Ascorbate injury and EDTA (or manganese) protection of D2-dopamine receptors

Eur J Pharmacol. 1982 Jun 16;81(1):111-6. doi: 10.1016/0014-2999(82)90607-0.

Abstract

Ascorbic acid, EDTA, and Mn2+ modulated neuroleptic binding to membrane receptors but not to solubilized receptors. Preincubation with ascorbic acid at 22 degrees C produced a profound time-dependent decline in [3H]spiperone binding to membrane receptors (prepared in Tris-ascorbate buffer). Ascorbate had minimal effect if introduced simultaneously with [3H]spiperone in the incubation medium, and receptor binding was performed and assayed at 0 degrees C. Binding to the solubilized receptor was not ascorbate sensitive. Both EDTA and Mn2+ blocked the ascorbate effect on membrane receptors but were without effect on solubilized receptors. The preparation and incubation buffers used for [3H]spiperone binding studies should include EDTA if ascorbate is present in the buffer.

MeSH terms

  • Animals
  • Antipsychotic Agents / metabolism
  • Ascorbic Acid / pharmacology*
  • Corpus Striatum / metabolism
  • Dogs
  • Edetic Acid / pharmacology*
  • In Vitro Techniques
  • Manganese / pharmacology*
  • Receptors, Dopamine / drug effects*
  • Receptors, Dopamine / metabolism
  • Tromethamine

Substances

  • Antipsychotic Agents
  • Receptors, Dopamine
  • Tromethamine
  • Manganese
  • Edetic Acid
  • Ascorbic Acid