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Chronic treatment with gabaa receptor antagonist bicuculline increasesefficacy of gabaergic synaptic transmission in rat hippocampal cell cultures
S.Y. Ivanova, P.G.Kostyuk
International Center of Molecular Physiology, NationalAcademy of Sciences of Ukraine, Kiev.
Abstract
It has been proposed to consider plasticity in neuronal net-
work as occurring in two forms: use-dependent plasticity which
modifies the network properties, and homeostatic plasticity
which may counteract use-dependent changes. Сhronic block
of some of transmitter receptors is often used as a model for
studying homeostatic plasticity. We studied whether chronic
block of GABAA receptors can affect GABAergic transmis-
sion. Using whole-cell voltage clamp recording and local extra-
cellular stimulation we investigated evoked inhibitory postsyn-
aptic currents (IPSCs) in cultured rat hippocampal neurons
grown in the presence of GABAA receptor antagonist –
bicuculline (20мM) and in control conditions. Cell for both
control and pretreated cultures were obtained from same dis-
section and were grown in parallel. We compared the ampli-
tudes of the evoked IPSC, the reversal potentials of the
responses IPSC coefficient of variation and depression evoked
by paired stimulation. Chronic bicuculline treatment did not
significantly affect the paired-pulse depression (PPD) and
IPSC reversal potentials. In contrast we found that amplitude
of evoked IPSCs was increased about two times in cultures
treated with bicuculline. However, IPSC coefficients of varia-
tion were not significantly different. We conclude that chronic
block of GABAA receptors enhances efficacy of GABAergic
synaptic transmission in rat hippocampal cell cultures and
this effect is likely to postsynaptic mechanism(s) because
IPSC increase was not accompanied with changes of IPSC
coefficient of variation. A possibility that the effect of chronic
block of GABAA receptors on GABAergic transmission is
mediated by neurotrophin BDNF is discussed.
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© National Academy of Sciences of Ukraine, Bogomoletz Institute of Physiology, 2014-2024.
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