Literature DB >> 11314982

Effect of arsenic trioxide on metallothionein and its conversion to different arsenic metabolites in hen liver.

I Falnoga1, E Stibilj, M Tusek-Znidaric, Z Slejkovec, D Mazej, R Jacimovic, J Scancar.   

Abstract

The metabolism of arsenic, its affinity to metallothionein (MT), its influence on selenium levels, and its biotransformation to different metabolites in the liver tissue of laying hens exposed to arsenic trioxide (As2O3) was investigated. The experiment was performed with two groups of hens fed for 19 d with either a standard diet or with the same diet enriched in arsenic (30 microg/g). The major findings were as follows: 1. After 19 d exposure, about 65% of the total liver As was found in the water-soluble phase (100,000g centrifuged supernatant). In liver supernatant, As binding was found mostly in the range of very low-molecular-weight proteins (Mr < 10,000). Although after exposure the amount of MT-like proteins increased, the As bound to it was only in trace amounts. The protein was identified by convential procedures as Zn,Cu-thionein with traces of selenium and arsenic. 2. Arsenic exposure resulted in almost unchanged Se levels regarding its tissue concentrations and distribution between supernatant and pellet, where about 10% of total Se was found in the supernatant. On the contrary, As exposure did affect Cd levels. Tissue Cd concentration was slightly diminished, but the percentage of tissue Cd found in the water-soluble phase was increased from 20% to 40%. 3. In methanol extracts of tissue and supernatant of the As-exposed group, only two arsenic compounds were detected, As(III) and dimethylarsinic acid (DMA), the latter prevailing.

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Year:  2000        PMID: 11314982     DOI: 10.1385/bter:78:1-3:241

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


  7 in total

1.  Antagonistic toxicity of arsenate and cadmium in a freshwater amphipod (Gammarus pulex).

Authors:  Céline Vellinger; Marc Parant; Philippe Rousselle; Philippe Usseglio-Polatera
Journal:  Ecotoxicology       Date:  2012-04-26       Impact factor: 2.823

Review 2.  Arsenic (+3 oxidation state) methyltransferase and the methylation of arsenicals.

Authors:  David J Thomas; Jiaxin Li; Stephen B Waters; Weibing Xing; Blakely M Adair; Zuzana Drobna; Vicenta Devesa; Miroslav Styblo
Journal:  Exp Biol Med (Maywood)       Date:  2007-01

3.  Nitric oxide donor, V-PROLI/NO, provides protection against arsenical induced toxicity in rat liver cells: requirement for Cyp1a1.

Authors:  Wei Qu; Lida Cheng; Anna L Dill; Joseph E Saavedra; Sam Y Hong; Larry K Keefer; Michael P Waalkes
Journal:  Chem Biol Interact       Date:  2011-05-20       Impact factor: 5.192

4.  The nitric oxide prodrug, V-PYRRO/NO, mitigates arsenic-induced liver cell toxicity and apoptosis.

Authors:  Wei Qu; Jie Liu; Richard Fuquay; Joseph E Saavedra; Larry K Keefer; Michael P Waalkes
Journal:  Cancer Lett       Date:  2007-07-20       Impact factor: 8.679

5.  V-PROLI/NO, a nitric oxide donor prodrug, protects liver cells from arsenic-induced toxicity.

Authors:  Wei Qu; Jie Liu; Anna L Dill; Joseph E Saavedra; Larry K Keefer; Michael P Waalkes
Journal:  Cancer Sci       Date:  2008-12-15       Impact factor: 6.716

6.  Experimental modeling of the acute toxicity and cytogenotoxic fate of composite mixtures of chromate, copper and arsenate oxides associated with CCA preservative using Clarias gariepinus (Burchell 1822).

Authors:  Olukunle S Fagbenro; Chibuisi G Alimba; Adekunle A Bakare
Journal:  Environ Anal Health Toxicol       Date:  2019-09-30

7.  Arsenic Species in Chicken Breast: Temporal Variations of Metabolites, Elimination Kinetics, and Residual Concentrations.

Authors:  Qingqing Liu; Hanyong Peng; Xiufen Lu; Martin J Zuidhof; Xing-Fang Li; X Chris Le
Journal:  Environ Health Perspect       Date:  2016-03-18       Impact factor: 9.031

  7 in total

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