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Intravenous self-injection of four novel phenethylamines in baboons

Christine A. Sannerud, B. Kaminski, Roland R. Griffiths

Behavioural Pharmacology August 1, 1996 DOI: 10.1097/00008877-199608000-00002 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical experimental study Peer reviewed
Population Baboons
Interventions MDE N-OH-MDA NNDMA BDMPEA
Dose 0.32 mg/kg/injection cocaine (training dose); doses of test compounds not specified in abstract
Duration 15 or more successive days of substitution for cocaine
Topics Serotonin
Keywords Phenethylamines Self-administration Pharmacology Amphetamine Phencyclidine Fenfluramine Decussation Toxicity Anesthesia Dopamine
Citations 9
Key findings High doses of MDE and N-OH-MDA maintained self-injection in baboons, while NNDMA did not reliably do so, and BDMPEA maintained self-injection in each of three baboons at one or more doses.

Abstract

The present study evaluated the intravenous self-administration of four substituted phenethylamines, using a substitution procedure in baboons. Baboons were trained to self-inject 0.32mg/kg/injection cocaine under a fixed-ration (FR) schedule, with a 3h timeout following each injection. Doses of (+/-)-N-ethyl-3, 4-methylenedioxyamphetamine HCI (MDE), (+/-)-N-hydroxy-3, 4-methylendioxyamphetamine HCI (N-OH-MDA), (+)-N-N-dimethylamphetamine HCI (NNDMA), and 4-bromo-2,5-dimethyoxy-beta-phenethylamine (BDMPEA) and their vehicles were substituted for cocaine for 15 or more successive days. High doses of MDE and N-OH-MDA maintained self-injection; however, NNDMA and BDMPEA self-injection was less consistent. NNDMA did not reliably maintain self-injection, whereas one or more doses of BDMPEA maintained self-injection in each of three baboons. Intermediate to high doses of all four compounds decreased food pellet intake maintained under a FR schedule of reinforcement on a different lever. In some baboons, high doses of N-OH-MDA, NNDMA and BDMPEA produced signs of behavioral toxicity (e.g. cyclic pattern of self-injection, behavioral agitation, stereotypical movements) that were similar to those previously observed after administration of high doses of classic psychomotor stimulants such as d-amphetamine; however, the severity and profile of this behavioral toxicity differed between compounds. Thus, the present study documents both similarities and differences in the behavioral profiles of these four phenethylamines.

Comparable studies

Other preclinical and animal studies on serotonin, most cited first.

Citations in the library

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