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M P Johnson

5 papers in the library · 152 citations · publishing 1989-1991

Papers

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Assessment of the role of alpha-methylepinine in the neurotoxicity of MDMA.

Pharmacology, biochemistry, and behavior February 1991 T D Steele, W K Brewster, M P Johnson et al.

To assess the potential involvement of metabolism of 3,4-methylenedioxymethamphetamine (MDMA) to the catechol alpha-methylepinine in producing serotonergic neurotoxicity, we attempted to correlate aspects of this reaction with the neurotoxicity profile of MDMA. In contrast to the stereoselectivity of S-(+)-MDMA in causing persistent declines in rat brain 5-hydroxyindole levels, no...

Amphetamine derivatives induce locomotor hyperactivity by acting as indirect serotonin agonists.

Psychopharmacology 1991 C W Callaway, M P Johnson, L H Gold et al. 70 citations

Derivatives of amphetamine are potent releasers of both dopamine (DA) and serotonin (5-HT), but the relative contributions of DA and 5-HT release to the behavioral effects of these drugs have not been established. Previously, S-(+)3,4-methylenedioxymethamphetamine (S-(+)MDMA) was found to produce locomotor hyperactivity in rats which was dependent on 5-HT release. The present study found that...

[125I]-2-(2,5-dimethoxy-4-iodophenyl)aminoethane ([125I]-2C-I) as a label for the 5-HT2 receptor in rat frontal cortex.

Pharmacology, biochemistry, and behavior 1990 M P Johnson, C A Mathis, Alexander T. Shulgin et al. 56 citations

Recent studies of 5-HT2 receptor binding have involved the use of radiolabeled agonists. This report describes the use of [125I]-2-(2,5-dimethoxy-4-iodophenyl)aminoethane ([125I]-2C-I) as a label for low-density 5-HT2 agonist binding sites. A nonhydrolyzable analog of GTP, GppNHp, was found to inhibit the high affinity binding of [125I]-2C-I. 5-HT and several 5-HT2 agonists and antagonists...

Studies of dioxole ring substituted 3,4-methylenedioxyamphetamine (MDA) analogues.

Pharmacology, biochemistry, and behavior November 1989 D E Nichols, R Oberlender, K Burris et al.

The 3,4-ethylidenedioxy and 3,4-isopropylidenedioxy analogues, EDA and IDA, respectively, of 3, 4-methylenedioxyamphetamine (MDA) were compared to MDA in drug-stimulated [3H]-serotonin overflow from prelabelled rat hippocampal slices, [3H]-dopamine overflow from prelabelled rat caudate slices, in their ability to displace the 5-HT2 agonist R-[125I]-DOI from rat brain cortical binding sites....

Neurotoxic effects of the alpha-ethyl homologue of MDMA following subacute administration.

Pharmacology, biochemistry, and behavior May 1, 1989 M P Johnson, D E Nichols 26 citations

The possible neurotoxic effects of the alpha-ethyl homologue of MDMA, N-methyl-1-(1,3-benzodioxol-5-yl)-2-butanamine (MBDB), were examined following a regimen of twice daily dosing for four days. The levels of norepinephrine, serotonin and its metabolite 5-HIAA were quantitated by standard HPLC-EC techniques. In addition, the number of 5-HT uptake sites was estimated by examining the binding of...