 Research article
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Theoretical analysis of effects of transcranial magnetoacoustical stimulation on neuronal spikefrequency adaptation
BMC Neuroscience volume 23, Article number: 26 (2022)
Abstract
Background
Transcranial magnetoacoustical stimulation (TMAS) is a noninvasive technique that has advantages in spatial resolution and penetration depth. It changes the firing properties of neurons through the current generated by focused ultrasound and a static magnetic field. Spikefrequency adaptation is an important dynamic characteristic of neural information processing.
Methods
To address the effects of TMAS on neural spikefrequency adaptation, this study employs some ultrasound and magnetic field parameters, such as magnetic flux density, ultrasonic intensity, fundamental ultrasonic frequency, modulation frequency, and duty cycle. Using these different ultrasound and magnetic field parameters, membrane potential curves, spikefrequency curves, and adapted onset spikefrequency curves are exhibited and analyzed.
Results
The results show that spikefrequency adaptation is strongly dependent on ultrasonic intensity and magnetic flux density and is rarely affected by other parameters. However, modulation frequency and duty cycle influence membrane potentials and spike frequencies to some degree.
Conclusions
This study reveals the mechanism of the effects of TMAS on neural spikefrequency adaptation and serves as theoretical guidance for TMAS experiments.
Background
Transcranial magnetoacoustical stimulation (TMAS) is a new brain stimulation technique that has been studied in the neuroscience field. TMAS noninvasively stimulates neurons by generating an electric current with ultrasonic waves and a static magnetic field [1,2,3,4,5]. TMAS has more advantages in spatial resolution and penetrability than transcranial direct current stimulation and repetitive transcranial magnetic stimulation, which have been used in neuropsychiatric disease therapy [6, 7]. The high spatial resolution of TMAS benefits from its small ultrasonic spot, which is approximately 2 mm in diameter [8]. Transcranial focused ultrasound stimulation (TFUS) is another noninvasive brain stimulation technique that has been demonstrated to have spatial resolution and penetration equally as good as that of TMAS [9, 10]. However, our previous studies have shown that TMAS improves the neuromodulation performance in vivo animal experiments compared with TFUS [11, 12].
Spikefrequency adaptation is a significant neurobiological phenomenon in neural information processing, in which the spike frequencies of neurons gradually decline under constant external stimulation [13,14,15]. This effect can be attributed to two common types of adaptation currents, voltagesensitive potassium currents (Mtype currents, I_{M}) and calciumsensitive afterhyperpolarization currents (AHPtype currents, I_{AHP}), which have different properties. Specifically, the Mtype ones are active even in the quiescent state, while the AHPtype ones are activated by firing activity. Both types affect the dynamics of neurons, which deserves to discuss [13, 16,17,18,19,20,21]. Previous studies examined spikefrequency adaptation. For example, Benda et al. found that fast spikefrequency adaptation can result in intensity invariance of neural responses [16]. They further studied cases in which spikefrequency adaptation is suitable to be modeled as an adaptation current or a dynamic firing threshold, respectively [17]. Yi et al. concluded that the dynamic characteristics of neurons in electrical fields can be determined by neuronal morphology and neuronal adaptability [18]. Ha et al. investigated the influence of the Ca\(^{2+}\)activated chloride channel anoctamin2 on spikefrequency adaptation in thalamocortical and central nervous system neurons [19, 20]. Barraca et al. studied the influence of spikefrequency adaptation on the dynamics of a balanced network of neuronal models [13]. Chang et al. investigated the effects of external electric fields at extremely low frequencies on the adaptability of neurons in the Ermentrout model [21]. However, the influences of TMAS on the spikefrequency adaptation of neurons are still unknown. Thus, we applied TMAS to the Ermentrout model to analyze the effects of TMAS on neuronal spikefrequency adaptation.
The Ermentrout model is a typical neuron model that can be considered as a reduced onecompartment counterpart of the Traub–Miles model [22]. Both Mtype current and AHPcurrent were introduced to the Ermentrout model during the neuronal spikefrequency adaptation simulations [17, 23, 24]. The membrane potentials of sensory neurons can be changed by external physical stimulation [16, 17]. Thus, when the Ermentrout model is stimulated by focused ultrasound waves in a static magnetic field, a stimulus current is added to the neuronal model, and a spike is emitted when the membrane potentials exceed the threshold. A spikefrequency curve is generated by assigning the inverse interspike interval from the membrane potential curve for each spike [25,26,27,28].
