Pacemaker activity in hydra is modulated by glycine receptor ligands

In the mammalian central nervous system, the neurotransmitter, glycine, acts both on an inhibitory, strychnine-sensitive receptor (GlyR) and an excitatory, strychnine-insensitive site at the NMDA receptor. Here we present electrophysiological evidence that the strychnine-sensitive glycine agonists,...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Comparative biochemistry and physiology. Part A, Molecular & integrative physiology Molecular & integrative physiology, 2004-06, Vol.138 (2), p.193-202
Hauptverfasser: Ruggieri, R.D, Pierobon, P, Kass-Simon, G
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 202
container_issue 2
container_start_page 193
container_title Comparative biochemistry and physiology. Part A, Molecular & integrative physiology
container_volume 138
creator Ruggieri, R.D
Pierobon, P
Kass-Simon, G
description In the mammalian central nervous system, the neurotransmitter, glycine, acts both on an inhibitory, strychnine-sensitive receptor (GlyR) and an excitatory, strychnine-insensitive site at the NMDA receptor. Here we present electrophysiological evidence that the strychnine-sensitive glycine agonists, glycine and taurine, and the antagonist, strychnine, affect the endodermal rhythmic potential (RP) system and that the ectodermal contraction burst (CB) pacemaker system is modulated by glycine and strychnine in hydra. The RP and CB pacemaker systems are responsible for the respective elongation and contraction of hydra's body column. Activity of the CB system, quantified by the rate of contraction bursts (CBs), the number of pulses per contraction burst (P/CB), and the duration of bursts, was decreased by glycine. Glycine, coadministered with the strychnine-insensitive glycine site blocker, indole-2-carboxylic acid (I2CA), decreased RPs but not CBs or P/CB. The effect was mimicked by taurine. Strychnine increased the duration of RP production, and decreased CB duration. The effect of glycine with I2CA was counteracted by strychnine. The results support the idea that a vertebrate-like GlyR may be involved in modulating activity of the endodermal RP system and suggest that a glycine site on an NMDA receptor may be involved in the CB system.
doi_str_mv 10.1016/j.cbpb.2004.03.015
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_19406830</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1095643304001151</els_id><sourcerecordid>19406830</sourcerecordid><originalsourceid>FETCH-LOGICAL-c449t-7731409544ce43d20ae51ac9f7a9938ba4ae4f5b5bf628eb6a25c32e92f7e0033</originalsourceid><addsrcrecordid>eNp9kMtOwzAQRS0EoqXwAyyQV-wS_EwaiQ3iLVWCBawt25kUl7ywk0r5e1y1EjtmMzPSvVczB6FLSlJKaHazSa3pTcoIESnhKaHyCM2p5DQRnLPjOJNCJllcZugshA2JJag4RTMqWS4zKebo4V1baPQ3eKzt4LZumLBr8ddUeo1dwE1XjrUeoMRmwut6sq4F7MFCP3Qe126t2zKco5NK1wEuDn2BPp8eP-5fktXb8-v93SqxQhRDkueciniSEBYELxnRIKm2RZXrouBLo4UGUUkjTZWxJZhMM2k5g4JVORDC-QJd73N73_2MEAbVuGChrnUL3RgULQTJlpxEIdsLre9C8FCp3rtG-0lRonbs1Ebt2KkdO0W4iuyi6eqQPpoGyj_LAVYU3O4FEH_cOvAqWAethdJFIoMqO_df_i9Bpn-Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19406830</pqid></control><display><type>article</type><title>Pacemaker activity in hydra is modulated by glycine receptor ligands</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Ruggieri, R.D ; Pierobon, P ; Kass-Simon, G</creator><creatorcontrib>Ruggieri, R.D ; Pierobon, P ; Kass-Simon, G</creatorcontrib><description>In the mammalian central nervous system, the neurotransmitter, glycine, acts both on an inhibitory, strychnine-sensitive receptor (GlyR) and an excitatory, strychnine-insensitive site at the NMDA receptor. Here we present electrophysiological evidence that the strychnine-sensitive