Intravenous butyrylcholinesterase administration and plasma and brain levels of cocaine and metabolites in rats

Gilberto N. Carmona, Charles W. Schindler, Nigel H. Greig, Harold W. Holloway, Rebecca A. Jufer, Edward J. Cone, David A. Gorelick

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


Butyrylcholinesterase is a major cocaine-metabolizing enzyme in humans and other primates, catalyzing hydrolysis to ecgonine methylester. Increasing butyrylcholinesterase activity may be a treatment for cocaine addiction. We evaluated the effect of 30-min pretreatment with horse-derived butyrylcholinesterase (5-15,000 U i.v.) or with the selective butyrylcholinesterase inhibitor cymserine (10 mg/kg i.v.) on the metabolism of cocaine (17 mg/kg i.p.) in anesthetized rats. Venous blood samples were collected for two hours after cocaine administration and later assayed for cocaine and metabolites by gas chromatography/mass spectroscopy. Whole brains were collected after the last blood sample and similarly assayed. Butyrylcholinesterase significantly increased plasma and brain ecgonine methylester levels and decreased cocaine plasma half-life from 26.2 min (saline) to 16.4 min (15,000 U). Butyrylcholinesterase had no significant effect on plasma or brain cocaine or benzoylecgonine levels. Cymserine had no effect on any variable. These findings suggest that butyrylcholinesterase treatment may have benefits in enhancing cocaine metabolism and in increasing levels of ecgonine methylester, which may have a protective action against cocaine.

Original languageEnglish (US)
Pages (from-to)186-190
Number of pages5
JournalEuropean Journal of Pharmacology
Issue number3
StatePublished - Jul 11 2005


  • (Rat)
  • Benzoylecgonine
  • Butyrylcholinesterase
  • Cocaine
  • Cymserine
  • Ecgonine methylester

ASJC Scopus subject areas

  • Pharmacology


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