1987
DOI: 10.1007/bf00972136
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Brain cortical amino acids measured by intracerebral dialysis in portacaval shunted rats

Abstract: The extracellular amino acid content was measured in the parietal cortex in portacaval and sham operated rats, using the brain dialysis technique. The amino acid content of the perfusate was determined for 10 min before and during stimulation with potassium chloride. Basal levels of aspartate, glutamine, glycine, methionie, valine, phenylalanine and leucine were 2-to 6-fold higher in the PC-shunted as compared to the sham operated rats. For glutamate, taurine, and GABA no differences were observed between the … Show more

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Cited by 76 publications
(23 citation statements)
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“…This evidence can be summarized as follows: (1) As already stated in this arti cle, exposure o f cultured astrocytes to concentrations of ammonia equivalent to those reported in brain in experi mental PSE results in decreased capacity for glutamate uptake [28]; (2) blood extracts from patients with PSE inhibit the high affinity glutamate uptake system in rat hippocampal slices [35]; (3) high-affinity uptake of gluta mate into rat brain synaptosomes is significantly de creased by exposure to 5 mM ammonia [36]; (4) electri cally stimulated, Ca2 f-dependent (i.e., neuronal) release of glutamate from hippocampal slices from portacaval shunted rats is significantly increased [37], consistent with decreased reuptake into the presynaptic terminal and perineuronal astrocyte; (5) K 4 -stimulated release of glutamate in vivo has been shown to be increased from the brains of portacaval shunted rats measured using either the cortical cup technique [38] or in vivo cerebral microdialysis [39], and (6) densities of 3H-glutamate binding sites are decreased in the brains of portacaval shunted rats [40] consistent with down-regulation of these sites following prolonged exposure to increased concentrations of endogenous ligand (glutamate).…”
Section: Glutamatergic Synaptic Regulationmentioning
confidence: 99%
“…This evidence can be summarized as follows: (1) As already stated in this arti cle, exposure o f cultured astrocytes to concentrations of ammonia equivalent to those reported in brain in experi mental PSE results in decreased capacity for glutamate uptake [28]; (2) blood extracts from patients with PSE inhibit the high affinity glutamate uptake system in rat hippocampal slices [35]; (3) high-affinity uptake of gluta mate into rat brain synaptosomes is significantly de creased by exposure to 5 mM ammonia [36]; (4) electri cally stimulated, Ca2 f-dependent (i.e., neuronal) release of glutamate from hippocampal slices from portacaval shunted rats is significantly increased [37], consistent with decreased reuptake into the presynaptic terminal and perineuronal astrocyte; (5) K 4 -stimulated release of glutamate in vivo has been shown to be increased from the brains of portacaval shunted rats measured using either the cortical cup technique [38] or in vivo cerebral microdialysis [39], and (6) densities of 3H-glutamate binding sites are decreased in the brains of portacaval shunted rats [40] consistent with down-regulation of these sites following prolonged exposure to increased concentrations of endogenous ligand (glutamate).…”
Section: Glutamatergic Synaptic Regulationmentioning
confidence: 99%
“…Thus, whereas total brain glutamate levels are decreased in various models of HE (Hindfelt et al, 1977;Bosman et al, 1990;Dejong et al, 1992), extracellular glutamate levels are consistently increased in rat models of acute liver failure (Moroni et al, 1983;Tossman et al, 1987;de Knegt et al, 1994). Ammonia has been shown to suppress high affinity glutamate uptake (Bender and Norenberg, 1996).…”
Section: Introductionmentioning
confidence: 99%
“…Reductions in brain GS activity, as observed in the present and a previous study (Girard et al, 1993), would therefore be expected to result in decreased astrocytic glutamate uptake following PCA. In favour of this possibility, several reports describe increases of extracellular brain concentrations of glutamate in the brains of PCA rats (Moroni et al, 1983;Tossman et al, 1987), a finding which is consistent with diminished astrocytic uptake in the brains of these animals.…”
Section: Discussionmentioning
confidence: 74%