Hypotaurine transport in brain slices: comparison with taurine and GABA
Hypotaurine uptake was compared to taurine and GABA uptakes in brain slices under identical experimental conditions. The slices effectively concentrated both hypotaurine and GABA from the medium, whereas taurine was taken up more slowly. The uptakes of these three structurally related amino acids we...
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Veröffentlicht in: | Neurochemical research 1981-11, Vol.6 (11), p.1179-1191 |
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description | Hypotaurine uptake was compared to taurine and GABA uptakes in brain slices under identical experimental conditions. The slices effectively concentrated both hypotaurine and GABA from the medium, whereas taurine was taken up more slowly. The uptakes of these three structurally related amino acids were all saturable, consisting of one low- and one high-affinity transport component. The kinetic parameters of hypotaurine uptake were of the same order of magnitude as those of GABA uptake. All uptake systems were sensitive to temperature, metabolic poisons, and sodium omission. Hypotaurine uptake was inhibited by GABA, L-2,4-diaminobutyric acid (L-DABA), cysteic acid, and beta-alanine, but not by taurine. Taurine uptake was strongly reduced by hypotaurine, beta-alanine, and L-DABA, as well as by GABA, whereas GABA uptake was affected only by cystamine, L-DABA, and nipecotic acid. The uptake processes of hypotaurine, taurine, and GABA were thus fairly similar and showed properties characteristic for neurotransmitter uptake. Hypotaurine uptake resembled more GABA than taurine uptake. The present inhibition studies suggest that there may exist only one common two-component transport system for these three amino acids. |
doi_str_mv | 10.1007/BF00966676 |
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The slices effectively concentrated both hypotaurine and GABA from the medium, whereas taurine was taken up more slowly. The uptakes of these three structurally related amino acids were all saturable, consisting of one low- and one high-affinity transport component. The kinetic parameters of hypotaurine uptake were of the same order of magnitude as those of GABA uptake. All uptake systems were sensitive to temperature, metabolic poisons, and sodium omission. Hypotaurine uptake was inhibited by GABA, L-2,4-diaminobutyric acid (L-DABA), cysteic acid, and beta-alanine, but not by taurine. Taurine uptake was strongly reduced by hypotaurine, beta-alanine, and L-DABA, as well as by GABA, whereas GABA uptake was affected only by cystamine, L-DABA, and nipecotic acid. The uptake processes of hypotaurine, taurine, and GABA were thus fairly similar and showed properties characteristic for neurotransmitter uptake. Hypotaurine uptake resembled more GABA than taurine uptake. The present inhibition studies suggest that there may exist only one common two-component transport system for these three amino acids.</description><identifier>ISSN: 0364-3190</identifier><identifier>EISSN: 1573-6903</identifier><identifier>DOI: 10.1007/BF00966676</identifier><identifier>PMID: 7343858</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Biological Transport, Active - drug effects ; Brain - metabolism ; gamma-Aminobutyric Acid - metabolism ; Kinetics ; Mice ; Sodium - metabolism ; Structure-Activity Relationship ; Taurine - analogs & derivatives ; Taurine - metabolism ; Temperature</subject><ispartof>Neurochemical research, 1981-11, Vol.6 (11), p.1179-1191</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c241t-91d70a6c1d11d9a03c7c032027c8a86f206befcfda9941908f6a40b37fce3f8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7343858$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kontro, P</creatorcontrib><creatorcontrib>Oja, S S</creatorcontrib><title>Hypotaurine transport in brain slices: comparison with taurine and GABA</title><title>Neurochemical research</title><addtitle>Neurochem Res</addtitle><description>Hypotaurine uptake was compared to taurine and GABA uptakes in brain slices under identical experimental conditions. The slices effectively concentrated both hypotaurine and GABA from the medium, whereas taurine was taken up more slowly. The uptakes of these three structurally related amino acids were all saturable, consisting of one low- and one high-affinity transport component. The kinetic parameters of hypotaurine uptake were of the same order of magnitude as those of GABA uptake. All uptake systems were sensitive to temperature, metabolic poisons, and sodium omission. Hypotaurine uptake was inhibited by GABA, L-2,4-diaminobutyric acid (L-DABA), cysteic acid, and beta-alanine, but not by taurine. Taurine uptake was strongly reduced by hypotaurine, beta-alanine, and L-DABA, as well as by GABA, whereas GABA uptake was affected only by cystamine, L-DABA, and nipecotic acid. The uptake processes of hypotaurine, taurine, and GABA were thus fairly similar and showed properties characteristic for neurotransmitter uptake. Hypotaurine uptake resembled more GABA than taurine uptake. The present inhibition studies suggest that there may exist only one common two-component transport system for these three amino acids.