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Serotonin research published in 2007

Page 2 of 2: studies 21 to 28 of 28, newest first. Back to the serotonin overview

Studies

The Effects of the Preferential 5-HT2A Agonist Psilocybin on Prepulse Inhibition of Startle in Healthy Human Volunteers Depend on Interstimulus Interval

Neuropsychopharmacology February 14, 2007 Franz X. Vollenweider, Philipp A Csomor, Bernhard Knappe et al. 194 citations

Schizophrenia patients exhibit impairments in prepulse inhibition (PPI) of the startle response. Hallucinogenic 5-HT(2A) receptor agonists are used for animal models of schizophrenia because they mimic some symptoms of schizophrenia in humans and induce PPI deficits in animals. Nevertheless, one report indicates that the 5-HT(2A) receptor agonist psilocybin increases PPI in healthy humans....

DOI: 10.1038/sj.npp.1301324 (opens in new tab) Full text (opens in new tab) Psilocybin Prepulse inhibition Hallucinogen Interstimulus interval +7

5-Hydroxytryptamine (serotonin)2A receptors in rat anterior cingulate cortex mediate the discriminative stimulus properties of d-lysergic acid diethylamide.

Journal of Pharmacology and Experimental Therapeutics February 2007 Paul J Gresch, Robert J. Barrett, Elaine Sanders‐bush et al.

d-Lysergic acid diethylamide (LSD), an indoleamine hallucinogen, produces profound alterations in mood, thought, and perception in humans. The brain site(s) that mediates the effects of LSD is currently unknown. In this study, we combine the drug discrimination paradigm with intracerebral microinjections to investigate the anatomical localization of the discriminative stimulus of LSD in rats....

Hallucinogens recruit specific cortical 5-HT(2A) receptor-mediated signaling pathways to affect behavior.

Neuron February 1, 2007 Javier González-Maeso, Noelia V Weisstaub, Mingming Zhou et al.

Hallucinogens, including mescaline, psilocybin, and lysergic acid diethylamide (LSD), profoundly affect perception, cognition, and mood. All known drugs of this class are 5-HT(2A) receptor (2AR) agonists, yet closely related 2AR agonists such as lisuride lack comparable psychoactive properties. Why only certain 2AR agonists are hallucinogens and which neural circuits mediate their effects are...

5-HT1A receptors are involved in the anxiolytic effect of Delta9-tetrahydrocannabinol and AM 404, the anandamide transport inhibitor, in Sprague-Dawley rats.

European Journal of Pharmacology January 26, 2007 Daniela Braida, Valeria Limonta, Lorenzo Malabarba et al.

The mechanism mediating the effects of cannabinoids on anxiety-related responses appear to involve cannabinoid CB1 and non-CB1 receptors. However, other neurotransmitters may play a role in such effect. This study shows evidence of an interaction between endocannabinoid system and serotonin (5-HT), 1A receptor subtype on anxiety-like behavior in Sprague-Dawley rats. The exogenous cannabinoid...

Psychedelic bliss : memory and risk taking during MDMA intoxication

2007 Kim P. C. Kuypers 2 citations

In addition to the positive effects, ecstasy use is also accompanied by short-term side effects occurring early, with respect to administration, and later on.Early short time side effects i.e. fatigue, lack of energy and difficulty concentrating, arise approximately 24 hours after MDMA ingestion.Late short-term side effects occur up to 7 days post-drug and are more or less comparable to early...

MDMA (Ecstasy)

Annals of Clinical Psychiatry 2007 Rif S El-Mallakh, Henry David Abraham 17 citations

BACKGROUND: 3,4-Methylenedioxymethamphetamine (MDMA or Ecstasy) is a synthetic amphetamine analogue that is recreationally used to obtain a psychological effect of enhanced affiliative emotional response. Its use in Western countries appears to be increasing, particularly among young individuals. METHODS: Pertinent basic and clinical literature is critically reviewed. RESULTS: A significant...

Effects of (±) 3,4-Methylenedioxymethamphetamine (MDMA) on Sleep and Circadian Rhythms

TheScientificWorldJournal 2007 Una D. Mccann, George A. Ricaurte 52 citations

Abuse of stimulant drugs invariably leads to a disruption in sleep-wake patterns by virtue of the arousing and sleep-preventing effects of these drugs. Certain stimulants, such as 3,4-methylenedioxymethamphetamine (MDMA), may also have the potential to produce persistent alterations in circadian regulation and sleep because they can be neurotoxic toward brain monoaminergic neurons involved in...

In Vitro Screening of Psychoactive Drugs by [35S]GTP.GAMMA.S Binding in Rat Brain Membranes

Biological and Pharmaceutical Bulletin 2007 Ryouichi Nonaka, Fumiko Nagai, Akio Ogata et al. 31 citations

We constructed a reproducible, simple, and small-scale determination method of the psychoactive drugs that acted directly on the monoamine receptor by measuring the activation of [(35)S]guanosine-5'-O-(3-thio)-triphosphate binding to guanine nucleotide-binding proteins (G proteins). This method can simultaneously measure the effects of three monoamines, namely dopamine (DA), serotonin (5-HT),...

DOI: 10.1248/bpb.30.2328 (opens in new tab) Serotonin Phenethylamines Monoamine neurotransmitter Tryptamines +5