Development of Action Potential‐dependent and Independent Spontaneous GABAA Receptor‐mediated Currents in Granule Cells of Postnatal Rat Cerebellum
- 1 March 1997
- journal article
- Published by Wiley in European Journal of Neuroscience
- Vol. 9 (3) , 533-548
- https://doi.org/10.1111/j.1460-9568.1997.tb01630.x
Abstract
The postnatal development of spontaneous GABAergic transmission between cerebellar Golgi cells and granule cells was investigated with voltage‐clamp recording from rat cerebellar slices, in symmetrical Cl‐conditions. Between postnatal days 7 and 14 (P7–14), bicuculline‐and TTX (tetrodotoxin)‐sensitive spontaneous inhibitory postsynaptic currents (sIPSCs), occurred at high frequency in 56% of granule cells. Between P10 and P14, sIPSCs were superimposed on tonic current of‐12 ± 1.8 pA at ‐70 mV, that was accompanied by noise with variance of 17 ± 3 pA2. Both the current and noise were inhibited by bicuculline. TTX blocked the bicuculline‐sensitive current and noise by˜60%. Between P18 and P25, sIPSCs were less frequent; all cells showed tonic, bicuculline‐sensitive currents, but these were partially inhibited by TTX (˜35%). Between P40 and P53, slPSCs were rare; tonic, bicuculline‐sensitive currents and noise were greater in amplitude, with mean values of‐17 pA and 22 pA2 at‐70 mV, they were present in all cells but they were not inhibited by TTX. Glycine receptor channels that were expressed in immature, but not adult cells, did not mediate spontaneous currents. Our results indicate that spontaneous transmission onto cerebellar granule cells in immature animals consists primarily of action potential‐dependent, phasic release of vesicular GABA. This generates GABAA receptor‐mediated slPSCs. The effects of GABA transporter blockers suggest that it also produces the TTX‐sensitive current‐noise, as GABA spills out of synapses to activate extrasynaptic receptors or receptors in neighbouring synapses. In older animals, action potential‐independent release of transmitter is predominant and results in tonic activation of GABAA receptors. This does not appear to be spontaneous vesicular release of GABA. Neither does it appear to be reversed uptake of GABA, although further work is required to rule out these possibilities.Keywords
This publication has 62 references indexed in Scilit:
- Tiagabine, SK&F 89976-A, CI-966, and NNC-711 are selective for the cloned GABA transporter GAT-1European Journal of Pharmacology: Molecular Pharmacology, 1994
- Functional diversity of GABA activated Cl− currents in Purkinje versus granule neurons in rat cerebellar slicesNeuron, 1994
- Estimated conductance of glutamate receptor channels activated during EPSCs at the cerebellar mossy fiber-granule cell synapseNeuron, 1993
- Differential expression of GABAA/benzodiazepine receptor ?1, ?2, and ?3 subunit mRNAs in the developing mouse cerebellumJournal of Comparative Neurology, 1992
- Postsynaptic action of endogenous GABA released by nipecotic acid in the hippocampusNeuroscience Letters, 1992
- Rapid-time-course miniature and evoked excitatory currents at cerebellar synapses in situNature, 1992
- Expression of GABAA/benzodiazepine receptor α1-subunit mRNA and [3H]flunitrazepam binding sites during postnatal development of the mouse cerebellumDevelopmental Brain Research, 1991
- Quantitative morphology and synaptology of cerebellar glomeruli in the ratBrain Structure and Function, 1988
- Effect of Nipecotic Acid, a γ‐Aminobutyric Acid Transport Inhibitor, on the Turnover and Release of γ‐Aminobutyric Acid in Rat Cortical SlicesJournal of Neurochemistry, 1982
- UPTAKE AND RELEASE OF NIPECOTIC ACID BY RAT BRAIN SLICESJournal of Neurochemistry, 1976