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POSTNATAL CHANGES IN THE HIGH AFFINITY UPTAKE OF GLYCINE and GABA IN THE RAT CENTRAL NERVOUS SYSTEM
68
Citations
25
References
1974
Year
Brain DevelopmentSynaptic TransmissionNeurotransmitterNeurotransmissionSynaptic SignalingSocial SciencesNeurobiology Of DiseaseGaba UptakeNeurochemistryAnimal PhysiologyNeuropharmacologyNervous SystemGlycine UptakePharmacologyInhibitory NeurotransmittersSynaptic PlasticityNeurophysiologyCellular NeurosciencePhysiologyNeuropeptide ReceptorNeuroscienceMolecular NeurobiologyCentral Nervous SystemMedicine
Abstract— High affinity uptake systems for GABA into slices of cerebral cortex and for glycine into slices of spinal cord have been demonstrated in rats of 1 and 10 days postnatal age and compared with the systems in tissue slices from adult rats. For both systems there was an increase in the maximal rate of uptake of the substrate with development. For glycine uptake there was no significant change in apparent K m during development, whereas there was a four‐fold increase in the apparent K m for GABA uptake. There were some changes with development in the apparent substrate specificity of the two systems suggesting increased specificity with maturation. Bicuculline and strychnine, antagonists of the postsynaptic inhibitory actions of GABA and glycine, produced convulsions in 1‐, 2‐ and 10‐day‐old rats following intraperitoneal injection of doses somewhat lower than those required to convulse adult rats. These findings are consistent with other evidence that glycine and GABA are functioning as inhibitory transmitters at least as soon as 1 day after birth.
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