</description><subject>Animals</subject><subject>Biological Transport, Active - drug effects</subject><subject>Brain - metabolism</subject><subject>gamma-Aminobutyric Acid - metabolism</subject><subject>Kinetics</subject><subject>Mice</subject><subject>Sodium - metabolism</subject><subject>Structure-Activity Relationship</subject><subject>Taurine - analogs & derivatives</subject><subject>Taurine - metabolism</subject><subject>Temperature</subject><issn>0364-3190</issn><issn>1573-6903</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1Lw0AQhhdRaqxevAt7FqKz2XQ_vKXFpkLBi57DZD8w0nywmyL990Za9TJzed6XmYeQWwYPDEA-LtcAWgghxRlJ2ELyVGjg5yQBLvKUMw2X5CrGT4AJz9iMzCTPuVqohJSbw9CPuA9N5-gYsItDH0badLQOOM24a4yLT9T07YChiX1Hv5rxg_5GsLO0LJbFNbnwuIvu5rTn5H39_LbapNvX8mVVbFOT5WxMNbMSUBhmGbMagRtpgGeQSaNQCZ-BqJ033qLW-XS38gJzqLn0xnGvkM_J_bHXhD7G4Hw1hKbFcKgYVD8yqn8ZE3x3hId93Tr7h56-59-EvllZ</recordid><startdate>198111</startdate><enddate>198111</enddate><creator>Kontro, P</creator><creator>Oja, S S</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>198111</creationdate><title>Hypotaurine transport in brain slices: comparison with taurine and GABA</title><author>Kontro, P ; Oja, S S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c241t-91d70a6c1d11d9a03c7c032027c8a86f206befcfda9941908f6a40b37fce3f8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Animals</topic><topic>Biological Transport, Active - drug effects</topic><topic>Brain - metabolism</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>Kinetics</topic><topic>Mice</topic><topic>Sodium - metabolism</topic><topic>Structure-Activity Relationship</topic><topic>Taurine - analogs & derivatives</topic><topic>Taurine - metabolism</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kontro, P</creatorcontrib><creatorcontrib>Oja, S S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Neurochemical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kontro, P</au><au>Oja, S S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypotaurine transport in brain slices: comparison with taurine and GABA</atitle><jtitle>Neurochemical research</jtitle><addtitle>Neurochem Res</addtitle><date>1981-11</date><risdate>1981</risdate><volume>6</volume><issue>11</issue><spage>1179</spage><epage>1191</epage><pages>1179-1191</pages><issn>0364-3190</issn><eissn>1573-6903</eissn><abstract>Hypotaurine uptake was compared to taurine and GABA uptakes in brain slices under identical experimental conditions. The slices effectively concentrated both hypotaurine and GABA from the medium, whereas taurine was taken up more slowly. The uptakes of these three structurally related amino acids were all saturable, consisting of one low- and one high-affinity transport component. The kinetic parameters of hypotaurine uptake were of the same order of magnitude as those of GABA uptake. All uptake systems were sensitive to temperature, metabolic poisons, and sodium omission. Hypotaurine uptake was inhibited by GABA, L-2,4-diaminobutyric acid (L-DABA), cysteic acid, and beta-alanine, but not by taurine. Taurine uptake was strongly reduced by hypotaurine, beta-alanine, and L-DABA, as well as by GABA, whereas GABA uptake was affected only by cystamine, L-DABA, and nipecotic acid. The uptake processes of hypotaurine, taurine, and GABA were thus fairly similar and showed properties characteristic for neurotransmitter uptake. Hypotaurine uptake resembled more GABA than taurine uptake. The present inhibition studies suggest that there may exist only one common two-component transport system for these three amino acids.</abstract><cop>United States</cop><pmid>7343858</pmid><doi>10.1007/BF00966676</doi><tpages>13</tpages></addata></record> |
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subjects | Animals Biological Transport, Active - drug effects Brain - metabolism gamma-Aminobutyric Acid - metabolism Kinetics Mice Sodium - metabolism Structure-Activity Relationship Taurine - analogs & derivatives Taurine - metabolism Temperature |
title | Hypotaurine transport in brain slices: comparison with taurine and GABA |
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