Literature DB >> 147255

Post-mortem changes in human central nervous tissue and the effects on quantitation of nucleic acids and enzymes.

D M Mann, C M Barton, J S Davies.   

Abstract

A study of post-mortem changes in human central nervous tissue has shown that within 100 h of death, no significant change occurs in the amount of nerve cell DNA and nucleolar RNA nor in some membrane-associated enzymes such as succinate dehydrogenase, NADH and NADPH diaphorase, and cytochrome oxidase. Low molecular weight RNA species, probably transfer and messenger RNA are quickly lost, but there is little alteration in ribosomal RNA content. Cytoplasmic enzymes show variable changes; phosphofructokinase activity is rapidly decreased; hexokinase is unaltered but lactate dehydrogenase, pyruvate kinase and glucose-6-phosphate dehydrogenase initially show increases in activity which subsequently decline. Oxygen uptake diminishes quickly. These findings indicate that mechanical alterations in cell structure, following death, render organelles physiologically ineffective long before any significant changes in certain constituent biochemicals are detected. This report emphasizes the great importance necessary in the selection of appropriately time matched post-mortem tissues if accurate comparative studies of many of the cells constituents are to be made.

Entities:  

Mesh:

Substances:

Year:  1978        PMID: 147255     DOI: 10.1007/bf01003298

Source DB:  PubMed          Journal:  Histochem J        ISSN: 0018-2214


  6 in total

1.  The cytochemistry of anoxic and anoxicischemic encephalopathy in rats. III. Alterations in the neuronal Golgi apparatus identified by nucleoside diphosphatase activity.

Authors:  N H BECKER
Journal:  Am J Pathol       Date:  1962-02       Impact factor: 4.307

2.  Lipoprotein pigments--their relationship to ageing in the human nervous system. I. The lipofuscin content of nerve cells.

Authors:  D M Mann; P O Yates
Journal:  Brain       Date:  1974-09       Impact factor: 13.501

3.  A method for in situ cytophotometric estimation of absolute amount of ribonucleic acid using azure B1.

Authors:  J R Shea
Journal:  J Histochem Cytochem       Date:  1970-02       Impact factor: 2.479

4.  Neuromelanin and RNA in cells of substantia nigra.

Authors:  D M Mann; P O Yates; C M Barton
Journal:  J Neuropathol Exp Neurol       Date:  1977 Mar-Apr       Impact factor: 3.685

5.  The activities of fructose 1,6-diphosphatase, phosphofructokinase and phosphoenolpyruvate carboxykinase in white muscle and red muscle.

Authors:  L H Opie; E A Newsholme
Journal:  Biochem J       Date:  1967-05       Impact factor: 3.857

6.  The cytochemical localization of oxidative enzymes. I. Diphosphopyridine nucleotide diaphorase and triphosphopyridine nucleotide diaphorase.

Authors:  D G SCARPELLI; R HESS; A G PEARSE
Journal:  J Biophys Biochem Cytol       Date:  1958-11-25
  6 in total
  6 in total

1.  Optimizing gene expression analysis in archival brain tissue.

Authors:  Vivianna M D Van Deerlin; Lisa H Gill; Peter T Nelson
Journal:  Neurochem Res       Date:  2002-10       Impact factor: 3.996

2.  Postmortem activity of the key enzymes of glycolysis. In rat brain regions in relation to time after death.

Authors:  A Pla; L Lemus; A Valenzuela; E Villanueva
Journal:  Z Rechtsmed       Date:  1986

Review 3.  Cell and tissue fixation, 1972-1982.

Authors:  D Hopwood
Journal:  Histochem J       Date:  1985-04

4.  Postmortem activity of lactate and malate dehydrogenase in human liver in relation to time after death.

Authors:  T Gos; S Raszeja
Journal:  Int J Legal Med       Date:  1993       Impact factor: 2.686

5.  Enzyme alterations in brain tissue during the early postmortal interval with reference to the histomorphology: review of the literature.

Authors:  M Oehmichen
Journal:  Z Rechtsmed       Date:  1980

6.  Nucleoside map of the human central nervous system.

Authors:  Zsolt Kovács; Arpád Dobolyi; Gábor Juhász; Katalin A Kékesi
Journal:  Neurochem Res       Date:  2009-10-24       Impact factor: 3.996

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.