l-3,4-Dihydroxyphenylalanine induces ptosis through a GPR143-independent mechanism in mice

J Pharmacol Sci. 2016 Sep;132(1):109-112. doi: 10.1016/j.jphs.2016.08.005. Epub 2016 Aug 30.

Abstract

Through its conversion to dopamine by aromatic l-amino acid decarboxylase (AADC), l-3,4-dihydroxyphenylalanine (l-DOPA) replenishes depleted brain dopamine in Parkinson's disease patients. We recently identified GPR143 as a candidate receptor for l-DOPA. In this study, we investigated the behavioral actions of l-DOPA in wild type (wt) and Gpr143-deficient mice. l-DOPA dose-dependently (10-100 mg/kg, i.p.) induced ptosis under treatment with 3-hydroxybenzylhydrazine, a centrally acting AADC inhibitor. This effect was not mimicked by 3-O-methyldopa. l-DOPA-induced ptosis in Gpr143-deficient mice to a similar extent as in wt mice. These results suggest that l-DOPA induces ptosis in a GPR143-independent fashion in mice.

Keywords: GPR143; Ptosis; l-DOPA.

MeSH terms

  • Animals
  • Behavior, Animal / drug effects
  • Blepharoptosis / chemically induced*
  • Blepharoptosis / metabolism
  • Eye Proteins / genetics
  • Eye Proteins / metabolism
  • Levodopa*
  • Male
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism

Substances

  • Eye Proteins
  • Gpr143 protein, mouse
  • Membrane Glycoproteins
  • Receptors, G-Protein-Coupled
  • Levodopa