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Department of Pharmaceutical Sciences (M.A.H.) and the
Pharmacology/Toxicology Graduate Program (M.A.H., W.-J.P.),
College of Pharmacy, Washington State University
We investigated the effect of intravenous alcohol coadministration
on the pharmacokinetics of cocaine in awake, freely moving rats using
the microdialysis technique. Alcohol coadministration resulted in
faster rate of cocaine absorption after intraperitoneal administration
leading to higher cocaine plasma concentration. The higher plasma
cocaine concentration resulted in a proportional increase in the
cocaine brain extracellular fluid concentration. However, cocaine brain
extracellular fluid/plasma distribution ratio, determined from the
ratio of the corresponding cocaine area under the concentration-time
curves, was not affected by alcohol coadministration. Cocaethylene was
detected only after administration of cocaine + alcohol. The brain
extracellular fluid/plasma distribution ratio of cocaethylene was
similar to that of cocaine. The higher cocaine concentrations in plasma
and brain extracellular fluid, in addition to the formation of the
pharmacologically active metabolite cocaethylene are, at least
partially, responsible for the increased cocaine effects produced after
administration of this drug combination.
This article has been cited by other articles:
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C. E. Lau and L. Sun The Pharmacokinetic Determinants of the Frequency and Pattern of Intravenous Cocaine Self-administration in Rats by Pharmacokinetic Modeling Drug Metab. Dispos., March 1, 2002; 30(3): 254 - 261. [Abstract] [Full Text] [PDF] |
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