Regular Article
Expression of UDP-Glucuronosyltransferases (UGTs) 2B7 and 1A6 in the Human Brain and Identification of 5-Hydroxytryptamine as a Substrate,☆☆

https://doi.org/10.1006/abbi.1999.1155Get rights and content

Abstract

The extrahepatic expression of UDP-glucuronosyltransferases (UGTs) is important in the detoxification of a number of endogenous and exogenous compounds, including 5-hydroxytryptamine and morphine. Studies were designed to investigate the extrahepatic expression of human UGTs using RT-PCR techniques and to determine the UGTs involved in the glucuronidation of 5-hydroxytryptamine. Human UGT2B7 expression was found in the human liver, kidney, pancreas, and brain, while UGT1A6 expression is found in the liver, kidney, and brain. This is the first observation of UGTs present in the human central nervous system. Using glucuronidation assays, a significant amount of 5-hydroxytryptamine glucuronide was found to be catalyzed by UGT1A6. These studies suggest that UGT2B7 may play an important role in the overall contribution of morphine analgesia by serving to generate the potent morphine-6-O-glucuronidein situ.UGT1A6 could play an important role in the glucuronidation of 5-hydroxytryptaminein vivo,therefore terminating the actions of the neurotransmitter.

References (59)

  • J.K. Ritter et al.

    J. Biol. Chem.

    (1992)
  • J.K. Ritter et al.

    J. Biol. Chem.

    (1991)
  • B. Mojarrabi et al.

    Biochem. Biophys. Res. Commun.

    (1996)
  • B. Mojarrabi et al.

    Biochem. Biophys. Res. Commun.

    (1998)
  • B. Mojarrabi et al.

    Biochem. Biophys. Res. Commun.

    (1997)
  • P.I. Mackenzie et al.

    J. Biol. Chem.

    (1990)
  • S. Fournel-Gigleux et al.

    FEBS Lett.

    (1989)
  • J.K. Ritter et al.

    J. Biol. Chem.

    (1990)
  • M. Beaulieu et al.

    J. Biol. Chem.

    (1996)
  • C.P. Strassburg et al.

    J Biol. Chem.

    (1998)
  • P.A. Münzel et al.

    Arch. Biochem. Biophys.

    (1996)
  • J-F. Ghersi-Egea et al.

    Neuropharmacology

    (1987)
  • F.G. Suleman et al.

    Neurosci. Lett.

    (1993)
  • A. Wahlström et al.

    Pain

    (1988)
  • C.N. Falany et al.

    Arch. Biochem. Biophys.

    (1983)
  • J.K. Ritter et al.

    J. Biol. Chem.

    (1992)
  • S.K. Bansal et al.

    Anal. Biochem.

    (1980)
  • C. Mignat et al.

    Life Sci.

    (1995)
  • Q-L. Gong et al.

    Eur. J. Pharmacol.

    (1991)
  • K.W. Bock et al.

    Biochem. Pharmacol.

    (1993)
  • T. Iyanagi et al.

    J. Biol. Chem.

    (1986)
  • G.J. Dutton

    Glucuronidation of Drugs and Other Compounds

    (1980)
  • P.I. Mackenzie et al.

    Pharmacogenetics

    (1997)
  • Y. Emi et al.

    J. Biochem.

    (1995)
  • M.D. Green et al.

    Drug Metab. Dispos.

    (1995)
  • T. Ebner et al.

    Drug Metab. Dispos.

    (1993)
  • Z. Cheng et al.

    Arch. Biochem. Biophys.

    (1998)
  • S.J. Haque et al.

    DNA Cell Biol.

    (1991)
  • C-J. Jin et al.

    J. Pharmacol. Exp. Ther.

    (1993)
  • Cited by (160)

    • Albumin is a secret factor involved in multidirectional interactions among the serotoninergic, immune and endocrine systems that supervises the mechanism of CYP1A and CYP3A regulation in the liver

      2020, Pharmacology and Therapeutics
      Citation Excerpt :

      In turn, up-regulation of AhR target genes, particularly UGT1A gene expression is an unexplored mechanism of serotonin deactivation. UDP-glucuronosyltransferase isoforms (UGTs) are important in the detoxification of 5- hydroxytryptamine via conjugation to glucuronic acid (King, Rios, Assouline, & Tephly, 1999). Thus, it seems that a decrase in the level of testosterone during a brief period of neonatal androgen exposure may block the development of autism.

    View all citing articles on Scopus

    This research was supported by NIH Grant GM26221.

    ☆☆

    Kosterlita, H. W.

    2

    To whom correspondence should be addressed at Department of Pharmacology, 2-452 BSB, University of Iowa, Iowa City, IA 52242. Fax: (319) 335-8930.

    View full text