Effects of auricular vagus nerve stimulation and electrical earlobe stimulation on motor‐evoked potential changes induced by paired associative stimulation

Author:

Haakana Piia123ORCID,Nätkynmäki Anna1,Kirveskari Erika14,Mäkelä Jyrki P.1,Kilgard Michael P.5,Tarvainen Mika P.67,Shulga Anastasia18ORCID

Affiliation:

1. BioMag Laboratory, HUS Diagnostic Center, Helsinki University Hospital University of Helsinki and Aalto University School of Science Helsinki Finland

2. Motion Analysis Laboratory, New Children's Hospital Helsinki University Hospital and University of Helsinki Helsinki Finland

3. Department of Physiology University of Helsinki Helsinki Finland

4. HUS Medical Imaging Center, Clinical Neurophysiology; Clinical Neurosciences Helsinki University Hospital and University of Helsinki Helsinki Finland

5. Texas Biomedical Device Center, School of Behavioral and Brain Sciences University of Texas at Dallas Richardson Texas USA

6. Department of Technical Physics University of Eastern Finland Kuopio Finland

7. Department of Clinical Physiology and Nuclear Medicine Kuopio University Hospital Kuopio Finland

8. Department of Physical and Rehabilitation Medicine Helsinki University Hospital and University of Helsinki Helsinki Finland

Abstract

AbstractPaired associative stimulation (PAS) is a combination of transcranial magnetic stimulation (TMS) and peripheral nerve stimulation (PNS). PAS can induce long‐term potentiation (LTP)‐like plasticity in humans, manifested as motor‐evoked potential (MEP) enhancement. We have developed a variant of PAS (“high‐PAS”), which consists of high‐frequency PNS and high‐intensity TMS and targets spinal plasticity and promotes rehabilitation after spinal cord injury (SCI). Vagus nerve stimulation (VNS) promotes LTP‐like plasticity and enhances recovery in SCI and stroke in humans and animals when combined with repetitive motor training. We combined high‐PAS with simultaneous noninvasive transcutaneous auricular VNS (aVNS) to determine if aVNS enhances the extent of PAS‐induced MEP amplitude increase. Sixteen healthy participants were stimulated for 20 min in four different sessions (PAS, PAS + aVNS, PAS + shamVNS, and aVNS) in a randomized single‐blind setup. MEPs were measured before, immediately after, and at 30, 60, and 90 min post‐stimulation. Stimulation protocols with PAS significantly potentiated MEPs (p = 0.005) when compared with aVNS (p = 0.642). Although not significant, MEP enhancement observed after PAS (43.5%) is further increased by aVNS (49.7%) and electrical earlobe stimulation (63.9%). Our aVNS setup failed to significantly enhance the effect of PAS, but sham VNS revealed a trend towards enhanced plasticity. Optimization of auricular VNS stimulation setup is required for possible tests of patients with SCI.

Funder

Wings for Life

Research Council of Finland

Publisher

Wiley

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