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  • 1
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: Stimulation of astrocytes with the excitatory neurotransmitter glutamate leads to the formation of inositol 1,4,5-trisphosphate and the subsequent increase of intracellular calcium content. Astrocytes express both ionotropic receptors and metabotropic glutamate (mGlu) receptors, of which mGlu5 receptors are probably involved in glutamate-induced calcium signaling. The mGlu5 receptor occurs as two splice variants, mGlu5a and mGlu5b, but it was hitherto unknown which splice variant is responsible for the glutamate-induced effects in astrocytes. We report here that both mRNAs encoding mGlu5 receptor splice variants are expressed by cultured astrocytes. The expression of mGlu5a receptor mRNA is much stronger than that of mGlu5b receptor mRNA in these cells. In situ hybridization experiments reveal neuronal expression of mGlu5b receptor mRNA in adult rat forebrain but a strong neuronal expression of mGlu5a mRNA only in olfactory bulb. Signals for mGlu5a receptor mRNA in the rest of the brain were diffuse and weak but consistently above background. Activation of mGlu5 receptors in astrocytes yields increases in inositol phosphate production and transient calcium responses. It is surprising that the rank order of agonist potency [quisqualate 〉 (2S, 1′S,2′S)-2-(carboxycyclopropyl)glycine = trans-(1S,3R)-1-amino-1,3-cyclopentanedicarboxylic acid (1S, 3R-ACPD) 〉 glutamate] differs from that reported for recombinantly expressed mGlu5a receptors. The expression of mGlu5a receptor mRNA and the occurrence of 1S, 3R-ACPD-induced calcium signaling were found also in cultured microglia, indicating for the first time expression of mGlu5a receptors in these macrophage-like cells.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 351 (1995), S. 565-568 
    ISSN: 1432-1912
    Keywords: Glutamate receptor ; Metabotropic ; Binding assay ; Phenylglycines ; Adenylate cyclase inhibition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A cDNA clone encoding the rat metabotropic glutamate receptor mGluR3 was stably transfected into human embryonic kidney 293 cells. Receptor-expressing cell lines were characterized by centrifugation binding assays using [3H]glutamate as radioligand. The rank order of affinity was l-glutamate〉(1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (1S,3R-ACPD)〉L(+)-2-amino-3-phosphonopropionic acid (L-AP3)〉quisqualic acid〉L(+)-2-amino-4-phosphonobutyric acid (L-AP4)〉ibotenic acid. The active enantiomers of several phenylglycines displayed Ki values of 300 to 400 μM. The nonactive enantiomers and the standard ionotropic glutamate receptor ligands N-methyl-d-aspartic acid (NMDA), (R,S)-α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and kainic acid only weakly displaced [3H]glutamate. In this cell line, l-glutamate and (2S,3S,4S)-α-(Carboxycyclopropyl)-glycine (L-CCG-I) reduced cAMP levels in a dose-dependent manner. The sensitivity of this system and its easy applicability make it feasible to envisage ligand binding assays on cell lines expressing cloned receptors as useful screening tools to discover and characterize new and specific agonists and antagonists.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 351 (1995), S. 565-568 
    ISSN: 1432-1912
    Keywords: Key words Glutamate receptor ; Metabotropic ; Binding assay ; Phenylglycines ; Adenylate cyclase inhibition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A cDNA clone encoding the rat metabotropic glutamate receptor mGluR3 was stably transfected into human embryonic kidney 293 cells. Receptor-expressing cell lines were characterized by centrifugation binding assays using [3H]glutamate as radioligand. The rank order of affinity was L-glutamate〉(1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (1S,3R-ACPD)〉L(+)-2-amino-3-phosphonopropionic acid (L-AP3)〉quisqualic acid〉L(+)-2-amino-4-phosphonobutyric acid (L-AP4)〉ibotenic acid. The active enantiomers of several phenylglycines displayed Ki values of 300 to 400 μM. The nonactive enantiomers and the standard ionotropic glutamate receptor ligands N-methyl-D-aspartic acid (NMDA), (R,S)-α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and kainic acid only weakly displaced [3H]glutamate. In this cell line, L-glutamate and (2S,3S,4S)-α-(Carboxycyclopropyl)-glycine (L-CCG-I) reduced cAMP levels in a dose-dependent manner. The sensitivity of this system and its easy applicability make it feasible to envisage ligand binding assays on cell lines expressing cloned receptors as useful screening tools to discover and characterize new and specific agonists and antagonists.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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