The Use of Naltrexone in Dermatology. Current Evidence and Future Directions

Curr Drug Targets. 2019;20(10):1058-1067. doi: 10.2174/1389450120666190318121122.

Abstract

Naltrexone is a competitive opioid receptor antagonist approved as supportive treatment in alcohol dependence and opioid addiction. At a dose of 50-100 mg daily, naltrexone is used off-label in dermatology for the treatment of trichotillomania and different types of pruritus. At a dose as low as 1- 5 mg per day, naltrexone demonstrates immunomodulatory action i.e. modulates Toll-like receptors signaling, decreases release of proinflammatory cytokines (tumor necrosis factor, interleukin-6, interleukin- 12), inhibits T lymphocyte proliferation, down-regulates the expression of chemokine receptors and adhesion molecules. The efficacy of standard and low doses of naltrexone in a variety of dermatological disorders has been reported. These include diseases such as familial benign chronic pemphigus (Hailey-Hailey disease), dermatomyositis, systemic sclerosis, psoriasis and lichen planopilaris. Optimistic preliminary findings, low cost of therapy and good tolerance make naltrexone a promising alternative therapy or adjunct drug in dermatology.

Keywords: Alopecia; low dose naltrexone; opioid growth factor; pruritus; psoriasis; toll-like receptor..

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytokines / metabolism
  • Dose-Response Relationship, Drug
  • Humans
  • Immunomodulation
  • Naltrexone / pharmacology
  • Naltrexone / therapeutic use*
  • Pruritus / drug therapy
  • Pruritus / immunology
  • Signal Transduction / drug effects
  • Skin Diseases / drug therapy*
  • Skin Diseases / immunology*
  • T-Lymphocytes / metabolism
  • Toll-Like Receptors / metabolism
  • Trichotillomania / drug therapy
  • Trichotillomania / immunology

Substances

  • Cytokines
  • Toll-Like Receptors
  • Naltrexone