Literature DB >> 6618912

The value of enzyme leakage for the prediction of necrosis in liver ischemia.

W M Frederiks, G L Myagkaya, K S Bosch, G M Fronik, H van Veen, I M Vogels, J James.   

Abstract

Following the clamping of the afferent vessels of the left lateral and median lobes in rat liver, a considerable part of these lobes show signs of necrosis 24 h after 90 min of ischemia, whereas no necrotic areas can be detected after 30 min interruption of the blood flow. The purpose of this study was to examine the value of an analysis of the leakage of enzymes from the liver parenchyma in the early phase after restoration of the blood flow after ischemia for a prediction of the occurrence of necrosis. Leakage of the enzymes GPT, GOT and LDH can be detected in the blood plasma with a maximum activity between 1 and 5 h both following 30 and 90 min of ischemia; a considerable difference in clearance is observed, however, in the period afterwards, the normal situation being reached after 24 h with the 30-min ischemic period, but not following the 90-min period. With use of an enzyme histochemical reaction, in situ a depletion of LDH-activity in the hepatocytes could be detected within a short period of time after 30 min temporary ischemia and a restoration during the following period of 24 h; the decrease in LDH-activity persisted during 24 h with a 90-min period of ischemia. Electronmicroscopically cytoplasmic blebs arisen from hepatocytes are observed in the lumen of sinusoids immediately after 30 min of ischemia, whereas after 90 min of ischemia actual leakage of cytoplasmic material takes place through the damaged surface of the hepatocytes. Enzyme leakage probably takes place via these both types of shedding of cytoplasm. It is concluded that the enzyme leakage as such cannot be used as a discriminating test between reversible and irreversible damage of the liver parenchyma.

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Year:  1983        PMID: 6618912     DOI: 10.1007/bf00496197

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


  14 in total

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Journal:  Am J Pathol       Date:  1948-05       Impact factor: 4.307

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Journal:  Arch Biochem Biophys       Date:  1977-04-15       Impact factor: 4.013

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Authors:  E F Farkouh; A M Daniel; J G Beaudoin; L D MacLean
Journal:  Surg Gynecol Obstet       Date:  1971-05

5.  Enzyme cytochemical staining of individual cells with the use of a polyacrylamide carrier. Studies on the synthetizing reaction technique, the indigogenic method, the metal salt method, the post-azo-coupling technique, and the tetrazolium salt technique.

Authors:  C J van Noorden; R D Bhattacharya; I M Vogels
Journal:  Acta Histochem       Date:  1983       Impact factor: 2.479

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Authors:  L Cossel
Journal:  Pathol Res Pract       Date:  1980-12       Impact factor: 3.250

7.  Bleb formation in hepatocytes during drug metabolism is caused by disturbances in thiol and calcium ion homeostasis.

Authors:  S A Jewell; G Bellomo; H Thor; S Orrenius; M Smith
Journal:  Science       Date:  1982-09-24       Impact factor: 47.728

8.  A model for provoking ischemic necrosis in rat liver parenchyma and its quantitative analysis.

Authors:  W M Frederiks; J James; K S Bosch; M J Schröder; H C Schuyt
Journal:  Exp Pathol       Date:  1982

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Journal:  J Cell Biol       Date:  1977-02       Impact factor: 10.539

10.  The ultrastructural localization of the isozymes of aspartate aminotransferase in murine tissues.

Authors:  J M Papadimitriou; P van Duijn
Journal:  J Cell Biol       Date:  1970-10       Impact factor: 10.539

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  17 in total

1.  Effects of ischaemia and reperfusion on NADH coenzyme Q reductase activity in rat liver.

Authors:  W M Frederiks; K S Bosch; H Vreeling-Sindelárová
Journal:  Histochem J       Date:  1999-09

Review 2.  HMGB1 and microparticles as mediators of the immune response to cell death.

Authors:  David S Pisetsky; Julie Gauley; Anirudh J Ullal
Journal:  Antioxid Redox Signal       Date:  2011-05-05       Impact factor: 8.401

Review 3.  Detection of metabolic changes in hepatocytes by quantitative cytochemistry.

Authors:  J James; W M Frederiks; C J van Noorden; J Tas
Journal:  Histochemistry       Date:  1986

4.  Plasma amino acids in four models of experimental liver injury in rats.

Authors:  M Holeček; J Mráz; I Tilšer
Journal:  Amino Acids       Date:  1996-09       Impact factor: 3.520

5.  Cytophotometric analysis of reaction rates of succinate and lactate dehydrogenase activity in rat liver, heart muscle and tracheal epithelium.

Authors:  C J Van Noorden; I M Vogels
Journal:  Histochem J       Date:  1989 Sep-Oct

6.  The effects of storage on the retention of enzyme activity in cryostat sections. A quantitative histochemical study on rat liver.

Authors:  W M Frederiks; I J Ouwerkerk; K S Bosch; F Marx; A Kooij; C J Van Noorden
Journal:  Histochem J       Date:  1993-02

7.  Quantitative aspects of enzyme histochemistry on sections of freeze-substituted glycol methacrylate-embedded rat liver.

Authors:  W M Frederiks; K S Bosch
Journal:  Histochemistry       Date:  1993-10

8.  Experimentally induced colon cancer metastases in rat liver increase the proliferation rate and capacity for purine catabolism in liver cells.

Authors:  G N Jonges; I M Vogels; K S Bosch; K P Dingemans; C J Van Noorden
Journal:  Histochemistry       Date:  1993-07

9.  The effect of ischaemia on xanthine oxidase activity in rat intestine and liver.

Authors:  W M Frederiks; F Marx; A Kooij
Journal:  Int J Exp Pathol       Date:  1993-02       Impact factor: 1.925

10.  Quantitative comparison between the gel-film and polyvinyl alcohol methods for dehydrogenase histochemistry reveals different intercellular distribution patterns of glucose-6-phosphate and lactate dehydrogenases in mouse liver.

Authors:  P Griffini; E Vigorelli; V Bertone; I Freitas; C J Van Noorden
Journal:  Histochem J       Date:  1994-06
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