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A novel metabolic activation associated with glutathione in dimethylmonothioarsinic acid (DMMTA(V))-induced toxicity obtained from in vitro reaction of DMMTA(V) with glutathione.
Kurosawa, Hidetoshi; Shimoda, Yasuyo; Miura, Motofumi; Kato, Koichi; Yamanaka, Kenzo; Hata, Akihisa; Yamano, Yuko; Endo, Yoko; Endo, Ginji.
Afiliação
  • Kurosawa H; Laboratory of Environmental Toxicology and Carcinogenesis, Nihon University School of Pharmacy, Chiba 274-8555, Japan; Criminal Investigation Laboratory, Metropolitan Police Department, Tokyo 100-8929, Japan.
  • Shimoda Y; Laboratory of Environmental Toxicology and Carcinogenesis, Nihon University School of Pharmacy, Chiba 274-8555, Japan.
  • Miura M; Laboratory of Molecular Chemistry, Nihon University School of Pharmacy, Chiba 274-8555, Japan.
  • Kato K; Laboratory of Environmental Toxicology and Carcinogenesis, Nihon University School of Pharmacy, Chiba 274-8555, Japan.
  • Yamanaka K; Laboratory of Environmental Toxicology and Carcinogenesis, Nihon University School of Pharmacy, Chiba 274-8555, Japan. Electronic address: yamanaka.kenzo@nihon-u.ac.jp.
  • Hata A; Department of Medical Risk Management, Graduate School of Risk and Crisis Management, Chiba Institute of Science, Chiba 288-0025, Japan.
  • Yamano Y; Department of Hygiene and Preventive Medicine, School of Medicine, Showa University, 142-8555, Japan.
  • Endo Y; Research Center for Occupational Poisoning, Kansai Rosai Hospital, Hyogo 660-8511, Japan.
  • Endo G; Department of Preventive Medicine and Environmental Health, Graduate School of Medicine, Osaka City University, Osaka 545-8585, Japan.
J Trace Elem Med Biol ; 33: 87-94, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26653748
ABSTRACT
The purpose of the present study was to elucidate the metabolic processing of dimethylmonothioarsinic acid (DMMTA(V)), which is a metabolite of inorganic arsenic and has received a great deal of attention recently due to its high toxicity. The metabolites produced from an in vitro reaction with GSH were analyzed by high performance liquid chromatography-time of flight mass spectrometer (HPLC-TOFMS), HPLC with a photodiode array detector (PDA), and also gas chromatography-mass spectrometry (GC-MS) and GC with a flame photometric detector (FPD). The reaction of dimethylarsinic acid (DMA(V)) with GSH did not generate DMA(V)-SG but did generate dimethylarsinous acid (DMA(III)) or DMA(III)-SG. On the contrary, we confirmed that the reaction of DMMTA(V) with GSH directly produced the stable complex of DMMTA(V)-SG without reduction through a trivalent dimethylated arsenic such as DMA(III) and DMA(III)-SG. Furthermore, the present study suggests the production of hydrogen sulfide (H2S) and dimethylmercaptoarsine (DMA(III)-SH), a trivalent dimethylated arsenic, as well as DMA(III) and DMA(III)-SG in the decomposition process of DMMTA(V)-SG. These results indicate that the toxicity of DMMTA(V) depends not only on the formation of DMA(III) but also on at least those of H2S and DMA(III)-SH.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ativação Metabólica / Glutationa Tipo de estudo: Risk_factors_studies Idioma: En Revista: J Trace Elem Med Biol Assunto da revista: METABOLISMO / SAUDE AMBIENTAL Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ativação Metabólica / Glutationa Tipo de estudo: Risk_factors_studies Idioma: En Revista: J Trace Elem Med Biol Assunto da revista: METABOLISMO / SAUDE AMBIENTAL Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão