Literature DB >> 2057452

Methyl mercuric chloride toxicokinetics in mice. II: Sexual differences in whole-body retention and deposition in blood, hair, skin, muscles and fat.

J B Nielsen1, O Andersen.   

Abstract

This article reports the time course for deposition of methyl mercury administered as a single oral dose in whole body, total carcass, liver, kidneys, brain, blood, fat, muscle, bone, skin and hair of male and female Bom:NMRI mice. The whole-body elimination initially approximated first order kinetics with half-times around 7 days and 12 days for males and females respectively, although a decreased elimination rate was observed during the last 10 days. The elimination of mercury from carcass was slower than the elimination from the whole-body, causing an increasing relative carcass deposition with time in both male and female mice and explaining the observed deviation from first order elimination kinetics. Thus, first order kinetics is observed only during 2-3 weeks after dosage. Throughout the experimental period, male mice had significantly lower levels of mercury in both blood, brain and muscles than had female mice, whereas renal deposition of mercury in male mice was significantly higher than in female mice. At day 30 the females had about twice as much mercury in liver, brain and hair (median values) as had male mice. Despite the fact that comparable whole-body retention and carcass deposition were observed in male and female mice, the blood concentrations in male mice was only about half that in female mice. Furthermore, half-times for mercury in blood did not differ much between male and female mice and were close to whole-body half-time in male mice, although the absolute amounts of mercury in both blood and whole-blood at day 20 were significantly different.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 2057452     DOI: 10.1111/j.1600-0773.1991.tb01224.x

Source DB:  PubMed          Journal:  Pharmacol Toxicol        ISSN: 0901-9928


  6 in total

1.  Sex-dependent and non-monotonic enhancement and unmasking of methylmercury neurotoxicity by prenatal stress.

Authors:  Hiromi I Weston; Marissa E Sobolewski; Joshua L Allen; Doug Weston; Katherine Conrad; Sean Pelkowski; Gene E Watson; Grazyna Zareba; Deborah A Cory-Slechta
Journal:  Neurotoxicology       Date:  2014-02-03       Impact factor: 4.294

2.  Developmental exposure to methylmercury and resultant muscle mercury accumulation and adult motor deficits in mice.

Authors:  Matthew D Rand; Katherine Conrad; Elena Marvin; Katherine Harvey; Don Henderson; Rabi Tawil; Marissa Sobolewski; Deborah A Cory-Slechta
Journal:  Neurotoxicology       Date:  2020-07-28       Impact factor: 4.294

3.  Evaluation of mercury in hair, blood and muscle as biomarkers for methylmercury exposure in male and female mice.

Authors:  J B Nielsen; O Andersen; P Grandjean
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

4.  Prenatal methylmercury exposure hampers glutathione antioxidant system ontogenesis and causes long-lasting oxidative stress in the mouse brain.

Authors:  James Stringari; Adriana K C Nunes; Jeferson L Franco; Denise Bohrer; Solange C Garcia; Alcir L Dafre; Dejan Milatovic; Diogo O Souza; João B T Rocha; Michael Aschner; Marcelo Farina
Journal:  Toxicol Appl Pharmacol       Date:  2007-10-22       Impact factor: 4.219

5.  Assessment of Total Mercury in Hair, Urine and Fingernails of Small-Scale Gold Miners in the Amansie West District, Ghana.

Authors:  Edward Ebow Kwaansa-Ansah; Edward Kwaku Armah; Francis Opoku
Journal:  J Health Pollut       Date:  2019-03-14

Review 6.  Evaluation of mercury exposure level, clinical diagnosis and treatment for mercury intoxication.

Authors:  Byeong-Jin Ye; Byoung-Gwon Kim; Man-Joong Jeon; Se-Yeong Kim; Hawn-Cheol Kim; Tae-Won Jang; Hong-Jae Chae; Won-Jun Choi; Mi-Na Ha; Young-Seoub Hong
Journal:  Ann Occup Environ Med       Date:  2016-01-22
  6 in total

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