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216 Détection de coïncidences dans les neurones bruités<br />

a b<br />

2 mV<br />

10%<br />

20 ms<br />

PSTH<br />

20 ms<br />

non-coincident<br />

EPSPs<br />

c d<br />

S<br />

2w<br />

w<br />

threshold<br />

0.53 extra<br />

spikes<br />

Coincidence sensitivity S<br />

coincident<br />

EPSPs<br />

σ = 2 mV<br />

σ = 3 mV<br />

0.49 extra<br />

spikes<br />

mean voltage (mV)<br />

Figure 8.6 – Coincidence sensitivity in the mean-driven vs. fluctuation-driven regime.<br />

a, b. As in Figure 8.4, we calculate the average extra number of output spikes due to<br />

two additional synchronous (b) or non-synchronous (a) spikes. The definition is identical but<br />

here the neuron is in a mean-driven regime, that is, the average drive exceeds threshold. c. In<br />

this regime, the membrane potential distribution is increasing near threshold. As a result, coincidence<br />

sensitivity S (red contour) is negative, meaning the neuron fires less to coincident than<br />

to non-coincident spikes. d. Coincidence sensitivity in a neuron model with background noise<br />

(with two different standard deviations σ, and w=1 mV) as a function of the mean membrane<br />

potential, measured in the absence of spikes. The neuron stops being sensitive to coincidences<br />

when the mean membrane potential approaches threshold.<br />

rious areas, extracted from a number of previous studies. In anesthetized preparations,<br />

these distributions are often bimodal, which reflects “up” and “down”<br />

states (Constantinople et Bruno 2011). Since down states are quiescent, only the<br />

depolarized mode (up state) is relevant to this study. In all cases, the membrane<br />

potential distribution decreases toward threshold, suggesting that neurons are in<br />

threshold

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