Literature DB >> 573618

Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) mice.

J R Mann, J Camakaris, D M Danks, E G Walliczek.   

Abstract

Copper therapy was applied to brindled mouse mutants, which suffer from lethal hypocupraemia, by using cuprous and cupric solutions. The method of treatment was a single subcutaneous injection of 50 microgram of copper at 7 days of age. Early effects of the dose were: prevention of the tremors and spasms seen in untreated mutants, raising to normal and near-normal of caeruloplasmin oxidase and lysyl oxidase activities and pigmentation of skin and fur. Growth of mutants was retarded up to 23 days of age, but thereafter they rapidly gained weight to be nearly normal by 60 days of age. At 3 days after injection, copper concentrations in previously deficient mutant organs apart from liver were at least as much as those of treated normals, which had remained unchanged. Copper in mutant livers had increased only slightly in comparison with the normal control. A state of copper deficiency recurred in mutant tissues by 25 days after injection. A solution of Cu+, retained as such by an alkyl polyether, and sebacic acid resulted in greater growth rates after 23 days than did three other copper treatments. Cu+ may have resulted in an improved growth response owing to it being more readily metabolized than C12+. Delayed release of copper from the site of injection may have played an important role.

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Year:  1979        PMID: 573618      PMCID: PMC1161100          DOI: 10.1042/bj1800605

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  13 in total

1.  Primary defect in copper transport underlies mottled mutants in the mouse.

Authors:  D M Hunt
Journal:  Nature       Date:  1974-06-28       Impact factor: 49.962

2.  Biological applications of the carbon rod atomizer in atomic absorption spectroscopy. 2. Determination of copper in small samples of tissue.

Authors:  B J Stevens
Journal:  Clin Chem       Date:  1972-11       Impact factor: 8.327

3.  Impaired copper homeostasis in neonatal male and adult female Brindled (Mobr) mice.

Authors:  G W Evans; B L Reis
Journal:  J Nutr       Date:  1978-04       Impact factor: 4.798

4.  Letter: Intravenous copper in Menkes' kinky-hair syndrome.

Authors:  H Wehinger; I Witt; I Lösel; G Denz-Seibert; C Sander
Journal:  Lancet       Date:  1975-05-17       Impact factor: 79.321

5.  64Cu metabolism in Menkes and normal cultured skin fibroblasts.

Authors:  N G Beratis; P Price; G Labadie; K Hirschhorn
Journal:  Pediatr Res       Date:  1978-06       Impact factor: 3.756

6.  Copper metabolism in mottled mouse mutants: copper concentrations in tissues during development.

Authors:  J Camakaris; J R Mann; D M Danks
Journal:  Biochem J       Date:  1979-06-15       Impact factor: 3.857

7.  Copper metabolism in mottled mouse mutants: distribution of 64Cu in brindled (Mobr) mice.

Authors:  J R Mann; J Camakaris; D M Danks
Journal:  Biochem J       Date:  1979-06-15       Impact factor: 3.857

8.  Copper incorporation studies on cultured cells for prenatal diagnosis of Menkes' disease.

Authors:  N Horn
Journal:  Lancet       Date:  1976-05-29       Impact factor: 79.321

9.  The biological role of ceruloplasmin and its oxidase activity.

Authors:  E Frieden; H S Hsieh
Journal:  Adv Exp Med Biol       Date:  1976       Impact factor: 2.622

10.  Menkes disease: a biochemical abnormality in cultured human fibroblasts.

Authors:  T J Goka; R E Stevenson; P M Hefferan; R R Howell
Journal:  Proc Natl Acad Sci U S A       Date:  1976-02       Impact factor: 11.205

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  24 in total

1.  Silencing of the Menkes copper-transporting ATPase (Atp7a) gene increases cyclin D1 protein expression and impairs proliferation of rat intestinal epithelial (IEC-6) cells.

Authors:  Sukru Gulec; James F Collins
Journal:  J Trace Elem Med Biol       Date:  2014-08-04       Impact factor: 3.849

2.  Golgi study on macular mutant mouse after copper therapy.

Authors:  H Kawasaki; T Yamano; S Iwane; M Shimada
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

3.  Cerebellar changes of the female mice heterozygous for brindled gene.

Authors:  T Yamano; K Suzuki
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

4.  Copper metabolism in mottled mouse mutants. The effect of copper therapy on lysyl oxidase activity in brindled (Mobr) mice.

Authors:  P M Royce; J Camakaris; J R Mann; D M Danks
Journal:  Biochem J       Date:  1982-02-15       Impact factor: 3.857

5.  Copper metabolism in mottled mouse mutants: copper concentrations in tissues during development.

Authors:  J Camakaris; J R Mann; D M Danks
Journal:  Biochem J       Date:  1979-06-15       Impact factor: 3.857

6.  Copper metabolism in mottled mouse mutants: distribution of 64Cu in brindled (Mobr) mice.

Authors:  J R Mann; J Camakaris; D M Danks
Journal:  Biochem J       Date:  1979-06-15       Impact factor: 3.857

7.  Cytosolic copper-binding proteins in rat and mouse hepatocytes incubated continuously with Cu(II).

Authors:  F A Palida; A Mas; L Arola; K Bethin; P A Lonergan; M J Ettinger
Journal:  Biochem J       Date:  1990-06-01       Impact factor: 3.857

8.  Hepatic metallothionein synthesis in neonatal Mottled-Brindled mutant mice.

Authors:  J E Piletz; H R Herschman
Journal:  Biochem Genet       Date:  1983-06       Impact factor: 1.890

9.  Copper metabolism in mottled mouse (Mus musculus) mutants. Studies of blotchy (Moblo) mice and a comparison with brindled (Mobr) mice.

Authors:  J R Mann; J Camakaris; N Francis; D M Danks
Journal:  Biochem J       Date:  1981-04-15       Impact factor: 3.857

10.  The relationship of excess copper accumulation by fibroblasts from the brindled mouse model of Menkes disease to the primary defect.

Authors:  G L Waldrop; M J Ettinger
Journal:  Biochem J       Date:  1990-04-15       Impact factor: 3.857

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