Literature DB >> 24387587

Modeling oscillatory dynamics in brain microcircuits as a way to help uncover neurological disease mechanisms: a proposal.

F K Skinner1, K A Ferguson1.   

Abstract

There is an undisputed need and requirement for theoretical and computational studies in Neuroscience today. Furthermore, it is clear that oscillatory dynamical output from brain networks is representative of various behavioural states, and it is becoming clear that one could consider these outputs as measures of normal and pathological brain states. Although mathematical modeling of oscillatory dynamics in the context of neurological disease exists, it is a highly challenging endeavour because of the many levels of organization in the nervous system. This challenge is coupled with the increasing knowledge of cellular specificity and network dysfunction that is associated with disease. Recently, whole hippocampus in vitro preparations from control animals have been shown to spontaneously express oscillatory activities. In addition, when using preparations derived from animal models of disease, these activities show particular alterations. These preparations present an opportunity to address challenges involved with using models to gain insight because of easier access to simultaneous cellular and network measurements, and pharmacological modulations. We propose that by developing and using models with direct links to experiment at multiple levels, which at least include cellular and microcircuit, a cycling can be set up and used to help us determine critical mechanisms underlying neurological disease. We illustrate our proposal using our previously developed inhibitory network models in the context of these whole hippocampus preparations and show the importance of having direct links at multiple levels.

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Year:  2013        PMID: 24387587     DOI: 10.1063/1.4829620

Source DB:  PubMed          Journal:  Chaos        ISSN: 1054-1500            Impact factor:   3.642


  5 in total

1.  Examining the limits of cellular adaptation bursting mechanisms in biologically-based excitatory networks of the hippocampus.

Authors:  K A Ferguson; F Njap; W Nicola; F K Skinner; S A Campbell
Journal:  J Comput Neurosci       Date:  2015-10-13       Impact factor: 1.621

2.  Introduction to focus issue: rhythms and dynamic transitions in neurological disease: modeling, computation, and experiment.

Authors:  Tasso J Kaper; Mark A Kramer; Horacio G Rotstein
Journal:  Chaos       Date:  2013-12       Impact factor: 3.642

3.  Simple, biologically-constrained CA1 pyramidal cell models using an intact, whole hippocampus context.

Authors:  Katie A Ferguson; Carey Y L Huh; Benedicte Amilhon; Sylvain Williams; Frances K Skinner
Journal:  F1000Res       Date:  2014-05-09

4.  Combining Theory, Model, and Experiment to Explain How Intrinsic Theta Rhythms Are Generated in an In Vitro Whole Hippocampus Preparation without Oscillatory Inputs.

Authors:  Katie A Ferguson; Alexandra P Chatzikalymniou; Frances K Skinner
Journal:  eNeuro       Date:  2017-08-07

5.  Inhibitory Network Bistability Explains Increased Interneuronal Activity Prior to Seizure Onset.

Authors:  Scott Rich; Homeira Moradi Chameh; Marjan Rafiee; Katie Ferguson; Frances K Skinner; Taufik A Valiante
Journal:  Front Neural Circuits       Date:  2020-01-14       Impact factor: 3.492

  5 in total

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