| 词条 | Beta-Hydroxybutyric acid |
| 释义 |
| Watchedfields = changed | verifiedrevid = 443420188 | Name = beta-Hydroxybutyric acid | ImageFile = Beta-Hydroxybutyric acid-2D-skeletal.svg | ImageSize = 200px | IUPACName = 3-Hydroxybutanoic acid | OtherNames = |Section1={{Chembox Identifiers | InChI = 1/C4H8O3/c1-3(5)2-4(6)7/h3,5H,2H2,1H3,(H,6,7) | InChIKey = WHBMMWSBFZVSSR-UHFFFAOYAO | SMILES1 = CC(CC(=O)O)O | ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL = 1162496 | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C4H8O3/c1-3(5)2-4(6)7/h3,5H,2H2,1H3,(H,6,7) | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = WHBMMWSBFZVSSR-UHFFFAOYSA-N | CASNo_Ref = {{cascite|correct|CAS}} | CASNo = 300-85-6 | PubChem = 441 | IUPHAR_ligand = 1593 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 428 | ChEBI_Ref = {{ebicite|correct|EBI}} | ChEBI = 20067 | Beilstein = 773861 | KEGG = C01089 | 3DMet = B00239 | SMILES = O=C(O)CC(O)C | MeSHName = beta-Hydroxybutyrate |Section2={{Chembox Properties | C=4 | H=8 | O=3 | Appearance = white solid | Density = | MeltingPt = 44-46 | BoilingPt = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = |Section4={{Chembox Related | OtherAnions = hydroxybutyrate | OtherFunction_label = carboxylic acids | OtherFunction = propionic acid lactic acid 3-hydroxypropanoic acid malonic acid hydroxypentanoic acid butyric acid β-methylbutyric acid β-hydroxy β-methylbutyric acid | OtherCompounds = erythrose threose 1,2-butanediol 1,3-butanediol 2,3-butanediol 1,4-butanediol }}β-Hydroxybutyric acid, also known as 3-hydroxybutyric acid, is an organic compound and a beta hydroxy acid with the chemical formula CH3CH(OH)CH2CO2H; its conjugate base is β-hydroxybutyrate, also known as 3-hydroxybutyrate. β-Hydroxybutyric acid is a chiral compound with two enantiomers: D-β-hydroxybutyric acid and L-β-hydroxybutyric acid. Its oxidized and polymeric derivatives occur widely in nature. In humans, D-β-hydroxybutyric acid is one of two primary endogenous agonists of hydroxycarboxylic acid receptor 2 (HCA2), a {{nowrap|Gi/o-coupled}} G protein-coupled receptor (GPCR).[1][2] BiosynthesisIn humans, {{nowrap|D-β-hydroxybutyrate}} can be synthesized in the liver via the metabolism of fatty acids (e.g., butyrate), {{nowrap|β-hydroxy}} {{nowrap|β-methylbutyrate}}, and ketogenic amino acids through a series of reactions that metabolize these compounds into acetoacetate, which is the first ketone body that is produced in the fasting state. The biosynthesis of {{nowrap|D-β-hydroxybutyrate}} from acetoacetate is catalyzed by the β-hydroxybutyrate dehydrogenase enzyme. Butyrate can also be metabolized into {{nowrap|D-β-hydroxybutyrate}} via a second metabolic pathway that does not involve acetoacetate as a metabolic intermediate. This metabolic pathway is as follows:[3] butyrate→butyryl-CoA→crotonyl-CoA→β-hydroxybutyryl-CoA→poly-β-hydroxybutyrate→{{nowrap|D-β-}}({{nowrap|D-β-hydroxybutyryloxy}}){{nowrap|-butyrate}}→{{nowrap|D-β-hydroxybutyrate}} The last reaction in this metabolic pathway, which involves the conversion of {{nowrap|D-β-}}({{nowrap|D-β-hydroxybutyryloxy}}){{nowrap|-butyrate}} into {{nowrap|D-β-hydroxybutyrate}}, is catalyzed by the hydroxybutyrate-dimer hydrolase enzyme.[3] The concentration of β-hydroxybutyrate in human blood plasma, as with other ketone bodies, increases through ketosis.[4] This elevated β-hydroxybutyrate level is naturally expected, as β-hydroxybutyrate is formed from acetoacetate. The compound can be used as an energy source by the brain when blood glucose is low.[5] Diabetic patients can have their ketone levels tested via urine or blood to indicate diabetic ketoacidosis. In alcoholic ketoacidosis, this ketone body is produced in greatest concentration. Ketogenesis occurs if oxaloacetate in the liver cells is depleted, a circumstance created by reduced carbohydrate intake (through diet or starvation), prolonged, excessive alcohol consumption, and/or insulin deficiency. Because oxaloacetate is crucial for entry of acetyl-CoA into the TCA cycle, the rapid production of acetyl-CoA from fatty acid oxidation in the absence of ample oxaloacetate overwhelms the decreased capacity of the TCA cycle, and the resultant excess of acetyl-CoA is shunted towards ketone body production.