Literature DB >> 15239389

Environmental distribution, analysis, and toxicity of organometal(loid) compounds.

E Dopp1, L M Hartmann, A M Florea, A W Rettenmeier, A V Hirner.   

Abstract

The biochemical modification of the metals and metalloids mercury, tin, arsenic, antimony, bismuth, selenium, and tellurium via formation of volatile metal hydrides and alkylated species (volatile and involatile) performs a fundamental role in determining the environmental processing of these elements. In most instances, the formation of such species increases the environmental mobility of the element, and can result in bioaccumulation in lipophilic environments. While inorganic forms of most of these compounds are well characterized (e.g., arsenic, mercury) and some of them exhibit low toxicity (e.g., tin, bismuth), the more lipid-soluble organometals can be highly toxic. Methylmercury poisoning (e.g., Minamata disease) and tumor development in rats after exposure to dimethylarsinic acid or tributyltin oxide are just some examples. Data on the genotoxicity (and the neurotoxicity) as well as the mechanisms of cellular action of organometal(loid) compounds are, however, scarce. Many studies have shown that the production of such organometal(loid) species is possible and likely whenever anaerobic conditions (at least on a microscale) are combined with available metal(loid)s and methyl donors in the presence of suitable organisms. Such anaerobic conditions can exist within natural environments (e.g., wetlands, pond sediments) as well as within anthropogenic environmental systems (e.g., waste disposal sites and sewage treatments plants). Some methylation can also take place under aerobic conditions. This article gives an overview about the environmental distribution of organometal(loid) compounds and the potential hazardous effects on animal and human health. Genotoxic effects in vivo and in vitro in particular are discussed.

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Year:  2004        PMID: 15239389     DOI: 10.1080/10408440490270160

Source DB:  PubMed          Journal:  Crit Rev Toxicol        ISSN: 1040-8444            Impact factor:   5.635


  19 in total

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2.  Simultaneously discrete biomineralization of magnetite and tellurium nanocrystals in magnetotactic bacteria.

Authors:  Masayoshi Tanaka; Atsushi Arakaki; Sarah S Staniland; Tadashi Matsunaga
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3.  Mercury analysis of acid- and alkaline-reduced biological samples: identification of meta-cinnabar as the major biotransformed compound in algae.

Authors:  David Kelly; Kenneth Budd; Daniel D Lefebvre
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4.  Novel lipid-soluble thiol-redox antioxidant and heavy metal chelator, N,N'-bis(2-mercaptoethyl)isophthalamide (NBMI) and phospholipase D-specific inhibitor, 5-fluoro-2-indolyl des-chlorohalopemide (FIPI) attenuate mercury-induced lipid signaling leading to protection against cytotoxicity in aortic endothelial cells.

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Review 5.  Comparative meta-analysis of organic contaminants in sewage sludge from the United States and China.

Authors:  Joshua C Steele; Xiang-Zhou Meng; Arjun K Venkatesan; Rolf U Halden
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6.  Role of intestinal microbiota in transformation of bismuth and other metals and metalloids into volatile methyl and hydride derivatives in humans and mice.

Authors:  Klaus Michalke; Annette Schmidt; Britta Huber; Jörg Meyer; Margareta Sulkowski; Alfred V Hirner; Jens Boertz; Frank Mosel; Philip Dammann; Gero Hilken; Hans J Hedrich; Martina Dorsch; Albert W Rettenmeier; Reinhard Hensel
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Review 7.  Heavy metal toxicity and the environment.

Authors:  Paul B Tchounwou; Clement G Yedjou; Anita K Patlolla; Dwayne J Sutton
Journal:  Exp Suppl       Date:  2012

8.  Toxicity of volatile methylated species of bismuth, arsenic, tin, and mercury in Mammalian cells in vitro.

Authors:  E Dopp; U von Recklinghausen; J Hippler; R A Diaz-Bone; J Richard; U Zimmermann; A W Rettenmeier; A V Hirner
Journal:  J Toxicol       Date:  2011-10-05

9.  Production of toxic volatile trimethylbismuth by the intestinal microbiota of mice.

Authors:  Britta Huber; Philip Dammann; Christine Krüger; Petra Kirsch; Beatrix Bialek; Roland A Diaz-Bone; Reinhard Hensel
Journal:  J Toxicol       Date:  2011-10-10

10.  Arsenic Methylation in Arabidopsis thaliana Expressing an Algal Arsenite Methyltransferase Gene Increases Arsenic Phytotoxicity.

Authors:  Zhong Tang; Yanling Lv; Fei Chen; Wenwen Zhang; Barry P Rosen; Fang-Jie Zhao
Journal:  J Agric Food Chem       Date:  2016-03-28       Impact factor: 5.279

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