Differential substitution for the discriminative stimulus effects of 3,4-methylenedioxymethamphetamine and methylphenidate in rats

• Published in: The Journal of pharmacology and experimental therapeutics Vol. 350; no. 2; pp. 403 - 411
• Main Authors: Mori, Tomohisa, Uzawa, Naoki, Kazawa, Haruyo, Watanabe, Hirohiko, Mochizuki, Ayano, Shibasaki, Masahiro, Yoshizawa, Kazumi, Higashiyama, Kimio, Suzuki, Tsutomu
• Format: Journal Article
• Language: English
• Published: United States 01.08.2014
• Subjects: Animals; Benzazepines - pharmacology; Central Nervous System Stimulants - pharmacology; Discrimination Learning - drug effects; Dose-Response Relationship, Drug; Male; Methylphenidate - pharmacology; N-Methyl-3,4-methylenedioxyamphetamine - pharmacology; Rats; Rats, Inbred F344; Receptor, Serotonin, 5-HT1A - physiology; Receptors, Serotonin, 5-HT2 - physiology; Receptors, sigma - physiology; Sigma-1 Receptor
• ISSN: 0022-3565; 1521-0103
• DOI: 10.1124/jpet.114.214288

Previous studies have demonstrated that methylphenidate, MDMA (3,4-methylenedioxymethamphetamine), and other psychostimulants exert stimulant-like subjective effects in humans. Furthermore, MDMA and methylphenidate substitute for the discriminative stimulus effects of psychostimulants, such as amphetamine and cocaine, in animals, which suggests that MDMA and methylphenidate may produce similar discriminative stimulus effects in rats. However, there is no evidence regarding the similarities between the discriminative stimulus effects of MDMA and methylphenidate. To explore this issue, cross-substitution, substitution, and combination tests were conducted in rats that had been trained to discriminate between MDMA (2.5 mg/kg) or methylphenidate (5.0 mg/kg) and saline. In the cross-substitution tests, MDMA and methylphenidate did not cross-substitute for each other. In the substitution test, methamphetamine substituted for the discriminative stimulus effects of methylphenidate, but not for those of MDMA. Furthermore, ephedrine and bupropion, which activate dopaminergic and noradrenergic systems, substituted for the discriminative stimulus effects of methylphenidate. On the other hand, serotonin (5-HT) receptor agonists 5-HT1A and 5-HT2 fully substituted for the discriminative stimulus effects of MDMA. These results suggest that activation of the noradrenergic and dopaminergic systems is important for the discriminative stimulus effects of methylphenidate, whereas activation of the serotonergic system is crucial for the discriminative stimulus effects of MDMA. Even though MDMA, like psychostimulants, exerts stimulant-like effects, our findings clearly indicate that the discriminative stimulus effects of MDMA are distinctly different from those of other psychostimulants in rats.