Ketogenesis Explained

Ketogenesis is the biochemical process through which organisms produce ketone bodies by breaking down fatty acids and ketogenic amino acids. The process supplies energy to certain organs, particularly the brain, heart and skeletal muscle, under specific scenarios including fasting, caloric restriction, sleep,[1] or others. (In rare metabolic diseases, insufficient gluconeogenesis can cause excessive ketogenesis and hypoglycemia, which may lead to the life-threatening condition known as non-diabetic ketoacidosis.)[2]

Ketone bodies are not obligately produced from fatty acids; rather a meaningful amount of them is synthesized only in a situation of carbohydrate and protein insufficiency, where only fatty acids are readily available as fuel for their production.

Recent evidence suggests that glial cells are ketogenic, supplying neurons with locally synthesized ketone bodies to sustain cognitive processes.[3]

Production

Ketone bodies are produced mainly in the mitochondria of liver cells, and synthesis can occur in response to an unavailability of blood glucose, such as during fasting.[2] Other cells, e.g. human astrocytes, are capable of carrying out ketogenesis, but they are not as effective at doing so.[4] Ketogenesis occurs constantly in a healthy individual.[5] Ketogenesis in healthy individuals is ultimately under the control of the master regulatory protein AMPK, which is activated during times of metabolic stress, such as carbohydrate insufficiency. Its activation in the liver inhibits lipogenesis, promotes fatty acid oxidation, switches off acetyl-CoA carboxylase, turns on malonyl-CoA decarboxylase, and consequently induces ketogenesis.[6] Ethanol is a potent AMPK inhibitor[7] and therefore can cause significant disruptions in the metabolic state of the liver, including halting of ketogenesis, even in the context of hypoglycemia.

Ketogenesis takes place in the setting of low glucose levels in the blood, after exhaustion of other cellular carbohydrate stores, such as glycogen.[8] It can also take place when there is insufficient insulin (e.g. in type 1 (and less commonly type 2) diabetes), particularly during periods of "ketogenic stress" such as intercurrent illness.[2]

The production of ketone bodies is then initiated to make available energy that is stored as fatty acids. Fatty acids are enzymatically broken down in β-oxidation to form acetyl-CoA. Under normal conditions, acetyl-CoA is further oxidized by the citric acid cycle (TCA/Krebs cycle) and then by the mitochondrial electron transport chain to release energy. However, if the amounts of acetyl-CoA generated in fatty-acid β-oxidation challenge the processing capacity of the TCA cycle; i.e. if activity in TCA cycle is low due to low amounts of intermediates such as oxaloacetate, acetyl-CoA is then used instead in biosynthesis of ketone bodies via acetoacetyl-CoA and β-hydroxy-β-methylglutaryl-CoA (HMG-CoA). Furthermore, since there is only a limited amount of coenzyme A in the liver, the production of ketogenesis allows some of the coenzyme to be freed to continue fatty-acid β-oxidation.[9] Depletion of glucose and oxaloacetate can be triggered by fasting, vigorous exercise, high-fat diets or other medical conditions, all of which enhance ketone production.[10] Deaminated amino acids that are ketogenic, such as leucine, also feed TCA cycle, forming acetoacetate & ACoA and thereby produce ketones.[11] Besides its role in the synthesis of ketone bodies, HMG-CoA is also an intermediate in the synthesis of cholesterol, but the steps are compartmentalised.[12] Ketogenesis occurs in the mitochondria, whereas cholesterol synthesis occurs in the cytosol, hence both processes are independently regulated.

Ketone bodies

The three ketone bodies, each synthesized from acetyl-CoA molecules, are:

β-Hydroxybutyrate and acetoacetate can pass through membranes easily, and are therefore a source of energy for the brain, which cannot directly metabolize fatty acids. The brain receives 60-70% of its required energy from ketone bodies when blood glucose levels are low. These bodies are transported into the brain by monocarboxylate transporters 1 and 2. Therefore, ketone bodies are a way to move energy from the liver to other cells. The liver does not have the critical enzyme, succinyl CoA transferase, to process ketone bodies, and therefore cannot undergo ketolysis. The result is that the liver only produces ketone bodies, but does not use a significant amount of them.[16]

Regulation

Ketogenesis may or may not occur, depending on levels of available carbohydrates in the cell or body. This is closely related to the paths of acetyl-CoA:[17]

