Enhancement of Dopamine Release In Vivo from the Rat Striatum by Dialytic Perfusion of 6R‐l‐erythro‐5,6,7,8‐Tetrahydrobiopterin

: We have previously reported that intracerebroventricular administration of 6R‐L‐erythro‐5,6,7,8‐tetrahydrobiopterin (6R‐BH4), a cofactor for tyrosine hydroxylase, enhances biosynthesis of 3,4‐dihydroxyphenylethylamine (dopamine) in the rat brain. In the present study, we have more precisely examin...

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Veröffentlicht in:Journal of neurochemistry 1990-04, Vol.54 (4), p.1391-1397
Hauptverfasser: Koshimura, Kunio, Miwa, Soichi, Lee, Ken, Fujiwara, Motohatsu, Watanabe, Yasuyoshi
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creator Koshimura, Kunio
Miwa, Soichi
Lee, Ken
Fujiwara, Motohatsu
Watanabe, Yasuyoshi
description : We have previously reported that intracerebroventricular administration of 6R‐L‐erythro‐5,6,7,8‐tetrahydrobiopterin (6R‐BH4), a cofactor for tyrosine hydroxylase, enhances biosynthesis of 3,4‐dihydroxyphenylethylamine (dopamine) in the rat brain. In the present study, we have more precisely examined the effects of 6R‐BH4 on dopamine release in vivo from the rat striatum using brain microdialysis. The amount of dopamine collected in striatal dialysates was determined using HPLC with electrochemical detection after purification with an alumina batch method. When the striatum was dialyzed with Ringer solution containing various concentrations of 6R‐BH4 (0.25,0.5, and 1.0 mM), dopamine levels in striatal dialysates increased in a concentration‐dependent manner. Biopterin had little effect on dopamine levels in dialysates. The 6R‐BH4‐induced increase in dopamine levels in dialysates was abolished after pretreatment with tetrodotoxin (50 μM) added to the perfusion fluid, but after pretreatment with nomifensine (100 mg/kg, intraperitoneal injection), an inhibitor of dopamine uptake mechanism, a larger increase was observed. After inhibition of tyrosine hydroxylase by pretreatment with α‐methyl‐p‐tyrosine (250 mg/kg, intraperitoneal injection), most of the increase persisted. These results suggest that 6R‐BH4 has a dopamine‐releasing action, which is not dependent on biosynthesis of dopamine.
doi_str_mv 10.1111/j.1471-4159.1990.tb01974.x
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In the present study, we have more precisely examined the effects of 6R‐BH4 on dopamine release in vivo from the rat striatum using brain microdialysis. The amount of dopamine collected in striatal dialysates was determined using HPLC with electrochemical detection after purification with an alumina batch method. When the striatum was dialyzed with Ringer solution containing various concentrations of 6R‐BH4 (0.25,0.5, and 1.0 mM), dopamine levels in striatal dialysates increased in a concentration‐dependent manner. Biopterin had little effect on dopamine levels in dialysates. The 6R‐BH4‐induced increase in dopamine levels in dialysates was abolished after pretreatment with tetrodotoxin (50 μM) added to the perfusion fluid, but after pretreatment with nomifensine (100 mg/kg, intraperitoneal injection), an inhibitor of dopamine uptake mechanism, a larger increase was observed. 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Pathways and receptors ; Chromatography ; Corpus Striatum - metabolism ; Dialysis - methods ; Dopamine ; Dopamine - biosynthesis ; Dopamine - metabolism ; Fundamental and applied biological sciences. Psychology ; Male ; Methyltyrosines - pharmacology ; Nomifensine - pharmacology ; Osmolar Concentration ; Perfusion ; Rats ; Rats, Inbred Strains ; Reference Standards ; Release ; Striatum ; Tetrahydrobiopterin ; Tetrodotoxin - pharmacology ; Tyrosine 3-Monooxygenase - antagonists &amp; inhibitors ; Vertebrates: nervous system and sense organs</subject><ispartof>Journal of neurochemistry, 1990-04, Vol.54 (4), p.1391-1397</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1471-4159.1990.tb01974.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1471-4159.1990.tb01974.