An electron microscopic and biochemical study of the effects of glucagon on glycogen autophagy in the liver and heart of newborn rats

التفاصيل البيبلوغرافية
العنوان: An electron microscopic and biochemical study of the effects of glucagon on glycogen autophagy in the liver and heart of newborn rats
المؤلفون: O. B. Kotoulas, Stefanos A. Kalamidas, D.J. Kondomerkos
المصدر: Microscopy Research and Technique. 63:87-93
بيانات النشر: Wiley, 2004.
سنة النشر: 2004
مصطلحات موضوعية: medicine.medical_specialty, Time Factors, Histology, Vacuole, Biology, Glucagon, Glucosidases/metabolism, chemistry.chemical_compound, Glycogen/*metabolism, Heart/drug effects/physiology, Internal medicine, Autophagy, medicine, Animals, Maltose, Instrumentation, Electron microscopic, Myocardium/*metabolism/ultrastructure, Protein Synthesis Inhibitors, chemistry.chemical_classification, Liver/drug effects/*metabolism/ultrastructure, Glycogen, Myocardium, Maltose/metabolism, Heart, Autophagy/*drug effects, Glucagon/*pharmacology, Rats, Cardiovascular physiology, Microscopy, Electron, Medical Laboratory Technology, Endocrinology, Enzyme, Animals, Newborn, Liver, chemistry, Hepatocytes/drug effects/metabolism/ultrastructure, Protein Synthesis Inhibitors/*pharmacology, Hepatocytes, Ultrastructure, Anatomy, Glucosidases
الوصف: The effects of glucagon on the ultrastructural appearance and acid glucosidase activities in the liver and heart of newborn rats were studied. Liver or heart glycogen-hydrolyzing activity of acid glucosidase increased 3 hours after birth and gradually decreased from 3 to 9 hours. Maltose-hydrolyzing activity of acid glucosidase also rose 3 hours after birth, maintained a plateau between 3 and 6 hours, and fell at 9 hours. The administration of glucagon increased autophagic activity in the hepatocytes at the age of 6 hours. Glycogen inside the autophagic vacuoles was decreased, apparently due to the increased glycogen degradation. Glycogen-hydrolyzing activity was elevated in both the liver and the heart. Maltose-hydrolyzing activity was elevated in the liver, but not in the heart. The results of this study suggest that the glycogen-hydrolyzing and maltose-hydrolyzing activities of acid glucosidase are due to different enzymes. Glucagon's effect on the glycogen-hydrolyzing acid glucosidase activity and autophagosomal morphology is similar in both the liver and the heart. Microsc Res Tech
تدمد: 1097-0029
1059-910X
DOI: 10.1002/jemt.20000
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea5e4f19fab8f6f448be282e56827532
https://doi.org/10.1002/jemt.20000
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....ea5e4f19fab8f6f448be282e56827532
قاعدة البيانات: OpenAIRE
الوصف
تدمد:10970029
1059910X
DOI:10.1002/jemt.20000