Literature DB >> 2989341

Hepatic copper distribution in primary biliary cirrhosis shown by the scanning proton microprobe.

D J Vaux, F Watt, G W Grime, J Takacs.   

Abstract

A number of conditions are associated with abnormalities of trace metal handling by the liver. We report the application of the Oxford scanning proton microprobe to the analysis of hepatic copper in one such condition, primary biliary cirrhosis. The scanning proton microprobe analyses conventional tissue sections (5-10 micron thickness) and produces simultaneous elemental distribution maps of biologically relevant elements with a spatial resolution of 1 micron and a detection limit better than 1 ppm. We have confirmed the localisation of excess copper to periportal areas and suggest that such accumulation is confined to a proportion of periportal hepatocytes. We have also shown a close spatial correlation between regions of copper accumulation and areas of high sulphur concentration. The copper to sulphur ratio in these areas is consistent with their identity as aggregates of copper loaded metallothionein, and the scanning proton microprobe was further able to show that the aggregates contain less than 30 ppm zinc.

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Year:  1985        PMID: 2989341      PMCID: PMC499263          DOI: 10.1136/jcp.38.6.653

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  11 in total

1.  ACUTE TUBERCULOSIS AND GRANULOCYTIC DISORDERS.

Authors:  N C OSWALD
Journal:  Br Med J       Date:  1963-12-14

2.  Histochemical localization of copper with rubeanic acid.

Authors:  L L UZMAN
Journal:  Lab Invest       Date:  1956 May-Jun       Impact factor: 5.662

3.  Copper and primary biliary cirrhosis.

Authors:  C R Fleming; E R Dickson; A H Baggenstoss; J T McCall
Journal:  Gastroenterology       Date:  1974-12       Impact factor: 22.682

4.  Liver-copper levels in liver disease: studies using neutron activation analysis.

Authors:  R A Smallwood; H A Williams; V M Rosenoer; S Sherlock
Journal:  Lancet       Date:  1968-12-21       Impact factor: 79.321

5.  Synthesis and function of metallothioneins.

Authors:  J Kägi; T L Coombs; J Overnell; M Webb
Journal:  Nature       Date:  1981-08-06       Impact factor: 49.962

6.  Preparation and properties of the major copper-binding component in human fetal liver. Its identification as metallothionein.

Authors:  L Rydén; H F Deutsch
Journal:  J Biol Chem       Date:  1978-01-25       Impact factor: 5.157

7.  Changes in the distribution of hepatic copper in relation to the progression of Wilson's disease (hepatolenticular degeneration).

Authors:  S Goldfischer; I Sternlieb
Journal:  Am J Pathol       Date:  1968-12       Impact factor: 4.307

8.  Human fetal liver contains both zinc- and copper-rich forms of metallothionein.

Authors:  J R Riordan; V Richards
Journal:  J Biol Chem       Date:  1980-06-10       Impact factor: 5.157

9.  Evidence for site-selective metal binding in calf liver metallothionein.

Authors:  R W Briggs; I M Armitage
Journal:  J Biol Chem       Date:  1982-02-10       Impact factor: 5.157

10.  Is copper hepatotoxic in primary biliary cirrhosis?

Authors:  O Epstein; B Arborgh; M Sagiv; R Wroblewski; P J Scheuer; S Sherlock
Journal:  J Clin Pathol       Date:  1981-10       Impact factor: 3.411

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  3 in total

1.  Some medical applications of the oxford scanning proton microprobe.

Authors:  D J Vaux; G W Grime; F Watt
Journal:  Biol Trace Elem Res       Date:  1987-08       Impact factor: 3.738

2.  Systemic amyloidosis of beta 2-microglobulin type: a complication of long-term haemodialysis.

Authors:  J M Theaker; A E Raine; A J Rainey; A Heryet; A Clark; D O Oliver
Journal:  J Clin Pathol       Date:  1987-10       Impact factor: 3.411

3.  A copper-sulfur complex in the liver of a patient with Wilson's disease.

Authors:  A Sasa; H Hayashi; A Yagi; S Ohguchi; R Kidokoro; Y Sato; N Sakamoto
Journal:  Gastroenterol Jpn       Date:  1986-12
  3 in total

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