Abstract
Sydnocarb (3-(β-phenylisopropyl)-N-phenylcarbamoylsydnonimine) is a psychostimulant in clinical practice in Russia as a primary and adjunct therapy for a host of psychiatric disorders, including schizophrenia and depression. It has been described as a stimulant with an addiction liability and toxicity less than that of amphetamines. The present study undertook to evaluate the psychomotor stimulant effects of sydnocarb in comparison to those of methamphetamine. Sydnocarb increased locomotor activity of mice with reduced potency (∼10-fold) and efficacy compared with methamphetamine. Sydnocarb blocked the locomotor depressant effects of haloperidol at doses that were inactive when given alone. The locomotor stimulant effects of both methamphetamine and sydnocarb were dose-dependently blocked by the dopamine D1 and D2 antagonists SCH 39166 and spiperone, respectively; blockade generally occurred at doses of the antagonists that did not depress locomotor activity when given alone. In mice trained to discriminate methamphetamine from saline, sydnocarb fully substituted for methamphetamine with a 9-fold lower potency. When substituted for methamphetamine under self-administration experiments in rats, 10-fold higher concentrations of sydnocarb maintained responding by its i.v. presentation. Sydnocarb engendered stereotypy in high doses with approximately a 2-fold lower potency than methamphetamine. However, sydnocarb was much less efficacious than methamphetamine in inducing stereotyped behavior. Both sydnocarb and methamphetamine increased dialysate levels of dopamine in mouse striatum; however, the potency and efficacy of sydnocarb was less than methamphetamine. The convulsive effects of cocaine were significantly enhanced by the coadministration of nontoxic doses of methamphetamine but not of sydnocarb. Taken together, the present findings indicate that sydnocarb has psychomotor stimulant effects that are shared by methamphetamine while demonstrating a reduced behavioral toxicity.
Footnotes
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Send reprint requests to: J.M. Witkin, Drug Development Group, National Institute on Drug Abuse Addiction Research Center, 5500 Nathan Shock Drive, Baltimore, MD 21224. E-mail:jwitkin{at}intra.nida.nih.gov
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↵1 Animals used in these studies were maintained in facilities fully accredited by the American Association for the Accreditation of Laboratory Animal Care. In conducting the research described in this report, the investigators adhered to the “Guide for the Care and Use of Laboratory Animals”, as promulgated by the Committee on the Care and Use of Laboratory Animals of the Institute of Laboratory Animal Resources, National Research Council. Some of the data presented here were published in abstract form: Chefer V, Shippenberg TS, He M, Savtchenko N, Gloushkov R and Witkin J (1997) Behavioral and neurochemical effects of sydnocarb: A novel psychomotor stimulant. Soc Neurosci Abst23:1090.
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↵2 Partly supported by the Netherlands Organization for Scientific Research (NWO). Present address: Department of Medicinal Chemistry, University Center of Pharmacy, Ant. Deusinglaan 1, 9713 AW Groningen, the Netherlands.
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↵3 Visiting Fellow in the National Institutes of Health Visiting Program granted from Fogarty International Center.
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↵4 A Visiting Fellow in the National Institutes of Health Visiting Program granted from Fogarty International Center, Bethesda, MD. Permanent address: Department of Pharmacology, Medical University School, Lublin, Poland.
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↵5 A Visiting Fellow in the National Institutes of Health Visiting Program granted from Fogarty International Center, Bethesda, MD. Permanent address: Pavlov Institute of Physiology, Russian Academy of Science, 6 Nab. Makarova, St.Petersburg, Russia, 199164.
- Abbreviations:
- DA
- dopamine
- DMSO
- dimethyl sulfoxide
- SCH 39166
- [(−)-trans-6,7,7a,8,9,13b-hexahydro-3-chloro-2-hydroxy-N-methyl-5H-benzo[d]naptho-{2–1-b}azepine]
- FR
- fixed ratio
- Received May 11, 1998.
- Accepted October 25, 1998.
- The American Society for Pharmacology and Experimental Therapeutics
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