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ACTIONS OF l- AND d-HOMOCYSTEATE IN RAT CNS: A CORRELATION BETWEEN LOW-AFFINITY UPTAKE AND THE TIME COURSES OF EXCITATION BY MICROELECTROPHORETICALLY APPLIED L-GLUTAMATE ANALOGUES
Authors:D W G Cox  M H Headley  J C Watkins
Institution:Departments of Physiology and Pharmacology, The Medical School, University Walk, Bristol BS8 1TD.
Abstract:Abstract— A correlation has been attempted between the uptake characteristics of l - and d -homocysteate and the time courses of neuronal excitation by these and other amino acids related to l -glutamate. The uptake of l - and d -homocysteate and of l -35S]homocysteate was studied in individual slices of rat cerebral cortex at 37°C. Tissue: medium ratios attained over l0 min for the unlabelled enantiomers at 2.5 mM were 3.7 for l -homocysteate but only 0.8 for the d -isomer. The uptake of l -35S]homocysteate over the concentration range 0.09 μm -2 mm can be attributed mainly to a low-affinity transport process with Km approx 3 mm and Vmax 1.7 μmol/g/min, but a high-affinity process of low Vmax may make a minor contribution at the lower concentrations within this range. In terms of dependence on energy metabolism and Na+], and on inhibition by p-chloromercuriphenylsulphonate, ouabain and structural analogues of the amino acid, the main uptake system for L-35S]homocysteate appears to be similar to that mediating low-affinity uptake of l -glutamate and other acidic amino acids. d -Homocysteate was but a weak inhibitor of this uptake system compared with other structural analogues. The time courses of excitation by 6 amino acids were determined by microelectrophoretic application to rat spinal neurones. d -Homocysteate induced responses with recovery times considerably longer than those of the other amino acids; this correlates with the absence of rapid uptake systems demonstrated for this amino acid in cortical tissue. d -Glutamate and l -homocysteate, which are only accumulated by low-affinity transport mechanisms, induced responses with recovery periods similar to those of l -glutamate, l -aspartate and d -aspartate, which are accumulated by both high- and low-affinity uptake systems. Although contributions of other factors to the observed time courses, such as rates of association and dissociation of the amino acid-receptor complexes, cannot be excluded, the present results are consistent with the hypothesis that low-affinity uptake systems of high Vmax play an important role in the rapid termination of the effects of amino acid excitants.
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