Purpose: Glucuronidation pathway is very important in the detoxification of endogenous and exogenous compounds. The objective of this study was to evaluate the activity and expression of various hepatic uridine diphosphate glucuronosyltransferases (UGTs) in rats at various time points after initiation of hepatic regeneration by partial hepatectomy (PHx).
Methods: The mRNA expression of various UGTs was evaluated using real-time polymerase chain reaction (real-time PCR) with specific primers. The in vitro activity of UGTs was evaluated using different substrates such as estradiol (UGT1A1), acetaminophen (UGT1A6/7), morphine (UGT2B1), testosterone (UGT2B1/3/6), androsterone (UGT2B2), and (-)-borneol (UGT2B12).
Results: Whereas the activity and mRNA expression of UGT1A1, UGT2B1, UGT2B1/3/6, UGT2B2, and UGT2B12 were lower, the activity and mRNA expression of UGT1A6/7 were preserved during hepatic regeneration. The mRNA expression of UGT2B8 was down-regulated, whereas the mRNA expression of UGT1A5 and UGT1A8 was not altered by PHx. The mRNA expression of UGT1A2 and UGT1A3 was increased during hepatic regeneration.
Conclusion: UGT-mediated drug-metabolizing ability of the liver was altered differentially in the regenerating rat liver. Individualized dosing regimen for different UGT substrates may be needed when using such substrates of these enzymes in patients with a regenerating liver, especially during the early postoperative period. However, the glucuronide conjugating capacity of the liver in the donor of a living donor liver transplantation is expected to completely return to normal with time after surgery.