ; Calcium - metabolism ; Central Nervous System - cytology ; Chromatography, High Pressure Liquid - methods ; CNS ; electrophysiology ; Electrophysiology - methods ; gastropods ; Helix ; Helix (Snails) ; histamine ; Histamine - metabolism ; immunocytochemistry ; Immunohistochemistry - methods ; Kinetics ; Lymnaea ; Membrane Potentials - drug effects ; molluscs ; Motor Activity - drug effects ; Motor Activity - physiology ; Neurons - metabolism ; Peripheral Nervous System - cytology ; PNS ; Potassium - pharmacology ; Tritium - metabolism</subject><ispartof>Journal of comparative neurology (1911), 2004-07, Vol.475 (3), p.391-405</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>Copyright 2004 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4251-d0769da46ab9dfea7f7e597b55c213645bd5f2beb1edf576afea86999a5ac3a73</citedby><cites>FETCH-LOGICAL-c4251-d0769da46ab9dfea7f7e597b55c213645bd5f2beb1edf576afea86999a5ac3a73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcne.20171$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.20171$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15221953$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hegedűs, Endre</creatorcontrib><creatorcontrib>Kaslin, Jan</creatorcontrib><creatorcontrib>Hiripi, László</creatorcontrib><creatorcontrib>Kiss, Tibor</creatorcontrib><creatorcontrib>Panula, Pertti</creatorcontrib><creatorcontrib>Elekes, Károly</creatorcontrib><title>Histaminergic neurons in the central and peripheral nervous system of gastropods (Helix, Lymnaea): An immunocytochemical, biochemical, and electrophysiological approach</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>Distribution, chemical‐neuroanatomy, concentration, and uptake‐release properties of histamine (HA)‐containing neurons and the possible physiological effects of HA in the central and peripheral nervous system of the pulmonate snails, Helix pomatia and Lymnaea stagnalis, are described. In the CNS of both species, the distribution pattern of HA‐immunoreactive (HA‐IR) neurons was similar. In both species the majority were located in the buccal, cerebral, and pedal ganglia. In Helix, ∼400 HA‐IR neurons were seen, whereas in Lymnaea ∼130 labeled cells were visualized. The neuropils, connectives, commissures, several peripheral nerves, and a part of the peripheral tissues (lip and foot of both species and the upper tentacles of Helix) were innervated by HA‐IR elements. Numerous sensory cells were found in the tentacles, lip, and statocysts. The HA concentration values assayed by HPLC ranged from 4.8 to 47.4 pmol/mg in the different central ganglia of Helix, and from 4.3 to 18.6 pmol/mg in Lymnaea CNS, whereas the peripheral tissues contained 0.33–1 pmol/mg HA in Helix and 0.26–0.46 pmol/mg in Lymnaea. In the Lymnaea CNS, a high‐affinity (37.6 μM), single component 3H‐HA uptake system was demonstrated. 3H‐HA release evoked by either electrical stimulation or 100 mM K+ could be prevented in Ca2+‐free physiological solution. Voltage‐clamp experiments indicated specific changes caused by HA in the membrane conductance of identified central neurons of Helix and Lymnaea. Exogenously applied 10‐5 M HA resulted in the acceleration of locomotion (gliding by foot cilia) of Lymnaea. The findings suggest an important signaling role of HA, described here for the first time, in the nervous system of higher‐order, pulmonate, gastropods, involving efferent, integrative, and sensory functions. The data can also be applied as a background for further specification of HA in the regulation of different behaviors in these species. J. Comp. Neurol. 