Abstract

Facial nerve damage can lead to partial or total facial nerve palsy. Photobiomodulation has been reported to improve and accelerate functional recovery following peripheral nerve lesion, depending on the type of lesion and the light exposure parameters used. The aim of this study was to investigate the effects of infrared exposure on functional and axonal regeneration after section-suture of the distal branches of the facial nerve: the buccal and marginal mandibular branches and the distal pes. The animals underwent surgery and were irradiated with infrared light at 850 nm twice daily from day 1 to day 16. The recovery of facial function was then studied at both the behavioral and morphological levels. Behavioral analyses were performed by videoscoring with a high-speed camera and using various devices to assess the recovery of whisker movement on the lesioned side from day 1 to day 30. We also assessed nasal deviation toward the intact side and the ability to close the ipsilateral eyelid completely from day 1 to day 38 and from day 1 to day 50, respectively. For morphological analyses, we assessed the re-establishment of facial motoneuron labeling with Fluorogold®, an immunofluorescent retrograde marker of axonal transport injected into the vibrissae, on D10, D14 and D30. We found that whisker movements recovery was significantly faster in treated than in control mice. A complete disappearance of nasal deviation was observed at 2 weeks in infrared-treated lesioned mice and at 5 weeks in controls. Complete eyelid closure was observed 3 weeks after surgery in treated animals and 6 weeks after surgery in controls. Finally, normal fluorogold labeling of the facial nuclei complex was restored 30 days after surgery in the treated animals, but no such restoration was ever observed in control animals. In conclusion, our data show that IR treatment at a distal site has a significant positive effect on facial nerve recovery. These findings pave the way for the clinical use of infrared photobiomodulation in patients with nerve lesions.

Highlights

  • Peripheral nerve lesions cause major motor and/or sensory disorders that can significantly impair quality of life

  • We studied first the dose-response relationship between PBM and facial nerve functional recovery

  • In the proximal facial nerve section model, the functional recovery was not observed before 3 months and very often the recovery was abnormal with synkinesia

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Summary

Introduction

Peripheral nerve lesions cause major motor and/or sensory disorders that can significantly impair quality of life. For example, is a severe handicap with severe consequences for the patient’s professional, social and family life. Damaged peripheral nerves can regenerate, but they often do so imperfectly, resulting in very difficult living conditions for the injured patients. The annual incidence of facial palsy is about 15 to 30 cases per 100,000 people. Bell’s palsy accounts for 80% of these cases. It occurs suddenly, generally improving after a few weeks, but sometimes with sensory or motor sequelae. Numerous studies have been performed with the goal of enhancing and accelerating the functional recovery of such peripheral nerve lesions [1–4]

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