Effect of phenazine methosulfate on electrophysiological activity of the semicircular canal: antioxidant properties of trimetazidine
Ischemia strokes appear to be the main source of cochleo-vestibular dysfunctions of peripheral origin. The present study aimed to investigate the action of oxygen free radicals on the bioelectric activity of the labyrinthine epithelium, using the frog semicircular canal as an in vitro preparation. W...
Gespeichert in:
Veröffentlicht in: | European journal of pharmacology 1989-12, Vol.174 (2), p.215-225 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 225 |
---|---|
container_issue | 2 |
container_start_page | 215 |
container_title | European journal of pharmacology |
container_volume | 174 |
creator | Aubert, Anne Bernard, Christian Clauser, Pascale Harpey, Catherine Vaudry, Hubert |
description | Ischemia strokes appear to be the main source of cochleo-vestibular dysfunctions of peripheral origin. The present study aimed to investigate the action of oxygen free radicals on the bioelectric activity of the labyrinthine epithelium, using the frog semicircular canal as an in vitro preparation. We also examined the possible effect of the antianginal drug, trimetazidine (TMZ), under physiological conditions and during the administration of phenazine methosulfate (PMS). The model allows the ionic composition of endolymphatic and perilymphatic fluids bathing the semicircular canal to be dealt with separately. Spontaneous afferent vestibular nerve activity and the endolymphatic potential were recorded under resting conditions. Three additional parameters were investigated during mechanical displacement of the endolymphatic fluid: the ampullar direct current, the nerve direct current and the frequency of the evoked afferent spikes. Addition of TMZ (10
−6 and 10
−5 M, 50 min) into the perilymphatic compartment did not induce significant modifications of the different bioelectrical signals. Generation of oxygen free radicals, through administration of PMS (10
−5 M, 15 min) into the perilymphatic compartment, caused an impairment of all bioelectrical signals, except the ampullar direct current. The spontaneous activity, nerve direct current and frequency of afferent evoked spikes signals were significantly reduced 75 min after the start of PMS administration (−64, −17 and −32%, respectively). In contrast, there was a marked increase of the endolymphatic potential signal (+51%). Addition of TMZ (10
−6 or 10
−5 M) into the perilymph solution reversed the effect of PMS on all bioeletrical signals. These results indicate that TMZ acts as an antioxidant molecule which is capable of protecting the labyrinthine epithelium from the deleterious effect of oxygen radicals. Our data suggest that the protective effect of TMZ on ischemia-induced cochleo-vestibular dysfunctions may be accounted for by the antioxidant properties of this antianginal drug. |
doi_str_mv | 10.1016/0014-2999(89)90314-2 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79504513</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0014299989903142</els_id><sourcerecordid>79504513</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-274fabe82730ca175b6cc912b7a6d63b15b573859896219376f59174f44d53283</originalsourceid><addsrcrecordid>eNp9kU2PFCEQhonRrOPqP9CEgzF6aOWjgWYPJmazfiSbeNEzoenCwTDNCPTG8ewPl96ZzNETgXreqsoDQs8peUsJle8IoX3HtNavB_1GE77eHqANHZTuiKLsIdqckcfoSSk_CSFCM3GBLpjkpL1v0N8b78FVnDzeb2G2f8IMeAd1m8oSva2A04whNiSn_fZQQorpR3A2YutquAv1sEbrFnCBXXAhuyXajJ2dbbzCdq4h_Q5TO_G-NYBcA5T7RA5tShs3tYFP0SNvY4Fnp_MSff948-36c3f79dOX6w-3neODrB1TvbcjDExx4ixVYpTOacpGZeUk-UjFKBQfhB60ZFRzJb3QtIX6fhKcDfwSvTr2bbv8WqBUswvFQYx2hrQUo7QgvaC8gf0RdDmVksGbfdvX5oOhxKzyzWrWrGbNoM29fMNa7MWp_zLuYDqHTrZb_eWpbktT6LOdXShnTEpFKSMNe3_EoLm4C5BNcQFmB1PI7SPMlML_9_gHLmainw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>79504513</pqid></control><display><type>article</type><title>Effect of phenazine methosulfate on electrophysiological activity of the semicircular canal: antioxidant properties of trimetazidine</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Aubert, Anne ; Bernard, Christian ; Clauser, Pascale ; Harpey, Catherine ; Vaudry, Hubert</creator><creatorcontrib>Aubert, Anne ; Bernard, Christian ; Clauser, Pascale ; Harpey, Catherine ; Vaudry, Hubert</creatorcontrib><description>Ischemia strokes appear to be the main source of cochleo-vestibular dysfunctions of peripheral origin. The present study aimed to investigate the action of oxygen free radicals on the bioelectric activity of the labyrinthine epithelium, using the frog semicircular canal as an in vitro preparation. We also examined the possible effect of the antianginal drug, trimetazidine (TMZ), under physiological conditions and during the administration of phenazine methosulfate (PMS). The model allows the ionic composition of endolymphatic and perilymphatic fluids bathing the semicircular canal to be dealt with separately. Spontaneous afferent vestibular nerve activity and the endolymphatic potential were recorded under resting conditions. Three additional parameters were investigated during mechanical displacement of the endolymphatic fluid: the ampullar direct current, the nerve direct current and the frequency of the evoked afferent spikes. Addition of TMZ (10
