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Intrinsic Network Properties Govern the Network Response to Repetitive Transcranial Magnetic Stimulation (rTMS) in a Neuronal Network Model Simulating the Effects of rTMS

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P64. Intrinsic network properties govern the network response to repetitive transcranial magnetic stimulation (rTMS) in a neuronal network model simulating the effects of rTMS—A. Bey, C.

Wienbruch (Universität Konstanz, Konstanz, Germany)

Since the underlying principles of the complex neuronal interac tion in the brain are still far from being understood, network models are widely used to simulate neural activity. Classic neural network models based on binary neurons have limited dynamics and are not suitable to explain the highly chaotic behavior observed in

Fig. 1.

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Konstanzer Online-Publikations-System (KOPS)

URL: http://nbn-resolving.de/urn:nbn:de:bsz:352-0-290032

Erschienen in: Clinical Neurophysiology ; 126 (2015), 8. - S. e125-e126

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measurement data. Yet, by adding the capability of summating the synaptic input over time, they offer chaotic dynamics in combination with computational efficiency (Bressloff, 1992). Models of spiking neurons consider the number of spikes and their timing and range from detailed biophysical representations of neuronal activity (Hodgkin and Huxley, 1952) based on differential equations (Izhikevich, 2003) to Integrate and Fire (IF) models. These networks exhibit rich dynamical properties(Brunel, 2000) and account for results in the field of neuroscience.

In spite of the vast number of models, there is still a gap between the theoretical findings and their mapping to neuropsychiatric and neurological disorders which are often characterized by an impaired resting state activity due to an altered connectivity. There is a need for models that account for the relation between local synaptic orga nization and transitions from normal to impaired neural activity.

In order to investigate the responsiveness of the resting state activity to external influences, such as medication or repetitive tran scranial magnetic stimulation (rTMS), we use a time summating binary network model for simulating the effect of synaptic layout and external influences, i.e. rTMS stimulation, on network activity with the following results:

(I) We observe two types of dynamics: a chaotic activity, and a seizure like periodic activity (Radhakrishnan and Gangadhar, 1998) with large groups of neurons alternately firing together (Fig. 1). (II) A perturbation can convert periodic into chaotic activity or vice versa depending on the synaptic layout. (III) We define a lower and upper parameter regime of the synaptic layout for which the chaotic activ ity is altered by perturbation but not zero or periodic. (IV) We calcu late the mean band power of the EEG frequency bands using the network output and state a rising band power in the alpha and gamma band after perturbation in the lower regime, whereas in the upper regime, the band power is stable (see Fig. 2).

In combination with our previous findings (Bey et al., 2012) it is further substantiated that the synaptic connectivity not only forms and maintains resting state activity but also affects the influence of rTMS application on resting state activity.

References

Bey A, Leue S, Wienbruch C. A neuronal network model for simulating the effects of repetitive transcranial magnetic stimulation on local field potential power spectra. PLoS ONE 2012;7:e49097.

Bressloff P. Complex dynamics of a discrete time model of a neuron. In: Taylor JG, Caianiello ER, Cotterill RMJ, Clark JW, editors. Neural network dynamics. London: Springer; 1992. p. 103–21.

Brunel N. Dynamics of sparsely connected networks of excitatory and inhibitory spiking neurons. J Comput Neurosci 2000;8:183–208.

Hodgkin AL, Huxley AF. A quantitative description of membrane current and its application to conduction and excitation in nerve. J Physiol 1952;117:500–44.

Izhikevich EM. Simple model of spiking neurons. IEEE 2003;4:1569–72.

Radhakrishnan N, Gangadhar BN. Estimating regularity in epileptic seizure time-series data. IEEE Eng Med Biol 1998:89–94.

Fig. 2.

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