Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control
EMG responses in the soleus muscles evoked by unipolar galvanic vestibular stimulation
Introduction
Transmastoid direct current (`galvanic') stimulation has long been used as a means of vestibular activation to induce both ocular and postural movements. It is only relatively recently that characteristic EMG changes occurring within postural muscles have been defined (e.g. Nashner and Wolfson, 1974; Iles and Pisini, 1992; Britton et al., 1993; Fitzpatrick et al., 1994). These studies have shown that in standing subjects lower limb EMG excitability changes of opposing types occur at short (approximately 60 ms) and medium (approximately 100 ms) latencies (Britton et al., 1993; Fitzpatrick et al., 1994) following the onset of the stimulus. These effects are profoundly influenced by polarity of stimulation, head and body posture and postural task (Nashner and Wolfson, 1974; Tokita et al., 1989; Britton et al., 1993; Fitzpatrick et al., 1994). Primary vestibular afferents are characterized by a high level of tonic discharge, and studies of the effects of DC current in monkeys have shown that both excitatory and inhibitory effects may follow stimulation, depending on its polarity (Goldberg et al., 1984). Thus transmastoid galvanic stimulation, as used in human subjects, has the potential to produce its effects through simultaneously exciting one vestibular apparatus and inhibiting the other.
Clearly, the ability to stimulate each vestibular apparatus separately would be advantageous, both in furthering our understanding of basic physiology, and also for any clinical applications. Such lateralized stimulation montages have been used in the past in studies of induced eye movements (e.g. Skurczynski and Ernst, 1989) and posture (e.g. Coats and Stoltz, 1969; Watanabe et al., 1989; Cass et al., 1996).
The object of the present experiments was to investigate the lower limb EMG responses to lateralized vestibular stimulation and to compare these to those occurring with transmastoid stimulation. In addition, we have studied a series of patients with unilateral vestibular nerve section. The absence of EMG responses with unipolar stimulation on the side of the sectioned nerve would provide strong evidence confirming that the responses are vestibular dependent, and that the DC current acts at, or distal to, the level of the vestibular nerve fibres.
Section snippets
Methods and materials
All techniques were approved by the University of New South Wales Ethics Committee, and all subjects gave informed consent. For all experiments, subjects stood leaning slightly forwards, with feet together, eyes closed, and with head rotated close to 90°, conditions under which the largest short latency (SL) and medium latency (ML) EMG responses in soleus are obtained (Britton et al., 1993; Fitzpatrick et al., 1994). The SL has a higher threshold (Fitzpatrick et al., 1994), while the ML is more
Results
Our results for transmastoid stimulation were consistent with previous reports: when the cathode was placed over the mastoid process ipsilateral to the direction of head rotation (and therefore with the anode facing forwards), a facilitatory SL response was followed by an inhibitory ML response, and both these responses inverted when the polarity of the stimulus was reversed (Britton et al., 1993; Fitzpatrick et al., 1994). Unipolar stimulation produced responses that were qualitatively similar
Discussion
A characteristic feature of vestibular primary afferents is their high resting discharge rate, approximately 90 spikes per second in humans (Goldberg and Fernandez, 1971; Goldberg and Fernandez, 1984). This property allows the afferents to code responses to head movements in opposite directions, by either an increase or a decrease in the resting discharge rate. Caloric testing of the lateral semicircular canals exploits this property: irrigation with warm and cool water causes opposite effects,
Acknowledgements
We thank Ms. D. Wagener for expert technical assistance and Dr. P. Fagan for referral of patients. S.R.D.W. was supported by the Whitmont Fellowship of the Australian Brain Foundation during the period of this study.
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