z-logo
Premium
Identification of mechano‐sensitive C fibre sensitization and contribution to nerve injury‐induced mechanical hyperalgesia
Author(s) -
Hulse R. P.
Publication year - 2016
Publication title -
european journal of pain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.305
H-Index - 109
eISSN - 1532-2149
pISSN - 1090-3801
DOI - 10.1002/ejp.779
Subject(s) - nerve conduction velocity , saphenous nerve , hyperalgesia , nerve injury , stimulation , nociception , sensitization , electrophysiology , sensory system , medicine , anesthesia , chemistry , neuroscience , anatomy , biology , receptor
Abstract Background C fibre hyperexcitability is fundamental to chronic pain development in humans and rodents; therefore, peripheral sensory neuronal sensitization plays a role in the development of mechanical hyperalgesia. However, the axonal properties and underlying mechanisms that are associated to these chronic pain states still require investigation. Methods Teased fibre electrophysiology of the saphenous nerve was used to identify C fibres in naïve and nerve‐injured rats. C fibres were identified using electrical stimulation which further provided conduction velocity slowing profiles. From these nerve filaments evoked responses to mechanical stimuli were recorded. Vehicle or galanin were applied directly to the saphenous nerve trunk prior to stimulation. Results Increased levels of mechanically evoked activity in mechano‐sensitive C fibres was associated to reduced conduction failure, enhanced conduction velocity latency recovery and reduced conduction velocity slowing. Mechanical hyperalgesia developed in nerve‐injured animals in which mechano‐sensitive C fibres demonstrated increased mechanically evoked responses and reduced rate of adaptation. Mechano‐sensitive C fibres in nerve‐injured animals had reduced levels of conduction velocity slowing, enhanced rate of conduction velocity recovery and reduced firing frequency failure versus naïve animals; all hallmarks of enhanced sensory neuronal excitability. Directly applying the antinociceptive agent galanin to the saphenous nerve trunk in naive animals led to increased conduction failure, reduced latency recovery rate and increased levels of conduction velocity slowing. Discussion Nerve injury‐induced enhanced neural responses to mechanical stimulation are associated to defined parameters setout by conduction velocity slowing, mediated via axonal processing. Application of galanin inhibits axonal excitability.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here