Glutamine transport in rat brain synaptic and non-synaptic mitochondria
Glutamine transport into rat brain mitochondria (synaptic and non-synaptic) was monitored by the uptake of [3H]glutamine as well as by mitochondrial swelling. The uptake is inversely correlated to medium osmolarity, temperature-dependent, saturable and inhibited by mersalyl, and glutamine is upconce...
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description | Glutamine transport into rat brain mitochondria (synaptic and non-synaptic) was monitored by the uptake of [3H]glutamine as well as by mitochondrial swelling. The uptake is inversely correlated to medium osmolarity, temperature-dependent, saturable and inhibited by mersalyl, and glutamine is upconcentrated in the mitochondria. These results indicate that glutamine is transported into an osmotically active space by a protein catalyzed mechanism. The uptake is slightly higher in synaptic mitochondria than in non-synaptic ones. It is inhibited both by rotenone and the protonophore carbonyl cyanide p-trifluoromethoxyphenylhydrazone, the latter at pH 6.5, showing that the transport is activated by an electrochemical proton gradient. The K+/H+ ionophore nigericin also inhibits the uptake at pH 6.5 in the presence of external K+, which indicates that glutamine, at least in part, is taken up by a proton symport transporter. In addition, glutamine uptake as measured by the swelling technique revealed an additional glutamine transport activity with at least 10 times higher Km value. This uptake is inhibited by valinomycin in the presence of K+ and is thus also activated by the membrane potential. Otherwise, the two methods show similar results. These data indicate that glutamine transport in brain mitochondria cannot be described by merely a simple electroneutral uniport mechanism, but are consistent with the uptake of both the anionic and the zwitterionic glutamine. |
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A ; KVAMME, E</creator><creatorcontrib>ROBERG, B ; TORGNER, I. A ; KVAMME, E</creatorcontrib><description>Glutamine transport into rat brain mitochondria (synaptic and non-synaptic) was monitored by the uptake of [3H]glutamine as well as by mitochondrial swelling. The uptake is inversely correlated to medium osmolarity, temperature-dependent, saturable and inhibited by mersalyl, and glutamine is upconcentrated in the mitochondria. These results indicate that glutamine is transported into an osmotically active space by a protein catalyzed mechanism. The uptake is slightly higher in synaptic mitochondria than in non-synaptic ones. It is inhibited both by rotenone and the protonophore carbonyl cyanide p-trifluoromethoxyphenylhydrazone, the latter at pH 6.5, showing that the transport is activated by an electrochemical proton gradient. The K+/H+ ionophore nigericin also inhibits the uptake at pH 6.5 in the presence of external K+, which indicates that glutamine, at least in part, is taken up by a proton symport transporter. In addition, glutamine uptake as measured by the swelling technique revealed an additional glutamine transport activity with at least 10 times higher Km value. This uptake is inhibited by valinomycin in the presence of K+ and is thus also activated by the membrane potential. Otherwise, the two methods show similar results. These data indicate that glutamine transport in brain mitochondria cannot be described by merely a simple electroneutral uniport mechanism, but are consistent with the uptake of both the anionic and the zwitterionic glutamine.