475:391–405, 2004. © 2004 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Behavior, Animal</subject><subject>biochemistry</subject><subject>Biochemistry - methods</subject><subject>Calcium - metabolism</subject><subject>Central Nervous System - cytology</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>CNS</subject><subject>electrophysiology</subject><subject>Electrophysiology - methods</subject><subject>gastropods</subject><subject>Helix</subject><subject>Helix (Snails)</subject><subject>histamine</subject><subject>Histamine - metabolism</subject><subject>immunocytochemistry</subject><subject>Immunohistochemistry - methods</subject><subject>Kinetics</subject><subject>Lymnaea</subject><subject>Membrane Potentials - drug effects</subject><subject>molluscs</subject><subject>Motor Activity - drug effects</subject><subject>Motor Activity - physiology</subject><subject>Neurons - metabolism</subject><subject>Peripheral Nervous System - cytology</subject><subject>PNS</subject><subject>Potassium - pharmacology</subject><subject>Tritium - metabolism</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc9u1DAQhy0EotvCgRdAPiEqNa2drO2YW7Vqu6irwqGIo-U4k11DYqd2As0b8Zg47PLngi_WaL75RqMfQq8oOaeE5BfGwXlOqKBP0IISyTNZcvoULVKPZlJycYSOY_xCCJGyKJ-jI8rynEpWLNCPtY2D7qyDsLUGOxiDdxFbh4cdYANuCLrF2tW4h2D7Hcxlgr_5MeI4xQE67Bu81XEIvvd1xG_X0NrHM7yZOqdBn77Dlw7brhudN9PgzQ46a3R7hiv7TzFvgBbMbNlN0frWb-cO1n0fvDa7F-hZo9sILw__Cfp0fXW_WmebDzfvV5ebzCxzRrOaCC5rveS6knUDWjQCmBQVYyanBV-yqmZNXkFFoW6Y4DoxJZdSaqZNoUVxgt7svWntwwhxUJ2NBtpWO0g3K54eLXmRwNM9aIKPMUCj-mA7HSZFiZpjUSkW9SuWxL4-SMeqg_ovecghARd74LttYfq_Sa3urn4rs_1Eyg8e_0zo8FVxUQimPt_dqM09uS1vP5ZKFD8BS7iq9Q</recordid><startdate>20040726</startdate><enddate>20040726</enddate><creator>Hegedűs, Endre</creator><creator>Kaslin, Jan</creator><creator>Hiripi, László</creator><creator>Kiss, Tibor</creator><creator>Panula, Pertti</creator><creator>Elekes, Károly</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>20040726</creationdate><title>Histaminergic neurons in the central and peripheral nervous system of gastropods (Helix, Lymnaea): An immunocytochemical, biochemical, and electrophysiological approach</title><author>Hegedűs, Endre ; Kaslin, Jan ; Hiripi, László ; Kiss, Tibor ; Panula, Pertti ; Elekes, Károly</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4251-d0769da46ab9dfea7f7e597b55c213645bd5f2beb1edf576afea86999a5ac3a73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Behavior, Animal</topic><topic>biochemistry</topic><topic>Biochemistry - methods</topic><topic>Calcium - metabolism</topic><topic>Central Nervous System - cytology</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>CNS</topic><topic>electrophysiology</topic><topic>Electrophysiology - methods</topic><topic>gastropods</topic><topic>Helix</topic><topic>Helix (Snails)</topic><topic>histamine</topic><topic>Histamine - metabolism</topic><topic>immunocytochemistry</topic><topic>Immunohistochemistry - methods</topic><topic>Kinetics</topic><topic>Lymnaea</topic><topic>Membrane Potentials - drug effects</topic><topic>molluscs</topic><topic>Motor Activity - drug effects</topic><topic>Motor Activity - physiology</topic><topic>Neurons - metabolism</topic><topic>Peripheral Nervous System - cytology</topic><topic>PNS</topic><topic>Potassium - pharmacology</topic><topic>Tritium - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hegedűs, Endre</creatorcontrib><creatorcontrib>Kaslin, Jan</creatorcontrib><creatorcontrib>Hiripi, László</creatorcontrib><creatorcontrib>Kiss, Tibor</creatorcontrib><creatorcontrib>Panula, Pertti</creatorcontrib><creatorcontrib>Elekes, Károly</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>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hegedűs, Endre</au><au>Kaslin, Jan</au><au>Hiripi, László</au><au>Kiss, Tibor</au><au>Panula, Pertti</au><au>Elekes, Károly</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histaminergic neurons in the central and peripheral nervous system of gastropods (Helix, Lymnaea): An immunocytochemical, biochemical, and electrophysiological approach</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>2004-07-26</date><risdate>2004</risdate><volume>475</volume><issue>3</issue><spage>391</spage><epage>405</epage><pages>391-405</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Distribution, chemical‐neuroanatomy, concentration, and