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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Veröffentlicht in:Neurochemical research 1999-03, Vol.24 (3), p.383-390
Hauptverfasser: ROBERG, B, TORGNER, I. A, KVAMME, E
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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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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. 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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. 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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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