−6 and 10
−5 M, 50 min) into the perilymphatic compartment did not induce significant modifications of the different bioelectrical signals. Generation of oxygen free radicals, through administration of PMS (10
−5 M, 15 min) into the perilymphatic compartment, caused an impairment of all bioelectrical signals, except the ampullar direct current. The spontaneous activity, nerve direct current and frequency of afferent evoked spikes signals were significantly reduced 75 min after the start of PMS administration (−64, −17 and −32%, respectively). In contrast, there was a marked increase of the endolymphatic potential signal (+51%). Addition of TMZ (10
−6 or 10
−5 M) into the perilymph solution reversed the effect of PMS on all bioeletrical signals. These results indicate that TMZ acts as an antioxidant molecule which is capable of protecting the labyrinthine epithelium from the deleterious effect of oxygen radicals. Our data suggest that the protective effect of TMZ on ischemia-induced cochleo-vestibular dysfunctions may be accounted for by the antioxidant properties of this antianginal drug.</description><identifier>ISSN: 0014-2999</identifier><identifier>EISSN: 1879-0712</identifier><identifier>DOI: 10.1016/0014-2999(89)90314-2</identifier><identifier>PMID: 2630299</identifier><identifier>CODEN: EJPHAZ</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animals ; Antioxidants - pharmacology ; Biological and medical sciences ; Drug toxicity and drugs side effects treatment ; Electrophysiology ; Evoked Potentials - drug effects ; Free radicals ; Hydrogen-Ion Concentration ; In Vitro Techniques ; Male ; Medical sciences ; Methylphenazonium Methosulfate - pharmacology ; Miscellaneous (drug allergy, mutagens, teratogens...) ; Neurons, Afferent - drug effects ; Pharmacology. Drug treatments ; Phenazine methosulfate ; Phenazines - pharmacology ; Physical Stimulation ; Piperazines - pharmacology ; Rana ridibunda ; Semicircular canal ; Semicircular Canals - drug effects ; Trimetazidine ; Trimetazidine - pharmacology ; Vestibular dysfunctions</subject><ispartof>European journal of pharmacology, 1989-12, Vol.174 (2), p.215-225</ispartof><rights>1989</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-274fabe82730ca175b6cc912b7a6d63b15b573859896219376f59174f44d53283</citedby><cites>FETCH-LOGICAL-c386t-274fabe82730ca175b6cc912b7a6d63b15b573859896219376f59174f44d53283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0014-2999(89)90314-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6671120$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2630299$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aubert, Anne</creatorcontrib><creatorcontrib>Bernard, Christian</creatorcontrib><creatorcontrib>Clauser, Pascale</creatorcontrib><creatorcontrib>Harpey, Catherine</creatorcontrib><creatorcontrib>Vaudry, Hubert</creatorcontrib><title>Effect of phenazine methosulfate on electrophysiological activity of the semicircular canal: antioxidant properties of trimetazidine</title><title>European journal of pharmacology</title><addtitle>Eur J Pharmacol</addtitle><description>Ischemia strokes appear to be the main source of cochleo-vestibular dysfunctions of peripheral origin. The present study aimed to investigate the action of oxygen free radicals on the bioelectric activity of the labyrinthine epithelium, using the frog semicircular canal as an in vitro preparation. We also examined the possible effect of the antianginal drug, trimetazidine (TMZ), under physiological conditions and during the administration of phenazine methosulfate (PMS). The model allows the ionic composition of endolymphatic and perilymphatic fluids bathing the semicircular canal to be dealt with separately. Spontaneous afferent vestibular nerve activity and the endolymphatic potential were recorded under resting conditions. Three additional parameters were investigated during mechanical displacement of the endolymphatic fluid: the ampullar direct current, the nerve direct current and the frequency of the evoked afferent spikes. Addition of TMZ (10
