Publication | Open Access
Subcellular Localization of Metabotropic GABA<sub>B</sub>Receptor Subunits GABA<sub>B1a/b</sub>and GABA<sub>B2</sub>in the Rat Hippocampus
204
Citations
71
References
2003
Year
Synaptic TransmissionNeurotransmitterSubcellular LocalizationNeurotransmissionCellular NeurobiologySynaptic SignalingSocial SciencesQuantitative AnalysisNeurologyNeurochemistryMolecular NeuroscienceCell BiologyGaba B2Rat HippocampusSynaptic PlasticityNeurobiological MechanismNeurophysiologyNeuroanatomyGaba B ReceptorsNeuroscienceMolecular NeurobiologyCentral Nervous SystemMedicine
Metabotropic GABA B receptors mediate slow inhibitory effects presynaptically and postsynaptically. Using preembedding immunohistochemical methods combined with quantitative analysis of GABA B receptor subunit immunoreactivity, this study provides a detailed description of the cellular and subcellular localization of GABA B1a/b and GABA B2 in the rat hippocampus. At the light microscopic level, an overlapping distribution of GABA B1a/b and GABA B2 was revealed in the dendritic layers of the hippocampus. In addition, expression of the GABA B1a/b subunit was found in somata of CA1 pyramidal cells and of a subset of GABAergic interneurons. At the electron microscopic level, immunoreactivity for both subunits was observed on presynaptic and, more abundantly, on postsynaptic elements. Presynaptically, subunits were mainly detected in the extrasynaptic membrane and occasionally over the presynaptic membrane specialization of putative glutamatergic and, to a lesser extent, GABAergic axon terminals. Postsynaptically, the majority of GABA B receptor subunits were localized to the extrasynaptic plasma membrane of spines and dendritic shafts of principal cells and shafts of interneuron dendrites. Quantitative analysis revealed enrichment of GABA B1a/b around putative glutamatergic synapses on spines and an even distribution on dendritic shafts of pyramidal cells contacted by GABAergic boutons. The association of GABA B receptors with glutamatergic synapses at both presynaptic and postsynaptic sides indicates their intimate involvement in the modulation of glutamatergic neurotransmission. The dominant extrasynaptic localization of GABA B receptor subunits suggests that their activation is dependent on spillover of GABA requiring simultaneous activity of populations of GABAergic cells as it occurs during population oscillations or epileptic seizures.
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