GDPbS Activates Excitatory Synapses in CA1 Pyramidal Cells by Disinhibiting the PKA Activating PathwayMohamed Ouardouz*
NRAC, Gatineau, Quebec, Canada
- Corresponding Author:
- Mohamed Ouardouz
NRAC, 39 du météore Gatineau
Quebec, J9A 3B5, Canada
E-mail: [email protected]
Received date: June 28, 2014; Accepted dat: September 29, 2014; Published date: October 06, 2014
Citation: Ouardouz M (2014) GDPßS Activates Excitatory Synapses in CA1 Pyramidal Cells by Disinhibiting the PKA Activating Pathway. J Neurol Neurophysiol 5:235. doi:10.4172/2155-9562.1000235
Copyright: © 2014 Ouardouz M. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Objective: During the early postnatal brain developmental stages, excitatory synapses mediated by AMPA
receptors are weak or silent. Activity-dependent insertion of AMPA receptors into synapses depends on the activation
of protein kinase A. In this work, we investigated the effect of Guanosine 5’-[βthiol] diphosphate (GDPßS) on excitatory
and inhibitory synaptic currents in CA1 pyramidal cells at postnatal days 9-12.
Methods: Whole-cell patch-clamp recordings from identified hippocampal CA1 pyramidal cells were used. GDPβS
Was applied through the recording electrode.
Results: GDPβS induces an increase in excitatory synaptic current amplitude, but not in the inhibitory synaptic
current amplitude. An analysis of the change in excitatory synaptic current amplitude in the presence of GDPβS revealed
a progressive increase, which is blocked by the protein kinase A inhibitor Rp-3’,5’-cyclic monophosphothioatetriethylamine
(Rp-cAMP), suggesting that GDPβS inhibits G-protein with a tonic negative control on a protein kinase A
activating pathway. In addition, GDPβS has no effect on paired-pulse facilitation, suggesting that the glutamate release
machinery is not affected. Moreover, as GDPβS was applied to postsynaptic neurons, the increase in excitatory
postsynaptic current amplitude is related to changes at the postsynaptic side.
Conclusion: Those results suggest that in developing hippocampal CA1 pyramidal cells, the tonic inhibition of a
protein kinase A activating pathway by a G-protein prevents the activation of excitatory synapses