Maturation of precise temporal control of spike timing by feedforward inhibition and associated developmental switch in the L4-L2/3 plasticity in the barrel cortex

2009 ◽  
Vol 65 ◽  
pp. S68
Author(s):  
Fumitaka Kimura ◽  
Chiaki Itami
2014 ◽  
Vol 2 (3) ◽  
pp. e00271 ◽  
Author(s):  
Abhishek Banerjee ◽  
Ana González-Rueda ◽  
Cassandra Sampaio-Baptista ◽  
Ole Paulsen ◽  
Antonio Rodríguez-Moreno

2013 ◽  
Vol 110 (8) ◽  
pp. 1930-1944 ◽  
Author(s):  
Franck Dubruc ◽  
David Dupret ◽  
Olivier Caillard

In the hippocampus, activity-dependent changes of synaptic transmission and spike-timing coordination are thought to mediate information processing for the purpose of memory formation. Here, we investigated the self-tuning of intrinsic excitability and spiking reliability by CA1 hippocampal pyramidal cells via changes of their GABAergic inhibitory inputs and endocannabinoid (eCB) signaling. Firing patterns of CA1 place cells, when replayed in vitro, induced an eCB-dependent transient reduction of spontaneous GABAergic activity, sharing the main features of depolarization-induced suppression of inhibition (DSI), and conditioned a transient improvement of spike-time precision during consecutive burst discharges. When evaluating the consequences of DSI on excitatory postsynaptic potential (EPSP)-spike coupling, we found that transient reductions of uncorrelated (spontaneous) or correlated (feedforward) inhibition improved EPSP-spike coupling probability. The relationship between EPSP-spike-timing reliability and inhibition was, however, more complex: transient reduction of correlated (feedforward) inhibition disrupted or improved spike-timing reliability according to the initial spike-coupling probability. Thus eCB-mediated tuning of pyramidal cell spike-time precision is governed not only by the initial level of global inhibition, but also by the ratio between spontaneous and feedforward GABAergic activities. These results reveal that eCB-mediated self-tuning of spike timing by the discharge of pyramidal cells can constitute an important contribution to place-cell assemblies and memory formation in the hippocampus.


2003 ◽  
pp. 229-240
Author(s):  
Daniel E. Feldman ◽  
Cara B. Allen ◽  
Tansu Celikel
Keyword(s):  

PLoS ONE ◽  
2013 ◽  
Vol 8 (11) ◽  
pp. e80749 ◽  
Author(s):  
Christoph M. Zehendner ◽  
Simeon Tsohataridis ◽  
Heiko J. Luhmann ◽  
Jenq-Wei Yang

2007 ◽  
Vol 98 (4) ◽  
pp. 1871-1882 ◽  
Author(s):  
Marcelo A. Montemurro ◽  
Stefano Panzeri ◽  
Miguel Maravall ◽  
Andrea Alenda ◽  
Michael R. Bale ◽  
...  

Rats discriminate texture by whisking their vibrissae across the surfaces of objects. This process induces corresponding vibrissa vibrations, which must be accurately represented by neurons in the somatosensory pathway. In this study, we investigated the neural code for vibrissa motion in the ventroposterior medial (VPm) nucleus of the thalamus by single-unit recording. We found that neurons conveyed a great deal of information (up to 77.9 bits/s) about vibrissa dynamics. The key was precise spike timing, which typically varied by less than a millisecond from trial to trial. The neural code was sparse, the average spike being remarkably informative (5.8 bits/spike). This implies that as few as four VPm spikes, coding independent information, might reliably differentiate between 106 textures. To probe the mechanism of information transmission, we compared the role of time-varying firing rate to that of temporally correlated spike patterns in two ways: 93.9% of the information encoded by a neuron could be accounted for by a hypothetical neuron with the same time-dependent firing rate but no correlations between spikes; moreover, ≥93.4% of the information in the spike trains could be decoded even if temporal correlations were ignored. Taken together, these results suggest that the essence of the VPm code for vibrissa motion is firing rate modulation on a submillisecond timescale. The significance of such a code may be that it enables a small number of neurons, firing only few spikes, to convey distinctions between very many different textures to the barrel cortex.


2009 ◽  
Vol 19 (12) ◽  
pp. 2959-2969 ◽  
Author(s):  
Abhishek Banerjee ◽  
Rhiannon M. Meredith ◽  
Antonio Rodríguez-Moreno ◽  
Susanna B. Mierau ◽  
Yves P. Auberson ◽  
...  

2021 ◽  
Vol 118 (35) ◽  
pp. e2107026118 ◽  
Author(s):  
Ricardo Gómez ◽  
Laura E. Maglio ◽  
Alberto J. Gonzalez-Hernandez ◽  
Belinda Rivero-Pérez ◽  
David Bartolomé-Martín ◽  
...  

Postsynaptic N-methyl-D-aspartate receptors (NMDARs) are crucial mediators of synaptic plasticity due to their ability to act as coincidence detectors of presynaptic and postsynaptic neuronal activity. However, NMDARs exist within the molecular context of a variety of postsynaptic signaling proteins, which can fine-tune their function. Here, we describe a form of NMDAR suppression by large-conductance Ca2+- and voltage-gated K+ (BK) channels in the basal dendrites of a subset of barrel cortex layer 5 pyramidal neurons. We show that NMDAR activation increases intracellular Ca2+ in the vicinity of BK channels, thus activating K+ efflux and strong negative feedback inhibition. We further show that neurons exhibiting such NMDAR–BK coupling serve as high-pass filters for incoming synaptic inputs, precluding the induction of spike timing–dependent plasticity. Together, these data suggest that NMDAR-localized BK channels regulate synaptic integration and provide input-specific synaptic diversity to a thalamocortical circuit.


Sign in / Sign up

Export Citation Format

Share Document