Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 May 11;293(19):7087-7088.
doi: 10.1074/jbc.TM118.002642. Epub 2018 Mar 7.

Introduction to the Thematic Minireview Series: Brain glycogen metabolism

Affiliations

Introduction to the Thematic Minireview Series: Brain glycogen metabolism

Gerald M Carlson et al. J Biol Chem. .

Abstract

The synthesis of glycogen allows for efficient intracellular storage of glucose molecules in a soluble form that can be rapidly released to enter glycolysis in response to energy demand. Intensive studies of glucose and glycogen metabolism, predominantly in skeletal muscle and liver, have produced innumerable insights into the mechanisms of hormone action, resulting in the award of several Nobel Prizes over the last one hundred years. Glycogen is actually present in all cells and tissues, albeit at much lower levels than found in muscle or liver. However, metabolic and physiological roles of glycogen in other tissues are poorly understood. This series of Minireviews summarizes what is known about the enzymes involved in brain glycogen metabolism and studies that have linked glycogen metabolism to multiple brain functions involving metabolic communication between astrocytes and neurons. Recent studies unexpectedly linking some forms of epilepsy to mutations in two poorly understood proteins involved in glycogen metabolism are also reviewed.

Keywords: Lafora disease (Lafora progressive myoclonic epilepsy, MELF); astrocyte; glycogen; neurochemistry; neuron.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no conflicts of interest with the contents of this article.

Similar articles

Cited by

References

    1. Kerr S. E. (1936) The carbohydrate metabolism of brain: I. The determination of glycogen in nerve tissue. J. Biol. Chem. 116, 1–7
    1. Kerr S. E. (1938) The carbohydrate metabolism of brain: VI. Isolation of glycogen. J. Biol. Chem. 123, 443–449
    1. Richter K., Hamprecht B., and Scheich H. (1996) Ultrastructural localization of glycogen phosphorylase predominantly in astrocytes of the gerbil brain. Glia 17, 263–273 10.1002/(SICI)1098-1136(199608)17:4%3C263::AID-GLIA1%3E3.0.CO%3B2-0 - DOI - PubMed
    1. Psarra A. M. G., Pfeiffer B., Giannakopoulou M., Sotiroudis T. G., Stylianopoulou F., and Hamprecht B. (1998) Immunocytochemical localization of glycogen phosphorylase kinase in rat brain sections and in glial and neuronal primary cultures. J. Neurocytol. 27, 779–790 10.1023/A:1006970429961 - DOI - PubMed
    1. Pfeiffer-Guglielmi B., Bröer S., Bröer A., and Hamprecht B. (2000) Isozyme pattern of glycogen phosphorylase in the rat nervous system and rat astroglia-rich primary cultures: electrophoretic and polymerase chain reaction studies. Neurochem. Res. 25, 1485–1491 10.1023/A:1007676109206 - DOI - PubMed

Publication types

LinkOut - more resources