alpha-Methyl-p-tyrosine inhibits latanoprost-induced melanogenesis in vitro

Exp Eye Res. 1999 Jan;68(1):85-90. doi: 10.1006/exer.1998.0581.

Abstract

The PGF2alpha derivative, latanoprost, is a recent anti-glaucoma drug that has been reported to induce a discrete incidence of increased iris pigmentation in men. The present experiments were made in order to study whether this phenomenon could be influenced by the tyrosinase inhibitor, alpha-methyl-p-tyrosine. Melanin content, melanin production and tyrosinase activity of cultured uveal melanocytes derived from irides of brown or brown-blue color were measured after adding latanoprost at different molar concentration with or without alpha-methyl-p-tyrosine (10(-5)m). It was shown that latanoprost stimulated melanin content, melanin production and tyrosinase activity in a molar range between 10(-7) and 10(-5)m in uveal melanocytes derived from irides of both brown and brown-blue color. The effect seemed to be more pronounced in melanocytes derived from irides of brown-blue color. The adding of alpha-methyl-p-tyrosine completely prevented latanoprost-induced stimulation of melanin production in uveal melanocytes derived from irides of both colors. These results suggest that latanoprost-induced stimulation of melanin production, follows the metabolic pathway involving tyrosinase activity and may be relevant for the therapeutic application of latanoprost in glaucoma in order to reduce its side-effect resulting in increased iris pigmentation.

MeSH terms

  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Eye Color
  • Humans
  • Latanoprost
  • Melanins / biosynthesis*
  • Melanocytes / drug effects*
  • Melanocytes / metabolism
  • Monophenol Monooxygenase / metabolism
  • Prostaglandins F, Synthetic / antagonists & inhibitors*
  • Prostaglandins F, Synthetic / pharmacology
  • Uvea / drug effects
  • Uvea / metabolism
  • alpha-Methyltyrosine / pharmacology*

Substances

  • Melanins
  • Prostaglandins F, Synthetic
  • alpha-Methyltyrosine
  • Latanoprost
  • Monophenol Monooxygenase