In our study, we extend the Ermentrout model by adding the electric current induced by TMAS to the membrane balance equation. We adopt an additional adaptation Mtype current to study the firing characteristics and analyze the membrane potential curves as well as the spikefrequency curves as we vary the ultrasound and magnetic field parameters, such as magnetic flux density, ultrasonic intensity, fundamental ultrasonic frequency, modulation frequency, and duty cycles. We also discuss the changes in adapted onset spikefrequency curves under magnetoacoustical parameters based on different initial values of adaptation variables. We investigate the characteristics of spikefrequency adaptation for the Ermentrout neuron under TMAS through computational simulation and provide some discussion.
Methods
TMAS principle
A schematic showing the principle of TMAS is presented in Fig. 1a. In TMAS, a lowintensity focused ultrasound beam can drive the charged ions in tissue fluid. Combined with the static magnetic field, Lorentz forces in opposite directions generated on positive and negative charges. The moving charged ions forced by the Lorentz force form an electric current, \(I_{ext}\), which is perpendicular to the direction of the static magnetic field and the ultrasound wave. In this study, we establish the Cartesian coordinate axes, in which ultrasound waves longitudinally propagate along the zaxis, the static magnetic field and the created current density are in the xaxis and the yaxis respectively. The relationship between the electric current density, \(J_{y}\), and the ultrasound and magnetic parameters can be expressed as follows [29, 30]:
where \(\sigma \) is the tissue conductivity, \(B_{x}\) is the magnetic flux density, \(\Gamma \) is the ultrasound intensity, \(\rho \) is the tissue density, \(c_{0}\) is the ultrasound speed, and \(f_{u}\) is the fundamental ultrasonic frequency. This electric current density, \(J_{y}\), can be represented as the external input current \(I_{ext}\) of the Ermentrout neuron under TMAS.
In the simulation, to generate a sodium current and action potentials through stimulation, the fundamental ultrasound wave must be a sine wave with a DC offset [12]. The ultrasonic intensity influence the current density in nerve tissue. In the literature, both continuous and modulated ultrasonic waves are applied to stimulate the motor cortex, and both can safely and repeatedly evoke local field potentials [8]. Thus, we used pulsed ultrasound waves modulated by a square wave and continuous waves in our computational study. These waves obey the following equation:
where RF and DC are the modulation frequency and the duty cycle, respectively. Thus, the stimulus current, \(I_{ext}\), generated by TMAS can be expressed as follows:
The fixed parameters of this mathematical expression are listed in Table 1 [12].
The Ermentrout model
The Ermentrout model is advantageous for describing voltage and current changes in the neuronal membrane. A circuit diagram of the Ermentrout model with external current, \(I_{ext}\), is exhibited in Fig. 1b. The expression of the membrane potential can be described as follows [22]:
where \(C_{m}\) is the membrane capacity, \(I_{ext}\) is the input stimulus current in tissue fluid, and V is the transmembrane voltage component generated by \(I_{ext}\). The voltagegated currents \(I_{Na}\), \(I_{K}\), and \(I_{Ca}\) are given by the following equations:
where \(g_{Na}\) and \(E_{Na}\) are the maximum conductance and the reversal potentials of sodium channels, respectively. Similarly, \(g_{K}\), \(E_{K}\), and \(g_{Ca}\), \(E_{Ca}\) represent the same parameters for the potassium and calcium channels, respectively. The kinetics of the gating variables \(x\in m,n,h\) are given by
The leak current can be expressed as follows:
where \(g_{L}\) and \(E_{L}\) represent the maximum conductance and the reversal potential of the chlorine channel, respectively.
The Mtype current is a kind of depolarizationactivated and hyperpolarizing potassium current that decays with the activation of muscarinic acetylcholine receptors. It obeys the following expression:
where \(g_M\) is the maximum conductance, and w is the gating variable.
