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Oscillations and Spiking Pairs: Behavior of a Neuronal Model with STDP Learning
Xi Shen, Xiaobin Lin, and Philippe De Wilde
Neural Computation 20 (8), 2037-69 (01 Aug 2008)
 
Self-organization and neuronal avalanches in networks of dissociated cortical neurons
V Pasquale et al.
Neuroscience, (2008)
 
Decoupling through Synchrony in Neuronal Circuits with Propagation Delays
Evgueniy Lubenov and Athanassios Siapas
Neuron 58 (1), 118-31 (2008)
 
Spatio-temporal dynamics of oscillatory network activity in the neonatal mouse cerebral cortex
Jyh-Jang Sun and Heiko Luhmann
European Journal of Neuroscience 26 (7), 1995-2004 (2007)
 
Large-scale oscillatory calcium waves in the immature cortex
Olga Garaschuk et al.
Nature Neuroscience 3 (5), 452-9 (2000)
 
Spontaneous oscillatory burst activity in the piriform–amygdala region and its relation to in vitro respiratory activity in newborn rats
H Onimaru and I Homma
Neuroscience 144 (1), 387-94 (05 Jan 2007)
he amygdala is important for the formation of emotions that are affected by olfactory information. The piriform cortex is involved in information processing related to olfaction. To investigate functional interactions between the piriform cortex and amygdala and their relation to medullary respiratory activity, we developed a novel in vitro preparation including the limbic system, brainstem, and spinal cord of newborn rats. With the use of optical and electrophysiologic recordings, we analyzed spontaneous neuronal activity in the piriform–amygdala complex in limbic–brainstem–spinal cord preparations from 0- to 1-day-old rats. For optical recordings, the preparation was stained with a voltage-sensitive dye, and inspiratory activity was monitored from the fourth cervical (C4) ventral root. Spontaneous oscillatory burst activity (up to 10/min) was detected from the rostral cut surface of limbic and para-limbic regions including the piriform cortex and amygdala. The burst activity initially appeared in the piriform cortex and then propagated to the amygdala. We averaged the imaging data in the limbic area with the use of C4 inspiratory activity as a trigger signal. The results suggest functional coupling of the rhythmic burst activity in the piriform–amygdala complex to medullary inspiratory activity, which was confirmed electrophysiologically by cross-correlation analysis of these signals. This rhythmic burst activity may be involved in the development of neuronal circuits that process information related to olfaction, emotion, and respiration.

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