What is Transcranial Magnetic Stimulation?Faraday was the first to discover the principle of mutual induction in 1831 and in his law, quantified the conversion of electrical energy into magnetic fields and vice versa. Magnetic stimulation was first used toward the end of the 19th century in experiments conducted by d’Arsonval (1896), the inventor of the galvanometer.

Given the technical limitations of the day, d’Arsonval could only stimulate his subject’s retinas, eliciting a phenomenon known as magneto phosphenes, which is characterized by the experience of seeing light, when in fact, light had not penetrated the eye.

It was not for over half a century from the pioneering works of d’Arsonval that the magnetic method was applied to neuromuscular stimulation. In 1965, Bickford and Fremming used an underpowered 500 Hz sinusoidal magnetic field in order to demonstrate muscular stimulation both in animals as well as in humans. This was subsequently replicated by Öberg (1973).

Polson et al. in 1982 were the first to successfully stimulate superficial nerves via magnetic fields. However, it was not until the end of the 20th century that a device, the first TMS device, capable of producing cortical depolarization via magnetic stimulation, was created (Barker, Jalinous, & Freeston, 1985) and subsequently used for clinical experimentation, mainly by neurologists, for mapping of the human cortex.

The first reported use of TMS on psychiatric patients in an open study was in 1993 by Hofflich et al. (Hofflich, Kasper, Hufnagel, Ruhrmann, & Moller, 1993), whose case report involving two treatment-resistant patients, reported modest antidepressant effect (Burt, Lisanby, & Sackeim, 2002). However, the early studies of the use of TMS in the treatment of depression were limited by a number of factors. Primarily among these was the low-frequency stimulation that was employed and imprecise coil placement, as scientific knowledge to the importance of prefrontal coil placement was lacking.

Transcranial magnetic stimulation can take the form of single-pulse, paired-pulse or repetitive TMS (Rossi, et. al, 2009). Each application has different uses, from the mapping of motor cortical outputs and studying of brain-behavior relationship (single pulse) to the study of corticocortical interactions (paired pulse). Repetitive pulses delivered in ‘trains’ is known as rTMS, a term which has now been universally accepted as replacing earlier terms such as rapid-rate TMS or rapid TMS and refers to single TMS pulses which are regularly applied.

In a further sub-classification, the frequency of the pulses is used to differentiate between ‘fast’ or ‘high’ frequency rTMS (rates of more than 1 Hz) and ‘slow’ or ‘low’ frequency rTMS (rates of less than 1 Hz). This differentiation has been defined secondary to criteria, including varying physiological effects and degrees of related risk.

A further subdivision known as patterned rTMS refers to short rTMS which is applied “in bursts at a high inner frequency interleaved by short pauses of no stimulation,” in protocols known as continuous (cTBS) or intermittent (iTBS) theta-burst transcranial magnetic stimulation. However, the technical protocols go beyond the scope of this work.

Basic Principles of TMS

TMS uses the principle of inductance in order for electrical energy to cross the scalp and skull in order to do avoid the pain of direct percutaneous electrical stimulation (Wassermann E. , 1998):

The process involves placing a small coil of wire on the scalp and passing a powerful and rapidly changing current through it. This produces a magnetic field that passes unimpeded and relatively painlessly through the tissues of the head. The peak strength of the magnetic field is related to the magnitude of the current and the number of turns of wire in the coil. The magnetic field, in turn, induces a much weaker electrical current in the brain. The strength of the induced current is a function of the rate of change of the magnetic field, which is determined by the rate of change of the current in the coil. In order to produce enough current to excite neurons in the brain, the current passed through the coil must change within a few hundred microseconds. (Wassermann, 1998 page 2)

The power of the stimulators and coils is measured in Tesla which is the International System of Units of magnetic-field strength or magnetic-flux density, commonly denoted as T, defined in 1960 in honor of the inventor of the Tesla Coil, Nikola Tesla. Modern devices develop 1.5 – 4 tesla (T) measured at the coil’s surface with studies showing that cortical neurons are activated beneath the scalp to a depth of 1.5 – 2 cm. (Epstein, Schwartzenberg, Davey, & Sudderth, 1990; Rudiak & Marg, 1994), which effectively means that TMS with contemporary equipment does not appear to penetrate deeper than the cortex.

Despite this, it has been shown that TMS has an effect on cells trans-synaptically beyond the site of stimulation, as evidenced by positron emission tomography studies, which show effects on distant cortical and subcortical sites (Kimbrell, Dunn, & Wassermann, 1997; Wassermann, et al., 1997).

As previously mentioned, TMS involves the administration on the scalp (in the primary motor cortex area) of a short (~ 200 ms) and powerful (0.2 to 4.0 Tesla) magnetic pulse through a coil, equal to 110-120 percent of the resting motor threshold (RMT), resulting in progressive increases in the amplitude of motor evoked potentials (MEPs) and duration of the cortical silent period (CSP) (Pascual-Leone, Valls-Sole, Wassermann, & Hallett, 1994; Berardelli, 1998).

