1973The Anatomical RecordRequires access

Correlation between structure and glycogen content of livers from rats on a controlled feeding schedule

Robert R. Cardell, Joseph Larner, Muriel B. Babcock

Open publisher page 37 citations

Abstract

Abstract Male rats were maintained on a controlled feeding schedule and groups of animals sacrificed at 2, 15, 21, 36, 48 and 72 hours of fasting. Chemical determinations of glycogen showed that livers of rats fasted two hours contained 8.7% glycogen; 15 hours, 6.2%; 21 hours, 0.7%; 36 hours, 0.7%; 48 hours, 0.8%; and 72 hours, 0.4%. After PA/S procedures, glycogen appeared in hepatocytes of rats fasted 2 and 15 hours as large masses intensely stained. At these time‐periods, almost all cells contained significant quantities of glycogen but hepatocytes located toward portal tracts showed larger and more intensely stained masses of glycogen than found in cells near central veins. After longer periods of fasting, glycogen masses decreased in size, number, and staining intensity. The fine structure of hepatocytes from rats fasted 2 or 15 hours showed abundant α and β particles of glycogen in the form of large masses throughout the cytosome. These correlated in position and shape to the masses of glycogen seen in the light microscope. As glycogen depletion occurred (fasted 21 hours and longer) the number of glycogen particles decreased in hepatocytes. It is concluded from this study that a good correlation exists between chemical determinations of hepatic glycogen, cytochemistry of glycogen in hepatocytes, fine structure of liver cells, and the fasting state of the animal.

About this research paper

What this paper is about

Abstract Male rats were maintained on a controlled feeding schedule and groups of animals sacrificed at 2, 15, 21, 36, 48 and 72 hours of fasting. Chemical determinations of glycogen showed that livers of rats fasted two hours contained 8.7% glycogen; 15 hours, 6.2%; 21 hours, 0.7%; 36 hours, 0.7%; 48 hours, 0.8%; and 72 hours, 0.4%. After PA/S procedures, glycogen appeared in hepatocytes of rats fasted 2 and 15 hours as large masses intensely stained. At these time‐periods, almost all cells contained significant quantities of glycogen but hepatocytes located toward portal tracts showed larger and more intensely stained masses of glycogen than found in cells near central veins. After longer periods of fasting, glycogen masses decreased in size, number, and staining intensity. The fine structure of hepatocytes from rats fasted 2 or 15 hours showed abundant α and β particles of glycogen in the form of large masses throughout the cytosome. These correlated in position and shape to the masses of glycogen seen in the light microscope. As glycogen depletion occurred (fasted 21 hours and longer) the number of glycogen particles decreased in hepatocytes. It is concluded from this study that a good correlation exists between chemical determinations of hepatic glycogen, cytochemistry of glycogen in hepatocytes, fine structure of liver cells, and the fasting state of the animal.

Why it matters

OpenAlex reports 37 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract Male rats were maintained on a controlled feeding schedule and groups of animals sacrificed at 2, 15, 21, 36, 48 and 72 hours of fasting. Chemical determinations of glycogen showed that livers of rats fasted two hours contained 8.7% glycogen; 15 hours, 6.2%; 21 hours, 0.7%; 36 hours, 0.7%; 48 hours, 0.8%; and 72 hours, 0.4%. After PA/S procedures, glycogen appeared in hepatocytes of rats fasted 2 and 15 hours as large masses intensely stained. At these time‐periods, almost all cells contained significant quantities of glycogen but hepatocytes located toward portal tracts showed larger and more intensely stained masses of glycogen than found in cells near central veins. After longer periods of fasting, glycogen masses decreased in size, number, and staining intensity. The fine structure of hepatocytes from rats fasted 2 or 15 hours showed abundant α and β particles of glycogen in the form of large masses throughout the cytosome. These correlated in position and shape to the masses of glycogen seen in the light microscope. As glycogen depletion occurred (fasted 21 hours and longer) the number of glycogen particles decreased in hepatocytes. It is concluded from this study that a good correlation exists between chemical determinations of hepatic glycogen, cytochemistry of glycogen in hepatocytes, fine structure of liver cells, and the fasting state of the animal.

Key concepts: Glycogen, Internal medicine, Endocrinology, Cytochemistry, Periodic acid–Schiff stain, Staining, Chemistry, Biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Correlation between structure and glycogen content of livers from rats on a controlled feeding schedule — Research Paper | ScholarLens