Effects of α-Asarone on the Neuronal Glutamate Transporter EAAC1

R2; Objective: α-asarone is a major effective component that can be isolated from Acorus tatarinowii Schott,a Chinese herbal medicine. Clinical investigations have shown that α-asarone has strong sedative and anti-convulsive action in the central nervous system. In recent years, several medicines co...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:针灸推拿医学(英文版) 2008, Vol.6 (6), p.372
Hauptverfasser: 顾全保, 杜慧明, Heike FOTIS, 马春辉, 黄成钢, Wolfgang SCHWARZ
Format: Artikel
Sprache:chi
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 6
container_start_page 372
container_title 针灸推拿医学(英文版)
container_volume 6
creator 顾全保
杜慧明
Heike FOTIS
马春辉
黄成钢
Wolfgang SCHWARZ
description R2; Objective: α-asarone is a major effective component that can be isolated from Acorus tatarinowii Schott,a Chinese herbal medicine. Clinical investigations have shown that α-asarone has strong sedative and anti-convulsive action in the central nervous system. In recent years, several medicines containing a-asarone were applied in treatment of asthma, bronchitis, expectorant, or epilepsy. However, the underlying cellular mechanism of ct-asarone is still unknown. Here the authors considered EAAC1, the transporter for the excitatory glutamate, as a possible target. Methods: Supercritical CO2 fluid extraction and silica gel column chromatography were used to obtain ct-asarone from the rhizomes of Acorus tatarinowii Schott. Xenopus oocytes with heterologously expressed EAAC 1 were used as a model system. Rate of glutamate uptake was measured by means of isotopic tracer technique. Glutamate-induced current was recorded under two-electrode voltage clamp. 40μg/mL of ct-asarone was used for testing its effect on EA
format Article
fullrecord <record><control><sourceid>wanfang_jour</sourceid><recordid>TN_cdi_wanfang_journals_zjtnyx_e200806005</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><wanfj_id>zjtnyx_e200806005</wanfj_id><sourcerecordid>zjtnyx_e200806005</sourcerecordid><originalsourceid>FETCH-wanfang_journals_zjtnyx_e2008060053</originalsourceid><addsrcrecordid>eNqVjDsKwkAUALdQMGju8FqLwEtks6YMIWpllT485a0a4q7sbvBzKy_imUzhBayGgWEmIkpzlSUrWaiZiL2_HBBzhVKqIhJlrTUfgwer4fNOSk_OGgZrIJwZ9jyMSj1s-yHQlQJD48j4m3WBHdRlWaULMdXUe45_nIvlpm6qXXIno8mc2s4Obnz49tUF83y0nCGuMUeUq3_aL5csPoo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Effects of α-Asarone on the Neuronal Glutamate Transporter EAAC1</title><source>ProQuest Central Essentials</source><source>Springer Journals</source><source>ProQuest Central (Alumni)</source><source>Alma/SFX Local Collection</source><source>ProQuest Central</source><creator>顾全保 ; 杜慧明 ; Heike FOTIS ; 马春辉 ; 黄成钢 ; Wolfgang SCHWARZ</creator><creatorcontrib>顾全保 ; 杜慧明 ; Heike FOTIS ; 马春辉 ; 黄成钢 ; Wolfgang SCHWARZ</creatorcontrib><description>R2; Objective: α-asarone is a major effective component that can be isolated from Acorus tatarinowii Schott,a Chinese herbal medicine. Clinical investigations have shown that α-asarone has strong sedative and anti-convulsive action in the central nervous system. In recent years, several medicines containing a-asarone were applied in treatment of asthma, bronchitis, expectorant, or epilepsy. However, the underlying cellular mechanism of ct-asarone is still unknown. Here the authors considered EAAC1, the transporter for the excitatory glutamate, as a possible target. Methods: Supercritical CO2 fluid extraction and silica gel column chromatography were used to obtain ct-asarone from the rhizomes of Acorus tatarinowii Schott. Xenopus oocytes with heterologously expressed EAAC 1 were used as a model system. Rate of glutamate uptake was measured by means of isotopic tracer technique. Glutamate-induced current was recorded under two-electrode voltage clamp. 40μg/mL of ct-asarone was used for testing its effect on EA</description><identifier>ISSN: 1672-3597</identifier><language>chi</language><ispartof>针灸推拿医学(英文版), 2008, Vol.6 (6), p.372</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/zjtnyx-e/zjtnyx-e.jpg</thumbnail><link.rule.ids>314,780,784,4014</link.rule.ids></links><search><creatorcontrib>顾全保</creatorcontrib><creatorcontrib>杜慧明</creatorcontrib><creatorcontrib>Heike FOTIS</creatorcontrib><creatorcontrib>马春辉</creatorcontrib><creatorcontrib>黄成钢</creatorcontrib><creatorcontrib>Wolfgang SCHWARZ</creatorcontrib><title>Effects of α-Asarone on the Neuronal Glutamate Transporter EAAC1</title><title>针灸推拿医学(英文版)</title><description>R2; Objective: α-asarone is a major effective component that can be isolated from Acorus tatarinowii Schott,a Chinese herbal