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Role of Cytochrome P4502B6 Polymorphisms in Ketamine Metabolism and Clearance.

Publication ,  Journal Article
Rao, LK; Flaker, AM; Friedel, CC; Kharasch, ED
Published in: Anesthesiology
December 2016

BACKGROUND: At therapeutic concentrations, cytochrome P4502B6 (CYP2B6) is the major P450 isoform catalyzing hepatic ketamine N-demethylation to norketamine in vitro. The CYP2B6 gene is highly polymorphic. The most common variant allele, CYP2B6*6, is associated with diminished hepatic CYP2B6 expression and catalytic activity compared with wild-type CYP2B6*1/*1. CYP2B6.6, the protein encoded by the CYP2B6*6 allele, and liver microsomes from CYP2B6*6 carriers had diminished ketamine metabolism in vitro. This investigation tested whether humans with the CYP2B6*6 allele would have decreased clinical ketamine metabolism and clearance. METHODS: Thirty volunteers with CYP2B6*1/*1, *1/*6, or *6/*6 genotypes (n = 10 each) received a subsedating dose of oral ketamine. Plasma and urine concentrations of ketamine and the major CYP2B6-dependent metabolites were determined by mass spectrometry. Subjects' self-assessment of ketamine effects were also recorded. The primary outcome was ketamine N-demethylation, measured as the plasma norketamine/ketamine area under the curve ratio. Secondary outcomes included plasma ketamine enantiomer and metabolite area under the plasma concentration-time curve, maximum concentrations, apparent oral clearance, and metabolite formation clearances. RESULTS: There was no significant difference between CYP2B6 genotypes in ketamine metabolism or any of the secondary outcome measures. Subjective self-assessment did reveal some differences in energy and level of awareness among subjects. CONCLUSIONS: These results show that while the CYP2B6*6 polymorphism results in diminished ketamine metabolism in vitro, this allelic variant did not affect single, low-dose ketamine metabolism, clearance, and pharmacokinetics in vivo. While in vitro drug metabolism studies may be informative, clinical investigations in general are needed to validate in vitro observations.

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Published In

Anesthesiology

DOI

EISSN

1528-1175

Publication Date

December 2016

Volume

125

Issue

6

Start / End Page

1103 / 1112

Location

United States

Related Subject Headings

  • Young Adult
  • Polymorphism, Genetic
  • Middle Aged
  • Male
  • Ketamine
  • Humans
  • Female
  • Cytochrome P-450 CYP2B6
  • Anesthetics, Dissociative
  • Anesthesiology
 

Citation

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Chicago
ICMJE
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Rao, L. K., Flaker, A. M., Friedel, C. C., & Kharasch, E. D. (2016). Role of Cytochrome P4502B6 Polymorphisms in Ketamine Metabolism and Clearance. Anesthesiology, 125(6), 1103–1112. https://doi.org/10.1097/ALN.0000000000001392
Rao, Lesley K., Alicia M. Flaker, Christina C. Friedel, and Evan D. Kharasch. “Role of Cytochrome P4502B6 Polymorphisms in Ketamine Metabolism and Clearance.Anesthesiology 125, no. 6 (December 2016): 1103–12. https://doi.org/10.1097/ALN.0000000000001392.
Rao LK, Flaker AM, Friedel CC, Kharasch ED. Role of Cytochrome P4502B6 Polymorphisms in Ketamine Metabolism and Clearance. Anesthesiology. 2016 Dec;125(6):1103–12.
Rao, Lesley K., et al. “Role of Cytochrome P4502B6 Polymorphisms in Ketamine Metabolism and Clearance.Anesthesiology, vol. 125, no. 6, Dec. 2016, pp. 1103–12. Pubmed, doi:10.1097/ALN.0000000000001392.
Rao LK, Flaker AM, Friedel CC, Kharasch ED. Role of Cytochrome P4502B6 Polymorphisms in Ketamine Metabolism and Clearance. Anesthesiology. 2016 Dec;125(6):1103–1112.

Published In

Anesthesiology

DOI

EISSN

1528-1175

Publication Date

December 2016

Volume

125

Issue

6

Start / End Page

1103 / 1112

Location

United States

Related Subject Headings

  • Young Adult
  • Polymorphism, Genetic
  • Middle Aged
  • Male
  • Ketamine
  • Humans
  • Female
  • Cytochrome P-450 CYP2B6
  • Anesthetics, Dissociative
  • Anesthesiology