p-methylthioamphetamine is a potent new non-neurotoxic serotonin-releasing agent

Eur J Pharmacol. 1992 Dec 8;229(1):31-8. doi: 10.1016/0014-2999(92)90282-9.

Abstract

p-Methylthioamphetamine (MTA), was compared to p-chloroamphetamine (PCA) in a number of pharmacological assays. MTA was about 2-fold more potent than PCA at inhibiting synaptosomal uptake of [3H]5-hydroxytryptamine ([3H]5-HT), and about 7-fold and 10-fold less potent than PCA at inhibiting synaptosomal uptake of [3H]dopamine and [3H]norepinephrine, respectively. In drug discrimination assays, MTA was nearly equipotent to PCA in animals trained to discriminate saline from 3,4-methylenedioxymethamphetamine (MDMA), or two related analogues S-(+)-N-methyl-1-(1,3-benzodioxol-5-yl)-2-butanamine (S-MBDB) or 5-methoxy-6-methyl-2-aminoindan (MMAI). MTA caused dose-dependent increases of tritium efflux from superfused rat frontal cortex slices preloaded with [3H]5-HT, comparable to that induced by an equal molar concentration of PCA. The potential neurotoxicity of MTA was examined by measuring monoamine and metabolite levels at one week following an acute dose. A 10 mg/kg dose of PCA caused a 70-90% decrease of cortical, hippocampal and striatal 5-HT and 5-hydoxyindoleacetic acid (5-HIAA) levels, while twice the molar dose of MTA (21.3 mg/kg) had no effect. Thus, MTA is a potent, selective, serotonin releaser, apparently devoid of serotonin neurotoxic effects. This work also supports the idea that catecholamine systems may play a critical role in the neurotoxicity of PCA-like compounds.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amphetamines / pharmacology*
  • Amphetamines / toxicity
  • Animals
  • Brain / drug effects*
  • Brain / metabolism
  • Chromatography, High Pressure Liquid
  • Corpus Striatum / drug effects
  • Discrimination, Psychological
  • Dopamine / metabolism
  • Frontal Lobe / drug effects
  • Hippocampus / drug effects
  • In Vitro Techniques
  • Male
  • Neurotransmitter Uptake Inhibitors / pharmacology*
  • Neurotransmitter Uptake Inhibitors / toxicity
  • Norepinephrine / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Serotonin Uptake Inhibitors / pharmacology*
  • Serotonin Uptake Inhibitors / toxicity
  • Structure-Activity Relationship
  • Synaptosomes / drug effects

Substances

  • Amphetamines
  • Neurotransmitter Uptake Inhibitors
  • Serotonin Uptake Inhibitors
  • 4-methylthioamphetamine
  • Dopamine
  • Norepinephrine