Literature DB >> 1749210

Detoxification pathways in the liver.

D M Grant1.   

Abstract

The liver plays an important rôle in protecting the organism from potentially toxic chemical insults through its capacity to convert lipophiles into more water-soluble metabolites which can be efficiently eliminated from the body via the urine. This protective ability of the liver stems from the expression of a wide variety of xenobiotic biotransforming enzymes whose common underlying feature is their ability to catalyse the oxidation, reduction and hydrolysis (Phase I) and/or conjugation (Phase II) of functional groups on drug and chemical molecules. The broad substrate specificity, isoenzyme multiplicity and inducibility of many of these enzyme systems make them particularly well adapted to handling the vast array of different chemical structures in the environment to which we are exposed daily. However, some chemicals may also be converted to more toxic metabolites by certain of these enzymes, implying that variations in the latter may be important predisposing factors for toxicity. Pharmacogenetic defects of xenobiotic biotransformation enzymes, a subclass of inborn errors of metabolism which are manifested only upon drug challenge, introduce marked variation into human populations for the pharmacokinetics and pharmacodynamics of therapeutic and toxic agents, and thus may have important clinical consequences for drug efficacy and toxicity.

Entities:  

Mesh:

Year:  1991        PMID: 1749210     DOI: 10.1007/bf01797915

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  15 in total

Review 1.  N-acetyltransferase.

Authors:  D A Evans
Journal:  Pharmacol Ther       Date:  1989       Impact factor: 12.310

Review 2.  Enzyme induction in the cytochrome P-450 system.

Authors:  A B Okey
Journal:  Pharmacol Ther       Date:  1990       Impact factor: 12.310

3.  Cloning and expression of cDNAs for polymorphic and monomorphic arylamine N-acetyltransferases from human liver.

Authors:  S Ohsako; T Deguchi
Journal:  J Biol Chem       Date:  1990-03-15       Impact factor: 5.157

4.  Acetylation pharmacogenetics. The slow acetylator phenotype is caused by decreased or absent arylamine N-acetyltransferase in human liver.

Authors:  D M Grant; K Mörike; M Eichelbaum; U A Meyer
Journal:  J Clin Invest       Date:  1990-03       Impact factor: 14.808

5.  Evidence for two closely related isozymes of arylamine N-acetyltransferase in human liver.

Authors:  D M Grant; F Lottspeich; U A Meyer
Journal:  FEBS Lett       Date:  1989-02-13       Impact factor: 4.124

Review 6.  Some current perspectives on chemical carcinogenesis in humans and experimental animals: Presidential Address.

Authors:  E C Miller
Journal:  Cancer Res       Date:  1978-06       Impact factor: 12.701

7.  Molecular mechanism of slow acetylation of drugs and carcinogens in humans.

Authors:  M Blum; A Demierre; D M Grant; M Heim; U A Meyer
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-15       Impact factor: 11.205

8.  N-acetylation pharmacogenetics: a gene deletion causes absence of arylamine N-acetyltransferase in liver of slow acetylator rabbits.

Authors:  M Blum; D M Grant; A Demierre; U A Meyer
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

Review 9.  Evolution of the cytochrome P450 genes.

Authors:  D W Nebert; D R Nelson; R Feyereisen
Journal:  Xenobiotica       Date:  1989-10       Impact factor: 1.908

10.  Monomorphic and polymorphic human arylamine N-acetyltransferases: a comparison of liver isozymes and expressed products of two cloned genes.

Authors:  D M Grant; M Blum; M Beer; U A Meyer
Journal:  Mol Pharmacol       Date:  1991-02       Impact factor: 4.436

View more
  30 in total

1.  Differential methylation pattern of xenobiotic metabolizing genes and susceptibility to Balkan endemic nephropathy, in a cohort of Romanian patients.

Authors:  Alexandra Ivan; Dilys Lam; Mirabela Iustina Cristea; Ada Telea; Alexandra Teodora Gruia; Camelia Oprean; Florin Margineanu; Florina Maria Bojin; Richard Saffery; Virgil Paunescu; Calin Adrian Tatu
Journal:  J Nephrol       Date:  2019-06-20       Impact factor: 3.902

Review 2.  A Change in Bile Flow: Looking Beyond Transporter Inhibition in the Development of Drug-induced Cholestasis.

Authors:  Brandy Garzel; Lei Zhang; Shiew-Mei Huang; Hongbing Wang
Journal:  Curr Drug Metab       Date:  2019       Impact factor: 3.731

Review 3.  Overview of extracellular microvesicles in drug metabolism.

Authors:  Javier Conde-Vancells; Esperanza Gonzalez; Shelly C Lu; Jose M Mato; Juan M Falcon-Perez
Journal:  Expert Opin Drug Metab Toxicol       Date:  2010-05       Impact factor: 4.481

4.  Age-associated changes in gene expression patterns in the liver.

Authors:  Robert P Thomas; Michelle Guigneaux; Thomas Wood; B Mark Evers
Journal:  J Gastrointest Surg       Date:  2002 May-Jun       Impact factor: 3.452

5.  Potent host-directed small-molecule inhibitors of myxovirus RNA-dependent RNA-polymerases.

Authors:  Stefanie A Krumm; J Maina Ndungu; Jeong-Joong Yoon; Melanie Dochow; Aiming Sun; Michael Natchus; James P Snyder; Richard K Plemper
Journal:  PLoS One       Date:  2011-05-16       Impact factor: 3.240

Review 6.  The Role of Extracellular Vesicles in Liver Pathogenesis.

Authors:  Gang Liu; Xiao-Ming Yin
Journal:  Am J Pathol       Date:  2022-06-22       Impact factor: 5.770

Review 7.  Potential Application of Living Microorganisms in the Detoxification of Heavy Metals.

Authors:  Runqiu Chen; Huaijun Tu; Tingtao Chen
Journal:  Foods       Date:  2022-06-27

8.  Acylated Quinic Acids Are the Main Salicortin Metabolites in the Lepidopteran Specialist Herbivore Cerura vinula.

Authors:  Felix Feistel; Christian Paetz; Riya C Menezes; Daniel Veit; Bernd Schneider
Journal:  J Chem Ecol       Date:  2018-03-17       Impact factor: 2.626

9.  Ceramide/protein phosphatase 2A axis is engaged in gap junction impairment elicited by PCB153 in liver stem-like progenitor cells.

Authors:  Roberta Squecco; Federica Pierucci; Eglantina Idrizaj; Alessia Frati; Elena Lenci; Catia Vicenti; Maria Chiara Iachini; Maria Martinesi; Rachele Garella; Maria Caterina Baccari; Fabio Francini; Elisabetta Meacci
Journal:  Mol Cell Biochem       Date:  2021-04-10       Impact factor: 3.396

10.  Hepatotoxic effects of melamine exposure from the weaning period in rats: a flow cytometric, electron microscopic, and histopathologic study.

Authors:  Zuleyha Erisgin; Hasan Serdar Mutlu; Yavuz Tekelioglu; Engin Deveci; Ugur Seker
Journal:  Toxicol Res (Camb)       Date:  2021-04-26       Impact factor: 3.524

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.