The magnetic pulse induces an electric current below the coil, over the cortical surface. This causes depolarization of cell membranes as well as trans-synaptic depolarization of cortical neurons (Barker, Jalinous, & Freeston, 1985; Barker, Freeston, Jalinous, & Jarratt, 1987). Originally, TMS was used in the field of clinical neurophysiology, for the functional evaluation of the cortico-spinal tract (Pellicciari, 2009; Barker, Freeston, Jalinous, & Jarratt, 1987). The procedure initially involved the administration of a single magnetic pulse, but by the mid-1990s, technological advances allowed for the development of machines capable of delivering streams of repetitive magnetic pulses in rapid succession, with a frequency that could reach 100 Hz.

This type of stimulation was called repetitive TMS (rTMS) and it was shown to be superior in its cortical interaction compared to single-pulse TMS.

Furthermore, rTMS can be applied at low or high frequency and, depending on the mode of application, may have different effects on cortical activity (Speer, Kimbrell, Wassermann, & Repella, 2000). The cutoff between high and low frequency is established empirically, on the basis of converging evidence indicating that rTMS at less than 1 Hz reduces cortical excitability both locally as well as in functionally related areas, while rTMS given at a frequency above 5 Hz, seems to have the opposite effect (Veniero, Brignani, Thut, & Minussi, 2011).

Therefore, it would seem that the modulation of neural excitability induced by rTMS, is transient, with a resulting effect that largely depends on the frequency of stimulation. These modulatory effects of cortical excitability, induced by rTMS at the level of motor cortical areas, depend on the modulation of cortical excitatory and inhibitory interneurons, through mechanisms of short and long-term synaptic potentiation, which is believed to play a decisive role in the voltage-gated ion channels and glutamate inotropic receptors (Castro-Alamancos & Connors, 1996).

References

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Barker, A., Jalinous, R., & Freeston, I. (1985). Non-invasive magnetic stimulation of the human motor cortex. Lancet, 1:1106-1107.

Berardelli, A. (1998). Facilitation of muscle evoked responses after repetitive cortical stimulation in man. Experimental Brain Research, 122, 79-84.

Burt, T., Lisanby, S., & Sackeim, H. (2002). Neuropsychiatric applications of transcranial magnetic stimulation : a meta analysis. International Journal of Neuropsychopharmacology, 5, 73-103.

Castro-Alamancos, M., & Connors, B. (1996). Short-term synaptic enhancement and long-term potentiation in neocortex. Proceedings of the National Academy of Sciences, 93, 1335-1339.

d’Arsonval, A. (1896). Dispositifs pour la mesure des courants alternatifs de toutes frequences. Comptes Rendus de Societe Biologique, 2, 450±451.

Epstein, C. M., Schwartzenberg, D. G., Davey, K. R., & Sudderth, D. B. (1990). Localizing the site of magnetic brain stimulation in humans. Neurology, 40: 666–670.

Hofflich, G., Kasper, S., Hufnagel, A., Ruhrmann, S., & Moller, H. (1993). Appication of transcranial magnetic stimulation in treatment of drug resistant major depression – a report of two cases. Human Psychopharmacology, 8, 361-365.

Kimbrell, T. A., Dunn, R. T., & Wassermann, E. M. (1997). Regional decreases in glucose metabolism with 1 Hz prefrontal transcranial magnetic stimulation: a new technique for tracing functional networks in the human brain. Soc. Neurosci. Abstr., 23: 1576.

Oberg, P. A. (1973). Magnetic stimulation of nerve tissue. Med Biol Eng, 11:55–64. 6.

Pascual-Leone, A., Valls-Sole, J., Wassermann, E., & Hallett, M. (1994). Responses to rapid-rate transcranial magnetic stimulation of the human motor cortex. Brain, 117, 847-858.

Pellicciari, M. (2009). Heritability of Intracortical Inhibition and Facilitation. The Journal of Neuroscience, 29(28):8897– 8900.

Rudiak, D., & Marg, E. (1994). Finding the depth of magnetic brain stimulation: a re-evaluation. Electroenceph. clin. Neurophysiol, 93: 358–71.

Speer, A., Kimbrell, T., Wassermann, E., & Repella, J. (2000). Opposite Effects of High and Low Frequency rTMS on Regional Brain Activity in Depressed Patients. Biological Psychiatry, 48:1133–1141.

Veniero, D., Brignani, D., Thut, G., & Minussi, C. (2011). Alpha-generation as basic response-signature to transcranial magnetic stimulation (TMS) targeting the human resting motor cortex: A TMS/EEG co-registration study. Psychophysiology, 48,1381–1389.

Wassermann, E. (1998). Risk and Safety of Repetitive Transcranial Magnetic Stimulation:Report and Suggested Guidelines From the International Workshop on the Safety of Repetitive Transcranial Magnetic Stimulation. Electroencephalogy and Clinical Neurophysiology, 108(1), 1-16.

Wassermann, E. M., Kimbrell, T. A., George, M. S., Danielson, A. L., Herscovitch, P., Hallett, M., & Post, R. M. (1997). Local and distant changes in cerebral glucose metabolism during repetitive transcranial magnetic stimulation (rTMS). Neurology, 48: A107.