The AHPtype current is activated by the influx of calcium that results from firing and can be expressed as
where \([Ca^{2+}]\) is the intracellular calcium concentration.
The kinetics of the Mtype current w can be expressed as follows:
where \(\tau \) is the time constant. The kinetics of \([Ca^{2+}]\) are:
The Ermentrout model is a reduced onecompartment counterpart of the Traub–Miles model. We introduce both Mtype currents and AHPtype currents to establish the modified Ermentrout model for adaptation. However, when we simulated the neuronal spikefrequency adaptation, either an Mtype current or an AHPcurrent was considered. In our simulation, we take the Mtype current model as an example. Therefore, we set \(I_{AHP}\) of the Ermentrout model constant in this paper. The fixed parameters used for the Ermentrout model in this study are listed in Table 2 [25].
The simulation was performed with MATLAB Simulink software (2018, MathWorks, USA). The main code used for the simulation has been deposited in a publicly available repository. It will be freely available to any scientist wishing to use them for noncommercial purposes.
Adaptation of the Ermentrout model
Adaptation is a significant phenomenon of neurons in neural signal processing. The membrane potentials of sensory neurons can be changed by external physical stimulation. Therefore, we pay close attention to the membrane potential curve of the adaptive model under TMAS. A spike occurs whenever the membrane potential exceeds its upper threshold. We can obtain spikefrequency by assigning each time the inverse interspike interval that contains this time. Both the membrane potential curves and spike frequency curves exhibit the adaptation processes. In the spikefrequency curve, two frequencies need special attention. One is the initial spikefrequency, \(f_{0}\), which denotes the inverse of the first interspike interval in the membrane potential curve; the other is the steadystate spikefrequency, \(f_{\infty }\), which represents the stable spikefrequency after an extended period. In addition, the time from the initial to steadystate spikefrequency, which is the settling time, is of interest for spikefrequency adaptation.
Other adaptive characteristics of neurons can be well captured by the onset spikefrequency curve. The onset spikefrequency curve, \(f_{0}\left( X\right) \), is obtained by mapping the corresponding initial firing frequency \(f_{0}\) to each input parameter X. Besides, to reveal the onset responses of neurons to stimulus intensity changes, we build the adapted onset spikefrequency curve, \(f_{0}\left( X, A_{0}\right) \), which consists of different onset spikefrequency curves under different initial stimulus inputs \(A_{0}\). The adapted curves indicate how the neuron being in a stable and fixed adaptation state will initially respond to new stimuli. While each neuron has exactly one onset and one steadystate spikefrequency curve, it has for each adaptation varaible a different adapted spikefrequency curve.
Results
Membrane potential curves and spikefrequency curves under different TMAS input parameters
To investigate the effects of different TMAS input signals on the spikefrequency adaptation, we discuss the membrane potential curves and the spikefrequency curves under different TMAS input parameters. As described in the section of methods, five variable parameters (\(B_x\), \(\Gamma \), \(f_{u}\), RF, and DC) of the modulated TMAS influence the spike frequency. To obtain the specific conclusions, we designate one as an adjustable parameter and fix the values of the others as follows: \(B_{x}=2\) T, \(\Gamma =3\) W/cm\(^{2}\), \(f_{u}=500\) kHz, \(RF=1\) Hz and \(DC=50\%\). Then, we discuss the characteristics of the membrane potential curves and the spikefrequency curves for different TMAS parameters.

i.
To investigate the influence of TMAS on the neural spike frequency, the membrane potential is simulated based on the Ermentrout model using a range of magnetic flux densities from 0.5 to 8 T. The other TMAS input parameters are set to fixed values. Figure 2a–c show the plots of membrane potentials for magnetic flux densities of 0.5 T, 1 T, and 2 T, respectively. One can see that the spikefrequency ultimately settles into a steady state after a long period in which the intervals tend to be the same value. As shown in Fig. 2d, as \(B_x\) increases, the spikefrequency curve shifts rightward and vertically toward those with a higher magnetic flux density, which means that the initial spikefrequency increases, and undergoes a longer transient process to attain the higher steadystate spikefrequency. In addition, the onset and steadystate spike frequencies of neurons, as well as the settling time, can be obtained through quantitative calculation, as shown in Table 3. We can conclude that as the magnetic flux density increases, both the onset and steadystate spike frequencies increase, and the transient process before the steady state requires more time.

