JPET

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by KUBENA, R. K.
Right arrow Articles by BARRY, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by KUBENA, R. K.
Right arrow Articles by BARRY, H., III
Journal of Pharmacology And Experimental Therapeutics, Vol. 173, Issue 1, 94-100, 1970
Copyright © 1970 by American Society for Pharmacology and Experimental Therapeutics


INTERACTIONS OF Dgr1-TETRAHYDROCANNABINOL WITH BARBITURATES AND METHAMPHETAMINE

ROBERT K. KUBENA 1 and HERBERT BARRY III 1

1 Department of Pharmacology, University of Pittsbvrgh School of Pharmacy, Pittsburgh, Pennsylvania

NIale albino rats were tested for interactions of Dgr1-tetrahvdrocannabinol (Dgr1-THC), a pure, synthesized compound thought to be the principal euphoric constituent of marihuana, with the depressant action of two barbiturates and with the stimulant action of methamphetamine. In a test of spontaneous motor activity in a photocell arena, Dgr1-THC (4 and 16 mg/kg) potentiated the depressant effect of both pentobarbital (10 mg/kg) and barbital (120 mg/kg). The same doses of Dgr1-THC also prolonged sleeping time under pentobarbital (30 mg/kg) and barbital (240 mg/kg). Since barbital is not metabolized, interaction with . Dgr1-THC is attributable to synergetic depressant actions in the central nervous system rather than inhibition of microsomal enzymes. The higher dose of Dgr1-THC (16 mg/kg), which by itself greatly decreased spontaneous motor activity, failed to diminish the stimulant effect of two doses of methamphetamine (0.5 and 2 mg/kg). However, the percentage of animals surviving a toxic dose of methamphetamine (25 mg/kg) was increased by Dgr1-THC (4 and 16 mg/kg). The findings suggest that Dgr1-THC has sedative or tranquilizing actions. enhancing depressant effects of barbiturates and counteracting toxic effects of methamphetamine stimulation. These interactions with other drugs were found even with a low dose of Dgr1-THC (4 mg/kg). which by itself had little effect on spontaneous motor activity.

Submitted on July 15, 1969
Accepted on December 18, 1969




This article has been cited by other articles:


Home page
Endocr. Rev.Home page
U. Pagotto, G. Marsicano, D. Cota, B. Lutz, and R. Pasquali
The Emerging Role of the Endocannabinoid System in Endocrine Regulation and Energy Balance
Endocr. Rev., February 1, 2006; 27(1): 73 - 100.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
L. M. Newman, M. P. Lutz, M. H. Gould, and E. F. Domino
Dgr9-Tetrahydrocannabinol and Ethyl Alcohol: Evidence for Cross-Tolerance in the Rat
Science, March 3, 1972; 175(4025): 1022 - 1023.
[Abstract] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1970 by the American Society for Pharmacology and Experimental Therapeutics.