1982
DOI: 10.1016/0045-6535(82)90152-7
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Evidence for the presence of arsenobetaine and another organoarsenical in shrimps

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Cited by 109 publications
(30 citation statements)
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“…Arsenocholine, a rather elusive member of the marine arsenic cycle, was reported to be present in shrimp, 5,27 lobsters, 28 mussels 27,29 and fish. 2,27 Arsenocholine represented 0.5-9% of the extractable arsenic in the livers of marine mammals.…”
Section: Arsenocholinementioning
confidence: 99%
“…Arsenocholine, a rather elusive member of the marine arsenic cycle, was reported to be present in shrimp, 5,27 lobsters, 28 mussels 27,29 and fish. 2,27 Arsenocholine represented 0.5-9% of the extractable arsenic in the livers of marine mammals.…”
Section: Arsenocholinementioning
confidence: 99%
“…4,18 They are further methylated and converted to trimethyl arsenic compounds, including AsCho, in marine animals. 5,6 It was reported that AsCho had a weak, but significant, in vivo acute toxicity in mice, 7 but we recently demonstrated that AsCho had no in vitro cytolethality on cultured mouse splenocytes, thymocytes, Peyer's patch lymphocytes, macrophages and bone marrow cells. 1,8,9 In this study, we examined whether AsCho has any in vivo immunotoxicity, and found that it was slightly, but significantly, immunotoxic in vivo.…”
Section: Discussionmentioning
confidence: 98%
“…Therefore, it is necessary to investigate the effects of organic arsenic compounds contained in marine animals on living systems; however, there have only been a few reports about them, because insufficient amounts of pure compounds for biological experiments have been obtained. Norin and Christakopoulos 5 and Shiomi et al 6 found a minor water-soluble trimethyl arsenic compound, namely arsenocholine (AsCho), from some kinds of shrimp 5 and conch. 6 The chemical structure of this trimethyl arsenic compound was the trimethyl(2-hydroxyethyl)arsonium cation.…”
Section: Introductionmentioning
confidence: 99%
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“…Methods used include TLC-AAS [44,143], paper chromatography-AAS [ 1441, paper electrophoresis-AAS [ 1451, ion exchange column chromatography-AAS for the separation and detection of arsenic(III), arsenic(V), MMAA, DMAA [146,147], GC with flame ionization detection (FID) and GC-MS of methylthioglycolate derivatives of MMAA and DMAA [148]. GC-MIP and GC alkali flame ionization for the estimation of the ethylene glycol derivative of MMAA [149], GC-FID and flame spectrometric detection of the trimethyl-silyl [150] and GC-electron capture detection of the diethyldithiocarbamate complex of MMAA and DMAA [150]; solvent extraction followed by detection by AAS [ 15 1,1521, and polarography/voltammetry to discriminate arsenic(II1) and arsenic(V) [ 153,1543.…”
Section: Other Methodsmentioning
confidence: 99%