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Wake Forest University Health Sciences, Department of Physiology and Pharmacology, Winston-Salem, North Carolina 27157
Submitted 23 December 2002; accepted in final form 8 March 2003
A number of recent studies have demonstrated that a well-known form of
short-term plasticity at hippocampal GABAergic synapses, called
depolarization-induced suppression of inhibition (DSI), is in fact
mediated by the retrograde actions of endocannabinoids released in response to
depolarization of the postsynaptic cells. These studies suggest that
endogenous cannabinoids may play an important role in regulating inhibitory
tone in the mammalian CNS. Despite the widespread interest and potential
physiological importance of DSI, many questions regarding the physiological
relevance of DSI remain. To that end, this study set out to define the
specific limiting conditions that could elicit DSI at GABAergic synapses in
CA1 hippocampal pyramidal neurons and to determine if DSI could be elicited
with pulse trains that mimic hippocampal cell-firing patterns that occur in
vivo. Whole cell recordings from hippocampal neurons under voltage-clamp
configuration were made in rat hippocampal slices. Spontaneous and evoked
-aminobutyric acid-A (GABAA) receptor-mediated inhibitory
postsynaptic currents (sIPSCs and eIPSCs, respectively) were recorded prior to
and following depolarization of CA1 hippocampal pyramidal cells. Depolarizing
voltage pulses were shaped to evoke currents in QX-314-treated cells similar
to those accompanying single spontaneous voltage-clamped action potentials
recorded from the soma. Attempts were made to elicit DSI with trains of these
pulses that mimicked hippocampal cell firing patterns in vivo, for instance,
when animals traverse place fields or are performing a short-term memory task.
DSI could not be elicited by such pulse trains or by a number of other
combinations of behaviorally specific firing parameters. The minimum duration
of depolarization necessary to elicit DSI in hippocampal neurons determined by
paired-pulse manipulation was 50 75 ms at a critical interval of 20
30 ms between pulse pairs. Under the conditions tested, the normal
firing patterns of hippocampal neurons that occur in vivo do not appear to
elicit DSI.
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