Literature DB >> 17527

Glucuronidation and deglucuronidation reactions in hepatic and extrahepatic tissues during perinatal development.

G W Lucier, B R Sonawane, O S McDaniel.   

Abstract

The relative activities of uridine diphosphoglucuronyltransferase (UDPGT) and beta-glucuronidase (betaG) were measured during perinatal development of hepatic and extrahepatic tissues to determine the balance between glucuronidation and deglucuronidation reactions at different developmental stages. Liver, lung, kidney, intestine, and placenta were studied in guinea pigs and rabbits. In general, betaG activities exceeded those of UDPGT in fetal tissues, whereas the converse was evident in adults. There were significant species and age differences in the onset of betaG and UDPGT activities and the occurrence of developmental peaks. A dramatic betaG developmental peak was observed in fetal guinea pig intestine and newborn rabbit intestine. Both microsomal and lysosomal betaG exhibited similar developmental patterns in all tissues tested. Hepatic nonsteroid UDPGT activities were higher at parturition than in adult animals, whereas no such developmental peak occurred for steroid UDPGT. Triton X-100 activated fetal UDPGT in vitro by approximately the same factor as it did for adult UDPGT.

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Year:  1977        PMID: 17527

Source DB:  PubMed          Journal:  Drug Metab Dispos        ISSN: 0090-9556            Impact factor:   3.922


  11 in total

1.  Second trimester amniotic fluid bisphenol A concentration is associated with decreased birth weight in term infants.

Authors:  Sara E Pinney; Clementina A Mesaros; Nathaniel W Snyder; Christine M Busch; Rui Xiao; Sara Aijaz; Naila Ijaz; Ian A Blair; Jeanne M Manson
Journal:  Reprod Toxicol       Date:  2016-11-06       Impact factor: 3.143

2.  Distribution of UDP-glucuronyltransferase in different human foetal tissues.

Authors:  G M Pacifici; A Rane
Journal:  Br J Clin Pharmacol       Date:  1982-05       Impact factor: 4.335

3.  Altered sexual differentiation of hepatic uridine diphosphate glucuronyltransferase by neonatal hormone treatment in rats.

Authors:  C A Lamartiniere; C S Dieringer; E Kita; G W Lucier
Journal:  Biochem J       Date:  1979-05-15       Impact factor: 3.857

Review 4.  Circulating levels of genistein in the neonate, apart from dose and route, predict future adverse female reproductive outcomes.

Authors:  Wendy N Jefferson; Carmen J Williams
Journal:  Reprod Toxicol       Date:  2010-10-15       Impact factor: 3.143

5.  Fetal liver bisphenol A concentrations and biotransformation gene expression reveal variable exposure and altered capacity for metabolism in humans.

Authors:  Muna S Nahar; Chunyang Liao; Kurunthachalam Kannan; Dana C Dolinoy
Journal:  J Biochem Mol Toxicol       Date:  2012-12-03       Impact factor: 3.642

6.  Assisted reproduction technologies impair placental steroid metabolism.

Authors:  Abby C Collier; Shogo J Miyagi; Yasuhiro Yamauchi; Monika A Ward
Journal:  J Steroid Biochem Mol Biol       Date:  2009-05-03       Impact factor: 4.292

7.  Fetal exposure to bisphenol A as a risk factor for the development of childhood asthma: an animal model study.

Authors:  Yoichi Nakajima; Randall M Goldblum; Terumi Midoro-Horiuti
Journal:  Environ Health       Date:  2012-02-21       Impact factor: 5.984

8.  Metabolic activation/deactivation reactions during perinatal development.

Authors:  G W Lucier; E M Lui; C A Lamartiniere
Journal:  Environ Health Perspect       Date:  1979-04       Impact factor: 9.031

9.  Does rapid metabolism ensure negligible risk from bisphenol A?

Authors:  Gary Ginsberg; Deborah C Rice
Journal:  Environ Health Perspect       Date:  2009-07-14       Impact factor: 9.031

10.  Pregnancy-specific physiologically-based toxicokinetic models for bisphenol A and bisphenol S.

Authors:  Jeremy Gingrich; David Filipovic; Rory Conolly; Sudin Bhattacharya; Almudena Veiga-Lopez
Journal:  Environ Int       Date:  2020-12-22       Impact factor: 9.621

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