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Neuropharmacology. 2002 Jan;42(1):34-47.

Pharmacological heterogeneity of gamma-aminobutyric acid receptors during development suggests distinct classes of rat cerebellar granule cells in situ.

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  • 1Department of Psychiatry, Clinical Research Group, University of Mainz, Untere Zahlbacher Strasse 8, 55131, Mainz, Germany. hevers@mail.uni-mainz.de

Abstract

The gamma-aminobutyric acid receptor (GABA(A)R) represents a ligand-gated Cl(-)-channel assembling as heteropentamere from 19 known subunits. Cerebellar granule cells contain a unique subset, namely the alpha1-, alpha6-, beta2-, gamma2- and delta-subunits. We studied their GABAergic pharmacology in situ using whole-cell patch-clamp recordings in brain slices and a modified Y-tube application system. The distribution of the EC50s for GABA in young (P8-P14) and medium aged animals (P15-P28) could be fitted with the sum of two Gaussian distributions with means of 60 and 185 microM and 27 and 214 microM, respectively. In older animals (P29-P48) the observed homogeneous range of sensitivities fitted a single Gaussian distribution (11 microM). In young animals (< or =P14) GABA-responses were largely insensitive towards 300 microM of the alpha6-specific inhibitor furosemide (82% of control response). The sensitivity increased in older animals at the EC5-20 of GABA (31% of control responses), supporting an increased expression of alpha6-subunits as molecular basis for the observed developmental changes. Approximately 50% of cells in the age range P15-P48 were potentiated by 1 microM diazepam and by 3 microM methyl-6,7-dimethoxy-4-ethyl-beta-carboline-3-carboxylate (DMCM), suggesting the concurrent presence of alpha1- and alpha6-containing receptors, whereas the remaining of cells were neither potentiated by diazepam nor did they show the alpha6-typical DMCM potentiation, though they were potentiated by loreclezole. These properties indicate unknown pharmacological characteristics of cerebellar receptor-subunit combinations in approximately 50% of granule cells in situ.

PMID:
11750914
[PubMed - indexed for MEDLINE]
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