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Serotonin research published in 2005

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Studies

Prenatal 3,4-methylenedioxymethamphetamine (ecstasy) exposure induces long-term alterations in the dopaminergic and serotonergic functions in the rat.

Brain research. Developmental brain research February 8, 2005 Laurent Galineau, Catherine Belzung, Ercem Kodas et al.

We investigated several aspects of the dopaminergic and serotonergic functions throughout brain development in rats prenatally exposed to MDMA ("ecstasy"). Pregnant rats were treated with MDMA (10 mg/kg s.c.) or saline from the 13th to the 20th day of gestation and studies were conducted on the progeny from both groups: (i) quantification of whole brain contents of DA, 5-HT and metabolites from...

Modulating the Rate and Rhythmicity of Perceptual Rivalry Alternations with the Mixed 5-HT2A and 5-HT1A Agonist Psilocybin

Neuropsychopharmacology January 26, 2005 Olivia Carter, John D. Pettigrew, Felix Hasler et al. 122 citations

Binocular rivalry occurs when different images are presented simultaneously to corresponding points within the left and right eyes. Under these conditions, the observer's perception will alternate between the two perceptual alternatives. Motivated by the reported link between the rate of perceptual alternations, symptoms of psychosis and an incidental observation that the rhythmicity of...

A comparative study on the acute and long‐term effects of MDMA and 3,4‐dihydroxymethamphetamine (HHMA) on brain monoamine levels after i.p. or striatal administration in mice

British Journal of Pharmacology 2005 Isabel Escobedo, Esther O’shea, Laura Orío et al. 68 citations

This study investigated whether the immediate and long‐term effects of 3,4‐methylenedioxymethamphetamine (MDMA) on monoamines in mouse brain are due to the parent compound and the possible contribution of a major reactive metabolite, 3,4‐dihydroxymethamphetamine (HHMA), to these changes. The acute effect of each compound on rectal temperature was also determined. MDMA given i.p. (30 mg kg −1 ,...

DOI: 10.1038/sj.bjp.0706071 (opens in new tab) MDMA Serotonin Dopamine Monoamine neurotransmitter +5

Repeated MDMA (“Ecstasy”) exposure in adolescent male rats alters temperature regulation, spontaneous motor activity, attention, and serotonin transporter binding

Developmental Psychobiology 2005 Brian J. Piper, Joseph B. Fraiman, Jerrold S. Meyer 71 citations

Previous research in our laboratory found that repeated exposure of adolescent rats to 3,4-methylenedioxymethamphetamine (MDMA) impaired working memory and reduced anxiety. The present experiment extended these findings by investigating the physiological, behavioral, and neurotoxic effects of a modified MDMA treatment regimen. Male Sprague-Dawley rats received 5 mg/kg of MDMA hourly for a...

DOI: 10.1002/dev.20085 (opens in new tab) MDMA Ecstasy Habituation Serotonin transporter +3

Interaction between LSD and dopamine D2/3 binding sites in pig brain

Synapse 2005 Luciano Minuzzi, George G. Nomikos, Mark Wade et al. 25 citations

The psychoactive properties of the hallucinogen LSD have frequently been attributed to high affinity interactions with serotonin 5HT2 receptors in brain. Possible effects of LSD on dopamine D2/3 receptor availability have not previously been investigated in living brain. Therefore, we used PET to map the binding potential (pB) of [11C]raclopride in brain of three pigs, first in a baseline...

DOI: 10.1002/syn.20141 (opens in new tab) Serotonin Raclopride Dopamine receptor d2 Pharmacology +4

Tryptamines as Ligands and Modulators of the Serotonin 5‑HT2A Receptor and the Isolation of Aeruginascin from the Hallucinogenic Mushroom Inocybe aeruginascens

2005 Niels Jensen 8 citations

Aeruginascin ist ein Naturstoff aus dem halluzinogenen Pilz Inocybe aeruginascens. Die Substanz wurde isoliert und als 4-Phosphoryloxy-N,N,N-trimethyl-tryptamin identifiziert. Aeruginascin ist das quartäre Trimethylammonium-Analogon der halluzinogenen Substanz Psilocybin. Synthetisches Aeruginascin war in allen Aspekten identisch mit der isolierten Probe. Zusätzlich wurden die Pilzalkaloide...