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European Journal of Clinical Pharmacology

, Volume 68, Issue 4, pp 397–406 | Cite as

Influence of sex on propofol metabolism, a pilot study: implications for propofol anesthesia

  • Irena Loryan
  • Marja Lindqvist
  • Inger Johansson
  • Masahiro Hiratsuka
  • Ilse van der Heiden
  • Ron HN van Schaik
  • Jan Jakobsson
  • Magnus Ingelman-SundbergEmail author
Pharmacokinetics and Disposition

Abstract

Purpose

The basis of high intersubject variability of propofol metabolism is unclear. Therefore, we examined the influence of genetic polymorphisms of the key metabolizing enzymes cytochrome P450 2B6 (CYP2B6) and uridine diphosphate (UDP)-glucuronosyltransferase 1A9 (UGT1A9), age, and sex on propofol biotransformation in vitro and in vivo.

Methods

Plasma concentrations of propofol, 4-hydroxypropofol, and their glucuronides were measured over 20 min in 105 patients after a single intravenous bolus of propofol. Propofol 4-hydroxylation activity, genotypes, and content of CYP2B6 protein in 68 human livers were determined. The common single nucleotide polymorphisms (SNPs) for the CYP2B6 and UGT1A9 genes were analyzed by polymerase chain reaction (PCR).

Results

Plasma levels of propofol metabolites showed high interindividual variability (range of coefficient of variation 89–128%). This was supported by in vitro data showing similar variability of propofol 4-hydroxylation in liver microsomes and 1.9-fold higher CYP2B6 protein content in the livers from women. No significant relationships were revealed between the SNPs studied and propofol metabolism. However, patients’ sex had a pronounced effect on propofol metabolism. Thus, women had higher amounts of propofol glucuronide (1.25-fold; p = 0.03), 4-hydroxypropofol-1-glucuronide (2.1-fold; p = 0.0009), and 4-hydroxypropofol-4-glucuronide (1.7-fold; p = 0.02) as shown by the weight-corrected area under the time–plasma concentration curve of metabolites. Additionally, the sexual dimorphism in 4-hydroxypropofol glucuronidation was prominent in the 35- to 64-year-old subgroup.

Conclusions

No significant effects of CYP2B6 and UGT1A9 SNPs or age on propofol metabolism were revealed in this pilot study, but there was a pronounced effect of sex, a finding that indicates an important factor for the previously described sex difference in systemic clearance of propofol seen.

Keywords

Propofol Anesthesia Metabolism Sex UGT1A9 CYP2B6 

Abbreviations list

CYP2B6

Cytochrome P450 2B6

UGT1A9

UDP-glucuronosyltransferase 1A9

SNP

Single nucleotide polymorphism

PG

Propofol glucuronide

1-OHPG

4-hydroxypropofol-1-glucuronide

4-OHPG

4-hydroxyporpofol-4-glucuronide

4-OHPGs

Sum of 4-hydroxypropofol-1-glucuronide and 4-hydroxyporpofol-4-glucuronide

4-OHP

4-hydroxypropofol (2,6-diisopropyl-1,4-quinol)

HLM

Human liver microsomes

AUC20min

Area under the time-plasma concentration curve measured over 20 min

ASA

American Society of Anesthesiologists

Notes

Acknowledgments

We thank Pharsight Corporation for approving the free Academic Research Node License for WinNonLin through the Pharsight Academic License program. This research was supported by grants from the Swedish Research Council and from Karolinska Institutet. We are indebted to Åsa Nordling for valuable aid in analyses of propofol metabolites.

Supplementary material

228_2011_1132_MOESM1_ESM.docx (13 kb)
Supplementary Material 1 (DOCX 13 kb)
228_2011_1132_MOESM2_ESM.docx (14 kb)
Supplementary Material 2 (DOCX 14 kb)
228_2011_1132_MOESM3_ESM.docx (18 kb)
Supplementary Material 3 (DOCX 18 kb)

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Copyright information

© Springer-Verlag 2011

Authors and Affiliations

  • Irena Loryan
    • 1
  • Marja Lindqvist
    • 1
  • Inger Johansson
    • 1
  • Masahiro Hiratsuka
    • 1
    • 3
  • Ilse van der Heiden
    • 2
  • Ron HN van Schaik
    • 2
  • Jan Jakobsson
    • 1
  • Magnus Ingelman-Sundberg
    • 1
    Email author
  1. 1.Section of Pharmacogenetics, Department of Physiology and PharmacologyKarolinska InstitutetStockholmSweden
  2. 2.Department of Clinical ChemistryErasmus MC RotterdamRotterdamThe Netherlands
  3. 3.Laboratory of Pharmacotherapy of Life-Style Related Diseases, Graduate School of Pharmaceutical SciencesTohoku UniversitySendaiJapan

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