Non-additive effects of electrical stimulation of the dorsolateral prefrontal cortex and the vestibular system on muscle sympathetic nerve activity in humans.
Brendan McCarthy, Sudipta Datta, Gianni Sesa-Ashton, Rebecca Wong, Luke A Henderson, Tye Dawood, Vaughan G Macefield
Author Information
Brendan McCarthy: Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Sudipta Datta: Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Gianni Sesa-Ashton: Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Rebecca Wong: Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Luke A Henderson: School of Medical Sciences (Neuroscience), Brain and Mind Centre, The University of Sydney, Camperdown, NSW, Australia.
Tye Dawood: Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Vaughan G Macefield: Baker Heart and Diabetes Institute, Melbourne, VIC, Australia. vaughan.macefield@monash.edu. ORCID
Sinusoidal galvanic vestibular stimulation (sGVS) induces robust modulation of muscle sympathetic nerve activity (MSNA) alongside perceptions of side-to-side movement, sometimes with an accompanying feeling of nausea. We recently showed that transcranial alternating current stimulation (tACS) of the dorsolateral prefrontal cortex (dlPFC) also modulates MSNA, but does not generate any perceptions. Here, we tested the hypothesis that when the two stimuli are given concurrently, the modulation of MSNA would be additive. MSNA was recorded from 11 awake participants via a tungsten microelectrode inserted percutaneously into the right common peroneal nerve at the fibular head. Sinusoidal stimuli (± 2 mA, 0.08 Hz, 100 cycles) were applied in randomised order as follows: (i) tACS of the dlPFC at electroencephalogram (EEG) site F4 and referenced to the nasion; (ii) bilateral sGVS applied to the vestibular apparatuses via the mastoid processes; and (iii) tACS and sGVS together. Previously obtained data from 12 participants supplemented the data for stimulation protocols (i) and (ii). Cross-correlation analysis revealed that each stimulation protocol caused significant modulation of MSNA (modulation index (paired data): 35.2 ± 19.4% for sGVS; 27.8 ± 15.2% for tACS), but there were no additive effects when tACS and sGVS were delivered concurrently (32.1 ± 18.5%). This implies that the vestibulosympathetic reflexes are attenuated with concurrent dlPFC stimulation. These results suggest that the dlPFC is capable of blocking the processing of vestibular inputs through the brainstem and, hence, the generation of vestibulosympathetic reflexes.
