Hepatic and skeletal muscle glycogen metabolism in rats with short-term cholestasis.

Détails

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Etat: Public
Version: Final published version
Licence: Non spécifiée
ID Serval
serval:BIB_C2427E4FFA23
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Hepatic and skeletal muscle glycogen metabolism in rats with short-term cholestasis.
Périodique
Journal of hepatology
Auteur⸱e⸱s
Lang C., Schäfer M., Varga L., Zimmermann A., Krähenbühl S., Krähenbühl L.
ISSN
0168-8278 (Print)
ISSN-L
0168-8278
Statut éditorial
Publié
Date de publication
01/2002
Peer-reviewed
Oui
Volume
36
Numéro
1
Pages
22-29
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
To study the effect of short-term cholestasis on glycogen metabolism.
Rats were bile duct ligated (BDL) for 4 or 8 days and compared to sham-operated control rats pair-fed to BDL (pair-fed CON) or fed ad libitum (ad libitum-fed CON).
Four days after surgery, the hepatic glycogen content was 21.6+/-7.6 mg/g in BDL, 21.2+/-8.5 mg/g in pair-fed CON and 72.9+/-7.7 mg/g in ad libitum-fed CON, respectively. Eight days after surgery, the hepatic glycogen content was reduced in BDL as compared to pair-fed (31.2+/-8.9 vs. 59.1+/-5.4 mg/g) or ad libitum-fed CON (58.3+/-4.7 mg/g). Similar findings were obtained with the glycogen content expressed per ml hepatocytes or per liver. Histological analysis of BDL livers showed that most hepatocytes were affected. As compared to CON, activities and mRNA levels of glycogen synthase and phosphorylase were reduced in BDL, whereas plasma glucagon and endotoxin levels were increased at both time points. In contrast to liver, skeletal muscle glycogen metabolism remained unaffected.
While reduced intake of food explains the decrease in the hepatic glycogen stores in BDL and pair-fed CON 4 days after surgery, reduced glycogen synthesis, possibly related to endotoxinemia, is the most probable cause of the decrease in the hepatic glycogen content in BDL 8 days after surgery.
Mots-clé
Acute Disease, Animals, Bile Ducts, Cholestasis, Extrahepatic/metabolism, Endotoxemia/metabolism, Gene Expression Regulation, Enzymologic, Glycogen/biosynthesis, Glycogen/metabolism, Glycogen Phosphorylase/genetics, Glycogen Phosphorylase/metabolism, Glycogen Synthase/genetics, Glycogen Synthase/metabolism, Ligation, Liver/metabolism, Male, Muscle, Skeletal/metabolism, RNA, Messenger/analysis, Rats, Rats, Sprague-Dawley
Pubmed
Web of science
Open Access
Oui
Création de la notice
11/12/2018 15:10
Dernière modification de la notice
03/05/2023 12:34
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