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The Journal of Neuroscience, July 2, 2003, 23(13):5906-5918
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Characterization of Depolarization-Induced Suppression of Inhibition Using Paired InterneuronPurkinje Cell Recordings
Marco A. Diana and
Alain Marty
Laboratoire de Physiologie Cérébrale, Université
Paris 5, 75006 Paris, France
Depolarization-induced suppression of inhibition (DSI) is a retrograde form
of synaptic inhibition involving the Ca2+-dependent release of
cannabinoids from the postsynaptic cell. DSI exerts multiple effects on
presynaptic neurons: here, we establish the breakdown of DSI in its individual
components at the synapses between basket and stellate cells and Purkinje
cells. In the presence of tetrodotoxin, the change in IPSC frequency entirely
accounted for the decrease of transmission during DSI; in contrast, without
tetrodotoxin, the reductions of frequency and average amplitude gave equal
contributions. In paired recordings, transmission displayed an irreversible
rundown unless interneurons were recorded from with the perforated patch
method. Under these conditions, a DSI of 68.8% was measured; the failure rate
and the paired pulse ratio (at 20 msec intervals) increased from 1.2 to 20.2
and 95.6 to 132.6%, respectively, and the variance to mean ratio augmented
2.17-fold. Presynaptic dialysis with Cs+ led to a major
potentiation of synaptic strength and to a marked reduction of DSI with
respect to control potassium conditions; DSI recovered only partially when
decreasing the extracellular Ca2+ concentration to match the
control IPSC amplitudes. These results, combined with those of Kreitzer et al.
(2002), indicate that three
distinct presynaptic processes contribute to DSI: reductions of miniature
frequency (13.4% of total DSI), of presynaptic action potential frequency
(23.2%), and of the probability that presynaptic depolarizations elicit
transmitter release (63.4%). The latter component involves a modulation of
K+ channels and trial-to-trial modifications of the presynaptic
signal.
Key words: DSI in various components; paired recordings; perforated patch; GABAergic interneurons; retrograde communication; cerebellum
Received Dec. 11, 2002;
revised Feb. 21, 2003;
accepted Apr. 12, 2003.
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