Tetanic stimulation of the peripheral nerve augments motor evoked potentials by re-exciting spinal anterior horn cells.
Yusuke YamamotoHideki ShigematsuMasahiko KawaguchiHironobu HayashiTsunenori TakataniMasato TanakaAkinori OkudaSachiko KawasakiKeisuke MasudaYuma SugaYasuhito TanakaPublished in: Journal of clinical monitoring and computing (2021)
Tetanic stimulation of the peripheral nerve, immediately prior to conducting transcranial electrical stimulation motor evoked potential (TES-MEP), increases MEP amplitudes in both innervated and uninnervated muscles by the stimulated peripheral nerve; this is known as the remote augmentation of MEPs. Nevertheless, the mechanisms underlying the remote augmentation of MEPs remain unclear. Although one hypothesis was that remote augmentation of MEPs results from increased motoneuronal excitability at the spinal cord level, the effect of spinal anterior horn cells has not yet been investigated. We aimed to investigate the effect of tetanic stimulation of the peripheral nerve on spinal cord anterior horn cells by analyzing the F-wave. We included 34 patients who underwent elective spinal surgeries and compared the changes in F-waves and TES-MEPs pre- and post-tetanic stimulation of the median nerve. F-wave analyses were recorded by stimulating the median and tibial nerves. TES-MEPs and F-wave analyses were compared between baseline and post-tetanic stimulation time periods using Wilcoxon signed-rank tests. A significant augmentation of MEPs, independent of the level corresponding to the median nerve, was demonstrated. Furthermore, F-wave persistence was significantly increased not only in the median nerve but also in the tibial nerve after tetanic stimulation of the median nerve. The increased F-wave persistence indicates an increase of re-excited motor units in spinal anterior horn cells. These results confirm the hypothesis that tetanic stimulation of the peripheral nerve may cause remote augmentation of MEPs, primarily by increasing the excitability of the anterior horn cells.
Keyphrases
- peripheral nerve
- spinal cord
- induced apoptosis
- neuropathic pain
- cell cycle arrest
- spinal cord injury
- chronic kidney disease
- end stage renal disease
- endoplasmic reticulum stress
- total knee arthroplasty
- oxidative stress
- cell death
- newly diagnosed
- ejection fraction
- soft tissue
- risk assessment
- prognostic factors
- climate change
- cell proliferation
- patient reported
- cerebral blood flow