Literature DB >> 15463201

Xenobiotic metabolism in helminths.

W Y Precious1, J Barrett.   

Abstract

During its life cycle a parasite, like mammals and other organisms, comes into contact with a variety of toxic molecules. In mammals the main line of defence against such compounds is a group of oxidative enzymes that occur predominantly in the liver. Many of these oxidations are dependent on the haemoprotein cytochrome P-450 which serves as a terminal oxidase accepting electrons from NADPH and cytochrome [Formula: see text] . This review by Wendy Precious and John Barrett illustrates that in contrast to mammals, xenobiotic metabolism in both parasitic and free-living platyhelminths and nematodes is predominantly reductive and hydrolytic as the cytochrome P-450 system is absent. This is surprising since it is present in many groups including bacteria, fungi and protozoa, which suggests an ancient origin. The absence of the cytochrome P-450 system not only severely limits the ability of helminths to detoxify compounds but also limits their ability to activate prodrugs.

Entities:  

Year:  1989        PMID: 15463201     DOI: 10.1016/0169-4758(89)90080-x

Source DB:  PubMed          Journal:  Parasitol Today        ISSN: 0169-4758


  12 in total

1.  In vitro antifilarial activity of glutathione S-transferase inhibitors.

Authors:  Lakshmy Srinivasan; Nisha Mathew; Kalyanasundaram Muthuswamy
Journal:  Parasitol Res       Date:  2009-06-28       Impact factor: 2.289

2.  Structure of glutathione S-transferase 1 from the major human hookworm parasite Necator americanus (Na-GST-1) in complex with glutathione.

Authors:  Oluwatoyin A Asojo; Christopher Ceccarelli
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2014-08-29       Impact factor: 1.056

Review 3.  The redox biology of schistosome parasites and applications for drug development.

Authors:  Hsin-Hung Huang; Coraline Rigouin; David L Williams
Journal:  Curr Pharm Des       Date:  2012       Impact factor: 3.116

4.  In vivo metabolism of aminopyrine by the larvae of the helminth Heligmosomoides polygyrus.

Authors:  D Kerboeuf; D Soubieux; R Guilluy; J L Brazier; J L Rivière
Journal:  Parasitol Res       Date:  1995       Impact factor: 2.289

5.  Structure of glutathione S-transferase of the filarial parasite Wuchereria bancrofti: a target for drug development against adult worm.

Authors:  Sivaramakrishnan Thirumalai Nathan; Nisha Mathew; Muthuswami Kalyanasundaram; Kothandapani Balaraman
Journal:  J Mol Model       Date:  2005-04-29       Impact factor: 1.810

6.  Structure of monomeric Na-GST-3, a glutathione S-transferase from the major human hookworm parasite Necator americanus.

Authors:  Alan Kelleher; Bin Zhan; Oluwatoyin A Asojo
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2013-07-27

7.  Glutathione transferases in the tapeworm Moniezia expansa.

Authors:  P M Brophy; C Southan; J Barrett
Journal:  Biochem J       Date:  1989-09-15       Impact factor: 3.857

8.  Albendazole enantiomeric metabolism and binding to cytosolic proteins in the liver fluke Fasciola hepatica.

Authors:  H Solana; S Scarcella; G Virkel; C Ceriani; J Rodríguez; C Lanusse
Journal:  Vet Res Commun       Date:  2008-08-26       Impact factor: 2.459

9.  Towards an understanding of the function of the phytochelatin synthase of Schistosoma mansoni.

Authors:  Coraline Rigouin; Elyse Nylin; Alexis A Cogswell; Dirk Schaumlöffel; Dirk Dobritzsch; David L Williams
Journal:  PLoS Negl Trop Dis       Date:  2013-01-31

10.  X-ray structures of Na-GST-1 and Na-GST-2 two glutathione S-transferase from the human hookworm Necator americanus.

Authors:  Oluwatoyin A Asojo; Kohei Homma; Meghan Sedlacek; Michelle Ngamelue; Gaddam N Goud; Bin Zhan; Vehid Deumic; Oluyomi Asojo; Peter J Hotez
Journal:  BMC Struct Biol       Date:  2007-06-26
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