ii
To evaluate the influence of ultrasonic intensity on the neural spikefrequency adaptation under TMAS, different ultrasonic intensities from 0.2 to 4 W/cm^{2} were deployed in this simulation, while the other parameters are fixed values. The membrane potential curves corresponding to ultrasonic intensities of 0.5 W/cm^{2}, 1 W/cm^{2}, and 3 W/cm^{2} are shown in Fig. 3a–c. Similar to the results exhibited in Fig. 2, the spikefrequency decays with time and ultimately enters to a steady state. We also computed the spike frequencies, and the results are shown in Fig. 3d. We find that the spikefrequency curve shifts rightward and horizontally as the ultrasound intensity increases, which means that as ultrasonic intensity increases, the onset spikefrequency \(f_{0}\) and the steadystate spikefrequency \(f_{\infty }\) increase, and the settling time becomes longer. The detailed data are shown in Table 4.

iii.
Next, we analyze the neural spikefrequency adaptation under TMAS with various fundamental ultrasonic frequencies from 200 to 700 kHz. The other parameters are fixed to preset values. Figure 4a–c show the membrane potential curves corresponding to the ultrasound fundamental frequencies of 300 kHz, 400 kHz, and 600 kHz, respectively. No significant change occurs in the membrane potential of the adaptive model as the fundamental ultrasonic frequency increases. The quantitative calculation of the spikefrequency curves in Fig. 4d shows that the onset spikefrequency is always 353.4 Hz, and it reaches a steadystate value of 122.8 Hz after 218 ms under different fundamental ultrasonic frequencies. These results show that the fundamental ultrasonic frequency has no influence on the spikefrequency adaptation.

iv
Because the stimulus current \(I_{ext}\) is generated by the modulated TMAS, the modulation frequency RF and the duty cycle DC have nonnegligible influences on the spike frequency. Different modulation frequencies from 1 to 100 Hz are deployed to the Ermentrout model to reveal the neuronal spikefrequency adaptation under the modulated TMAS. The values of duty cycles, ultrasonic intensity, magnetic flux density, and fundamental ultrasonic frequency are preset and fixed. The membrane potential curves corresponding to modulation frequencies of 20 Hz, 50 Hz, 80 Hz, and 100 Hz are shown in Fig. 5a–d, respectively. The spike frequencies settling time of neurons can be obtained through quantitative calculation, as shown in Table 5. Clearly, the interspike interval decreases as the modulation frequency RF increases. From Fig. 5e, f, we can see that the spikefrequency curves under different modulation frequencies have the same initial spikefrequency, and reach higher steady values more quickly with increasing modulation frequencies. However, when the modulation frequencies are too small, the spike frequency in both the transient and steady states fluctuates with time. In addition, the frequency of the spikefrequency curve increases as the modulation frequency increases, while the amplitude decreases.

V.
We also investigate the neuronal spikefrequency adaptation under TMAS using various duty cycles, from \(10\) to \(95\%\). We set the modulation frequency, ultrasonic intensity, magnetic flux density, and fundamental ultrasonic frequency using the fixed values mentioned above. The membrane potential curves with duty cycles of \(30\%\), \(50\%\), \(70\%\), and \(90\%\) are shown in Fig. 6a–d. The detailed spike frequencies and settling time with different duty cycles are shown in Table 6. The results indicate that a gap between a cluster decreases as the duty cycle increases. The membrane potentials produce bursting activities with the same initial spike frequency, but the spike frequency within each cluster decreases with both increasing time and increasing duty cycle, as shown in Fig. 6e, f.
