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<item>
  <id>05716099</id>
  <dt>j</dt>
  <an>05716099</an>
  <augroup>
    <au>Pospischil, Martin</au>
    <au>Piwkowska, Zuzanna</au>
    <au>Rudolph, Michelle</au>
    <au>Bal, Thierry</au>
    <au>Destexhe, Alain</au>
  </augroup>
  <ti>Inhibitory conductance dynamics in cortical neurons during activated states.</ti>
  <so>Neurocomputing 70, No. 10-12, 1602-1604 (2007).</so>
  <py>2007</py>
  <pu>Elsevier Science Publishers B.V., Amsterdam</pu>
  <lagroup>
    <la>EN</la>
  </lagroup>
  <ccgroup>
  </ccgroup>
  <utgroup>
    <ut>spike-triggered average</ut>
    <ut>conductance dynamics</ut>
    <ut>dynamic-clamp</ut>
  </utgroup>
  <cigroup>
  </cigroup>
  <ligroup>
    <li>doi:10.1016/j.neucom.2006.10.040</li>
  </ligroup>
  <abgroup>
    <ab>Summary: During activated states in vivo, neocortical neurons are subject to intense synaptic activity and high-amplitude membrane potential $(V_{m})$ fluctuations. These ``high-conductance'' states may strongly affect the integrative properties of cortical neurons. We investigated the responsiveness of cortical neurons during different states using a combination of computational models and in vitro experiments (dynamic-clamp) in the visual cortex of adult guinea pigs. Spike responses were monitored following stochastic conductance injection in both experiments and models. We found that cortical neurons can operate in a continuum between two different modes: during states with equal excitatory and inhibitory conductances, the firing is mostly correlated with an increase in excitatory conductance, which is a rather classic scenario. In contrast, during states dominated by inhibition, the firing is mostly related to a decrease in inhibitory conductances (dis-inhibition). This model prediction was tested experimentally using dynamic-clamp, and the same modes of firing were identified. We also found that the signature of spikes evoked by dis-inhibition is a transient drop of the total membrane conductance prior to the spike, which is typical of states with dominant inhibitory conductances. Such a drop should be identifiable from intracellular recordings in vivo, which would provide an important test for the presence of inhibition-dominated states. In conclusion, we show that in artificial activated states, not only inhibition can determine the conductance state of the membrane, but inhibitory inputs may also have a determinant influence on spiking. Future analyses and models should focus on verifying if such a determinant influence of inhibitory conductance dynamics is also present in vivo.</ab>
    <rv></rv>
  </abgroup>
</item>