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=6886952$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1968962$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koshimura, Kunio</creatorcontrib><creatorcontrib>Miwa, Soichi</creatorcontrib><creatorcontrib>Lee, Ken</creatorcontrib><creatorcontrib>Fujiwara, Motohatsu</creatorcontrib><creatorcontrib>Watanabe, Yasuyoshi</creatorcontrib><title>Enhancement of Dopamine Release In Vivo from the Rat Striatum by Dialytic Perfusion of 6R‐l‐erythro‐5,6,7,8‐Tetrahydrobiopterin</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>: We have previously reported that intracerebroventricular administration of 6R‐L‐erythro‐5,6,7,8‐tetrahydrobiopterin (6R‐BH4), a cofactor for tyrosine hydroxylase, enhances biosynthesis of 3,4‐dihydroxyphenylethylamine (dopamine) in the rat brain. In the present study, we have more precisely examined the effects of 6R‐BH4 on dopamine release in vivo from the rat striatum using brain microdialysis. The amount of dopamine collected in striatal dialysates was determined using HPLC with electrochemical detection after purification with an alumina batch method. When the striatum was dialyzed with Ringer solution containing various concentrations of 6R‐BH4 (0.25,0.5, and 1.0 mM), dopamine levels in striatal dialysates increased in a concentration‐dependent manner. Biopterin had little effect on dopamine levels in dialysates. The 6R‐BH4‐induced increase in dopamine levels in dialysates was abolished after pretreatment with tetrodotoxin (50 μM) added to the perfusion fluid, but after pretreatment with nomifensine (100 mg/kg, intraperitoneal injection), an inhibitor of dopamine uptake mechanism, a larger increase was observed. After inhibition of tyrosine hydroxylase by pretreatment with α‐methyl‐p‐tyrosine (250 mg/kg, intraperitoneal injection), most of the increase persisted. These results suggest that 6R‐BH4 has a dopamine‐releasing action, which is not dependent on biosynthesis of dopamine.</description><subject>alpha-Methyltyrosine</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biopterins - analogs &amp; derivatives</subject><subject>Biopterins - pharmacology</subject><subject>Brain microdialysis</subject><subject>Central nervous system</subject><subject>Central neurotransmission. Neuromudulation. Pathways and receptors</subject><subject>Chromatography</subject><subject>Corpus Striatum - metabolism</subject><subject>Dialysis - methods</subject><subject>Dopamine</subject><subject>Dopamine - biosynthesis</subject><subject>Dopamine - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Male</subject><subject>Methyltyrosines - pharmacology</subject><subject>Nomifensine - pharmacology</subject><subject>Osmolar Concentration</subject><subject>Perfusion</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Reference Standards</subject><subject>Release</subject><subject>Striatum</subject><subject>Tetrahydrobiopterin</subject><subject>Tetrodotoxin - pharmacology</subject><subject>Tyrosine 3-Monooxygenase - antagonists &amp; inhibitors</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc1u1DAURi0EKkPhEZAshFhNgn8SJ14hNC1QVAEqha11J3Oj8SiJp7YDzY4dW56RJ8FRo2LL8pW-o29xDyEvOMt5Oq8POS8qnhW81DnXmuVxy7iuivz2AVndRw_JijEhMskK8Zg8CeHAGFeF4ifkhGtVayVW5Pf5sIehwR6HSF1Lz9wRejsgvcIOISC9GOh3-8PR1ruexn0KINKv0VuIY0-3Ez2z0E3RNvQL-nYM1g1zj7r6--tPlx76Ke69S1O5VutqXafpGqOH_bTzbmvdMaK3w1PyqIUu4LPlPyXf3p1fbz5kl5_fX2zeXmYHySTPAACZrnlRc2ihBLFTqmZKqUpiKQq9a5CVslBtugyl1lpIUaDiQkLDy1qekld3vUfvbkYM0fQ2NNh1MKAbg-FlWelSsAQ-X8Bx2-POHL3twU9m2VzKXy45hAa61qct2nCPqbpWqSdhb-6wn7bD6X8LM7NJczCzLjPrMrNJs5g0t-bjpw2Xmst_zcmVqw</recordid><startdate>199004</startdate><enddate>199004</enddate><creator>Koshimura, Kunio</creator><creator>Miwa, Soichi</creator><creator>Lee, Ken</creator><creator>Fujiwara, Motohatsu</creator><creator>Watanabe, Yasuyoshi</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope></search><sort><creationdate>199004</creationdate><title>Enhancement of Dopamine Release In Vivo from the Rat Striatum by Dialytic Perfusion of 6R‐l‐erythro‐5,6,7,8‐Tetrahydrobiopterin</title><author>Koshimura, Kunio ; Miwa, Soichi ; Lee, Ken ; Fujiwara, Motohatsu ; Watanabe, Yasuyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j3031-aaae0981481afa5a2d668066673e5249dce05346f6f60e39992324e6123ac1583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>alpha-Methyltyrosine</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biopterins - analogs &amp; derivatives</topic><topic>Biopterins - pharmacology</topic><topic>Brain microdialysis</topic><topic>Central nervous system</topic><topic>Central neurotransmission. Neuromudulation. Pathways and receptors</topic><topic>Chromatography</topic><topic>Corpus Striatum - metabolism</topic><topic>Dialysis - methods</topic><topic>Dopamine</topic><topic>Dopamine - biosynthesis</topic><topic>Dopamine - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Methyltyrosines - pharmacology</topic><topic>Nomifensine - pharmacology</topic><topic>Osmolar Concentration</topic><topic>Perfusion</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Reference Standards</topic><topic>Release</topic><topic>Striatum</topic><topic>Tetrahydrobiopterin</topic><topic>Tetrodotoxin - pharmacology</topic><topic>Tyrosine 3-Monooxygenase - antagonists &amp; inhibitors</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koshimura, Kunio</creatorcontrib><creatorcontrib>Miwa, Soichi</creatorcontrib><creatorcontrib>Lee, Ken</creatorcontrib><creatorcontrib>Fujiwara, Motohatsu</creatorcontrib><creatorcontrib>Watanabe, Yasuyoshi</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>Neurosciences Abstracts</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koshimura, Kunio</au><au>Miwa, Soichi</au><au>Lee, Ken</au><au>Fujiwara, Motohatsu</au><au>Watanabe, Yasuyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhancement of Dopamine Release In Vivo from the Rat Striatum by Dialytic Perfusion of 6R‐l‐erythro‐5,6,7,8‐Tetrahydrobiopterin</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1990-04</date><risdate>1990</risdate><volume>54</volume><issue>4</issue><spage>1391</spage><epage>1397</epage><pages>1391-1397</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: We have previously reported that intracerebroventricular administration of 6R‐L‐erythro‐5,6,7,8‐tetrahydrobiopterin (6R‐BH4), a cofactor for tyrosine hydroxylase, enhances biosynthesis of 3,4‐dihydroxyphenylethylamine (dopamine) in the rat brain. In the present study, we have more precisely examined the effects of 6R‐BH4 on dopamine release in vivo from the rat striatum using brain microdialysis. The amount of dopamine collected in striatal dialysates was determined using HPLC with electrochemical detection after purification with an alumina batch method. When the striatum was dialyzed with Ringer solution containing various concentrations of 6R‐BH4 (0.25,0.5, and 1.0 mM), dopamine levels in striatal dialysates increased in a concentration‐dependent manner. Biopterin had little effect on dopamine levels in dialysates. The 6R‐BH4‐induced increase in dopamine levels in dialysates was abolished after pretreatment with tetrodotoxin (50 μM) added to the perfusion fluid, but after pretreatment with nomifensine (100 mg/kg, intraperitoneal injection), an inhibitor of dopamine uptake mechanism, a larger increase was observed. After inhibition of tyrosine hydroxylase by pretreatment with α‐methyl‐p‐tyrosine (250 mg/kg, intraperitoneal injection), most of the increase persisted. These results suggest that 6R‐BH4 has a dopamine‐releasing action, which is not dependent on biosynthesis of dopamine.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1968962</pmid><doi>10.1111/j.1471-4159.1990.tb01974.x</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects alpha-Methyltyrosine
Animals
Biological and medical sciences
Biopterins - analogs & derivatives
Biopterins - pharmacology
Brain microdialysis
Central nervous system
Central neurotransmission. Neuromudulation. Pathways and receptors
Chromatography
Corpus Striatum - metabolism
Dialysis - methods
Dopamine
Dopamine - biosynthesis
Dopamine - metabolism
Fundamental and applied biological sciences. Psychology
Male
Methyltyrosines - pharmacology
Nomifensine - pharmacology
Osmolar Concentration
Perfusion
Rats
Rats, Inbred Strains
Reference Standards
Release
Striatum
Tetrahydrobiopterin
Tetrodotoxin - pharmacology
Tyrosine 3-Monooxygenase - antagonists & inhibitors
Vertebrates: nervous system and sense organs
title Enhancement of Dopamine Release In Vivo from the Rat Striatum by Dialytic Perfusion of 6R‐l‐erythro‐5,6,7,8‐Tetrahydrobiopterin
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