Glycogen

Schematic two-dimensional cross-sectional view of glycogen: A core protein of glycogenin is surrounded by branches of glucose units. The entire globular granule may contain around 30,000 glucose units.[1]
A view of the atomic structure of a single branched strand of glucose units in a glycogen molecule.
Glycogen (black granules) in spermatozoa of a flatworm; transmission electron microscopy, scale: 0.3 μm

Glycogen is a multibranched polysaccharide of glucose that serves as a form of energy storage in animals,[2] fungi, and bacteria.[3] It is the main storage form of glucose in the human body.

Glycogen functions as one of three regularly used forms of energy reserves, creatine phosphate being for very short-term, glycogen being for short-term and the triglyceride stores in adipose tissue (i.e., body fat) being for long-term storage. Protein, broken down into amino acids, is seldom used as a main energy source except during starvation and glycolytic crisis (see bioenergetic systems).

In humans, glycogen is made and stored primarily in the cells of the liver and skeletal muscle.[4][5] In the liver, glycogen can make up 5–6% of the organ's fresh weight: the liver of an adult, weighing 1.5 kg, can store roughly 100–120 grams of glycogen.[4][6] In skeletal muscle, glycogen is found in a low concentration (1–2% of the muscle mass): the skeletal muscle of an adult weighing 70 kg stores roughly 400 grams of glycogen.[4] Small amounts of glycogen are also found in other tissues and cells, including the kidneys, red blood cells,[7][8][9] white blood cells,[10] and glial cells in the brain.[11] The uterus also stores glycogen during pregnancy to nourish the embryo.[12]

The amount of glycogen stored in the body mostly depends on oxidative type 1 fibres,[13][14] physical training, basal metabolic rate, and eating habits.[15] Different levels of resting muscle glycogen are reached by changing the number of glycogen particles, rather than increasing the size of existing particles[14] though most glycogen particles at rest are smaller than their theoretical maximum.[16]

Approximately 4 grams of glucose are present in the blood of humans at all times;[4] in fasting individuals, blood glucose is maintained constant at this level at the expense of glycogen stores, primarily from the liver (glycogen in skeletal muscle is mainly used as an immediate source of energy for that muscle rather than being used to maintain physiological blood glucose levels).[4] Glycogen stores in skeletal muscle serve as a form of energy storage for the muscle itself;[4] however, the breakdown of muscle glycogen impedes muscle glucose uptake from the blood, thereby increasing the amount of blood glucose available for use in other tissues.[4] Liver glycogen stores serve as a store of glucose for use throughout the body, particularly the central nervous system.[4] The human brain consumes approximately 60% of blood glucose in fasted, sedentary individuals.[4]

Glycogen is an analogue of starch, a glucose polymer that functions as energy storage in plants. It has a structure similar to amylopectin (a component of starch), but is more extensively branched and compact than starch. Both are white powders in their dry state. Glycogen is found in the form of granules in the cytosol/cytoplasm in many cell types, and plays an important role in the glucose cycle. Glycogen forms an energy reserve that can be quickly mobilized to meet a sudden need for glucose, but one that is less compact than the energy reserves of triglycerides (lipids). As such it is also found as storage reserve in many parasitic protozoa.[17][18][19]