−6 and 10
−5 M, 50 min) into the perilymphatic compartment did not induce significant modifications of the different bioelectrical signals. Generation of oxygen free radicals, through administration of PMS (10
−5 M, 15 min) into the perilymphatic compartment, caused an impairment of all bioelectrical signals, except the ampullar direct current. The spontaneous activity, nerve direct current and frequency of afferent evoked spikes signals were significantly reduced 75 min after the start of PMS administration (−64, −17 and −32%, respectively). In contrast, there was a marked increase of the endolymphatic potential signal (+51%). Addition of TMZ (10
−6 or 10
−5 M) into the perilymph solution reversed the effect of PMS on all bioeletrical signals. These results indicate that TMZ acts as an antioxidant molecule which is capable of protecting the labyrinthine epithelium from the deleterious effect of oxygen radicals. Our data suggest that the protective effect of TMZ on ischemia-induced cochleo-vestibular dysfunctions may be accounted for by the antioxidant properties of this antianginal drug.</description><subject>Animals</subject><subject>Antioxidants - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Electrophysiology</subject><subject>Evoked Potentials - drug effects</subject><subject>Free radicals</subject><subject>Hydrogen-Ion Concentration</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methylphenazonium Methosulfate - pharmacology</subject><subject>Miscellaneous (drug allergy, mutagens, teratogens...)</subject><subject>Neurons, Afferent - drug effects</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenazine methosulfate</subject><subject>Phenazines - pharmacology</subject><subject>Physical Stimulation</subject><subject>Piperazines - pharmacology</subject><subject>Rana ridibunda</subject><subject>Semicircular canal</subject><subject>Semicircular Canals - drug effects</subject><subject>Trimetazidine</subject><subject>Trimetazidine - pharmacology</subject><subject>Vestibular dysfunctions</subject><issn>0014-2999</issn><issn>1879-0712</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2PFCEQhonRrOPqP9CEgzF6aOWjgWYPJmazfiSbeNEzoenCwTDNCPTG8ewPl96ZzNETgXreqsoDQs8peUsJle8IoX3HtNavB_1GE77eHqANHZTuiKLsIdqckcfoSSk_CSFCM3GBLpjkpL1v0N8b78FVnDzeb2G2f8IMeAd1m8oSva2A04whNiSn_fZQQorpR3A2YutquAv1sEbrFnCBXXAhuyXajJ2dbbzCdq4h_Q5TO_G-NYBcA5T7RA5tShs3tYFP0SNvY4Fnp_MSff948-36c3f79dOX6w-3neODrB1TvbcjDExx4ixVYpTOacpGZeUk-UjFKBQfhB60ZFRzJb3QtIX6fhKcDfwSvTr2bbv8WqBUswvFQYx2hrQUo7QgvaC8gf0RdDmVksGbfdvX5oOhxKzyzWrWrGbNoM29fMNa7MWp_zLuYDqHTrZb_eWpbktT6LOdXShnTEpFKSMNe3_EoLm4C5BNcQFmB1PI7SPMlML_9_gHLmainw</recordid><startdate>19891219</startdate><enddate>19891219</enddate><creator>Aubert, Anne</creator><creator>Bernard, Christian</creator><creator>Clauser, Pascale</creator><creator>Harpey, Catherine</creator><creator>Vaudry, Hubert</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</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>19891219</creationdate><title>Effect of phenazine methosulfate on electrophysiological activity of the semicircular canal: antioxidant properties of trimetazidine</title><author>Aubert, Anne ; Bernard, Christian ; Clauser, Pascale ; Harpey, Catherine ; Vaudry, Hubert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-274fabe82730ca175b6cc912b7a6d63b15b573859896219376f59174f44d53283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Animals</topic><topic>Antioxidants - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Electrophysiology</topic><topic>Evoked Potentials - drug effects</topic><topic>Free radicals</topic><topic>Hydrogen-Ion Concentration</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methylphenazonium Methosulfate - pharmacology</topic><topic>Miscellaneous (drug allergy, mutagens, teratogens...)</topic><topic>Neurons, Afferent - drug effects</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenazine methosulfate</topic><topic>Phenazines - pharmacology</topic><topic>Physical Stimulation</topic><topic>Piperazines - pharmacology</topic><topic>Rana ridibunda</topic><topic>Semicircular canal</topic><topic>Semicircular Canals - drug effects</topic><topic>Trimetazidine</topic><topic>Trimetazidine - pharmacology</topic><topic>Vestibular dysfunctions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aubert, Anne</creatorcontrib><creatorcontrib>Bernard, Christian</creatorcontrib><creatorcontrib>Clauser, Pascale</creatorcontrib><creatorcontrib>Harpey, Catherine</creatorcontrib><creatorcontrib>Vaudry, Hubert</creatorcontrib><collection>Pascal-Francis</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>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aubert, Anne</au><au>Bernard, Christian</au><au>Clauser, Pascale</au><au>Harpey, Catherine</au><au>Vaudry, Hubert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of