Lifting the veil on the dynamics of neuronal activities evoked by transcranial magnetic stimulation.
Lifting the veil on the dynamics of neuronal activities evoked by transcranial magnetic stimulation.
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DOI:
10.7554/elife.30552
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发表时间:
2017-11-22
期刊:
影响因子:
7.7
通讯作者:
Benali A
中科院分区:
文献类型:
--
作者:
Li B;Virtanen JP;Oeltermann A;Schwarz C;Giese MA;Ziemann U;Benali A
Transcranial magnetic stimulation (TMS) is a widely used non-invasive tool to study and modulate human brain functions. However, TMS-evoked activity of individual neurons has remained largely inaccessible due to the large TMS-induced electromagnetic fields. Here, we present a general method providing direct in vivo electrophysiological access to TMS-evoked neuronal activity 0.8–1 ms after TMS onset. We translated human single-pulse TMS to rodents and unveiled time-grained evoked activities of motor cortex layer V neurons that show high-frequency spiking within the first 6 ms depending on TMS-induced current orientation and a multiphasic spike-rhythm alternating between excitation and inhibition in the 6–300 ms epoch, all of which can be linked to various human TMS responses recorded at the level of spinal cord and muscles. The advance here facilitates a new level of insight into the TMS-brain interaction that is vital for developing this non-invasive tool to purposefully explore and effectively treat the human brain. Being able to tap into someone’s brain activity by holding loops of wires above their head sounds a little like the stuff of science fiction. And yet this technique, known as transcranial magnetic stimulation or TMS, is used in research and to treat many brain disorders. TMS emits a pulsed magnetic field that induces tiny electrical currents in the underlying brain tissue, activating that region of the brain. But exactly how these currents affect the individual neurons and networks within activated brain regions remains unclear. The main reason for this is that we cannot use conventional electrode-based techniques to study neuronal activity during TMS because its strong electromagnetic interferences mask the signals from the electrodes. Several groups have found ways to overcome this problem. However, their methods are technically demanding and specific to one single animal model –limitations that could present an obstacle for many laboratories. Li et al. therefore set out to develop a simple and widely accessible method to study neuronal activities under TMS. The resulting method makes it possible to measure the activity of individual neurons roughly 1/1,000th of a second after applying TMS. To show that the technique works, Li et al. induced small movements in the forelimbs of rats by applying TMS to the brain region that controls the forelimbs, while measuring the activity of neurons at the same time. This revealed, for the first time, how the neurons responsible for the forelimb movements responded to TMS. The observed TMS-triggered neuronal activity continued long after the TMS pulse had ended. The activity also varied depending on the direction of TMS-induced currents in the brain. This new method opens up the possibility to conveniently study – in rodents or other animals – how TMS procedures that are used in patients affect neuronal activity. Li et al. hope this will make it easier to develop, study and refine these procedures, and lead to advances in TMS therapies.