Effect of Minocycline on Traumatic Facial Nerve Injury: An Experimental Study

Bugra Celik1, Ozge Caglar Cil1, Erkan Tezcan2

  • 1Department of Otorhinolaryngology, Onsekiz Mart University Medical School, Çanakkale, Türkiye.

Abstract

Insights

Minocycline (M) and methylprednisolone (MP) show promise in treating facial nerve (FN) trauma. Combination therapy (M + MP) yielded the best results in rat models, suggesting potential human applications.

Area of Science:

  • Neuroscience
  • Pharmacology
  • Regenerative Medicine

Background:

  • Facial nerve (FN) injuries can lead to significant functional deficits.
  • Current treatment options for traumatic FN injury are limited.
  • Investigating novel therapeutic agents is crucial for improving patient outcomes.

Purpose of the Study:

  • To evaluate the efficacy of minocycline (M) and methylprednisolone (MP) in treating experimental facial nerve trauma.
  • To compare the effects of M, MP, and their combination in a rat model.

Main Methods:

  • 35 male Wistar albino rats underwent surgical trauma to the buccal branches of the facial nerve.
  • Rats were divided into five groups: sham, saline control, minocycline (M) alone, methylprednisolone (MP) alone, and combination (M + MP).
  • Electrophysiological tests (nerve excitability test [NET] and maximum stimulation test [MST]) and histopathological examinations were performed.

Main Results:

  • Histopathological analysis revealed superior outcomes in axonal diameter and reduced myelin sheath degeneration in the M + MP group compared to controls.
  • Electrophysiological tests showed significant improvements in NET and MST values in groups treated with M, MP, or both, compared to the saline group.
  • The combination therapy (M + MP) demonstrated the most favorable results, closely followed by MP alone.

Conclusions:

  • Minocycline (M), both alone and in combination with methylprednisolone (MP), positively impacts nerve fiber regeneration after facial nerve trauma.
  • M represents a potential therapeutic agent for traumatic FN injury, warranting further clinical investigation.
  • Advanced comparative studies are recommended to further elucidate the therapeutic potential of M and MP in FN regeneration.

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