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Discriminative stimulus properties of alpha-ethyltryptamine optical isomers.

S S Hong, R Young, R A Glennon

Pharmacology, biochemistry, and behavior January 1, 2001 DOI: 10.1016/s0091-3057(01)00605-0 via PubMed

Summary

AI-generated from the abstract

The optical isomers of alpha-ethyltryptamine (alpha-ET) produce distinct psychoactive effects in rats. The (-)isomer produced amphetamine-like effects, while the (+)isomer produced hallucinogen-like effects. Both isomers produced effects similar to MDMA and PMMA at comparable doses. The findings suggest that alpha-ET's stimulant character resides primarily with its (-)isomer and its hallucinogenic character with the (+)enantiomer.

Study at a glance

Characteristics Animal study Peer reviewed
Population Rats trained to discriminate drugs from vehicle
Dose ED(50)=7.8 mg/kg for (-)alpha-ET in amphetamine-trained rats; ED(50)=2.7 mg/kg for (+)alpha-ET in DOM-trained rats; ED(50)=1.6 and 1.4 mg/kg for (-)alpha-ET and (+)alpha-ET in PMMA-trained rats; ED(50)=1.3 and 2.0 mg/kg for (-)alpha-ET and (+)alpha-ET in MDMA-trained rats
Key finding The (-)isomer of alpha-ET produces amphetamine-like effects, the (+)isomer produces hallucinogen-like effects, and both produce MDMA/PMMA-like effects.

Abstract

alpha-Ethyltryptamine (alpha-ET) possesses central stimulant and hallucinogenic activity. Also, in tests of stimulus generalization using rats trained to discriminate the controlled substance analog (i.e., designer drug) N-methyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane (MDMA) from vehicle, alpha-ET substituted for MDMA. These previous studies employed racemic alpha-ET. Because psychoactive phenylalkylamines with abuse potential can produce one or more of three distinct stimulus effects (i.e., amphetamine-, DOM- and/or PMMA-like effects) in animals trained to discriminate either the stimulant (+)amphetamine, the hallucinogen 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM), or N-methyl-1-(4-methoxyphenyl)-2-aminopropane (PMMA) from vehicle, and because these effects can be stereoselective, the individual optical isomers of alpha-ET were examined in groups of animals trained to discriminate (+)amphetamine, DOM, PMMA and MDMA from saline vehicle. (-)alpha-ET (ED(50)=7.8 mg/kg), but not (+)alpha-ET (maximum of 53% drug-appropriate responding), substituted for (+)amphetamine, whereas (+)alpha-ET (ED(50)=2.7 mg/kg), but not (-)alpha-ET (maximum of 33% drug-appropriate responding), substituted for DOM. Both optical isomers of alpha-ET substituted for PMMA and MDMA with ED(50) values of 1.6 and 1.4 mg/kg (PMMA-trained animals) and 1.3 and 2.0 mg/kg (MDMA-trained animals) for (-)alpha-ET and (+)alpha-ET, respectively. The results of this investigation suggest that both optical isomers of alpha-ET are capable of producing an MDMA/PMMA-like effect at nearly comparable doses, and that the stimulant or amphetamine-like nature of alpha-ET resides primarily with its (-)isomer whereas hallucinogenic or DOM-like character resides primarily with the (+)enantiomer.

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