Adapted spikefrequency curves with various initial stimulus inputs
Adapted spikefrequency curves \(f_{0}\left( X, A_{0}\right) \) represent the onset response of the neuron to input changes. They can be obtained by taking the different values of \(A_{0}\), which represent the initial value of stimulus input. Figure 7a–e shows the adapted spikefrequency curves changing with the magnetic flux density, ultrasonic intensity, fundamental ultrasonic frequency, modulation frequency, and duty cycle, respectively. In these figures, the initial values of the stimulus input \(A_{0}\) were equal to 0 mA, 3 mA, 6 mA, or 9 mA, respectively. Each adapting stimulus \(A_{0}\) results in one adapted spikefrequency curve \(f_{0}\left( X, A_{0}\right) \). Adapted spikefrequency curves indicate how the neuron being in a stable adaptation state will initially respond to new stimuli. All the curves together characterize the spikefrequency response of an adapting neuron.
The adapted spikefrequency curves under different magnetic flux densities and ultrasonic intensity are shown in Fig. 7a, b. When magnetic flux density varies from 0.5 to 4 T, and ultrasonic intensity varies from 0.2 to 2 W/cm^{2}, the adapted spikefrequency curves have the same form, and the spikefrequency intervals distribute uniformly, which means the neuron has strong adaptation. However, as these two input parameters further increase, the adapted spikefrequency curves, \(f_{0}\left( B_{x}, A_{0}\right) \) and \(f_{0}\left( \Gamma , A_{0}\right) \), do not match the onset ones (\(A_{0}\) = 0). We can conclude that the neuron has weak adaptation.
Other adapted spikefrequency curves under changing fundamental ultrasonic frequency, modulation frequency, and duty cycle are presented in Fig. 7c–e. We can observe that the initial spike frequencies do not change as the adaptation variables vary, whereas these onset spike frequencies decrease as the initial stimulation input increase. We can conclude that the fundamental ultrasonic frequency, modulation frequency, and duty cycle have no significant influence on the spikefrequency adaptation.
Discussions
Based on the simulation results in the section of results, we analyzed the influence of different TMAS parameters on the adaptation process of the Ermentrout neuron. The conclusions demonstrate that both the initial and steadystate spike frequencies of the neuron increase with the increase of magnetic flux density or ultrasonic intensity of TMAS. According to the physiological mechanism of TMAS, the amplitude of the stimulus input increases as the magnetic flux density and ultrasound intensity increase, thus shortening the time required for membrane potential to reach the threshold. Therefore, both the initial spike frequency and the steadystate spike frequency of the neuron increase. The fundamental ultrasonic frequency of TMAS is in kilohertz level. Such a highfrequency transformation of the input intensity has little influence on the current in the tissue fluid of a neuron. Therefore, changes in the fundamental ultrasonic frequency of TMAS do not affect the neural spike frequency. Besides, we used a square wave to modulate the sinusoidal ultrasonic wave with offset in our simulation. Changes in the modulation frequency and duty cycle alter the current waveform of TMAS and then affect the frequency of the stimulus input acted on neurons. Therefore, changes in the modulation frequency and duty cycle lead to changes in the firing mode and the firing rhythm of the neurons.
We analyze the influence of different TMAS parameters on the spikefrequency adaptation of the Ermentrout neuron based on the adapted spikefrequency curves with various initial stimulus inputs in the section of results. The results show that the fundamental ultrasonic frequency, modulation frequency, and duty cycle do not affect the neural spikefrequency adaptation. The adaptation state usually alters with the slowly changing stimulus input and is subtracted from the stimulus input, so that the average value of the stimulus input changes. As a result, only rapidly fluctuating stimulus signals can be transmitted. In other words, the higher the alternating frequency, the strong adaptation the neuron exhibits. TMAS used highfrequency ultrasound to act on neurons. Therefore, there is no effect on the neural spike frequency adaptation of the fundamental ultrasonic frequency, modulation frequency, or duty cycle. However, the increase of magnetic flux density and ultrasonic intensity directly causes the enhancement of the stimulus strength, and the adaptation current strongly fluctuates between spikes. Therefore, the stronger the TMAS input, the worse the adaptation exhibits. According to Kirchhoff’s current theorem, the dynamic equation of membrane potential is derived from the vector sum of ionic currents. Therefore, with the increase of adaptation current, the onset spike frequency of neurons decreased.
