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Related Experiment Video

Updated: Jul 13, 2026

Measurement of Fatty Acid β-Oxidation in a Suspension of Freshly Isolated Mouse Hepatocytes
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Measurement of Fatty Acid β-Oxidation in a Suspension of Freshly Isolated Mouse Hepatocytes

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Inter-individual variability in esterases in human liver.

Christopher Jewell1, Phillippa Bennett, Elaine Mutch

  • 1Toxicology Unit, School of Clinical and Laboratory Sciences, 4th Floor, Devonshire Building, Devonshire Terrace, University of Newcastle upon Tyne, Newcastle upon Tyne NE2 4EA, UK.

Biochemical Pharmacology
|July 27, 2007
PubMed
Summary

Human liver carboxylesterases metabolize esters, including drugs. Studies show varying hydrolysis rates in liver fractions, with smaller leaving groups and phenylvalerate correlating with specific enzyme activity (hCE1).

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Area of Science:

  • Biochemistry
  • Pharmacology
  • Enzymology

Background:

  • Human liver possesses numerous hydrolytic enzymes crucial for metabolizing endogenous and exogenous esters.
  • Carboxylesterases (EC 3.1.1.1) are a key enzyme group, capable of hydrolyzing diverse ester substrates, including pro-ester prodrugs.

Purpose of the Study:

  • To investigate carboxylesterase activity in human liver subcellular fractions.
  • To compare intra- and inter-individual variations in the metabolism of phenylvalerate and a series of paraben esters.
  • To explore the relationship between substrate structure and enzyme involvement, particularly distinguishing between carboxylesterase 1 (hCE1) and carboxylesterase 2 (hCE2).

Main Methods:

  • Assessed carboxylesterase activity in liver subcellular fractions from 22 individuals.
  • Utilized phenylvalerate as a general carboxylesterase substrate.
  • Employed a homologous series of paraben esters (methyl-, ethyl-, propyl-, butyl-, and benzylparaben) to examine substrate specificity.
  • Compared hydrolysis rates between microsomal and cytosolic fractions.

Main Results:

  • Hydrolysis rates were consistently higher in microsomal fractions compared to cytosolic fractions for all tested ester substrates.
  • Paraben hydrolysis rates decreased with increasing size of the alcohol leaving group.
  • Individuals exhibiting high hydrolysis rates for methyl paraben also showed high rates for other parabens and phenylvalerate.
  • Phenylvalerate hydrolysis strongly correlated with small alcohol leaving group parabens, indicating significant involvement of human carboxylesterase 1 (hCE1).
  • Lower correlations with larger alcohol leaving group parabens suggest increased involvement of human carboxylesterase 2 (hCE2).

Conclusions:

  • Carboxylesterase activity in human liver exhibits significant inter-individual variability.
  • The size of the ester leaving group influences the rate of hydrolysis, with smaller groups being processed more rapidly.
  • Phenylvalerate serves as a reliable substrate for assessing hCE1 activity, while larger parabens may involve hCE2, providing insights into enzyme specificity.