Literature DB >> 26202038

Hepatocytes of cirrhotic rat liver accumulate glycogen more slowly than normal ones.

Natalia N Bezborodkina1, Sergey V Okovity2, Anna Yu Chestnova3, Boris N Kudryavtsev4.   

Abstract

PURPOSE: To investigate the accumulation of glycogen in cirrhotic rat liver at several time intervals after per os administration of glucose to fasted animals.
METHODS: Liver cirrhosis was produced by inhalation of the hepatotropic poison CCl4. Glycogen concentration in the liver was determined biochemically. Glycogen content in hepatocytes was measured cytofluorimetrically in the smears stained with a fluorescent PAS reaction. Glycogen content in the hepatocytes of the portal and the central zone of the liver lobule was determined by absorption cytophotometry.
RESULTS: Rats poisoned with CCl4 for 6 months developed typical liver cirrhosis characterized by a fourfold (p < 0.001) increase in the proportion of the connective tissue. In the cirrhotic rats fasted for 48 h, glycogen concentration in the liver and glycogen content in hepatocytes were lower as compared with the control by 36 and 27 % (p < 0.01), respectively. According to data obtained by different methods, the control animals accumulated glycogen at a high rate. In particular, the glycogen content in hepatocytes increased by 34 % after 10 min (p < 0.01). In the cirrhotic rats, glycogen content remained at the same level for 20 min. In both groups of animals, hepatocytes of the portal zone accumulated more glycogen than those of the central zone.
CONCLUSIONS: Glycogen accumulation in cirrhotic rats starts after a delay and proceeds at a lower rate than in the norm.

Entities:  

Keywords:  Glucose; Glycogen; Hepatocytes; Liver cirrhosis

Year:  2013        PMID: 26202038     DOI: 10.1007/s12072-013-9458-8

Source DB:  PubMed          Journal:  Hepatol Int        ISSN: 1936-0533            Impact factor:   6.047


  23 in total

1.  Microspectrophotometric study of the binding of the anionic dye, naphthol yellow S, by tissue sections and by purified proteins.

Authors:  A D DEITCH
Journal:  Lab Invest       Date:  1955 Sep-Oct       Impact factor: 5.662

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Authors:  M Kudryavtseva; N N Bezborodkina; S V Okovity; B N Kudryavtsev
Journal:  Eur J Gastroenterol Hepatol       Date:  2001-06       Impact factor: 2.566

3.  Cytology and cytochemistry of adenomas of the human hypophysis.

Authors:  A G PEARSE
Journal:  Acta Unio Int Contra Cancrum       Date:  1962

Review 4.  Glucose metabolism in cirrhosis: a review with some perspectives for the future.

Authors:  A S Petrides; R A DeFronzo
Journal:  Diabetes Metab Rev       Date:  1989-12

5.  Determination of glycogen in small tissue samples.

Authors:  S Lo; J C Russell; A W Taylor
Journal:  J Appl Physiol       Date:  1970-02       Impact factor: 3.531

6.  Hepatic nonoxidative disposal of an oral glucose meal in patients with liver cirrhosis.

Authors:  P Schneiter; M Gillet; R Chioléro; E Jéquier; L Tappy
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7.  Contributions of net hepatic glycogenolysis and gluconeogenesis to glucose production in cirrhosis.

Authors:  K F Petersen; M Krssak; V Navarro; V Chandramouli; R Hundal; W C Schumann; B R Landau; G I Shulman
Journal:  Am J Physiol       Date:  1999-03

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Authors:  Margarita V Kudryavtseva; Natalia N Bezborodkina; Sergey V Okovity; Boris N Kudryavtsey
Journal:  Exp Toxicol Pathol       Date:  2003-03

9.  Metabolic handling of orally administered glucose in cirrhosis.

Authors:  Y T Kruszynska; A Meyer-Alber; F Darakhshan; P D Home; N McIntyre
Journal:  J Clin Invest       Date:  1993-03       Impact factor: 14.808

10.  Kinetic analysis of glycogen synthase and PDC in cirrhotic rat liver and skeletal muscle.

Authors:  M G Giardina; M Matarazzo; L Sacca
Journal:  Am J Physiol       Date:  1994-12
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