Literature DB >> 7681309

The differential modulation of the enzymes of glutathione metabolism. Indication of overlapping effects of toxicity and repair in mouse liver and kidney after dietary treatment with methyl mercury and sodium selenite.

P Di Simplicio1, M Gorelli, R Vignani, C Leonzio.   

Abstract

The effect of methylmercury (MM) and MM plus sodium selenite (SE) on the activity of various GSH-dependent enzymes was studied in the liver and kidney of mice. Ten groups of mice were fed diets containing graded proportions of MM, alone or with graded quantities of SE. GST, GSH-Px, and GSSG-RED were assayed in the cytosolic fraction of liver and kidney homogenates. After treatment with MM, instead of the expected decrease in enzyme activities, an increase was observed in the kidney and a small decrease in the liver with no dose-response relation in either organ. In protected groups, a general pattern of induction was observed in both organs, but again there was little evidence of dose-response relationships. Detailed analysis of the results suggests that the effects observed were not directly caused by MM or SE but are the resultant of complex interactions presumably related to contemporaneous mechanisms of damage and repair.

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Year:  1993        PMID: 7681309     DOI: 10.1007/BF02783176

Source DB:  PubMed          Journal:  Biol Trace Elem Res        ISSN: 0163-4984            Impact factor:   3.738


  23 in total

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Journal:  Annu Rev Pharmacol       Date:  1972       Impact factor: 13.820

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Journal:  Bull Environ Contam Toxicol       Date:  1974-07       Impact factor: 2.151

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Authors:  S Potter; G Matrone
Journal:  J Nutr       Date:  1974-05       Impact factor: 4.798

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Authors:  A S Chung; M D Maines
Journal:  Biochem Pharmacol       Date:  1981-12-01       Impact factor: 5.858

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Authors:  Y Hirota; S Yamaguchi; N Shimojoh; K I Sano
Journal:  Toxicol Appl Pharmacol       Date:  1980-03-30       Impact factor: 4.219

6.  Disruption of cytoskeleton by methylmercury in cultured CHO cells.

Authors:  R Vignani; C Milanesi; P Di Simplicio
Journal:  Toxicol In Vitro       Date:  1992-01       Impact factor: 3.500

Review 7.  Mechanism of methylmercury cytotoxicity.

Authors:  K Miura; N Imura
Journal:  Crit Rev Toxicol       Date:  1987       Impact factor: 5.635

8.  Effects of inducers of drug metabolism on basic hepatic forms of mouse glutathione transferase.

Authors:  P Di Simplicio; H Jensson; B Mannervik
Journal:  Biochem J       Date:  1989-11-01       Impact factor: 3.857

9.  Selenium and drug metabolism--III. Relation of glutathione-peroxidase and other hepatic enzyme modulations to dietary supplements.

Authors:  R Reiter; A Wendel
Journal:  Biochem Pharmacol       Date:  1985-07-01       Impact factor: 5.858

10.  Identification of three classes of cytosolic glutathione transferase common to several mammalian species: correlation between structural data and enzymatic properties.

Authors:  B Mannervik; P Alin; C Guthenberg; H Jensson; M K Tahir; M Warholm; H Jörnvall
Journal:  Proc Natl Acad Sci U S A       Date:  1985-11       Impact factor: 11.205

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  4 in total

1.  Lipid peroxidation in liver of rats administrated with methyl mercuric chloride.

Authors:  T H Lin; Y L Huang; S F Huang
Journal:  Biol Trace Elem Res       Date:  1996-07       Impact factor: 3.738

2.  SKN-1/Nrf2 inhibits dopamine neuron degeneration in a Caenorhabditis elegans model of methylmercury toxicity.

Authors:  Natalia Vanduyn; Raja Settivari; Garry Wong; Richard Nass
Journal:  Toxicol Sci       Date:  2010-09-20       Impact factor: 4.849

3.  The putative multidrug resistance protein MRP-7 inhibits methylmercury-associated animal toxicity and dopaminergic neurodegeneration in Caenorhabditis elegans.

Authors:  Natalia VanDuyn; Richard Nass
Journal:  J Neurochem       Date:  2013-11-25       Impact factor: 5.372

Review 4.  The influence of nutrition on methyl mercury intoxication.

Authors:  L Chapman; H M Chan
Journal:  Environ Health Perspect       Date:  2000-03       Impact factor: 9.031

  4 in total

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