Delayed Nerve Repair Is Associated with Diminished Neuroenhancement by FK506

Michael J. Brenner, Ida K. Fox, David H. Kawamura, Vivian M. Yu, James B. Lowe, Daniel A. Hunter, Susan E. Mackinnon

Research output: Contribution to journalArticle

17 Scopus citations


Objectives/Hypothesis: The immunosuppressive agent FK506 has been shown in many studies to enhance nerve regeneration and to accelerate functional recovery after immediate nerve repair. However, in clinical practice the diagnosis and treatment of patients with peripheral nerve injuries is often delayed. The study investigated whether FK506 would retain its neuroregenerative properties when nerve repair and initiation of FK506 therapy were delayed for 7 days. Study Design: In vivo laboratory study. Methods: Thirty-two Lewis rats underwent tibial nerve transection and were randomly assigned to four experimental groups: immediate repair with FK506 treatment, immediate repair without FK506 treatment, 7-day delayed repair with FK506 treatment, and 7-day delayed repair without FK506 treatment. Treated animals received daily subcutaneous injections of 2 mg/kg FK506. Serial walking track measurements were performed at 14, 16, and 18 days after nerve repair. On day 18 after repair, peripheral nerves were injected with a fluorescent tracer for retrograde labeling. On day 21, peripheral nerves and spinal cords were harvested for histomorphometric analysis and motor neuron cell body counts, respectively. Results: Animals that underwent immediate repair with FK506 had significantly higher fiber counts and percentages of nerve than the other three groups (P < .05) but did not show statistically significant earlier functional recovery. The remaining three groups had intermediate levels of nerve regeneration that were not significantly different. Retrograde abled motor neurons counts were decreased in animals with delayed nerve repair that received no FK506 (P < .05). Conclusion: In a rat tibial nerve transection model, the neuroregenerative effects of FK506 diminished markedly when repair and initiation of FK506 therapy were delayed by 7 days.

Original languageEnglish
Pages (from-to)570-576
Number of pages7
Issue number3
StatePublished - Mar 1 2004


  • FK506
  • Functional recovery
  • Nerve regeneration
  • Rat
  • Tacrolimus

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