Literature DB >> 3732995

Strain-related patterns of biliary excretion and hepatic distribution of copper in the rat.

H Nederbragt, A J Lagerwerf.   

Abstract

Biliary copper excretion was studied in male, bile-cannulated rats of the inbred strains Fischer, Brown Norway, WAG/Rij and Lewis. After intravenous injection of 10, 30 and 50 micrograms copper per 100 gm body weight, two patterns of copper excretion were observed; their profiles varied with the copper dose and the strain of the rats used. The lowest amounts of copper were excreted by Fischer rats, the highest by WAG/Rij rats; this was related to the effect of the copper dose on both patterns. The subcellular distribution of copper in the liver was studied in Fischer and Brown Norway rats after doses of 50, 100, and 200 micrograms per 100 gm body weight. Brown Norway rats accumulated more copper in the liver, although the copper concentration was the same in both strains 1 hr after injection of all doses. Fischer rats accumulated proportionally more copper in lysosomal and nuclear mitochondrial fractions whereas Brown Norway rats accumulated proportionally more copper in the cytosol. Gel filtration of liver supernatants revealed that the amount of copper accumulating in the protein presumed to be metallothionein was 2 to 3 times higher in Brown Norway rats, whereas in the Fischer rats more copper eluted in the void volume fraction. We conclude that both biliary copper excretion and copper distribution in the liver are under genetic control. Because of its low copper excretion and reduced binding of copper to metallothionein the Fischer rat, compared to other strains, may be a suitable model for studying the involvement of the liver in copper intoxication.

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Year:  1986        PMID: 3732995     DOI: 10.1002/hep.1840060409

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  5 in total

1.  Strain differences in kidney copper concentrations of male rats.

Authors:  H Nederbragt; L F van Zutphen
Journal:  Biol Trace Elem Res       Date:  1987-12       Impact factor: 3.738

2.  Copper absorption, endogenous excretion, and distribution in Sprague-Dawley and lean (Fa/Fa) Zucker rats.

Authors:  G D Miller; C L Keen; J S Stern; J Y Uriu-Hare
Journal:  Biol Trace Elem Res       Date:  1996       Impact factor: 3.738

3.  The failure of selenium supplementation to prevent copper-induced liver damage in Fischer 344 rats.

Authors:  E M Aburto; A Cribb; I C Fuentealba; B O Ikede; F S Kibenge; F Markham
Journal:  Can J Vet Res       Date:  2001-04       Impact factor: 1.310

4.  Morphological and biochemical assessment of the liver response to excess dietary copper in Fischer 344 rats.

Authors:  E M Aburto; A E Cribb; I C Fuentealba; B O Ikede; F S Kibenge; F Markham
Journal:  Can J Vet Res       Date:  2001-04       Impact factor: 1.310

5.  Copper biodistribution after acute systemic administration of copper gluconate to rats.

Authors:  Betzabeth Anali García-Martínez; Sergio Montes; Luis Tristán-López; David Quintanar-Guerrero; Luz María Melgoza; Verónica Baron-Flores; Camilo Ríos
Journal:  Biometals       Date:  2021-04-26       Impact factor: 2.949

  5 in total

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