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Methcathinone: a new and potent amphetamine-like agent.

R A Glennon, M Yousif, N Naiman, P Kalix

Pharmacology, biochemistry, and behavior March 1, 1987 DOI: 10.1016/0091-3057(87)90164-x via PubMed

Summary

AI-generated from the abstract

N-monomethylation of phenylisopropylamine derivatives does not uniformly increase amphetamine-like activity. In rats trained to discriminate amphetamine from saline, N-monomethyl derivatives of several dimethoxy and trimethoxy compounds failed to produce amphetamine-appropriate responding, but the N-monomethyl derivative of cathinone (methcathinone) did. Methcathinone was more potent than racemic cathinone or amphetamine (ED50 = 0.37 mg/kg vs. 0.71 mg/kg), induced dopamine release from rat caudate nucleus tissue, and was a more potent locomotor stimulant in mice. These results support a structural and pharmacological analogy between amphetamine/methamphetamine and cathinone/methcathinone.

Study at a glance

Characteristics Observational study Peer reviewed
Population Rats and mice
Interventions 4-DMA 3 2 4 MMDA-2) methcathinone cathinone amphetamine methamphetamine
Dose 1.0 mg/kg of (+)-amphetamine
Key finding Methcathinone is more potent than cathinone or amphetamine in producing amphetamine-like stimulus effects and dopamine release.

Abstract

The purpose of the present investigation was to examine the effect of N-monomethylation of phenylisopropylamine derivatives on amphetamine-like activity. In tests of stimulus generalization using rats trained to discriminate 1.0 mg/kg of (+)-amphetamine from saline, the N-monomethyl derivatives of 1-(X-phenyl)-2-aminopropane, where X = 2,4-dimethoxy (2,4-DMA), 3,4-dimethoxy (3,4-DMA), 2,4,5-trimethoxy (2,4,5,-TMA), and 2-methoxy-4,5-methylenedioxy (MMDA-2), did not produce amphetamine-appropriate responding at the doses evaluated. However, the N-monomethyl derivative of cathinone (i.e., methcathinone), like cathinone, resulted in stimulus generalization. Further studies with this agent revealed that (a) in the amphetamine-trained animals, methcathinone (ED50 = 0.37 mg/kg) is more potent than racemic cathinone or racemic amphetamine (ED50 = 0.71 mg/kg in both cases), (b) methcathinone is capable of inducing release of radioactivity from [3H]dopamine-prelabeled tissue of rat caudate nucleus in a manner similar to that observed with cathinone, amphetamine, and methamphetamine, and (c) methcathinone is more potent than cathinone as a locomotor stimulant in mice as determined by their effect on spontaneous activity. The results of the present study provide evidence for a structural analogy between the prototypic psychostimulants amphetamine/methamphetamine and cathinone/methcathinone, and lend further support to the concept that amphetamine and cathinone correspond in their pharmacological effects.

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