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1.
Phys Rev E Stat Nonlin Soft Matter Phys ; 82(3 Pt 1): 031910, 2010 Sep.
Article in English | MEDLINE | ID: mdl-21230111

ABSTRACT

Living organisms use waves that propagate through excitable media to transport information. Ca2+ waves are a paradigmatic example of this type of processes. A large hierarchy of Ca2+ signals that range from localized release events to global waves has been observed in Xenopus laevis oocytes. In these cells, Ca2+ release occurs trough inositol 1,4,5-trisphosphate receptors (IP3Rs) which are organized in clusters of channels located on the membrane of the endoplasmic reticulum. In this article we construct a stochastic model for a cluster of IP3R 's that replicates the experimental observations reported in [D. Fraiman, Biophys. J. 90, 3897 (2006)]. We then couple this phenomenological cluster model with a reaction-diffusion equation, so as to have a discrete stochastic model for calcium dynamics. The model we propose describes the transition regimes between isolated release and steadily propagating waves as the IP3 concentration is increased.


Subject(s)
Calcium Signaling , Models, Biological , Animals , Calcium/metabolism , Diffusion , Inositol 1,4,5-Trisphosphate Receptors/metabolism , Ion Channel Gating , Kinetics , Stochastic Processes , Time Factors , Xenopus laevis/metabolism
2.
J Physiol Paris ; 102(4-6): 173-80, 2008.
Article in English | MEDLINE | ID: mdl-18996475

ABSTRACT

Electrosensory systems comprise extensive feedback pathways. It is also well known that these pathways exhibit synaptic plasticity on a wide-range of time scales. Recent in vitro brain slice studies have characterized synaptic plasticity in the two main feedback pathways to the electrosensory lateral line lobe (ELL), a primary electrosensory nucleus in Apteronotus leptorhynchus. Currently-used slice preparations, involving networks in open-loop conditions, allow feedback inputs to be studied in isolation, a critical step in determining their synaptic properties. However, to fully understand electrosensory processing, we must understand how dynamic feedback modulates neuronal responses under closed-loop conditions. To bridge the gap between current in vitro approaches and more complex in vivo work, we present two new in vitro approaches for studying the roles of closed-loop feedback in electrosensory processing. The first involves a hybrid-network approach using dynamic clamp, and the second involves a new slice preparation that preserves one of the feedback pathways to ELL in a closed-loop condition.


Subject(s)
Electric Fish/physiology , Electric Organ/physiology , Feedback, Physiological/physiology , Nerve Net/physiology , Animals , Electric Fish/anatomy & histology , In Vitro Techniques , Models, Neurological , Nerve Net/anatomy & histology , Neural Pathways/physiology , Nonlinear Dynamics , Synapses/physiology
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