phenazine methosulfate on electrophysiological activity of the semicircular canal: antioxidant properties of trimetazidine</atitle><jtitle>European journal of pharmacology</jtitle><addtitle>Eur J Pharmacol</addtitle><date>1989-12-19</date><risdate>1989</risdate><volume>174</volume><issue>2</issue><spage>215</spage><epage>225</epage><pages>215-225</pages><issn>0014-2999</issn><eissn>1879-0712</eissn><coden>EJPHAZ</coden><abstract>Ischemia strokes appear to be the main source of cochleo-vestibular dysfunctions of peripheral origin. The present study aimed to investigate the action of oxygen free radicals on the bioelectric activity of the labyrinthine epithelium, using the frog semicircular canal as an in vitro preparation. We also examined the possible effect of the antianginal drug, trimetazidine (TMZ), under physiological conditions and during the administration of phenazine methosulfate (PMS). The model allows the ionic composition of endolymphatic and perilymphatic fluids bathing the semicircular canal to be dealt with separately. Spontaneous afferent vestibular nerve activity and the endolymphatic potential were recorded under resting conditions. Three additional parameters were investigated during mechanical displacement of the endolymphatic fluid: the ampullar direct current, the nerve direct current and the frequency of the evoked afferent spikes. Addition of TMZ (10
−6 and 10
−5 M, 50 min) into the perilymphatic compartment did not induce significant modifications of the different bioelectrical signals. Generation of oxygen free radicals, through administration of PMS (10
−5 M, 15 min) into the perilymphatic compartment, caused an impairment of all bioelectrical signals, except the ampullar direct current. The spontaneous activity, nerve direct current and frequency of afferent evoked spikes signals were significantly reduced 75 min after the start of PMS administration (−64, −17 and −32%, respectively). In contrast, there was a marked increase of the endolymphatic potential signal (+51%). Addition of TMZ (10
−6 or 10
−5 M) into the perilymph solution reversed the effect of PMS on all bioeletrical signals. These results indicate that TMZ acts as an antioxidant molecule which is capable of protecting the labyrinthine epithelium from the deleterious effect of oxygen radicals. Our data suggest that the protective effect of TMZ on ischemia-induced cochleo-vestibular dysfunctions may be accounted for by the antioxidant properties of this antianginal drug.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>2630299</pmid><doi>10.1016/0014-2999(89)90314-2</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0014-2999 |
ispartof | European journal of pharmacology, 1989-12, Vol.174 (2), p.215-225 |
issn | 0014-2999 1879-0712 |
language | eng |
recordid | cdi_proquest_miscellaneous_79504513 |
source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Animals Antioxidants - pharmacology Biological and medical sciences Drug toxicity and drugs side effects treatment Electrophysiology Evoked Potentials - drug effects Free radicals Hydrogen-Ion Concentration In Vitro Techniques Male Medical sciences Methylphenazonium Methosulfate - pharmacology Miscellaneous (drug allergy, mutagens, teratogens...) Neurons, Afferent - drug effects Pharmacology. Drug treatments Phenazine methosulfate Phenazines - pharmacology Physical Stimulation Piperazines - pharmacology Rana ridibunda Semicircular canal Semicircular Canals - drug effects Trimetazidine Trimetazidine - pharmacology Vestibular dysfunctions |
title | Effect of phenazine methosulfate on electrophysiological activity of the semicircular canal: antioxidant properties of trimetazidine |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T05%3A33%3A14IST&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=Effect%20of%20phenazine%20methosulfate%20on%20electrophysiological%20activity%20of%20the%20semicircular%20canal:%20antioxidant%20properties%20of%20trimetazidine&rft.jtitle=European%20journal%20of%20pharmacology&rft.au=Aubert,%20Anne&rft.date=1989-12-19&rft.volume=174&rft.issue=2&rft.spage=215&rft.epage=225&rft.pages=215-225&rft.issn=0014-2999&rft.eissn=1879-0712&rft.coden=EJPHAZ&rft_id=info:doi/10.1016/0014-2999(89)90314-2&rft_dat=%3Cproquest_cross%3E79504513%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=79504513&rft_id=info:pmid/2630299&rft_els_id=0014299989903142&rfr_iscdi=true |