Table 1.
Parameters of neuron model.
Table 2.
Parameters of static and plastic network models.
Table 3.
Parameters of structural plasticity model.
Fig 1.
Transcranial magnetic stimulation (TMS) has an immediate effect on the membrane potential dynamics of single neurons.
(A) Schematic illustration of TMS in humans and neurons. The TMS-induced electric fields cause depolarization of neurons in the target region. We implemented TMS as rectangular pulse current injections with a duration of 0.5 ms (c.f., output parameters of conventional TMS devices). (B) Single stimuli produce changes in the membrane potential in a dose-dependent manner. (C) A linear relationship is evident between applied effective stimulation strength (in nA) and the resulting membrane potential deviation, as predicted by Ohm’s law (See Methods). (D) Suprathreshold stimulation at different frequencies elicits spiking responses from the stimulated neurons. Created with BioRender.com.
Table 4.
Parameters of Transcranial Magnetic Stimulation (TMS).
Fig 2.
Repetitive transcranial magnetic stimulation (rTMS) changes network activity in a static network.
(A) Illustration of the recurrent neuronal network with sparsely connected excitatory [E] and inhibitory [I] neurons used in this study. A subset of excitatory neurons [S] is stimulated. (B) rTMS influences the firing state of the stimulated neurons [S], causing them to fire in a more synchronous manner. (C) Change in the average firing rate in response to different stimulation intensities and frequencies of 10% of excitatory neurons. Four intensities (a: weak, c: peak, d: strong, and b: strong-equivalent) were selected to represent different stimulation intensities. (D) Firing rate histograms for populations E, I, and S at stimulation intensities a, b, c, and d, respectively. (E) Heatmaps summarizing the response of stimulated neurons to rTMS applied to 10% (top) and 30% (bottom) of excitatory neurons.
Fig 3.
rTMS induces structural remodeling of stimulated networks.
(A) Homeostatic structural plasticity assumes negative feedback of neuronal activity on its connectivity with other neurons: A high firing rate removes synapses between excitatory neurons, and a low firing rate promotes synapse formation. (B) Poisson input stabilizes the firing rate and connection probability prior to stimulation. (C) Effects of a 10 Hz stimulation protocol consisting of 900 pulses on the firing rate and structural remodeling [i.e., connectivity between stimulated neurons (S–S), between non-stimulated excitatory neurons (E–E), and between stimulated and non-stimulated neurons (S–E and E–S)]. (D) Effects of the same stimulation protocol on the firing rate of stimulated neurons and connectivity between stimulated neurons at the four representative amplitudes from Fig 2C [i.e., weak (a), strong-equivalent (b), peak (c), and strong (d)].
Fig 4.
rTMS intensity and pulse number affect the structural remodeling of the stimulated population (S).
(A) Interrelation between the S − S connectivity drop during stimulation (ΔCstim) and S − S connectivity increase post stimulation (ΔCpost). (B) S − S connectivity changes from different pulse numbers of 10 Hz stimulation at peak stimulation intensity (c, as defined in Fig 2C). (C) Saturation points of S − S connectivity, expressed in the form of total pulse numbers required to reach saturation, are summarized for a range of frequencies. (D) Time constants of connectivity decay (τdecay) were extracted by fitting an exponential function to connectivity drop among stimulated neurons (S–S).
Fig 5.
rTMS leads to duration and intensity dependant overstimulation for intermittent Theta Burst Stimulation (iTBS).
(A) US FDA approved iTBS protocol consists of 600 pulses distributed across ON times of 2 s and OFF times of 8 s. The ON times consist of ten bursts of stimulus pulses at 5 Hz, where each burst consists of 3 pulses occurring at 50 Hz. (B) iTBS applied at peak amplitude (c, as defined in Fig 2C) resulted in the strongest firing rate response and the largest network connectivity upshoot. (C) iTBS at increasing stimulation duration (i.e., pulse numbers) was found to cause increasing values of post-stimulation connectivity upshoot among stimulated neurons. This trend was tested for iTBS, cTBS and 10 Hz and is summarised as log-log plots in (D).