Abstract

Recent work found that experimental pain appeared to negate alterations in cortical somatosensory evoked potentials (SEPs) that occurred in response to motor learning acquisition of a novel tracing task. The goal of this experiment was to further investigate the interactive effects of pain stimulus location on motor learning acquisition, retention, and sensorimotor processing. Three groups of twelve participants (n = 36) were randomly assigned to either a local capsaicin group, remote capsaicin group or contralateral capsaicin group. SEPs were collected at baseline, post-application of capsaicin cream, and following a motor learning task. Participants performed a motor tracing acquisition task followed by a pain-free retention task 24–48 h later while accuracy data was recorded. The P25 (p < 0.001) SEP peak significantly decreased following capsaicin application for all groups. Following motor learning acquisition, the N18 SEP peak decreased for the remote capsaicin group (p = 0.02) while the N30 (p = 0.002) SEP peaks increased significantly following motor learning acquisition for all groups. The local, remote and contralateral capsaicin groups improved in accuracy following motor learning (p < 0.001) with no significant differences between the groups. Early SEP alterations are markers of the neuroplasticity that accompanies acute pain and motor learning acquisition. Improved motor learning while in acute pain may be due to an increase in arousal, as opposed to increased attention to the limb performing the task.

Highlights

  • Motor learning difficulties are a significant problem for many people undergoing chronic pain rehabilitation but are often thought to be a consequence of pain present during the rehabilitation process

  • The use of an acute cutaneous tonic pain model is an important first step prior to the study of a chronic pain population. This will allow us to understand the effects of pain on motor learning acquisition and retention as we it allows the impact of pain to be studied independently of the chronic changes in motor control that occur in a chronic pain population [1]

  • The N18 somatosensory evoked potentials (SEPs) peak decreased for the remote capsaicin group while the amplitude of the N30

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Summary

Introduction

Motor learning difficulties are a significant problem for many people undergoing chronic pain rehabilitation but are often thought to be a consequence of pain present during the rehabilitation process. The use of an acute cutaneous tonic pain model is an important first step prior to the study of a chronic pain population This will allow us to understand the effects of pain on motor learning acquisition and retention as we it allows the impact of pain to be studied independently of the chronic changes in motor control that occur in a chronic pain population [1]. While motor learning acquisition occurred for both groups, the participants in the capsaicin group did not learn the task as well as the control group [2] This corroborates animal research demonstrating that acute pain interferes with the neuroplasticity that underlies learning [3,4]. A limitation of their conclusion was that the capsaicin applied locally over the area performing the task caused the movement to be altered so that it was no longer the same motor task, making it impossible to accurately compare motor performance between the pain and pain-free conditions

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