Binding of Inhibitory Fatty Acids Is Responsible for the Enhancement of UDP-Glucuronosyltransferase 2B7 Activity by Albumin: Implications for in Vitro-in Vivo Extrapolation

• Published in: The Journal of pharmacology and experimental therapeutics 2007-04, Vol.321 (1), p.137-147
• Main Authors: Rowland, Andrew, Gaganis, Paraskevi, Elliot, David J, Mackenzie, Peter I, Knights, Kathleen M, Miners, John O
• Format: Article
• Language: English
• Subjects: Albumins - pharmacology; Animals; Anti-HIV Agents - metabolism; Blotting, Western; Cattle; Chromatography, High Pressure Liquid; Data Interpretation, Statistical; Fatty Acids - metabolism; Glucuronides - metabolism; Glucuronosyltransferase - metabolism; Humans; Hymecromone - analogs & derivatives; Hymecromone - metabolism; In Vitro Techniques; Kinetics; Microsomes - metabolism; Protein Binding; Recombinant Proteins - metabolism; Serum Albumin - pharmacology; Serum Albumin, Bovine - pharmacology; Zidovudine - metabolism
• ISSN: 0022-3565; 1521-0103
• DOI: 10.1124/jpet.106.118216

Studies were performed to elucidate the mechanism responsible for the reduction in K m values of UDP-glucuronosyltransferase 2B7 (UGT2B7) substrates observed for incubations conducted in the presence of albumin. Addition of bovine serum albumin (BSA) and fatty acid-free human serum albumin (HSA-FAF), but not “crude” HSA, resulted in an approximate 90% reduction in the K m values for the glucuronidation of zidovudine (AZT) by human liver microsomes (HLM) and UGT2B7 and a 50 to 75% reduction in the S 50 for 4-methylumbelliferone (4MU) glucuronidation by UGT2B7, without affecting V max . Oleic, linoleic, and arachidonic acids were shown to be the most abundant unsaturated long-chain fatty acids present in crude HSA and in the membranes of HLM and human embryonic kidney (HEK)293 cells, and it was demonstrated that these and other unsaturated long-chain fatty acids were UGT2B7 substrates. Glucuronides with R f (retention factor) values corresponding to the glucuronides of linoleic and arachidonic acid were detected when HLM and HEK293 cell lysates were incubated with radiolabeled cofactor, and the intensity of the bands was modulated by the presence of crude HSA (increased) and BSA or HSA-FAF (decreased). Oleic, linoleic, and arachidonic acid inhibited AZT and 4MU glucuronidation by HLM and/or UGT2B7, due to an increase in K m /S 50 without a change in V max . Addition of BSA and HSA-FAF reversed the inhibition. Likewise, coexpression of UGT2B7 and HSA in HEK293 cells reduced the K m /S 50 values of these substrates. It is postulated that BSA and HSA-FAF sequester inhibitory fatty acids released during incubations, and the apparent high K m values observed for UGT2B7 substrates arise from the presence of these endogenous inhibitors.