Chemistry:Glyconeogenesis

From HandWiki

Glyconeogenesis is the synthesis of glycogen without using glucose or other carbohydrates, instead using substances like proteins and fats. This includes substrates like glycerol, lactate, glutamine and alanine.[1] It's used in replenishing glycogen stores when glucose is limited,[2] like after long periods of fasting.[3] In the liver and kidneys, it uses the enzymes phosphoenolpyruvate carboxykinase 2 (PCK2), fructose-1,6-bisphosphatase 1 (FBP1),[1] and fructose-1,6-bisphosphatase 2 in skeletal muscle.[2] One example is the conversion of lactic acid to glycogen in the liver.[4] Lactic acid is converted to alanine, the alanine is transferred to the liver, and once in the liver is it converted back to alanine where it is free to be transformed into glucose.[3]

Role in tumor survival

Outside of the liver, M1 class macrophages, a pro-inflammatory white blood cell, use glyconeogenesis through the same enzymes, PCK2 and FBP1.[1] M1 cells concentrate in inflammation, infection, and cancerous sites. These harsh environments are described as being hypoglycemic or waste-rich in compounds such as lactic acid, making glyconeogenesis particularly resourceful. In lung cancer, tumor-associated macrophages are found to exhibit M1-type properties such as the use of glyconeogenesis.[1] The tumor microenvironment is rich in lactic acid, signaling cytokine release to TAMs for the conversion of surrounding lactic acid into glycogen.

Fasting

Research on fasting using crustacean animal models, particularly the Chasmagnathus granulatus, show for differences in glyconeogenic activity based on diet. The study looked at the effects of a fast while being on a high-carbohydrate diet compared to a high-protein diet. After two weeks, the high-protein diet increased glyconeogenic activity while the high-carbohydrate diet showed a reduction in overall glyconeogenic capacity.[5]

See also

References

  1. 1.0 1.1 1.2 1.3 Jeroundi, Najia; Roy, Charlotte; Basset, Laetitia; Pignon, Pascale; Preisser, Laurence; Blanchard, Simon; Bocca, Cinzia; Abadie, Cyril et al. (18 October 2024). "Glycogenesis and glyconeogenesis from glutamine, lactate and glycerol support human macrophage functions". EMBO Reports 25 (12): 5383–5407. doi:10.1038/s44319-024-00278-4. PMID 39424955. 
  2. 2.0 2.1 Park, Hyun-Jun; Jang, Hye Rim; Park, Shi-Young; Kim, Young-Bum; Lee, Hui-Young; Choi, Cheol Soo (March 2020). "The essential role of fructose-1,6-bisphosphatase 2 enzyme in thermal homeostasis upon cold stress". Experimental & Molecular Medicine 52 (3): 485–496. doi:10.1038/s12276-020-0402-4. PMID 32203098. 
  3. 3.0 3.1 Komoda, Tsugikazu; Matsunaga, Toshiyuki (2015). Biochemistry for Medical Professionals. doi:10.1016/C2014-0-01063-5. ISBN 978-0-12-801918-4. [page needed]
  4. Komoda, Tsugikazu; Matsunaga, Toshiyuki (2015). "Metabolic Pathways in the Human Body". Biochemistry for Medical Professionals. pp. 25–63. doi:10.1016/B978-0-12-801918-4.00004-9. ISBN 978-0-12-801918-4. "Glyconeogenesis is a shunt for the synthesis of sugars such as glucose and glycogen from substances other than sugars. An example is the conversion from lactic acid to glucose. It passes through the following process, from the lactic acid elevated by a glycolytic shunt to make glucose by glyconeogenesis: lactic acid is converted into alanine and then carried into the liver. Alanine in the liver is changed back to lactic acid and synthesized to glucose by glyconeogenesis. However, glyconeogenesis occurs partly in the kidney. If enzymes are involved in the reaction of the glycolytic shunt, it is possible to make glucose by glyconeogenesis except for three one-way (irreversible) reactions in the glycolytic shunt." 
  5. Pellegrino, Ricardo; Kucharski, Luiz Carlos; Da Silva, Roselis Silveira Martins (2008-04-18). "Effect of fasting and refeeding on gluconeogenesis and glyconeogenesis in the muscle of the crab Chasmagnathus granulatus previously fed a protein- or carbohydrate-rich diet". Journal of Experimental Marine Biology and Ecology 358 (2): 144–150. doi:10.1016/j.jembe.2008.02.005. ISSN 0022-0981. https://www.sciencedirect.com/science/article/pii/S0022098108000877.