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Interactions of partial LSD analogs with behavioral disrupting effects of LSD and DMT in the rat.

B Kovacic, L J Wang Lu, D Ruffing, E F Domino

European Journal of Pharmacology January 1, 1978 DOI: 10.1016/0014-2999(78)90371-0 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Animal behavioral pharmacology experiment (preclinical) Peer reviewed
Population Adult male Holtzman rats
Interventions LSD DMT N N-diethylnipecotamide derivatives N-diethylbutyramide (DBA) 1-methyl-1 2 5 6-tetrahydropyridine-3-(N N-diethylcarboxamide) (THPC)
Dose LSD 0.1 mg/kg; DMT 3.2 or 10 mg/kg; pretreatment compounds 5–40 mg/kg
Topics DMT LSD
Key findings LSD (0.1 mg/kg) and DMT (3.2 or 10 mg/kg) completely abolished FR4 bar-pressing for sweetened milk, with responding usually resuming within an hour at near control rates. Pretreatment with N,N-diethylnipecotamide derivatives, DBA, or THPC (5–40 mg/kg) either did not affect or prolonged the hallucinogen-induced suppression of bar-pressing; none shortened it.

Abstract

Adult male Holtzman rats were trained to barpress on a schedule whereby every fourth press earned a reward of 0.01 ml of sugar-sweetened milk (FR4). After an i.p. injection of LSD (0.1 mg/kg) or DMT (3.2 or 10 mg/kg) such barpressing is abolished completely and resumed, usually within an hour, at a rate near the preinjection control rate of pressing. It continues at a steady, uninterrupted pace until the animals are removed from the operant chamber one-half hour later. A series of N,N-diethylnipecotamide derivatives were synthesized and tested for their ability to modify the disruptive effect of these hallucinogens. N,N-diethylbutyramide (DBA) and 1-methyl-1,2,5,6-tetrahydropyridine-3-(N,N-diethylcarboxamide) (THPC) were also tested. Pretreatment with a single i.p. injection of any of these compounds (5--40 mg/kg) either had no effect on or else prolonged the duration of hallucinogen-induced cessation of barpressing.

Comparable studies

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