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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004324naa a2200565 4500
001oai:DiVA.org:uu-50723
003SwePub
008081017s1996 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:1945810
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-507232 URI
024a https://doi.org/10.1046/j.1471-4159.1996.66041726.x2 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:19458102 URI
040 a (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Herrera-Marschitz, M4 aut
2451 0a On the origin of extracellular glutamate levels monitored in the basal ganglia of the rat by in vivo microdialysis
264 c 2002-11-23
264 1b Wiley,c 1996
338 a print2 rdacarrier
520 a Several putative neurotransmitters and metabolites were monitored simultaneously in the extracellular space of neostriatum, substantia nigra, and cortex and in subcutaneous tissue of the rat by in vivo microdialysis. Glutamate (Glu) and aspartate (Asp) were at submicromolar and gamma-aminobutyric acid (GABA) was at nanomolar concentrations in all brain regions. The highest concentration of dopamine (DA) was in the neostriatum. Dynorphin B (Dyn B) was in the picomolar range in all brain regions. Although no GABA, DA, or Dyn B could be detected in subcutaneous tissue, Glu and Asp levels were 5 and approximately 5 and approximately 0.4 microM, respectively. Lactate and pyruvate concentrations were approximately 200 and approximately 10 microM in all regions. The following criteria were applied to ascertain the neuronal origin of substances quantified by microdialysis: sensitivity to (a) K+ depolarization, (b) Na+ channel blockade, (c) removal of extracellular Ca2+, and (d) depletion of presynaptic vesicles by local administration of alpha-latrotoxin. DA, Dyn B, and GABA largely satisfied all these criteria. In contrast, Glu and Asp levels were not greatly affected by K+ depolarization and were increased by perfusing with tetrodotoxin or with Ca2+-free medium, arguing against a neuronal origin. However, Glu and Asp, as well as DA and GABA, levels were decreased under both basal and K+-depolarizing conditions by alpha-latrotoxin. Because the effect of K+ depolarization on Glu and Asp could be masked by reuptake into nerve terminals and glial cells, the reuptake blocker dihydrokainic acid (DHKA) or L-trans-pyrrolidine-2,4-dicarboxylic acid (PDC) was included in the microdialysis perfusion medium. The effect of K+ depolarization on Glu and Asp levels was increased by DHKA, but GABA levels were also affected. In contrast, PDC increased only Glu levels. It is concluded that there is pool of releasable Glu and Asp in the rat brain. However, extracellular levels of amino acids monitored by in vivo microdialysis reflect the balance between neuronal release and reuptake into surrounding nerve terminals and glial elements.
653 a microdialysis
653 a excitatory amino acids
653 a monoamines
653 a neuropeptides
653 a rat
653 a MEDICINE
653 a MEDICIN
700a You, Z-B4 aut
700a Goiny, Mu Karolinska Institutet4 aut
700a Meana, J J4 aut
700a Silveira, R4 aut
700a Godukhin, O V4 aut
700a Chen, Y4 aut
700a Espinoza, S4 aut
700a Pettersson, E4 aut
700a Loidl, C F4 aut
700a Lubec, G4 aut
700a Andersson, K4 aut
700a Nylander, Ingridu Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden4 aut0 (Swepub:uu)iny08577
700a Terenius, Lu Karolinska Institutet4 aut
700a Ungerstedt, Uu Karolinska Institutet4 aut
700a HerreraMarschitz, M4 aut
710a Karolinska Institutetb Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden4 org
773t Journal of Neurochemistryd : Wileyg 66:4, s. 1726-1735q 66:4<1726-1735x 0022-3042x 1471-4159
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-50723
8564 8u https://doi.org/10.1046/j.1471-4159.1996.66041726.x
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:1945810

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