  1. ^ McArdle, William D.; Katch, Frank I.; Katch, Victor L. (2006). Exercise physiology: Energy, nutrition, and human performance (6th ed.). Lippincott Williams & Wilkins. p. 12. ISBN 978-0-7817-4990-9.
  2. ^ Sadava, David E.; Purves, William K.; Hillis, David M.; Orians, Gordon H.; Heller, H. Craig (2011). Life (9th ed.). W. H. Freeman. ISBN 9781429254311.
  3. ^ Berg JM, Tymoczko JL, Gatto GJ, Stryer L (8 April 2015). Biochemistry (8th ed.). New York: W. H. Freeman. ISBN 9781464126109. OCLC 913469736.
  4. ^ a b c d e f g h i Wasserman DH (January 2009). "Four grams of glucose". American Journal of Physiology. Endocrinology and Metabolism. 296 (1): E11–21. doi:10.1152/ajpendo.90563.2008. PMC 2636990. PMID 18840763. Four grams of glucose circulates in the blood of a person weighing 70 kg. This glucose is critical for normal function in many cell types. In accordance with the importance of these 4 g of glucose, a sophisticated control system is in place to maintain blood glucose constant. Our focus has been on the mechanisms by which the flux of glucose from liver to blood and from blood to skeletal muscle is regulated. ... The brain consumes ~60% of the blood glucose used in the sedentary, fasted person. ... The amount of glucose in the blood is preserved at the expense of glycogen reservoirs (Fig. 2). In postabsorptive humans, there are ~100 g of glycogen in the liver and ~400 g of glycogen in muscle. Carbohydrate oxidation by the working muscle can go up by ~10 fold with exercise, and yet after 1 h, blood glucose is maintained at ~4 g.
  5. ^ Cite error: The named reference pmid1615908 was invoked but never defined (see the help page).
  6. ^ Guyton, Arthur C.; Hall, John Edward (2011). Guyton and Hall Textbook of Medical Physiology. New York, New York: Saunders/Elsevier. ISBN 978-5-98657-013-6.
  7. ^ Moses SW, Bashan N, Gutman A (December 1972). "Glycogen metabolism in the normal red blood cell". Blood. 40 (6): 836–843. doi:10.1182/blood.V40.6.836.836. PMID 5083874.
  8. ^ Ingermann RL, Virgin GL (1987). "Glycogen content and release of glucose from red blood cells of the sipunculan worm themiste dyscrita" (PDF). J Exp Biol. 129: 141–149. doi:10.1242/jeb.129.1.141.
  9. ^ Miwa I, Suzuki S (November 2002). "An improved quantitative assay of glycogen in erythrocytes". Annals of Clinical Biochemistry. 39 (Pt 6): 612–13. doi:10.1258/000456302760413432. PMID 12564847.
  10. ^ Murray, Bob (April 2018). "Fundamentals of glycogen metabolism for coaches and athletes". Nutrition Reviews. 76 (4): 243–259. doi:10.1093/nutrit/nuy001. PMC 6019055. PMID 29444266.
  11. ^ Oe Y, Baba O, Ashida H, Nakamura KC, Hirase H (June 2016). "Glycogen distribution in the microwave-fixed mouse brain reveals heterogeneous astrocytic patterns". Glia. 64 (9): 1532–1545. doi:10.1002/glia.23020. PMC 5094520. PMID 27353480.
  12. ^ Campbell, Neil A.; Williamson, Brad; Heyden, Robin J. (2006). Biology: Exploring Life. Boston, MA: Pearson Prentice Hall. ISBN 978-0-13-250882-7.
  13. ^ Jensen, Rasmus; Ørtenblad, Niels; Stausholm, Marie-Louise Holleufer; Skjærbæk, Mette Carina; Larsen, Daniel Nykvist; Hansen, Mette; Holmberg, Hans-Christer; Plomgaard, Peter; Nielsen, Joachim (1 October 2020). "Heterogeneity in subcellular muscle glycogen utilisation during exercise impacts endurance capacity in men". The Journal of Physiology. 598 (19): 4271–4292. doi:10.1113/JP280247. ISSN 1469-7793. PMID 32686845. S2CID 220653138.
  14. ^ a b Jensen, Rasmus; Ørtenblad, Niels; Stausholm, Marie-Louise H.; Skjærbæk, Mette C.; Larsen, Daniel N.; Hansen, Mette; Holmberg, Hans-Christer; Plomgaard, Peter; Nielsen, Joachim (1 May 2021). "Glycogen supercompensation is due to increased number, not size, of glycogen particles in human skeletal muscle". Experimental Physiology. 106 (5): 1272–1284. doi:10.1113/EP089317. ISSN 0958-0670. PMID 33675088. S2CID 232131416.
  15. ^ Bergström, Jonas; Hermansen, Lars; Hultman, Eric; Saltin, Bengt (October 1967). "Diet, Muscle Glycogen and Physical Performance". Acta Physiologica Scandinavica. 71 (2–3): 140–150. doi:10.1111/j.1748-1716.1967.tb03720.x. ISSN 1365-201X. PMID 5584523.
  16. ^ Marchand, I.; Chorneyko, K.; Tarnopolsky, M.; Hamilton, S.; Shearer, J.; Potvin, J.; Graham, T. E. (1 November 2002). "Quantification of subcellular glycogen in resting human muscle: granule size, number, and location". Journal of Applied Physiology. 93 (5): 1598–1607. doi:10.1152/japplphysiol.00585.2001. ISSN 8750-7587. PMID 12381743.
  17. ^ Ryley, J.F. (March 1955). "Studies on the metabolism of the protozoa. 5: Metabolism of the parasitic flagellate Trichomonas foetus". The Biochemical Journal. 59 (3): 361–369. doi:10.1042/bj0590361. PMC 1216250. PMID 14363101.
  18. ^ Benchimol, Marlene; Elias, Cezar Antonio; de Souza, Wanderley (December 1982). "Tritrichomonas foetus: Ultrastructural localization of calcium in the plasma membrane and in the hydrogenosome". Experimental Parasitology. 54 (3): 277–284. doi:10.1016/0014-4894(82)90036-4. ISSN 0014-4894. PMID 7151939.
  19. ^ Mielewczik, Michael; Mehlhorn, Heinz; al Quraishy, Saleh; Grabensteiner, E.; Hess, M. (1 September 2008). "Transmission electron microscopic studies of stages of histomonas meleagridis from clonal cultures". Parasitology Research. 103 (4): 745–750. doi:10.1007/s00436-008-1009-1. ISSN 0932-0113. PMID 18626664. S2CID 2331300.

© MMXXIII Rich X Search. We shall prevail. All rights reserved. Rich X Search