Insulin and glucagon are key regulating hormones of ketogenesis, with insulin being the primary regulator. Both hormones regulate hormone-sensitive lipase and acetyl-CoA carboxylase. Hormone-sensitive lipase produces diglycerides from triglycerides, freeing a fatty acid molecule for oxidation. Acetyl-CoA carboxylase catalyzes the production of malonyl-CoA from acetyl-CoA. Malonyl-CoA reduces the activity of carnitine palmitoyltransferase I, an enzyme that brings fatty acids into the mitochondria for β-oxidation. Insulin inhibits hormone-sensitive lipase and activates acetyl-CoA carboxylase, thereby reducing the amount of starting materials for fatty acid oxidation and inhibiting their capacity to enter the mitochondria. Glucagon activates hormone-sensitive lipase and inhibits acetyl-CoA carboxylase, thereby stimulating ketone body production, and making passage into the mitochondria for β-oxidation easier. Insulin also inhibits HMG-CoA lyase, further inhibiting ketone body production. Similarly, cortisol, catecholamines, epinephrine, norepinephrine, and thyroid hormones can increase the amount of ketone bodies produced, by activating lipolysis (the mobilization of fatty acids out of fat tissue) and thereby increasing the concentration of fatty acids available for β-oxidation. Unlike glucagon, catecholamines are capable of inducing lipolysis even in the presence of insulin for use by peripheral tissues during acute stress.

Peroxisome Proliferator Activated Receptor alpha (PPARα) also has the ability to upregulate ketogenesis, as it has some control over a number of genes involved in ketogenesis. For example, monocarboxylate transporter 1,[18] which is involved in transporting ketone bodies over membranes (including the blood–brain barrier), is regulated by PPARα, thus affecting ketone body transportation into the brain. Carnitine palmitoyltransferase is also upregulated by PPARα, which can affect fatty acid transportation into the mitochondria.

Pathology

Both acetoacetate and beta-hydroxybutyrate are acidic, and, if levels of these ketone bodies are too high, the pH of the blood drops, resulting in ketoacidosis. Ketoacidosis is known to occur in untreated type I diabetes (see diabetic ketoacidosis) and in alcoholics after prolonged binge-drinking without intake of sufficient carbohydrates (see alcoholic ketoacidosis).

The production and use of ketones can be ineffective in people with defects in the pathway for beta-oxidation, in the genes for ketogenesis (HMGCS2 and HMGCL), for ketolysis (OXCT1, ACAT1). Defects in this pathway can cause varying degrees of inability to cope with fasting. HMGCS2 deficiency, for example, can cause hypoglycemic crises that lead to brain damage, and death.[2]

Individuals with diabetes mellitus can experience overproduction of ketone bodies due to a lack of insulin. Without insulin to help extract glucose from the blood, tissues the levels of malonyl-CoA are reduced, and it becomes easier for fatty acids to be transported into mitochondria, causing the accumulation of excess acetyl-CoA. The accumulation of acetyl-CoA in turn produces excess ketone bodies through ketogenesis. The result is a rate of ketone production higher than the rate of ketone disposal, and a decrease in blood pH. In extreme cases the resulting acetone can be detected in the patient's breath as a faint, sweet odor.

There are some health benefits to ketone bodies and ketogenesis as well. It has been suggested that a low-carb, high fat ketogenic diet can be used to help treat epilepsy in children. Additionally, ketone bodies can be anti-inflammatory.[19] Some kinds of cancer cells are unable to use ketone bodies, as they do not have the necessary enzymes to engage in ketolysis. It has been proposed that actively engaging in behaviors that promote ketogenesis could help manage the effects of some cancers.