Adaptation, which represents not only the current state of adaptation but also the process of dynamic change, plays a significant role in neural information processing. In particular, a variety of firing currents lead to spikefrequency adaptation and can explain many phenomena, such as weak stimulation and enhanced rapid response to stimulation. Therefore, the adaptation current can be combined with TMAS and neurons to study the influence of TMAS on the adaptability of the neural network. This knowledge can help in exploring how TMAS regulates the biological nervous system.
Conclusions
In this paper, we investigated how TMAS influences neuronal spikefrequency adaptation by exploring different ultrasonic and magnetic field parameters, and furthermore, how it affects neural information transmission. Based on a numerical analysis, the magnetic flux density and ultrasonic intensity are found to be the determining parameters of spikefrequency adaptation. In addition, while the different modulation frequencies and duty cycles may lead to different membrane potentials and spike frequencies, they have no influence on spikefrequency adaptation. Based on the numerical analysis of neuron model, this paper explores the adaptation of neurons to the TMAS input and the effect of the stimulus current on the discharge activity of biological nervous system. These results enrich the theoretical basis of TMAS as a potential clinical treatment of nervous system diseases.
Availability of data and materials
All data generated or analyzed during this study are included in this published article. The main simulation code that support the findings of this study are available in ’Github’ with the identifier [https://zenodo.org/badge/latestdoi/428488703].
Abbreviations
 TMAS:

Transcranial magnetoacoustical stimulation
 TFUS:

Transcranial focused ultrasound stimulation
 Mtype currents:

Voltagesensitive potassium currents
 AHPtype currents:

Calciumsensitive afterhyperpolarization currents
References
Yuan Y, Chen Y, Li X. A new brain stimulation method: noninvasive transcranial magnetoacoustical stimulation. Chin Phys B. 2016;25(8):084301.
Wang Y, Feng L, Liu S, Zhou X, Yin T, Liu Z, Yang Z. Transcranial magnetoacoustic stimulation improves neuroplasticity in hippocampus of Parkinson’s disease model mice. Neurotherapeutics. 2019;16(4):1210–24.
Liu D, Zhao S, Luo X, Yuan Y. Synchronization for fractionalorder extended hindmarshrose neuronal models with magnetoacoustical stimulation input. Chaos Solitons Fractals. 2021;144(18):110635.
Liu D, Zhao S, Yuan Y, Luo X. Dynamic analysis of the extended hindmarshrose neuron model under transcranial magnetoacoustical stimulation. In: 2020 39th Chinese control conference (CCC). 2020.
Liu D, Zhao S, Luo X. Adaptive fuzzy control for the generalized projective synchronization of fractionalorder extended HindmarshRose neurons. IEEE Access. 2020;8:190689–99.
Halsey G, Wu Y, Guo L. Transcranial magnetic stimulation. In: Neural interface engineering. Cham: Springer; 2020. pp. 49–65.
Guillouët E, Cogné M, Saverot E, Roche N. Impact of combined transcranial direct current stimulation and speechlanguage therapy on spontaneous speech in aphasia: a randomized controlled doubleblind study. J Int Neuropsychol Soc. 2020;26(1):7–18.
Tufail Y, Matyushov A, Baldwin N, Tauchmann ML, Georges J, Yoshihiro A, HelmsTillery SI, Tyler WJ. Transcranial pulsed ultrasound stimulates intact brain circuits. Neuron. 2010;66(5):681–94.
Zhang D, Li H, Sun J, Hu W, Jin W, Li S, Tong S. Antidepressantlike effect of lowintensity transcranial ultrasound stimulation. IEEE Trans Biomed Eng. 2018;66(2):411–20.
Lee W, Kim HC, Jung Y, Chung YA, Song IU, Lee JH, Yoo SS. Transcranial focused ultrasound stimulation of human primary visual cortex. Sci Rep. 2016;6(1):34026.
Yuan Y, Chen Y, Li X. Noninvasive transcranial focused ultrasonicmagnetic stimulation for modulating brain oscillatory activity. Eur Phys J Appl Phys. 2016;73(2):21201.
Yuan Y, Chen Y, Li X. Theoretical analysis of transcranial magnetoacoustical stimulation with HodgkinHuxley neuron model. Front Comput Neurosci. 2016;10:35.
