Corneal safety of topically applied naltrexone

J Ocul Pharmacol Ther. 2006 Oct;22(5):377-87. doi: 10.1089/jop.2006.22.377.

Abstract

Purpose: Naltrexone (NTX), an opioid antagonist, accelerates wound healing of corneal epithelium in normal and diabetic animals. This study examined the safety of NTX by topical application in the cornea.

Methods: NTX in concentrations of 10(-3), 10(-4), 10(-5), 10(-6), or 10(-7) M was administered topically 4 times/daily for 7 d to the eye of Type 1 diabetic rats (glucose levels >400 mg/dL) (DB), DB animals receiving insulin to maintain normoglycemia (DB-IN), and normal (nondiabetic) (Normal) subjects beginning 8 weeks after onset of diabetes.

Results: No differences in intraocular pressures, corneal thickness, endothelial cell number, or epithelial apoptosis, necrosis, or organization were observed between DB, DB-IN, and Normal groups with and without treatment with NTX. The DB group had a twofold decrease in corneal sensitivity from the Normal and DB-IN groups prior to NTX treatment but were comparable to the Normal and DB-IN groups for at least 2 weeks after chronic exposure to 10(-3) to 10(-7) M NTX was terminated. No differences between Normal and DB-IN groups were noted.

Conclusions: Topical application of NTX over a 10,000-fold range of dosage had no overt toxicity for the parameters studied, indicating that efficacy studies for the use of NTX in corneal wound healing are warranted.

Publication types

  • Comparative Study
  • Evaluation Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Administration, Topical
  • Animals
  • Apoptosis / drug effects
  • Cell Count
  • Cornea / drug effects*
  • Cornea / pathology
  • Diabetes Mellitus, Experimental / complications
  • Diabetic Retinopathy / drug therapy*
  • Diabetic Retinopathy / etiology
  • Diabetic Retinopathy / pathology
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Endothelium, Corneal / drug effects
  • Male
  • Naltrexone / administration & dosage*
  • Naltrexone / adverse effects*
  • Narcotic Antagonists / administration & dosage
  • Necrosis
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Narcotic Antagonists
  • Naltrexone