glycine agonists, glycine and taurine, and the antagonist, strychnine, affect the endodermal rhythmic potential (RP) system and that the ectodermal contraction burst (CB) pacemaker system is modulated by glycine and strychnine in hydra. The RP and CB pacemaker systems are responsible for the respective elongation and contraction of hydra's body column. Activity of the CB system, quantified by the rate of contraction bursts (CBs), the number of pulses per contraction burst (P/CB), and the duration of bursts, was decreased by glycine. Glycine, coadministered with the strychnine-insensitive glycine site blocker, indole-2-carboxylic acid (I2CA), decreased RPs but not CBs or P/CB. The effect was mimicked by taurine. Strychnine increased the duration of RP production, and decreased CB duration. The effect of glycine with I2CA was counteracted by strychnine. The results support the idea that a vertebrate-like GlyR may be involved in modulating activity of the endodermal RP system and suggest that a glycine site on an NMDA receptor may be involved in the CB system.</description><identifier>ISSN: 1095-6433</identifier><identifier>EISSN: 1531-4332</identifier><identifier>DOI: 10.1016/j.cbpb.2004.03.015</identifier><identifier>PMID: 15275654</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Amino acid receptors ; Animals ; Biological Clocks - drug effects ; Biological Clocks - physiology ; Cnidarian ; Glycine ; Glycine - pharmacology ; Glycine Agents - pharmacology ; Hydra ; Hydra - drug effects ; Hydra - physiology ; I2CA ; Indoles - pharmacology ; Ligands ; Membrane Potentials - drug effects ; Muscle Contraction - drug effects ; NMDA ; Pacemakers ; Periodicity ; Receptors, Glycine - drug effects ; Receptors, Glycine - metabolism ; Species Specificity ; Strychnine ; Strychnine - pharmacology ; Taurine ; Taurine - pharmacology</subject><ispartof>Comparative biochemistry and physiology. Part A, Molecular &amp; integrative physiology, 2004-06, Vol.138 (2), p.193-202</ispartof><rights>2004 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c449t-7731409544ce43d20ae51ac9f7a9938ba4ae4f5b5bf628eb6a25c32e92f7e0033</citedby><cites>FETCH-LOGICAL-c449t-7731409544ce43d20ae51ac9f7a9938ba4ae4f5b5bf628eb6a25c32e92f7e0033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cbpb.2004.03.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15275654$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ruggieri, R.D</creatorcontrib><creatorcontrib>Pierobon, P</creatorcontrib><creatorcontrib>Kass-Simon, G</creatorcontrib><title>Pacemaker activity in hydra is modulated by glycine receptor ligands</title><title>Comparative biochemistry and physiology. Part A, Molecular &amp; integrative physiology</title><addtitle>Comp Biochem Physiol A Mol Integr Physiol</addtitle><description>In the mammalian central nervous system, the neurotransmitter, glycine, acts both on an inhibitory, strychnine-sensitive receptor (GlyR) and an excitatory, strychnine-insensitive site at the NMDA receptor. Here we present electrophysiological evidence that the strychnine-sensitive glycine agonists, glycine and taurine, and the antagonist, strychnine, affect the endodermal rhythmic potential (RP) system and that the ectodermal contraction burst (CB) pacemaker system is modulated by glycine and strychnine in hydra. The RP and CB pacemaker systems are responsible for the respective elongation and contraction of hydra's body column. Activity of the CB system, quantified by the rate of contraction bursts (CBs), the number of pulses per contraction burst (P/CB), and the duration of bursts, was decreased by glycine. Glycine, coadministered with the strychnine-insensitive glycine site blocker, indole-2-carboxylic acid (I2CA), decreased RPs but not CBs or P/CB. The effect was mimicked by taurine. Strychnine increased the duration of RP production, and decreased CB duration. The effect of glycine with I2CA was counteracted by strychnine. The results support the idea that a vertebrate-like GlyR may be involved in modulating activity of the endodermal RP system and suggest that a glycine site on an NMDA receptor may be involved in the CB system.