</description><identifier>ISSN: 0364-3190</identifier><identifier>EISSN: 1573-6903</identifier><identifier>DOI: 10.1023/A:1020985600422</identifier><identifier>PMID: 10215512</identifier><identifier>CODEN: NEREDZ</identifier><language>eng</language><publisher>New York, NY: Springer</publisher><subject>Animals ; Biological and medical sciences ; Biological Transport - drug effects ; Brain - metabolism ; Brain - ultrastructure ; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology ; Cell physiology ; Ethylmaleimide - pharmacology ; Fundamental and applied biological sciences. Psychology ; Glutamine - metabolism ; Hydrogen-Ion Concentration ; Kinetics ; Membrane and intracellular transports ; Mersalyl - pharmacology ; Mitochondria - metabolism ; Mitochondrial Swelling ; Molecular and cellular biology ; Rats ; Rotenone - pharmacology ; Sulfhydryl Reagents - pharmacology ; Synapses - metabolism ; Synapses - ultrastructure ; Tritium ; Uncoupling Agents - pharmacology</subject><ispartof>Neurochemical research, 1999-03, Vol.24 (3), p.383-390</ispartof><rights>1999 INIST-CNRS</rights><rights>Copyright Kluwer Academic Publishers Mar 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-39536f3ddd818a8d5cf62f53e0ff26c16d8ff63070546d821e4405ca97237b6f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1661385$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10215512$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ROBERG, B</creatorcontrib><creatorcontrib>TORGNER, I. A</creatorcontrib><creatorcontrib>KVAMME, E</creatorcontrib><title>Glutamine transport in rat brain synaptic and non-synaptic mitochondria</title><title>Neurochemical research</title><addtitle>Neurochem Res</addtitle><description>Glutamine transport into rat brain mitochondria (synaptic and non-synaptic) was monitored by the uptake of [3H]glutamine as well as by mitochondrial swelling. The uptake is inversely correlated to medium osmolarity, temperature-dependent, saturable and inhibited by mersalyl, and glutamine is upconcentrated in the mitochondria. These results indicate that glutamine is transported into an osmotically active space by a protein catalyzed mechanism. The uptake is slightly higher in synaptic mitochondria than in non-synaptic ones. It is inhibited both by rotenone and the protonophore carbonyl cyanide p-trifluoromethoxyphenylhydrazone, the latter at pH 6.5, showing that the transport is activated by an electrochemical proton gradient. The K+/H+ ionophore nigericin also inhibits the uptake at pH 6.5 in the presence of external K+, which indicates that glutamine, at least in part, is taken up by a proton symport transporter. In addition, glutamine uptake as measured by the swelling technique revealed an additional glutamine transport activity with at least 10 times higher Km value. This uptake is inhibited by valinomycin in the presence of K+ and is thus also activated by the membrane potential. Otherwise, the two methods show similar results. These data indicate that glutamine transport in brain mitochondria cannot be described by merely a simple electroneutral uniport mechanism, but are consistent with the uptake of both the anionic and the zwitterionic glutamine.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biological Transport - drug effects</subject><subject>Brain - metabolism</subject><subject>Brain - ultrastructure</subject><subject>Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology</subject><subject>Cell physiology</subject><subject>Ethylmaleimide - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glutamine - metabolism</subject><subject>Hydrogen-Ion Concentration</subject><subject>Kinetics</subject><subject>Membrane and intracellular transports</subject><subject>Mersalyl - pharmacology</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondrial Swelling</subject><subject>Molecular and cellular biology</subject><subject>Rats</subject><subject>Rotenone - pharmacology</subject><subject>Sulfhydryl Reagents - pharmacology</subject><subject>Synapses - metabolism</subject><subject>Synapses - ultrastructure</subject><subject>Tritium</subject><subject>Uncoupling Agents - pharmacology</subject><issn>0364-3190</issn><issn>1573-6903</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqF0E1LxDAQBuAgiruunr1JEfFWnSTNR70ti67Cghc9l2zSYJY2rUl68N8bcFXw4mmG4ZmBeRE6x3CDgdDb5V0uUEvGASpCDtAcM0FLXgM9RHOgvCoprmGGTmLcAWAAgo_RLC9hxjCZo_W6m5LqnW-LFJSP4xBS4XwRVCq2QeUufng1JqcL5U3hB1_-DHqXBv02eBOcOkVHVnWxPdvXBXp9uH9ZPZab5_XTarkpNa0glbRmlFtqjJFYKmmYtpxYRluwlnCNuZHWcgoCWJV7gtuqAqZVLQgV27y5QNdfd8cwvE9tTE3vom67Tvl2mGLDayawxOJfiAUBQSTN8PIP3A1T8PmJhhAsgRHCM7rYo2nbt6YZg-tV-Gi-g8zgag9U1KqzOUvt4q_jHFPJ6CedA4AD</recordid><startdate>19990301</startdate><enddate>19990301</enddate><creator>ROBERG, B</creator><creator>TORGNER, I. 