medicine. Clinical investigations have shown that α-asarone has strong sedative and anti-convulsive action in the central nervous system. In recent years, several medicines containing a-asarone were applied in treatment of asthma, bronchitis, expectorant, or epilepsy. However, the underlying cellular mechanism of ct-asarone is still unknown. Here the authors considered EAAC1, the transporter for the excitatory glutamate, as a possible target. Methods: Supercritical CO2 fluid extraction and silica gel column chromatography were used to obtain ct-asarone from the rhizomes of Acorus tatarinowii Schott. Xenopus oocytes with heterologously expressed EAAC 1 were used as a model system. Rate of glutamate uptake was measured by means of isotopic tracer technique. Glutamate-induced current was recorded under two-electrode voltage clamp. 40μg/mL of ct-asarone was used for testing its effect on EA</description><issn>1672-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqVjDsKwkAUALdQMGju8FqLwEtks6YMIWpllT485a0a4q7sbvBzKy_imUzhBayGgWEmIkpzlSUrWaiZiL2_HBBzhVKqIhJlrTUfgwer4fNOSk_OGgZrIJwZ9jyMSj1s-yHQlQJD48j4m3WBHdRlWaULMdXUe45_nIvlpm6qXXIno8mc2s4Obnz49tUF83y0nCGuMUeUq3_aL5csPoo</recordid><startdate>2008</startdate><enddate>2008</enddate><creator>顾全保</creator><creator>杜慧明</creator><creator>Heike FOTIS</creator><creator>马春辉</creator><creator>黄成钢</creator><creator>Wolfgang SCHWARZ</creator><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>2008</creationdate><title>Effects of α-Asarone on the Neuronal Glutamate Transporter EAAC1</title><author>顾全保 ; 杜慧明 ; Heike FOTIS ; 马春辉 ; 黄成钢 ; Wolfgang SCHWARZ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-wanfang_journals_zjtnyx_e2008060053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>chi</language><creationdate>2008</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>顾全保</creatorcontrib><creatorcontrib>杜慧明</creatorcontrib><creatorcontrib>Heike FOTIS</creatorcontrib><creatorcontrib>马春辉</creatorcontrib><creatorcontrib>黄成钢</creatorcontrib><creatorcontrib>Wolfgang SCHWARZ</creatorcontrib><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>针灸推拿医学(英文版)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>顾全保</au><au>杜慧明</au><au>Heike FOTIS</au><au>马春辉</au><au>黄成钢</au><au>Wolfgang SCHWARZ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of α-Asarone on the Neuronal Glutamate Transporter EAAC1</atitle><jtitle>针灸推拿医学(英文版)</jtitle><date>2008</date><risdate>2008</risdate><volume>6</volume><issue>6</issue><spage>372</spage><pages>372-</pages><issn>1672-3597</issn><abstract>R2; Objective: α-asarone is a major effective component that can be isolated from Acorus tatarinowii Schott,a Chinese herbal medicine. Clinical investigations have shown that α-asarone has strong sedative and anti-convulsive action in the central nervous system. In recent years, several medicines containing a-asarone were applied in treatment of asthma, bronchitis, expectorant, or epilepsy. However, the underlying cellular mechanism of ct-asarone is still unknown. Here the authors considered EAAC1, the transporter for the excitatory glutamate, as a possible target. Methods: Supercritical CO2 fluid extraction and silica gel column chromatography were used to obtain ct-asarone from the rhizomes of Acorus tatarinowii Schott. Xenopus oocytes with heterologously expressed EAAC 1 were used as a model system. Rate of glutamate uptake was measured by means of isotopic tracer technique. Glutamate-induced current was recorded under two-electrode voltage clamp. 40μg/mL of ct-asarone was used for testing its effect on EA</abstract></addata></record>
fulltext fulltext
identifier ISSN: 1672-3597
ispartof 针灸推拿医学(英文版), 2008, Vol.6 (6), p.372
issn 1672-3597
language chi
recordid cdi_wanfang_journals_zjtnyx_e200806005
source ProQuest Central Essentials; Springer Journals; ProQuest Central (Alumni); Alma/SFX Local Collection; ProQuest Central
title Effects of α-Asarone on the Neuronal Glutamate Transporter EAAC1
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T20%3A28%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wanfang_jour&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20%CE%B1-Asarone%20on%20the%20Neuronal%20Glutamate%20Transporter%20EAAC1&rft.jtitle=%E9%92%88%E7%81%B8%E6%8E%A8%E6%8B%BF%E5%8C%BB%E5%AD%A6(%E8%8B%B1%E6%96%87%E7%89%88)&rft.au=%E9%A1%BE%E5%85%A8%E4%BF%9D&rft.date=2008&rft.volume=6&rft.issue=6&rft.spage=372&rft.pages=372-&rft.issn=1672-3597&rft_id=info:doi/&rft_dat=%3Cwanfang_jour%3Ezjtnyx_e200806005%3C/wanfang_jour%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_wanfj_id=zjtnyx_e200806005&rfr_iscdi=true