</description><subject>Amino acid receptors</subject><subject>Animals</subject><subject>Biological Clocks - drug effects</subject><subject>Biological Clocks - physiology</subject><subject>Cnidarian</subject><subject>Glycine</subject><subject>Glycine - pharmacology</subject><subject>Glycine Agents - pharmacology</subject><subject>Hydra</subject><subject>Hydra - drug effects</subject><subject>Hydra - physiology</subject><subject>I2CA</subject><subject>Indoles - pharmacology</subject><subject>Ligands</subject><subject>Membrane Potentials - drug effects</subject><subject>Muscle Contraction - drug effects</subject><subject>NMDA</subject><subject>Pacemakers</subject><subject>Periodicity</subject><subject>Receptors, Glycine - drug effects</subject><subject>Receptors, Glycine - metabolism</subject><subject>Species Specificity</subject><subject>Strychnine</subject><subject>Strychnine - pharmacology</subject><subject>Taurine</subject><subject>Taurine - pharmacology</subject><issn>1095-6433</issn><issn>1531-4332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqXwAyyQV-wS_EwaiQ3iLVWCBawt25kUl7ywk0r5e1y1EjtmMzPSvVczB6FLSlJKaHazSa3pTcoIESnhKaHyCM2p5DQRnLPjOJNCJllcZugshA2JJag4RTMqWS4zKebo4V1baPQ3eKzt4LZumLBr8ddUeo1dwE1XjrUeoMRmwut6sq4F7MFCP3Qe126t2zKco5NK1wEuDn2BPp8eP-5fktXb8-v93SqxQhRDkueciniSEBYELxnRIKm2RZXrouBLo4UGUUkjTZWxJZhMM2k5g4JVORDC-QJd73N73_2MEAbVuGChrnUL3RgULQTJlpxEIdsLre9C8FCp3rtG-0lRonbs1Ebt2KkdO0W4iuyi6eqQPpoGyj_LAVYU3O4FEH_cOvAqWAethdJFIoMqO_df_i9Bpn-Q</recordid><startdate>20040601</startdate><enddate>20040601</enddate><creator>Ruggieri, R.D</creator><creator>Pierobon, P</creator><creator>Kass-Simon, G</creator><general>Elsevier Inc</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>F1W</scope><scope>H95</scope><scope>L.G</scope></search><sort><creationdate>20040601</creationdate><title>Pacemaker activity in hydra is modulated by glycine receptor ligands</title><author>Ruggieri, R.D ; Pierobon, P ; Kass-Simon, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c449t-7731409544ce43d20ae51ac9f7a9938ba4ae4f5b5bf628eb6a25c32e92f7e0033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Amino acid receptors</topic><topic>Animals</topic><topic>Biological Clocks - drug effects</topic><topic>Biological Clocks - physiology</topic><topic>Cnidarian</topic><topic>Glycine</topic><topic>Glycine - pharmacology</topic><topic>Glycine Agents - pharmacology</topic><topic>Hydra</topic><topic>Hydra - drug effects</topic><topic>Hydra - physiology</topic><topic>I2CA</topic><topic>Indoles - pharmacology</topic><topic>Ligands</topic><topic>Membrane Potentials - drug effects</topic><topic>Muscle Contraction - drug effects</topic><topic>NMDA</topic><topic>Pacemakers</topic><topic>Periodicity</topic><topic>Receptors, Glycine - drug effects</topic><topic>Receptors, Glycine - metabolism</topic><topic>Species Specificity</topic><topic>Strychnine</topic><topic>Strychnine - pharmacology</topic><topic>Taurine</topic><topic>Taurine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ruggieri, R.D</creatorcontrib><creatorcontrib>Pierobon, P</creatorcontrib><creatorcontrib>Kass-Simon, G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 1: Biological Sciences &amp; Living Resources</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><jtitle>Comparative