1. Academic Validation
  2. beta-Carbolines as selective monoamine oxidase inhibitors: in vivo implications

beta-Carbolines as selective monoamine oxidase inhibitors: in vivo implications

  • J Neural Transm. 1982;54(3-4):209-18. doi: 10.1007/BF01254930.
V Glover J Liebowitz I Armando M Sandler
Abstract

The inhibitory action of a range of beta-carbolines on human and rat Monoamine Oxidase (MAO) A and B has been studied. Concentrations of 5-hydroxytryptamine and phenylethylamine, approximately at their Km values, were used as substrates for MAO A and B respectively. A wide variation in selectivity was found, with harmaline being 10,000 times more potent an inhibitor of A than B whereas, using tetrahydro-beta-carboline and harmane, the difference was nearer to ten-fold. Of the carbolines which have been found endogenously, tetrahydro-beta-carboline, 6-methoxytetrahydro-beta-carboline and harmane are all sufficiently potent inhibitors of human MAO A, with I50 values of 5 X 10(-6), 10(-6), 5 X 10(-7) M respectively, for this property to be of possible physiological significance. Harmane, with an I50 of 5 X 10(-6) M, might also play a role as an inhibitor of MAO B.

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