Literature DB >> 3753197

Strain difference in mercury excretion in methylmercury-treated mice.

A Yasutake, K Hirayama.   

Abstract

The strain differences in mercury excretion and organ distribution after administration of methylmercuric chloride (5 mg/kg) were studied in male mice of four strains, C57BL/6N, BALB/cA, C3H/HeN and AKR. The urinary excretion rate of mercury for 5 days following administration was 3.9-4.7 times higher in the C57BL strain than in the other three strains, whereas the mercury level in feces was highest in the AKR strain. Although the blood mercury concentration in the C57BL strain was almost half that in the others up to the 5th day, the plasma levels did not vary so widely. C57BL showed the highest ratio of plasma to whole blood mercury level, which was thought to originate from the lower affinity of methylmercury for hemoglobin. The variation of the plasma/whole blood ratios was rather small throughout the experimental period in each strain examined. In the C57BL strain, the mercury levels in brain, liver, kidney and blood were significantly lower on and after the 5th day than in the other three strains, probably because of the rapid elimination of body mercury into urine, but the mercury uptake by the brain and kidney 5 min after administration was at a rather higher rate than in the other strains. On the other hand, the highest tissue levels were shown by the C3H strain in the brain and liver, and by the BALB/c strain in the kidney. It was suggested that in the C57BL strain, the higher mercury distribution in plasma and rapid uptake by the kidney might result in higher urinary excretion.

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Year:  1986        PMID: 3753197     DOI: 10.1007/bf00286731

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  10 in total

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Journal:  Am Ind Hyg Assoc J       Date:  1960-12

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Authors:  F Iverson; R H Downie; C Paul; H L Trenholm
Journal:  Toxicol Appl Pharmacol       Date:  1973-04       Impact factor: 4.219

3.  Methylmercury: exposure duration and regional distribution as determinants of neurotoxicity in nonhuman primates.

Authors:  H L Evans; R H Garman; B Weiss
Journal:  Toxicol Appl Pharmacol       Date:  1977-07       Impact factor: 4.219

4.  Developmental changes in the biliary excretion of methylmercury and glutathione.

Authors:  N Ballatori; T W Clarkson
Journal:  Science       Date:  1982-04-02       Impact factor: 47.728

5.  Differences in elimination rates of methylmercury between two genetic variant strains of mice.

Authors:  P J Kostyniak
Journal:  Toxicol Lett       Date:  1980-10       Impact factor: 4.372

6.  Organ distribution and biological half-time of methylmercury in four strains of mice.

Authors:  R Doi; T Kobayashi
Journal:  Jpn J Exp Med       Date:  1982-12

7.  Elimination of 203Hg-methylmercury in man.

Authors:  J K Miettinen; T Rahola; T Hattula; K Rissanen; M Tillander
Journal:  Ann Clin Res       Date:  1971-04

8.  Hereditary analysis of the strain difference of methylmercury distribution in mice.

Authors:  R Doi; M Tagawa; H Tanaka; K Nakaya
Journal:  Toxicol Appl Pharmacol       Date:  1983-07       Impact factor: 4.219

9.  Effects of diet on mercury metabolism and excretion in mice given methylmercury: role of gut flora.

Authors:  I R Rowland; R D Robinson; R A Doherty
Journal:  Arch Environ Health       Date:  1984 Nov-Dec

10.  [Methylmercury toxicosis. I. Relationship between the onset of motor incoordination and mercury contents in the brain (author's transl)].

Authors:  E Tagashira; T Urano; S Yanaura
Journal:  Nihon Yakurigaku Zasshi       Date:  1980-03
  10 in total
  5 in total

1.  Mechanism of urinary excretion of methylmercury in mice.

Authors:  A Yasutake; K Hirayama; M Inoue
Journal:  Arch Toxicol       Date:  1989       Impact factor: 5.153

2.  Phagocytic cells as a contributor to in vivo degradation of alkyl mercury.

Authors:  I Suda; M Suda; K Hirayama
Journal:  Bull Environ Contam Toxicol       Date:  1993-09       Impact factor: 2.151

3.  Interaction of methylmercury compounds with albumin.

Authors:  A Yasutake; K Hirayama; M Inoue
Journal:  Arch Toxicol       Date:  1990       Impact factor: 5.153

4.  Influence of sodium selenite on 203Hg absorption, distribution, and elimination in male mice exposed to methyl203Hg.

Authors:  A W Glynn; N G Ilbäck; D Brabencova; L Carlsson; E C Enqvist; E Netzel; A Oskarsson
Journal:  Biol Trace Elem Res       Date:  1993-10       Impact factor: 3.738

5.  Metabolism of methylmercury in rabbits and hamsters.

Authors:  K Petersson; L Dock; M Vahter
Journal:  Biol Trace Elem Res       Date:  1989 Jul-Sep       Impact factor: 3.738

  5 in total

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