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Ibogaine enhances the expression of locomotor sensitization in rats chronically treated with cocaine.

Karen K. Szumlinski, Isabelle M Maisonneuve, Stanley D Glick

Pharmacology, Biochemistry, and Behavior July 1, 1999 DOI: 10.1016/s0091-3057(99)00038-6 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Rats
Interventions Ibogaine Cocaine
Dose 40 mg/kg ibogaine, 7.5 mg/kg cocaine challenge, 15 mg/kg cocaine for chronic treatment
Duration 19-hour pretreatment interval; 5-day chronic cocaine treatment; two series of treatments with 3-4 day interval; 24-hour follow-up after second series
Topics Ibogaine
Keywords Anti-addiction compound Cocaine Stimulant Stimulating effects Drug interaction Drug synergy Drug potentiation Drug effects Heightened sensitivity Drug response Drug history Prior drug exposure Chronic drug use Drug experience
Citations 14
Key findings Ibogaine pretreatment potentiates cocaine-induced locomotion more strongly in rats with a history of chronic cocaine exposure than in cocaine-naive rats, and the effect increases with a second ibogaine treatment but dissipates within 24 hours.

Abstract

Pretreatment (19 h) with the putative antiaddictive agent, ibogaine, has been shown previously to potentiate cocaine-induced locomotion in rats. The present study demonstrates that the magnitude of this effect of ibogaine is dependent on the previous cocaine history of the animal, on the time following ibogaine treatment, and on the number of ibogaine treatments. Compared to rats with no previous cocaine experience, ibogaine pretreatment (40 mg/kg, IP, 19 h earlier) markedly enhanced the expression of locomotor sensitization in response to a cocaine challenge injection (7.5 mg/kg) in rats that were chronically treated with cocaine (15 mg/ kg, IP, daily for 5 days). Tolerance to cocaine-induced locomotor sensitization appeared to occur in vehicle-pretreated chronic cocaine controls. Following a second series of identical treatments (beginning 3-4 days after the initial treatment series), locomotor responding to the cocaine challenge was further enhanced by a second ibogaine injection in chronically cocaine-treated animals. Twenty-four hours later, when animals were challenged again with cocaine in the absence of any further ibogaine pretreatment, the effect of ibogaine had dissipated. Consistent with previous studies from this laboratory, these data demonstrate that ibogaine can enhance sensitivity to the psychomotor stimulant effect of cocaine. The results of the present study further indicate that the extent of this effect depends on the animal's history of exposure to both ibogaine and cocaine.

Comparable studies

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

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