uptake‐release properties of histamine (HA)‐containing neurons and the possible physiological effects of HA in the central and peripheral nervous system of the pulmonate snails, Helix pomatia and Lymnaea stagnalis, are described. In the CNS of both species, the distribution pattern of HA‐immunoreactive (HA‐IR) neurons was similar. In both species the majority were located in the buccal, cerebral, and pedal ganglia. In Helix, ∼400 HA‐IR neurons were seen, whereas in Lymnaea ∼130 labeled cells were visualized. The neuropils, connectives, commissures, several peripheral nerves, and a part of the peripheral tissues (lip and foot of both species and the upper tentacles of Helix) were innervated by HA‐IR elements. Numerous sensory cells were found in the tentacles, lip, and statocysts. The HA concentration values assayed by HPLC ranged from 4.8 to 47.4 pmol/mg in the different central ganglia of Helix, and from 4.3 to 18.6 pmol/mg in Lymnaea CNS, whereas the peripheral tissues contained 0.33–1 pmol/mg HA in Helix and 0.26–0.46 pmol/mg in Lymnaea. In the Lymnaea CNS, a high‐affinity (37.6 μM), single component 3H‐HA uptake system was demonstrated. 3H‐HA release evoked by either electrical stimulation or 100 mM K+ could be prevented in Ca2+‐free physiological solution. Voltage‐clamp experiments indicated specific changes caused by HA in the membrane conductance of identified central neurons of Helix and Lymnaea. Exogenously applied 10‐5 M HA resulted in the acceleration of locomotion (gliding by foot cilia) of Lymnaea. The findings suggest an important signaling role of HA, described here for the first time, in the nervous system of higher‐order, pulmonate, gastropods, involving efferent, integrative, and sensory functions. The data can also be applied as a background for further specification of HA in the regulation of different behaviors in these species. J. Comp. Neurol. 475:391–405, 2004. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15221953</pmid><doi>10.1002/cne.20171</doi><tpages>15</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9967 |
ispartof | Journal of comparative neurology (1911), 2004-07, Vol.475 (3), p.391-405 |
issn | 0021-9967 1096-9861 |
language | eng |
recordid | cdi_proquest_miscellaneous_66661863 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Animals Behavior, Animal biochemistry Biochemistry - methods Calcium - metabolism Central Nervous System - cytology Chromatography, High Pressure Liquid - methods CNS electrophysiology Electrophysiology - methods gastropods Helix Helix (Snails) histamine Histamine - metabolism immunocytochemistry Immunohistochemistry - methods Kinetics Lymnaea Membrane Potentials - drug effects molluscs Motor Activity - drug effects Motor Activity - physiology Neurons - metabolism Peripheral Nervous System - cytology PNS Potassium - pharmacology Tritium - metabolism |
title | Histaminergic neurons in the central and peripheral nervous system of gastropods (Helix, Lymnaea): An immunocytochemical, biochemical, and electrophysiological approach |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T14%3A22%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Histaminergic%20neurons%20in%20the%20central%20and%20peripheral%20nervous%20system%20of%20gastropods%20(Helix,%20Lymnaea):%20An%20immunocytochemical,%20biochemical,%20and%20electrophysiological%20approach&rft.jtitle=Journal%20of%20comparative%20neurology%20(1911)&rft.au=Heged%C5%B1s,%20Endre&rft.date=2004-07-26&rft.volume=475&rft.issue=3&rft.spage=391&rft.epage=405&rft.pages=391-405&rft.issn=0021-9967&rft.eissn=1096-9861&rft_id=info:doi/10.1002/cne.20171&rft_dat=%3Cproquest_cross%3E66661863%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=66661863&rft_id=info:pmid/15221953&rfr_iscdi=true |