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Changes in Glycogen Structure over Feeding Cycle Sheds New Light on Blood-Glucose Control
Author(s) -
Mitchell A. Sullivan,
Samuel T. N. Aroney,
Shihan Li,
Frederick J. Warren,
Jin Suk Joo,
Ka Sin Mak,
David Stapleton,
Kim BellAnderson,
Robert G. Gilbert
Publication year - 2013
Publication title -
biomacromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.689
H-Index - 220
eISSN - 1526-4602
pISSN - 1525-7797
DOI - 10.1021/bm401714v
Subject(s) - glycogen , diabetes mellitus , endocrinology , medicine , glycogen synthase , glucose homeostasis , chemistry , biology , biochemistry , insulin resistance
Liver glycogen, a highly branched polymer of glucose, is important for maintaining blood-glucose homeostasis. It was recently shown that db/db mice, a model for Type 2 diabetes, are unable to form the large composite glycogen α particles present in normal, healthy mice. In this study, the structure of healthy mouse-liver glycogen over the diurnal cycle was characterized using size exclusion chromatography and transmission electron microscopy. Glycogen was found to be formed as smaller β particles, and then only assembled into large α particles, with a broad size distribution, significantly after the time when glycogen content had reached a maximum. This pathway, missing in diabetic animals, is likely to give optimal blood-glucose control during the daily feeding cycle. Lack of this control may contribute to, or result from, diabetes. This discovery suggests novel approaches to diabetes management.

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