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1.
Int J Neural Syst ; 26(8): 1650028, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27389003

ABSTRACT

Epilepsy is a condition in which periods of ongoing normal EEG activity alternate with periods of oscillatory behavior characteristic of epileptic seizures. The dynamics of the transitions between the two states are still unclear. Computational models provide a powerful tool to explore the underlying mechanisms of such transitions, with the purpose of eventually finding therapeutic interventions for this debilitating condition. In this study, the possibility to postpone seizures elicited by a decrease of inhibition is investigated by using external stimulation in a realistic bistable neuronal model consisting of two interconnected neuronal populations representing pyramidal cells and interneurons. In the simulations, seizures are induced by slowly decreasing the conductivity of GABA[Formula: see text] synaptic channels over time. Since the model is bistable, the system will change state from the initial steady state (SS) to the limit cycle (LS) state because of internal noise, when the inhibition falls below a certain threshold. Several state-independent stimulations paradigms are simulated. Their effectiveness is analyzed for various stimulation frequencies and intensities in combination with periodic and random stimulation sequences. The distributions of the time to first seizure in the presence of stimulation are compared with the situation without stimulation. In addition, stimulation protocols targeted to specific subsystems are applied with the objective of counteracting the baseline shift due to decreased inhibition in the system. Furthermore, an analytical model is used to investigate the effects of random noise. The relation between the strength of random noise stimulation, the control parameter of the system and the transitions between steady state and limit cycle are investigated. The study shows that it is possible to postpone epileptic activity by targeted stimulation in a realistic neuronal model featuring bistability and that it is possible to stop seizures by random noise in an analytical model.


Subject(s)
Computer Simulation , Electric Stimulation Therapy/methods , Epilepsy/therapy , Models, Neurological , Algorithms , Brain/physiopathology , Epilepsy/physiopathology , Humans , Interneurons/physiology , Membrane Potentials/physiology , Neural Inhibition/physiology , Pyramidal Cells/physiology , Receptors, GABA-A/metabolism , Seizures/physiopathology , Seizures/therapy , Synapses/physiology , Time Factors
2.
Int J Neural Syst ; 25(6): 1550021, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26058401

ABSTRACT

High frequency oscillations (HFO) appear to be a promising marker for delineating the seizure onset zone (SOZ) in patients with localization related epilepsy. It remains, however, a purely observational phenomenon and no common mechanism has been proposed to relate HFOs and seizure generation. In this work we show that a cascade of two computational models, one on detailed compartmental scale and a second one on neural mass scale can explain both the autonomous generation of HFOs and the presence of epileptic seizures as emergent properties. To this end we introduce axonal-axonal gap junctions on a microscopic level and explore their impact on the higher level neural mass model (NMM). We show that the addition of gap junctions can generate HFOs and simultaneously shift the operational point of the NMM from a steady state network into bistable behavior that can autonomously generate epileptic seizures. The epileptic properties of the system, or the probability to generate epileptic type of activity, increases gradually with the increase of the density of axonal-axonal gap junctions. We further demonstrate that ad hoc HFO detectors used in previous studies are applicable to our simulated data.


Subject(s)
Brain Waves , Computer Simulation , Epilepsy/pathology , Gap Junctions/metabolism , Models, Neurological , Nerve Net
3.
Int J Neural Syst ; 24(2): 1430004, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24475896

ABSTRACT

In this study, we investigate the correspondence between dynamic patterns of behavior in two types of computational models of neuronal activity. The first model type is the realistic neuronal model; the second model type is the phenomenological or analytical model. In the simplest model set-up of two interconnected units, we define a parameter space for both types of systems where their behavior is similar. Next we expand the analytical model to two sets of 90 fully interconnected units with some overlap, which can display multi-stable behavior. This system can be in three classes of states: (i) a class consisting of a single resting state, where all units of a set are in steady state, (ii) a class consisting of multiple preserving states, where subsets of the units of a set participate in limit cycle, and (iii) a class consisting of a single saturated state, where all units of a set are recruited in a global limit cycle. In the third and final part of the work, we demonstrate that phase synchronization of units can be detected by a single output unit.


Subject(s)
Epilepsy/physiopathology , Models, Neurological , Neurons/physiology , Algorithms , Computer Simulation , Humans , Pyramidal Cells/physiopathology , Time Factors
4.
Int J Neural Syst ; 23(1): 1250032, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23273128

ABSTRACT

We aim to derive fully autonomous seizure suppression paradigms based on reactive control of neuronal dynamics. A previously derived computational model of seizure generation describing collective degrees of freedom and featuring bistable dynamics is used. A novel technique for real-time control of epileptogenicity is introduced. The reactive control reduces practically all seizures in the model. The study indicates which parameters provide the maximal seizure reduction with minimal intervention. An adaptive scheme is proposed that optimizes the stimulation parameters in nonstationary situations.


Subject(s)
Computer Simulation , Equipment Design/methods , Equipment Design/standards , Models, Neurological , Neurons/physiology , Seizures/physiopathology , Humans , Seizures/therapy
5.
Ann Biomed Eng ; 37(7): 1263-72, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19415496

ABSTRACT

Load-bearing soft tissues predominantly consist of collagen and exhibit anisotropic, non-linear visco-elastic behavior, coupled to the organization of the collagen fibers. Mimicking native mechanical behavior forms a major goal in cardiovascular tissue engineering. Engineered tissues often lack properly organized collagen and consequently do not meet in vivo mechanical demands. To improve collagen architecture and mechanical properties, mechanical stimulation of the tissue during in vitro tissue growth is crucial. This study describes the evolution of collagen fiber orientation with culture time in engineered tissue constructs in response to mechanical loading. To achieve this, a novel technique for the quantification of collagen fiber orientation is used, based on 3D vital imaging using multiphoton microscopy combined with image analysis. The engineered tissue constructs consisted of cell-seeded biodegradable rectangular scaffolds, which were either constrained or intermittently strained in longitudinal direction. Collagen fiber orientation analyses revealed that mechanical loading induced collagen alignment. The alignment shifted from oblique at the surface of the construct towards parallel to the straining direction in deeper tissue layers. Most importantly, intermittent straining improved and accelerated the alignment of the collagen fibers, as compared to constraining the constructs. Both the method and the results are relevant to create and monitor load-bearing tissues with an organized anisotropic collagen network.


Subject(s)
Bioartificial Organs , Collagen/chemistry , Collagen/ultrastructure , Heart, Artificial , Models, Chemical , Models, Molecular , Tissue Engineering/methods , Computer Simulation , Multiprotein Complexes/chemistry , Multiprotein Complexes/ultrastructure , Protein Conformation , Stress, Mechanical
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