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Multiple modes of GABAergic inhibition of rat cerebellar granule cells
Cerebellar granule cells are inhibited phasically by GABA released synaptically from Golgi cells, but are inhibited more powerfully by tonic activity of high affinity α 6 subunit-containing GABA A receptors. During development the tonic activity is generated by the accumulation of GABA released by...
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Published in: | The Journal of physiology 2003-04, Vol.548 (1), p.97-110 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Cerebellar granule cells are inhibited phasically by GABA released synaptically from Golgi cells, but are inhibited more powerfully
by tonic activity of high affinity α 6 subunit-containing GABA A receptors. During development the tonic activity is generated by the accumulation of GABA released by action potentials,
but in the adult the tonic activity is independent of action potentials. Here we show that in adult rats the tonic activation
of GABA A receptors is produced by non-vesicular transmitter release and is reduced by the activity of GAT-1 and GAT-3 GABA transporters,
demonstrating that alterations of GABA uptake will modulate information flow through granule cells. Acetylcholine (ACh) evokes
a large Ca 2+ -dependent but action potential-independent release of GABA, which activates α 6 subunit-containing GABA A receptors. These data show that three separate modes of transmitter release can activate GABA A receptors in adult cerebellar granule cells: action potential-evoked exocytotic GABA release, non-vesicular release, and
ACh-evoked Ca 2+ -dependent release independent of action potentials. The relative magnitudes of the inhibitory charge transfers generated
by action potential-evoked release (during high frequency stimulation of the mossy fibres), tonic inhibition and superfused
ACh are 1:3:12, indicating that tonic and ACh-mediated inhibition may play a major role in regulating granule cell firing. |
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ISSN: | 0022-3751 1469-7793 |
DOI: | 10.1113/jphysiol.2002.036459 |