Autotomy prevention by amitriptyline after peripheral nerve section in different strains of mice

X Navarro1, M Butí, E Verdú

  • 1Department of Cell Biology and Physiology, School of Medicine, Universitat Autònoma de Barcelona, E-08193 Bellaterra, Spain.

Insights

This study investigated autotomy behavior in mice after nerve injury. Amitriptyline treatment initiated 14 days pre-operation significantly reduced self-mutilation in OF1 and NMRI mouse strains.

Area of Science:

  • Neuroscience
  • Pharmacology

Background:

  • Anesthesia dolorosa, a neuropathic pain condition, can lead to self-mutilating behaviors.
  • Autotomy, or self-mutilation, is a common consequence of peripheral nerve injury in animal models.

Purpose of the Study:

  • To evaluate the degree of autotomy induced by sciatic and saphenous nerve transection in four mouse strains.
  • To assess the efficacy of amitriptyline in mitigating autotomy in selected mouse strains.

Main Methods:

  • Sciatic and saphenous nerves were transected in OF1, Balb-C, NMRI, and B6CBAF1 mice.
  • Autotomy was scored for one month post-denervation.
  • Amitriptyline (8 mg/kg/day) was administered to OF1 and NMRI mice at varying pre-operative intervals.

Main Results:

  • Autotomy onset typically occurred within the first week, progressing from nails proximally.
  • Significant strain-dependent differences in autotomy were observed: OF1 (88%), Balb-C (61%), NMRI (35%), and B6CBAF1 (15%).
  • Pre-operative amitriptyline administration, particularly starting 14 days before nerve injury, effectively reduced autotomy in OF1 and NMRI mice.

Conclusions:

  • Mouse strain significantly influences the development of autotomy following nerve injury.
  • Early pre-operative administration of amitriptyline is a promising therapeutic strategy for reducing neuropathic pain-induced autotomy.

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