Literature DB >> 35401870

Modeling plasticity during epileptogenesis by long short term memory neural networks.

Marzieh Shahpari1, Morteza Hajji2, Javad Mirnajafi-Zadeh3, Peyman Setoodeh2.   

Abstract

Understanding the pathogenesis of epilepsy including changes in synaptic pathways can improve our knowledge about epilepsy and development of new treatments. In this regard, data-driven models such as artificial neural networks, which are able to capture the effects of synaptic plasticity, can play an important role. This paper proposes long short term memory (LSTM) as the ideal architecture for modeling plasticity changes, and validates this proposal via experimental data. As a special class of recurrent neural networks (RNNs), LSTM is able to track information through time and control its flow via several gating mechanisms, which allow for maintaining the relevant and forgetting the irrelevant information. In our experiments, potentiation and depotentiation of motor circuit and perforant pathway as two forms of plasticity were respectively induced by kindled and kindled + transcranial magnetic stimulation of animal groups. In kindling, both procedure duration and gradual synaptic changes play critical roles. The stimulation of both groups continued for six days. Both after-discharge (AD) and seizure behavior as two biologically measurable effects of plasticity were recorded immediately post each stimulation. Three classes of artificial neural networks-LSTM, RNN, and feedforward neural network (FFNN)-were trained to predict AD and seizure behavior as indicators of plasticity during these six days. Results obtained from the collected data confirm the superiority of LSTM. For seizure behavior, the prediction accuracies achieved by these three models were 0.91 ± 0.01, 0.77 ± 0.02, and 0.59 ± 0.02%, respectively, and for AD, the prediction accuracies were 0.82 ± 0.01, 0.74 ± 0.08 and 0.42 ± 0.1, respectively.
© The Author(s), under exclusive licence to Springer Nature B.V. 2021.

Entities:  

Keywords:  Deep learning; Epilepsy model; Kindling; LSTM

Year:  2021        PMID: 35401870      PMCID: PMC8934824          DOI: 10.1007/s11571-021-09698-7

Source DB:  PubMed          Journal:  Cogn Neurodyn        ISSN: 1871-4080            Impact factor:   5.082


  48 in total

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7.  The Pilocarpine Model of Temporal Lobe Epilepsy and EEG Monitoring Using Radiotelemetry System in Mice.

Authors:  Ji-Eun Kim; Kyung-Ok Cho
Journal:  J Vis Exp       Date:  2018-02-27       Impact factor: 1.355

Review 8.  Kindling and status epilepticus models of epilepsy: rewiring the brain.

Authors:  Kiyoshi Morimoto; Margaret Fahnestock; Ronald J Racine
Journal:  Prog Neurobiol       Date:  2004-05       Impact factor: 11.685

Review 9.  Local Field Potentials: Myths and Misunderstandings.

Authors:  Oscar Herreras
Journal:  Front Neural Circuits       Date:  2016-12-15       Impact factor: 3.492

Review 10.  Deep Learning With Spiking Neurons: Opportunities and Challenges.

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Journal:  Front Neurosci       Date:  2018-10-25       Impact factor: 4.677

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