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Glenn D. Newport

4 papers in the library · 46 citations · publishing 1993-2003

Papers

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Plasma levels of parent compound and metabolites after doses of either d-fenfluramine or d-3,4-methylenedioxymethamphetamine (MDMA) that produce long-term serotonergic alterations.

Neurotoxicology June 2003 John F Bowyer, John F Young, William Slikker et al.

Plasma levels of parent compounds and metabolites were determined in adult rhesus monkeys after doses of either 5mg/kg d-fenfluramine (FEN) or 10mg/kg d-3, 4-methylenedioxymethamphetamine (MDMA) i.m. twice daily for four consecutive days. These treatment regimens have been previously shown to produce long-term serotonin (5-HT) depletions. Peak plasma levels of 2.0+/-0.4 microM FEN were reached...

Ibogaine blocked methamphetamine-induced hyperthermia and induction of heat shock protein in mice.

Brain Research March 27, 1999 X Yu, Syed Z. Imam, Glenn D. Newport et al. 17 citations

Body temperature changes and heat shock protein (HSP-72) induction in the caudate nucleus were studied in female C57BL/6N mice pretreated with ibogaine (50 mg/kg) and sacrificed 48 h. after a single dose of methamphetamine (20 mg/kg). Methamphetamine injection resulted in hyperthermia and induced HSP-72 expression, whereas treatment with ibogaine alone produced hypothermia. The ibogaine...

DOI: 10.1016/s0006-8993(99)01154-3 (opens in new tab) Full text (opens in new tab) Ibogaine: ibogaine This compound Methamphetamine: methamphetamine Counteract methamphetamine's impact +4

Neuroendocrine and neurochemical effects of acute ibogaine administration: a time course evaluation.

Brain Research October 21, 1996 S F Ali, Glenn D. Newport, William Slikker et al. 29 citations

Ibogaine (IBO) is an indole alkaloid that is reported to facilitate drug abstinence in substance abusers. Despite considerable investigation, the mechanism of IBO action in vivo and its suitability as a treatment for drug addiction remains unclear. The present study was designed to evaluate the time-course effects of acute IBO on neuroendocrine and neurochemical indices. Adult male rats were...

Oral administration of 3,4-methylenedioxymethamphetamine (MDMA) produces selective serotonergic depletion in the nonhuman primate.

Neurotoxicology and Teratology March 1, 1993 S F Ali, Glenn D. Newport, Andrew C. Scallet et al.

MDMA (3,4-methylenedioxymethamphetamine) has been reported to produce serotonergic depletion in nonhuman primates at doses as low as 2.5 mg/kg (1-2 times the typical human dose). The current study evaluated the dose-response relationships of MDMA (1.25-20.0 mg/kg) using regional concentrations of serotonin (5-HT) and its metabolite, 5-hydroxyindoleacetic acid (5-HIAA), and home cage behavior as...