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DMT: all studies

Page 154 of 160: studies 1,531 to 1,540 of 1,593, newest first. Back to the DMT overview

Research

Antagonism of the effects of the hallucinogen DOM and the purported 5-HT agonist quipazine by 5-HT2 antagonists.

European Journal of Pharmacology July 1, 1983

Rats trained to discriminate 1.0 mg/kg of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM) from saline in a two-lever operant choice task were administered doses of mescaline, LSD, 5-methoxy-N,N-dimethyltryptamine (5-OMe DMT), quipazine, TFMPP and RU-24969. The DOM-stimulus generalized to the three hallucinogenic agents and to quipazine, but not to the purported serotonin agonists TFMPP or...

Serotonin receptor activation in rats previously deprived of REM sleep.

Pharmacology, Biochemistry, and Behavior April 1, 1983 R Santos, E A Carlini 25 citations

The effects of serotonin precursors (L-5-hydroxytryptophan and L-tryptophan, with or without MAO inhibitors) and of agonists (quipazine and 5-methoxy-N,N-dimethyltryptamine-MeO-DMT) were studied in 3 day REM-deprived or control rats, by recording the presence of the serotonin syndrome and the number of head shakes. The REM sleep-deprived rats showed a larger incidence of the serotonin syndrome...

Effects of chronic administration of antidepressant drugs on central serotonergic receptor mechanisms

Palgrave Macmillan UK eBooks 1983 Sven Ove Ögren, Kjell Fuxé, Odd‐geir Berge et al. 11 citations

The present studies have shown that chronic antidepressant treatment with desipramine (DMI), imipramine (IMI) and zimelidine produced behavioral evidence for sub- and supersensitivity depending on 5-HT agonist dose and types of behavior examined. Thus, chronic treatment with all three drugs reduced head twitches induced by a high dose of the 5-HT agonist 5-methoxy-N,N-dimethyltryptamine...

DOI: 10.1007/978-1-349-06689-6_7 (opens in new tab) Serotonergic Desipramine Imipramine Antidepressant +4

Serotonin involvement in aversive conditioning: reversal of the fear retention deficit by long-term p-chloroamphetamine but not p-chlorophenylalanine.

Neuroscience Letters December 23, 1982 T Archer, S O Ogren, S B Ross 24 citations

5-Methoxy-N,N-dimethyltryptamine (5-MeO-DMT), a serotonin (5-HT) agonist, fenfluramine and p-chloroamphetamine (PCA), which are 5-HT releasers, produce deficits in fear retention as indicated by a notable lack of the immobility resulting from inescapable shocks. Depletion of central 5-HT neurones after long-term PCA treatment (2 X 10 mg/kg) completely blocked the retention impairment resulting...

Inhibition of prolactin release by stimulation of presynaptic serotonin autoreceptors.

Life Sciences December 6, 1982 J A Clemens, M E Roush 8 citations

The effects of 5-methoxy-N,N-dimethyltryptamine (5-MeODMT), a serotonin agonist with a preferential action on presynaptic autoreceptors, on prolactin release in male rats was determined. Basal serum prolactin levels were not altered after administration of 1.0, 2.0, 5.0, 10.0 or 20.0 mg/kg of 5-MeODMT. Pretreatment with 5-MeODMT reduced prolactin release by agents that depend on serotonergic...

Drug interactions do not support reduction in serotonin turnover as the mechanism of action of benzodiazepines.

Neuropharmacology October 1, 1982 R A Shephard, D A Buxton, P L Broadhurst 59 citations

Interactions between 5-methoxy, N,N-dimethyltryptamine (5-MeODMT), chlordiazepoxide and para-chlorophenylalanine (pCPA) on conflict behaviour were studied. 5-Methoxy, N,N-dimethyltryptamine (1.0 and 3.0 mg/kg), induced observable effects and reduced unpunished response rates but did not affect punished behaviour either alone, on in the presence of 5 or 10 mg/kg chlordiazepoxide. However,...

Medullary serotonergic neurons are insensitive to 5-MeoDMT and LSD.

European Journal of Pharmacology July 30, 1982 J Heym, G F Steinfels, Barry L. Jacobs 21 citations

A comparison was made of the effects of 5-MeoDMT or LSD on serotonergic unit activity in the dorsal raphe nucleus (DRN) and nucleus raphe pallidus (NRP) of freely moving cats. NRP neurons were substantially less responsive than DRN neurons to both drugs. NRP neurons were unresponsive to behaviorally effective low doses of these drugs whereas the activity of DRN neurons was strongly depressed....

Effects of diazepam and of serotonin agonists on hyponeophagia in rats.

Neuropharmacology April 1, 1982 R A Shephard, P L Broadhurst 53 citations

The effects of serotonin agonists, fenfluramine (2 mg/kg) and 5-methoxy N,N dimethyltryptamine (5-MeODMT, 2.5 mg/kg) on hyponeophagia were studied both alone and in combination with diazepam (1 mg/kg). Male and female rats were used but sex differences were not found. The serotonin agonists enhanced hyponeophagia while diazepam attenuated it and antagonised the actions of both serotonin...

Intracellular studies on the effects of systemic administration of serotonin agonists on rat facial motoneurons.

European Journal of Pharmacology February 26, 1982 C P Vandermaelen, George K. Aghajanian 37 citations

Intracellular recordings were made from facial motoneurons of anesthetized rats during systemic administration of 5-methoxy-N,-N-dimethyltryptamine (5-MeODMT) and p-chloroamphetamine (PCA), drugs which elicit the behavioral serotonin syndrome. Both drugs caused a slow depolarization, increased input resistance, and increased excitability of facial motoneurons. These changes are identical to...

Psilocybin as a discriminative stimulus: Lack of specificity in an animal behavior model for ?hallucinogens?

Psychopharmacology February 1, 1982 Jon Koerner, James B. Appel 19 citations

Fifteen rats were trained to discriminate between the tryptamine hallucinogen psilocybin (4-phosphoryloxy-N,N-dimethyltryptamine; 1.0 mg/kg) and saline in a two-lever choice task. Dose-response and time-response curves were obtained. The psilocybin cue generalized to psilocin (the dephosphorylated congener of psilocybin) and to the prototypical indoleamine hallucinogen LSD, but not to the...