Literature DB >> 3759507

A highly sensitive method for the histochemical demonstration of copper in normal rat tissues.

P Szerdahelyi, P Kása.   

Abstract

Earlier, widely used histochemical methods for the demonstration of copper are capable of detecting only extremely high tissue levels of this metal (generally only in pathological states, e.g. Wilson's disease, or in cases of copper intoxication), because of their low sensitivity. The specificity of these methods has also proved to be unsatisfactory. We present a new method based on the release of bound (unreactive) copper by trichloroacetic acid, its primary precipitation using magnesium dithizonate, and intensification of the staining (secondary precipitation) using silver nitrate. Using this method, copper is demonstrable in various tissues of normal rats (brain, stomach, liver, small intestine, spleen, pancreas, kidneys) in the form of reddish to pink staining. This method can also be applied to locate pathologically high levels of copper.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3759507     DOI: 10.1007/bf00493488

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  22 in total

1.  [LIGHT SENSITIVITY OF METAL DITHIZONATE].

Authors:  R SCHMIDT; R RAUTSCHKE
Journal:  Acta Histochem       Date:  1963-06-30       Impact factor: 2.479

2.  THE INTRAHEPATIC AND INTRACELLULAR DISTRIBUTION OF COPPER FOLLOWING CHRONIC ADMINISTRATION OF THE METAL IN THE DIET.

Authors:  W F MCNARY
Journal:  Anat Rec       Date:  1963-07

3.  Histochemical demonstration of copper in a case of hepatolenticular degeneration.

Authors:  C L GREEN
Journal:  Am J Pathol       Date:  1955 May-Jun       Impact factor: 4.307

4.  [The histochemical demonstration of normal heavy metals in the liver].

Authors:  F TIMM
Journal:  Z Zellforch Microsk Anat Histochem       Date:  1960

5.  Histochemical localization of copper with rubeanic acid.

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

6.  Studies on copper metabolism. XIII. Hepatolenticular degeneration.

Authors:  G E CARTWRIGHT; R E HODGES; C J GUBLER; J P MAHONEY; K DAUM; M M WINTROBE; W B BEAN
Journal:  J Clin Invest       Date:  1954-11       Impact factor: 14.808

7.  Pathogenesis of hepatocerebral disease. II. Histochemical study of copper of liver and brain in Wilson's disease.

Authors:  S OKINAKA; M YOSHIKAWA; M TOYODA; T MOZAI; Y TOYOKURA; M KAMEYAMA
Journal:  AMA Arch Neurol Psychiatry       Date:  1954-11

8.  Fixing and staining methods for lead and copper in tissues.

Authors:  F B Mallory; F Parker
Journal:  Am J Pathol       Date:  1939-09       Impact factor: 4.307

9.  Copper deficiency in the developing rat brain: a possible model for Menkes' steely-hair disease.

Authors:  J R Prohaska; W W Wells
Journal:  J Neurochem       Date:  1974-07       Impact factor: 5.372

10.  Trace metal patterns in disease states. II. Copper storage diseases, with consideration of juvenile cirrhosis, Wilson's disease, and hepatic copper of the newborn.

Authors:  E M BUTT; R E NUSBAUM; T C GILMOUR; S L DIDIO
Journal:  Am J Clin Pathol       Date:  1958-12       Impact factor: 2.493

View more
  3 in total

1.  Histochemical demonstration of copper in normal rat brain and spinal cord. Evidence of localization in glial cells.

Authors:  P Szerdahelyi; P Kása
Journal:  Histochemistry       Date:  1986

2.  Regional differences in the uptake of exogenous copper into rat brain after acute treatment with sodium diethyldithiocarbamate. A histochemical and atomic absorption spectrophotometric study.

Authors:  P Szerdahelyi; P Kása
Journal:  Histochemistry       Date:  1987

3.  Inhibition of angiogenesis and tumor growth in the brain. Suppression of endothelial cell turnover by penicillamine and the depletion of copper, an angiogenic cofactor.

Authors:  S S Brem; D Zagzag; A M Tsanaclis; S Gately; M P Elkouby; S E Brien
Journal:  Am J Pathol       Date:  1990-11       Impact factor: 4.307

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.