Inhibition of brain mitochondrial monoamine oxidases by the endogenous compound 5-hydroxyoxindole

Biochem Pharmacol. 2004 Mar 1;67(5):977-9. doi: 10.1016/j.bcp.2003.10.021.

Abstract

5-Hydroxyoxindole is a recently identified endogenous compound. Its physiological role remains unclear but certain evidence exists, that it may share some regulatory properties with isatin, a known endogenous inhibitor of monoamine oxidase (MAO) type B (MAO-B). In this study several oxidized indoles were tested for their in vitro inhibition of MAO type A (MAO-A) and B of rat brain non-synaptic mitochondria. 5-Hydroxyoxindole was less potent MAO-A inhibitor (IC50 56.8 microM) than isatin (31.8 microM) and especially 5-hydroxyisatin (6.5 microM), but it was the only highly selective MAO-A inhibitor among the all compounds studied (IC50 MAO-A:IC50 MAO-B = 0.044). Thus, the in vitro data suggest that MAO-A may represent potential target for 5-hydroxyoxindole.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / cytology
  • Indoles / pharmacology*
  • Isatin / analogs & derivatives*
  • Isatin / chemistry
  • Isatin / pharmacology
  • Mitochondria / drug effects*
  • Mitochondria / enzymology
  • Monoamine Oxidase / drug effects
  • Monoamine Oxidase / metabolism*
  • Monoamine Oxidase Inhibitors / chemistry
  • Monoamine Oxidase Inhibitors / pharmacology*
  • Oxindoles
  • Rats

Substances

  • 5-hydroxyisatin
  • 5-hydroxyoxindole
  • Indoles
  • Monoamine Oxidase Inhibitors
  • Oxindoles
  • Isatin
  • Monoamine Oxidase