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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular neurobiology 1 (1981), S. 115-120 
    ISSN: 1573-6830
    Keywords: glutamate ; aspartate ; 2-amino-4-phosphonobutyric acid ; kainic acid,N-methyl-DL-aspartate ; pyriform cortex slice ; lateral olfactory tract ; homocysteic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Aspartate and glutamate are the principal candidates for the excitatory neurotransmitter released by the lateral olfactory tract (LOT) in prepyriform cortex of the rat. Identity of action of the natural transmitter with exogenous glutamate and/or aspartate, however, has not yet been demonstrated. We show that bath-applied 2-amino-4-phosphonobutyric acid, a presumed specific glutamate antagonist, blocks LOT-stimulated prepyriform field potentials and single unit activity but not the single unit response to ionophoretically applied glutamate or aspartate in rat olfactory cortex slices. These results suggest that neither aspartate nor glutamate is the LOT transmitter. Responses to ionophoretically applied N-methyl-DL-aspartate, kainic acid, and DL-homocysteate were clearly decreased by 2-amino-4-phosphono-butyric acid. This suggests that these agents, usually presumed to be aspartate or glutamate agonists, act at different receptors than aspartate and glutamate.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular neurobiology 4 (1984), S. 185-190 
    ISSN: 1573-6830
    Keywords: excitatory amino acids ; aspartate ; N-methyl-dl-aspartate ; 2-amino-5-phosphonovalerate ; receptors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. The effects of ionophoretically appliedN-methyl-dl-aspartate (NMDA) and aspartate on identified pyramidal neurons in rat piriform cortex were examined in isolated, submerged, and perfused brain slices. 2. NMDA was more potent than aspartate in eliciting neuronal discharge. Perfusion of the acidic amino acid antagonists,dl-2-amino-5-phosphonovalerate (APV), 10−6 or 10−5 M,dl-2-amino-7-phosphonoheptanoate (APH), 10−5 M, andγ-d-glutamylglycine (γDGG), 10−5 M, selectively blocked the response to NMDA without effect on the response to aspartate. 3. At higher concentrations which blocked responses to both NMDA and aspartate,γDGG blocked kainate responses and depressed glutamate and quisqualate responses. 4. These results suggest that in piriform neurons NMDA and aspartate act at distinct receptor sites, not a common receptor site, and that both of these sites are distinct from those that mediate responses to glutamate, quisqualate, and kainate.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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