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A ; KVAMME, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-39536f3ddd818a8d5cf62f53e0ff26c16d8ff63070546d821e4405ca97237b6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biological Transport - drug effects</topic><topic>Brain - metabolism</topic><topic>Brain - ultrastructure</topic><topic>Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology</topic><topic>Cell physiology</topic><topic>Ethylmaleimide - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glutamine - metabolism</topic><topic>Hydrogen-Ion Concentration</topic><topic>Kinetics</topic><topic>Membrane and intracellular transports</topic><topic>Mersalyl - pharmacology</topic><topic>Mitochondria - metabolism</topic><topic>Mitochondrial Swelling</topic><topic>Molecular and cellular biology</topic><topic>Rats</topic><topic>Rotenone - pharmacology</topic><topic>Sulfhydryl Reagents - pharmacology</topic><topic>Synapses - metabolism</topic><topic>Synapses - ultrastructure</topic><topic>Tritium</topic><topic>Uncoupling Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ROBERG, B</creatorcontrib><creatorcontrib>TORGNER, I. 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A</au><au>KVAMME, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glutamine transport in rat brain synaptic and non-synaptic mitochondria</atitle><jtitle>Neurochemical research</jtitle><addtitle>Neurochem Res</addtitle><date>1999-03-01</date><risdate>1999</risdate><volume>24</volume><issue>3</issue><spage>383</spage><epage>390</epage><pages>383-390</pages><issn>0364-3190</issn><eissn>1573-6903</eissn><coden>NEREDZ</coden><abstract>Glutamine transport into rat brain mitochondria (synaptic and non-synaptic) was monitored by the uptake of [3H]glutamine as well as by mitochondrial swelling. The uptake is inversely correlated to medium osmolarity, temperature-dependent, saturable and inhibited by mersalyl, and glutamine is upconcentrated in the mitochondria. These results indicate that glutamine is transported into an osmotically active space by a protein catalyzed mechanism. The uptake is slightly higher in synaptic mitochondria than in non-synaptic ones. It is inhibited both by rotenone and the protonophore carbonyl cyanide p-trifluoromethoxyphenylhydrazone, the latter at pH 6.5, showing that the transport is activated by an electrochemical proton gradient. The K+/H+ ionophore nigericin also inhibits the uptake at pH 6.5 in the presence of external K+, which indicates that glutamine, at least in part, is taken up by a proton symport transporter. In addition, glutamine uptake as measured by the swelling technique revealed an additional glutamine transport activity with at least 10 times higher Km value. This uptake is inhibited by valinomycin in the presence of K+ and is thus also activated by the membrane potential. Otherwise, the two methods show similar results. These data indicate that glutamine transport in brain mitochondria cannot be described by merely a simple electroneutral uniport mechanism, but are consistent with the uptake of both the anionic and the zwitterionic glutamine.</abstract><cop>New York, NY</cop><pub>Springer</pub><pmid>10215512</pmid><doi>10.1023/A:1020985600422</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Biological Transport - drug effects Brain - metabolism Brain - ultrastructure Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology Cell physiology Ethylmaleimide - pharmacology Fundamental and applied biological sciences. Psychology Glutamine - metabolism Hydrogen-Ion Concentration Kinetics Membrane and intracellular transports Mersalyl - pharmacology Mitochondria - metabolism Mitochondrial Swelling Molecular and cellular biology Rats Rotenone - pharmacology Sulfhydryl Reagents - pharmacology Synapses - metabolism Synapses - ultrastructure Tritium Uncoupling Agents - pharmacology |
title | Glutamine transport in rat brain synaptic and non-synaptic mitochondria |
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