Literature DB >> 7086438

Postmortem stability of enzymes detoxifying peroxide in brain.

T S Brannan, H S Maker, M Bernstein.   

Abstract

Glutathione peroxidase, glutathione reductase, and catalase activities were measured to 48 h after death in mouse brains held at temperatures replicating the cooling occurring in human cadaver brain. Glutathione peroxidase was stable for 48 h; catalase was stable for 24 h and then declined 20% in activity. Glutathione reductase was stable for 4 h and then decreased to 55% of its initial activity by 48 h. Perfusion of mouse brain with 0.9% (wt/vol) NaCl did not decrease enzyme activities, indicating that erythrocyte contamination has little effect on measured brain activities. The results suggest that glutathione peroxidase would not be affected by moderate time delays in obtaining human postmortem brains but catalase activity may be affected if brains are not promptly removed. Glutathione reductase is not stable and measurements would require controls carefully matched for postmortem conditions.

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Year:  1982        PMID: 7086438     DOI: 10.1111/j.1471-4159.1982.tb03988.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  3 in total

1.  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

2.  Oxygen toxicity protecting enzymes in the human brain.

Authors:  R J Marttila; M Röyttä; H Lorentz; U K Rinne
Journal:  J Neural Transm       Date:  1988       Impact factor: 3.575

3.  Glutathione peroxidase activity in surgical and autopsied human brains.

Authors:  K A Ansari; D Bigelow; E Kaplan
Journal:  Neurochem Res       Date:  1985-05       Impact factor: 3.996

  3 in total

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