Increases in glycogenin and glycogenin mRNA accompany glycogen resynthesis in human skeletal muscle
Abstract
Glycogenin is the self-glycosylating protein primer that initiates glycogen granule formation. To examine the role of this protein during glycogen resynthesis, eight male subjects exercised to exhaustion on a cycle ergometer at 75% V̇o 2 max followed by five 30-s sprints at maximal capacity to further deplete glycogen stores. During recovery, carbohydrate (75 g/h) was supplied to promote rapid glycogen repletion, and muscle biopsies were obtained from the vastus lateralis at 0, 30, 120, and 300 min postexercise. At time 0, no free (deglycosylated) glycogenin was detected in muscle, indicating that all glycogenin was complexed to carbohydrate. Glycogenin activity, a measure of the glycosylating ability of the protein, increased at 30 min and remained elevated for the remainder of the study. Quantitative RT-PCR showed elevated glycogenin mRNA at 120 min followed by increases in protein levels at 300 min. Glycogenin specific activity (glycogenin activity/relative protein content) was also elevated at 120 min. Proglycogen increased at all time points, with the highest rate of resynthesis occurring between 0 and 30 min. In comparison, macroglycogen levels did not significantly increase until 300 min postexercise. Together, these results show that, during recovery from prolonged exhaustive exercise, glycogenin mRNA and protein content and activity increase in muscle. This may facilitate rapid glycogen resynthesis by providing the glycogenin backbone of proglycogen, the major component of glycogen synthesized in early recovery.
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A modified glycogen loading protocol of high carbohydrate intake and exercise taper, deleting the depletion phase, was similarly successful in athletes in the study by Sherman and colleagues.
“A 'modified' protocol of high CHO intake and exercise taper, deleting the depletion phase, was found to be similarly successful in athletes in the latter study (96).”
From Postexercise muscle glycogen resynthesis in humans. (2017) · cites this paper as [96]
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- Authors
- Shearer, J., Wilson, R. J., Battram, D. S., Richter, E. A., Robinson, D. L., Bakovic, M., & Graham, T. E.
- Affiliations
- University of Guelph (CA)
- Venue
- American Journal of Physiology-Endocrinology and Metabolism
- Publisher
- American Physiological Society
- Published
- 2005-09
- Volume
- 289
- Issue
- 3
- Pages
- E508-E514
- ISSN
- 0193-1849 (ISSN-L)
- 1522-1555
- OpenAlex
- W2151408372
- Cited by
- 32
- References
- 36
- Citations by year
- 2023: 1 · 2021: 1 · 2019: 1 · 2018: 2 · 2017: 1 · 2016: 1 · 2015: 1 · 2014: 1 · 2013: 1 · 2012: 5
- FWCI
- 1.22
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Funders
- University of Guelph
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Health Sciences › Medicine › Rheumatology › Glycogen Storage Diseases and Myoclonus
- Keywords
- glycogenin, glycogen resynthesis, skeletal muscle, carbohydrate supplementation, exhaustive exercise, post-exercise recovery, vastus lateralis, glycogen synthesis
- MeSH terms
- Adult, Blood Glucose, Exercise Test, Glucosyltransferases, Glycogen, Glycoproteins, Humans, Insulin, Male, Oxygen Consumption, RNA, Messenger, Transcription, Genetic, Gene Expression, Muscle, Skeletal
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