Literature DB >> 11599937

Animal species difference in the uptake of dimethylarsinous acid (DMA(III)) by red blood cells.

Y Shiobara1, Y Ogra, K T Suzuki.   

Abstract

The animal species difference in the metabolism of arsenic was studied from the viewpoint of the mechanism underlying its distribution in the form of dimethylated arsenic in red blood cells (RBCs). Dimethylarsinic (DMA(V)) and dimethylarsinous (DMA(III)) acids were incubated with rat, hamster, mouse, and human RBCs, and the uptake rates and chemical forms of arsenic were determined. Although DMA(V) was practically not or taken up slowly by RBCs of all the present animal species, DMA(III) was taken efficiently in the order of rat > hamster > human, RBCs of mice taking it up less efficiently and with a different pattern from the former three animals. Further, although DMA(III) taken up by rat RBCs was retained, that by hamster ones was effluxed in the form of DMA(V). The uptake of DMA(III) and efflux of DMA(V) took place much more slowly in human RBCs than rat and hamster ones. The uptake of DMA(III) by RBCs was inhibited on the oxidation of glutathione with diamide. Incubation of DMA(III), but not of DMA(V), with a hemolysate produced a high molecular weight complex, which increases in the presence of glutathione, suggesting that DMA(III) taken up by RBCs is retained through the formation of a complex with protein(s) specific to animal species, and effluxed from RBCs after being oxidized to DMA(V). These results indicate that DMA is taken up by RBCs in the form of DMA(III), and that the uptake and efflux rates are dependent on the animal species, the effluxed arsenic being DMA(V). The present results suggest that the uptake of DMA by RBCs is an additional contributing factor to the animal species difference in the metabolism of arsenic in addition to the reduction and methylation capacity in the liver.

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Year:  2001        PMID: 11599937     DOI: 10.1021/tx015537k

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  8 in total

1.  Using mathematical modeling to infer the valence state of arsenicals in tissues: A PBPK model for dimethylarsinic acid (DMAV) and dimethylarsinous acid (DMAIII) in mice.

Authors:  Lydia M Bilinsky; David J Thomas; Jeffrey W Fisher
Journal:  J Theor Biol       Date:  2018-10-26       Impact factor: 2.691

2.  Tissue dosimetry, metabolism and excretion of pentavalent and trivalent dimethylated arsenic in mice after oral administration.

Authors:  Michael F Hughes; Vicenta Devesa; Blakely M Adair; Sean D Conklin; John T Creed; Miroslav Styblo; Elaina M Kenyon; David J Thomas
Journal:  Toxicol Appl Pharmacol       Date:  2007-10-22       Impact factor: 4.219

Review 3.  Origins, fate, and actions of methylated trivalent metabolites of inorganic arsenic: progress and prospects.

Authors:  Miroslav Stýblo; Abhishek Venkatratnam; Rebecca C Fry; David J Thomas
Journal:  Arch Toxicol       Date:  2021-03-26       Impact factor: 5.153

Review 4.  Arsenic binding to proteins.

Authors:  Shengwen Shen; Xing-Fang Li; William R Cullen; Michael Weinfeld; X Chris Le
Journal:  Chem Rev       Date:  2013-06-28       Impact factor: 60.622

Review 5.  Methylated Organic Metabolites of Arsenic and their Cardiovascular Toxicities.

Authors:  Ok-Nam Bae; Kyung-Min Lim; Ji-Yoon Noh; Keun-Young Kim; Eun-Kyung Lim; Jin-Ho Chung
Journal:  Toxicol Res       Date:  2008-09-01

6.  Pentoxifylline Attenuates Arsenic Trioxide-Induced Cardiac Oxidative Damage in Mice.

Authors:  Atefeh Gholami; Sara Ataei; Davoud Ahmadimoghaddam; Navid Omidifar; Amir Nili-Ahmadabadi
Journal:  Oxid Med Cell Longev       Date:  2021-01-07       Impact factor: 6.543

7.  Urinary trivalent methylated arsenic species in a population chronically exposed to inorganic arsenic.

Authors:  Olga L Valenzuela; Victor H Borja-Aburto; Gonzalo G Garcia-Vargas; Martha B Cruz-Gonzalez; Eliud A Garcia-Montalvo; Emma S Calderon-Aranda; Luz M Del Razo
Journal:  Environ Health Perspect       Date:  2005-03       Impact factor: 9.031

8.  Chronic Exposure to Arsenic in Drinking Water Causes Alterations in Locomotor Activity and Decreases Striatal mRNA for the D2 Dopamine Receptor in CD1 Male Mice.

Authors:  Claudia Leticia Moreno Ávila; Jorge H Limón-Pacheco; Magda Giordano; Verónica M Rodríguez
Journal:  J Toxicol       Date:  2016-06-08
  8 in total

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