See also

External links

Notes and References

  1. Aalling . Nadia Nielsen . Nedergaard . Maiken . DiNuzzo . Mauro . Cerebral Metabolic Changes During Sleep. . Current Neurology and Neuroscience Reports . July 16, 2018 . 18 . 9 . 57 . 10.1007/s11910-018-0868-9 . 30014344 . 6688614 .
  2. Fukao. Toshiyuki. Mitchell. Grant. Sass. Jörn Oliver. Hori. Tomohiro. Orii. Kenji. Aoyama. Yuka. Ketone body metabolism and its defects. Journal of Inherited Metabolic Disease. 8 April 2014. 37. 4. 541–551. 10.1007/s10545-014-9704-9. 24706027. 21840932.
  3. Silva . Bryon . Mantha . Olivier L. . Schor . Johann . Pascual . Alberto . Plaçais . Pierre-Yves . Pavlowsky . Alice . Preat . Thomas . Glia fuel neurons with locally synthesized ketone bodies to sustain memory under starvation . Nature Metabolism . 17 February 2022 . 4 . 2 . 213–224 . 10.1038/s42255-022-00528-6. 35177854 . 8885408 .
  4. Grabacka M, Pierzchalska M, Dean M, Reiss K . Regulation of Ketone Body Metabolism and the Role of PPARα . . 17 . 12 . E2093 . 2016 . 10.3390/ijms17122093 . 5187893 . 27983603. free .
  5. Book: C., Engel, Paul. Pain-free biochemistry : an essential guide for the health sciences. 2010. Wiley-Blackwell. 9780470060469. 938920491.
  6. Viollet B, Foretz M, Guigas B, Horman S, Dentin R, Bertrand L, Hue L, Andreelli F. Activation of AMP-activated protein kinase in the liver: a new strategy for the management of metabolic hepatic disorders. The Journal of Physiology. 574. 1. 41–53. 10.1113/jphysiol.2006.108506. 16644802. 1817784. 2006. free.
  7. Ceni E, Mello T, Galli A . Pathogenesis of alcoholic liver disease: role of oxidative metabolism . . 20 . 47 . 17756–17772 . 2014 . 10.3748/wjg.v20.i47.17756 . 4273126 . 25548474 . free .
  8. Web site: Ketogensis in Low Glucose Levels . 2018-11-22 . 2021-10-23 . https://web.archive.org/web/20211023065113/https://www.shortcutketo.com/ketogenesis-in-low-glucose-levels/ . dead .
  9. Book: Lehninger Principles of biochemistry. Nelson, David Lee. M.. Cox, Michael. 2013. W.H. Freeman. 9781429234146. 828664654.
  10. Laffel. Lori. 1999-11-01. Ketone bodies: a review of physiology, pathophysiology and application of monitoring to diabetes. Diabetes/Metabolism Research and Reviews. en. 15. 6. 412–426. 10.1002/(sici)1520-7560(199911/12)15:6<412::aid-dmrr72>3.0.co;2-8. 1520-7560. 10634967. free.
  11. Book: Kohlmeier M . Nutrient Metabolism: Structures, Functions, and Genes . 2015 . Academic Press . 9780123877840 . 385–388 . 2nd . https://books.google.com/books?id=aTQTAAAAQBAJ&q=beta-hydroxy%20beta-methylbutyrate%20HMB&pg=PA387 . Leucine . Figure 8.57: Metabolism of L-leucine.
  12. Book: Kohlmeier M . Nutrient Metabolism: Structures, Functions, and Genes . 2015 . Academic Press . 9780123877840 . 150–151 . 2nd . https://books.google.com/books?id=aTQTAAAAQBAJ&pg=PA150 . Fatty acids .
  13. Web site: You Can Get There From Here: Acetone, Anionic Ketones and Even-Carbon Fatty Acids can Provide Substrates for Gluconeogenesis. Glew, Robert H. 8 March 2014. https://web.archive.org/web/20130926031021/http://www.bioline.org.br/request?np10002. 26 September 2013. dead.
  14. Miller DN, Bazzano G . 1965 . Propanediol metabolism and its relation to lactic acid metabolism . Ann NY Acad Sci . 119 . 957–973 . 1965NYASA.119..957M . Bazzano . 10.1111/j.1749-6632.1965.tb47455.x . 4285478 . 3. 37769342 .
  15. Ruddick JA . 1972 . Toxicology, metabolism, and biochemistry of 1,2-propanediol . Toxicol Appl Pharmacol . 21 . 1 . 102–111 . 10.1016/0041-008X(72)90032-4. 4553872 .
  16. J D McGarry. Foster. and D. W.. 1980-01-01. Regulation of Hepatic Fatty Acid Oxidation and Ketone Body Production. Annual Review of Biochemistry. 49. 1. 395–420. 10.1146/annurev.bi.49.070180.002143. 6157353.
  17. Web site: Ketogenesis. snst-hu.lzu.edu.cn. 2020-02-04. 2020-02-04. https://web.archive.org/web/20200204152958/http://snst-hu.lzu.edu.cn/zhangyi/ndata/Ketogenesis.html. dead.
  18. Felmlee MA, Jones RS, Morris ME . Monocarboxylate Transporters (SLC16): Function, Regulation, and Role in Health and Disease . . 72 . 2 . 466–485 . 2020 . 10.1124/pr.119.018762 . 7062045 . 32144120.
  19. Dupuis. Nina. Curatolo. Niccolo. Benoist. Jean-François. Auvin. Stéphane. 2015. Ketogenic diet exhibits anti-inflammatory properties. Epilepsia. en. 56. 7. e95–e98. 10.1111/epi.13038. 26011473. 1528-1167. free.