Barranca VJ, Huang H, Li S. The impact of spikefrequency adaptation on balanced network dynamics. Cogn Neurodyn. 2019;13(1):105–20.
Park Y, Ermentrout GB. Scalar reduction of a neural field model with spike frequency adaptation. Siam J Appl Dyn Syst. 2018;17(1):1–60.
Roach JP, Sander LM, Zochowski MR. Memory recall and spikefrequency adaptation. Phys Rev E. 2016;93(5):052307.
Benda J, Maler L, Longtin A. Linear versus nonlinear signal transmission in neuron models with adaptation currents or dynamic thresholds. J Neurophysiol. 2010;104(5):2806–20.
Benda J, Hennig RM. Spikefrequency adaptation generates intensity invariance in a primary auditory interneuron. J Comput Neurosci. 2008;24(2):113–36.
Yi G, Wang J, Tsang KM, Wei X, Deng B, Han C. Spikefrequency adaptation of a twocompartment neuron modulated by extracellular electric fields. Biol Cybern. 2015;109(3):287–306.
Ha GE, Lee J, Kwak H, Song K, Kwon J, Jung SY, Hong J, Chang GE, Hwang EM, Shin HS, Lee CJ, Cheong E. The Ca\(^{2+}\)activated chloride channel anoctamin2 mediates spikefrequency adaptation and regulates sensory transmission in thalamocortical neurons. Nat Commun. 2016;7:13791.
Ha GE, Cheong E. Spike frequency adaptation in neurons of the central nervous system. Exp Neurobiol. 2017;26(4):179–85.
Chang L, Wang J, Deng B, Wei X, Li H. The effect of extreme low frequency external electric field on the adaptability in the Ermentrout model. Neurocomputing. 2012;81(1):67–74.
Ermentrout B. Linearization of \(f\)I curves by adaptation. Neural Comput. 1998;10(7):1721–9.
Benda J, Longtin A, Maler L. Spikefrequency adaptation separates transient communication signals from background oscillations. J Neurosci. 2005;25(9):2312–21.
Prescott SA, Sejnowski TJ. Spikerate coding and spiketime coding are affected oppositely by different adaptation mechanisms. J Neurosci. 2008;28(50):13649–61.
Ermentrout B, Pascal M, Gutkin B. The effects of spike frequency adaptation and negative feedback on the synchronization of neural oscillators. Neural Comput. 2001;13(6):1285–310.
Benda J, Herz AVM. A universal model for spikefrequency adaptation. Neural Comput. 2005;25(9):2312–21.
Gigante G, Del GP, Mattia M. Frequencydependent response properties of adapting spiking neurons. Math Biosci. 2007;207(2):336–51.
Benda J, Tabak J. Spikefrequency adaptation. Encycl Comput Neurosci. 2014;15(11):1–12.
Norton SJ. Can ultrasound be used to stimulate nerve tissue? Biomed Eng Online. 2003;2(1):6.
Liu D, Zhao S, Luo X, Yuan Y. Unidirectional synchronization of hodgkinhuxley neurons with prescribed performance under transcranial magnetoacoustical simulation. Front Neurosci. 2019;13:1061.
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This work was supported in part by the National Natural Science Foundation of China (61873228), Technology and People’s Livelihood Project of Key Research and Development Program of Hebei Province (20377789D), and Key Science and Technology Research Project of Hebei Provincial Health Commission (20210446).
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SZ, DL, and YY contributed to the conception and design of the study. SZ, DL, ML, and XL acquired the data and performed the data analysis. SZ, DL, ML, XL, and YY interpreted the results. SZ and DL drafted the manuscript. SZ, DL, and ML edited and revised the manuscript. All authors read and approved the final manuscript.
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Zhao, S., Liu, D., Liu, M. et al. Theoretical analysis of effects of transcranial magnetoacoustical stimulation on neuronal spikefrequency adaptation. BMC Neurosci 23, 26 (2022). https://0doiorg.brum.beds.ac.uk/10.1186/s12868022007099
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DOI: https://0doiorg.brum.beds.ac.uk/10.1186/s12868022007099
Keywords
 Spikefrequency adaptation
 TMAS
 Ermentrout model