Neuropsychopharmacology
August 1996
J H Kehne, H J Ketteler, T C McCloskey et al.
(+/-)3,4-Methylenedioxymethamphetamine (MDMA) releases dopamine and serotonin in vivo and stimulates locomotor activity. Previous work demonstrated that MDMA-stimulated dopamine release could be reduced by the selective 5-HT2A receptor antagonist [R-(+)-a- (2,3-dimethoxyphenyl)-1-[2-(4-fluorophenylethyl)]-4-piperidinem ethanol] (MDL 100,907). In the present study MDL 100,907 significantly...
Psychopharmacology
March 1996
J H Kehne, R A Padich, T C McCloskey et al.
Increasing evidence suggests an important role for serotonin (5-HT) neurons in the etiology and treatment of schizophrenia. The prepulse inhibition paradigm is used as a model for sensorimotor gating processes that are disrupted in schizophrenia. The present study assessed the general role of 5-HT in modulating auditory and visual prepulse inhibition in Wistar rats. A general overactivation of...
Journal of Pharmacology and Experimental Therapeutics
1992
J H Kehne, T C McCloskey, Vicki L. Taylor et al.
The substituted amphetamines 4-chloroamphetamine (PCA), 3,4-methylenedioxymethamphetamine (MDMA) and fenfluramine (FEN) share the common neurochemical action of acutely releasing central serotonin (5-HT), and yet their behavioral effects are quite different. The present study evaluated the effects of these compounds on acoustic and tactile startle reflexes. PCA and MDMA were qualitatively...
European Journal of Pharmacology
November 27, 1990
C J Schmidt, C K Black, G M Abbate et al.
We report that maintaining rats under chloral hydrate anesthesia for the first 3 h following the administration of 3,4-methylenedioxymethamphetamine (MDMA) blocks the decrease in forebrain concentrations of 5-hydroxytryptamine (5-HT) measured 1 week later. In contrast, the acute effect of MDMA (3 h) on forebrain 5-HT was not altered by the anesthetic. This protective effect of chloral hydrate...
European Journal of Pharmacology
May 31, 1990
C J Schmidt, C K Black, V L Taylor
The role of transmitter release in the serotonergic neurotoxicity of methylenedioxymethamphetamine (MDMA) was examined using treatments altering MDMA-induced release or its consequences. The long-term decrease in 5-HT concentrations and tryptophan hydroxylase activity produced by MDMA was antagonized by depletion of vesicular monoamines with reserpine or interruption of monoamine synthesis with...
European Journal of Pharmacology
October 26, 1988
C J Schmidt, V L Taylor
Acute peripheral administration of either the (+) or (-) stereoisomer of methylenedioxymethamphetamine (MDMA) to rats results in a rapid loss of tryptophan hydroxylase (TPH) activity in several brain regions. This decline in enzyme activity precedes a decrease in serotonin (5-HT) concentrations in the same areas. An initial rise in the concentration of 5-hydroxyindole acetic acid after drug...
European Journal of Pharmacology
April 7, 1987
C J Schmidt
The acute and long-term neurochemical effects of three methylenedioxyamphetamine analogs were examined in the serotonergic system of the rat brain. Methylenedioxymethamphetamine as well as its N-desmethyl and N-ethyl derivatives depleted cortical serotonin (5HT) concentrations to less than 30% of control 3 h after drug administration. All three compounds were also very similar in their effects...
Journal of Pharmacology and Experimental Therapeutics
1987
C J Schmidt
530 citations
The neurochemical effects of the unique psychedelic agent, methylenedioxymethamphetamine (MDMA), indicate it may be a serotonergic neurotoxin related to agents such as p-chloroamphetamine. MDMA had a biphasic effect on cortical serotonin concentrations beginning with an acute depletion of the transmitter which reached a maximum between 3 and 6 hr after drug administration. This early phase of...