biochemistry and physiology. Part A, Molecular &amp; integrative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ruggieri, R.D</au><au>Pierobon, P</au><au>Kass-Simon, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pacemaker activity in hydra is modulated by glycine receptor ligands</atitle><jtitle>Comparative biochemistry and physiology. Part A, Molecular &amp; integrative physiology</jtitle><addtitle>Comp Biochem Physiol A Mol Integr Physiol</addtitle><date>2004-06-01</date><risdate>2004</risdate><volume>138</volume><issue>2</issue><spage>193</spage><epage>202</epage><pages>193-202</pages><issn>1095-6433</issn><eissn>1531-4332</eissn><abstract>In the mammalian central nervous system, the neurotransmitter, glycine, acts both on an inhibitory, strychnine-sensitive receptor (GlyR) and an excitatory, strychnine-insensitive site at the NMDA receptor. Here we present electrophysiological evidence that the strychnine-sensitive glycine agonists, glycine and taurine, and the antagonist, strychnine, affect the endodermal rhythmic potential (RP) system and that the ectodermal contraction burst (CB) pacemaker system is modulated by glycine and strychnine in hydra. The RP and CB pacemaker systems are responsible for the respective elongation and contraction of hydra's body column. Activity of the CB system, quantified by the rate of contraction bursts (CBs), the number of pulses per contraction burst (P/CB), and the duration of bursts, was decreased by glycine. Glycine, coadministered with the strychnine-insensitive glycine site blocker, indole-2-carboxylic acid (I2CA), decreased RPs but not CBs or P/CB. The effect was mimicked by taurine. Strychnine increased the duration of RP production, and decreased CB duration. The effect of glycine with I2CA was counteracted by strychnine. The results support the idea that a vertebrate-like GlyR may be involved in modulating activity of the endodermal RP system and suggest that a glycine site on an NMDA receptor may be involved in the CB system.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15275654</pmid><doi>10.1016/j.cbpb.2004.03.015</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1095-6433
ispartof Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 2004-06, Vol.138 (2), p.193-202
issn 1095-6433
1531-4332
language eng
recordid cdi_proquest_miscellaneous_19406830
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Amino acid receptors
Animals
Biological Clocks - drug effects
Biological Clocks - physiology
Cnidarian
Glycine
Glycine - pharmacology
Glycine Agents - pharmacology
Hydra
Hydra - drug effects
Hydra - physiology
I2CA
Indoles - pharmacology
Ligands
Membrane Potentials - drug effects
Muscle Contraction - drug effects
NMDA
Pacemakers
Periodicity
Receptors, Glycine - drug effects
Receptors, Glycine - metabolism
Species Specificity
Strychnine
Strychnine - pharmacology
Taurine
Taurine - pharmacology
title Pacemaker activity in hydra is modulated by glycine receptor ligands
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T16%3A27%3A21IST&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=Pacemaker%20activity%20in%20hydra%20is%20modulated%20by%20glycine%20receptor%20ligands&rft.jtitle=Comparative%20biochemistry%20and%20physiology.%20Part%20A,%20Molecular%20&%20integrative%20physiology&rft.au=Ruggieri,%20R.D&rft.date=2004-06-01&rft.volume=138&rft.issue=2&rft.spage=193&rft.epage=202&rft.pages=193-202&rft.issn=1095-6433&rft.eissn=1531-4332&rft_id=info:doi/10.1016/j.cbpb.2004.03.015&rft_dat=%3Cproquest_cross%3E19406830%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=19406830&rft_id=info:pmid/15275654&rft_els_id=S1095643304001151&rfr_iscdi=true