Initial characterization of PMMA as a discriminative stimulus.
R A Glennon, R Young, M Dukat, Y Cheng
Pharmacology, biochemistry, and behavior January 1, 1997 DOI: 10.1016/s0091-3057(96)00306-1 via PubMed
Summary
AI-generated from the abstractThe drug PMMA, a hybrid of PMA and methamphetamine, produces effects in rats similar to MDMA (Ecstasy) but lacks the stimulant or hallucinogen-like properties of amphetamine or DOM. Rats trained to distinguish PMMA from saline did not respond to amphetamine or DOM, but did respond to MDMA and its S(+) isomer. Partial responses occurred with several related compounds. These results suggest PMMA acts like MDMA without amphetamine-like stimulation, supporting the idea that PMMA is the structural parent of MDMA-like designer drugs.
Study at a glance
| Characteristics | Animal discrimination study Peer reviewed |
|---|---|
| Sample size | 6 |
| Population | Sprague-Dawley rats |
| Intervention | PMMA |
| Dose | 1.25 mg/kg |
| Citations | 48 |
| Key finding | PMMA produces MDMA-like stimulus effects in rats without amphetamine-like stimulation. |
Abstract
The phenylisopropylamine PMMA or N-methyl-1-(4-methoxyphenyl)-2-aminopropane, a structural hybrid of paramethoxyamphetamine (PMA) and methamphetamine, has been previously shown to unexpectedly lack amphetamine-like or hallucinogen-like stimulus properties in animals. For example, in tests of stimulus generalization, neither a (+)amphetamine stimulus nor a DOM stimulus generalized to PMMA. It has also been shown, however, that stimulus generalization does occur in animals trained to discriminate the designer drug MDMA ("Ecstasy" or N-methyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane) from vehicle. In order to further characterize this unique agent, we trained a group of six Sprague-Dawley rats to discriminate 1.25 mg/kg of PMMA (ED50 = 0.44 mg/kg) from saline vehicle. The PMMA stimulus failed to generalize to the phenylisopropylamine stimulant (+)amphetamine, or to the phenylisopropylamine hallucinogen DOM. Stimulus generalization occurred to (+/-)MDMA (ED50 = 1.32 mg/kg) and S(+)MDMA (ED50 = 0.48 mg/kg). Partial generalization occurred with R(+)MDMA, PMA, 3.4-DMA, and fenfluramine. The PMMA stimulus also generalized to the alpha-ethyl homolog of PMMA (EH/PMMA, ED50 = 1.29 mg/kg). Taken together, the results of these studies suggest that PMMA is an MDMA-like agent that lacks the amphetamine-like stimulant character of MDMA. These findings support our previous suggestion that PMMA be considered the structural parent of the MDMA-like family of designer drugs.