{{citation needed|date=June 2016}}{{Leucine metabolism in humans|note=yes|align=left|caption=Acetoacetate, the metabolic precursor of β-hydroxybutyrate, is a metabolite of fatty acids, ketogenic amino acids such as leucine[7] and isoleucine,[6] and {{nowrap|β-hydroxy}} {{nowrap|β-methylbutyrate}}.}}{{clear}} Biological activity{{expand section|transporter proteins[9] that move it across lipid membranes|date=February 2018|small=no}}D-β-Hydroxybutyric acid, along with butyric acid, are the two primary endogenous agonists of hydroxycarboxylic acid receptor 2 (HCA2), a {{nowrap|Gi/o-coupled}} GPCR.[1][2][7]β-Hydroxybutyric acid is able to cross the blood-brain-barrier into the central nervous system.[8] Levels of β-hydroxybutyric acid increase in the liver, heart, muscle, brain, and other tissues with exercise, calorie restriction, fasting, and ketogenic diets.[8] The compound has been found to act as a histone deacetylase (HDAC) inhibitor.[8] Through inhibition of the HDAC class I isoenzymes HDAC2 and HDAC3, β-hydroxybutyric acid has been found to increase brain-derived neurotrophic factor (BDNF) levels and TrkB signaling in the hippocampus.[8] Moreover, a rodent study found that prolonged exercise increases plasma β-hydroxybutyrate concentrations, which induces promoters of the BDNF gene in the hippocampus.[8] These findings may have clinical relevance in the treatment of depression, anxiety, and cognitive impairment.[8] In epilepsy patients on the ketogenic diet, blood β-hydroxybutyrate levels correlate best with degree of seizure control. The threshold for optimal anticonvulsant effect appears to be approximately 4 mmol/L.[9] Laboratory and industrial chemistryβ-Hydroxybutyric acid is the precursor to polyesters, which are biodegradable plastics. This polymer, poly(3-hydroxybutyrate), is also naturally produced by the bacteria Alcaligenes eutrophus.[10] β-Hydroxybutyrate can be extracted from poly(3-hydroxybutyrate) by acid hydrolysis.[11] The concentration of {{nowrap|β-hydroxybutyrate}} in blood plasma is measured through a test that uses β-hydroxybutyrate dehydrogenase, with NAD+ as an electron-accepting cofactor. The conversion of {{nowrap|β-hydroxybutyrate}} to acetoacetate, which is catalyzed by this enzyme, reduces the NAD+ to NADH, generating an electrical change; the magnitude of this change can then be used to extrapolate the amount of {{nowrap|β-hydroxybutyrate}} in the sample. See also
Notes1. ^1 {{cite journal | vauthors = Offermanns S, Colletti SL, Lovenberg TW, Semple G, Wise A, IJzerman AP | title = International Union of Basic and Clinical Pharmacology. LXXXII: Nomenclature and Classification of Hydroxy-carboxylic Acid Receptors (GPR81, GPR109A, and GPR109B) | journal = Pharmacological Reviews | volume = 63 | issue = 2 | pages = 269–90 | date = June 2011 | pmid = 21454438 | doi = 10.1124/pr.110.003301 | quote = }} 2. ^1 {{cite web |vauthors = Offermanns S, Colletti SL, IJzerman AP, Lovenberg TW, Semple G, Wise A, Waters MG |title=Hydroxycarboxylic acid receptors |url=http://www.guidetopharmacology.org/GRAC/FamilyDisplayForward?familyId=48 |website=IUPHAR/BPS Guide to Pharmacology |publisher=International Union of Basic and Clinical Pharmacology |accessdate=13 July 2018}} 3. ^1 {{cite web|title=Butanoate metabolism - Reference pathway|url=http://www.genome.jp/kegg-bin/show_pathway?map00650|website=Kyoto Encyclopedia of Genes and Genomes|publisher=Kanehisa Laboratories|date=1 November 2017|accessdate=1 February 2018}} 4. ^{{Cite journal |url= https://emedicine.medscape.com/article/2087381-overview#a4|title = Beta-Hydroxybutyrate |vauthors = Perelas A, Staros EB |date=October 30, 2015 |website= Medscape |publisher = WebMD LLC. |access-date= February 8, 2017}} 5. ^{{cite journal|author=O. E. Owen|title=Brain Metabolism during Fasting|journal=The Journal of Clinical Investigation|volume=46|issue=10|year=1967|pages=1589–1595|pmid=6061736|doi=10.1172/JCI105650|pmc=292907|display-authors=etal}} 6. ^1 {{cite web|title=Valine, leucine and isoleucine degradation - Reference pathway|url=http://www.genome.jp/kegg-bin/show_pathway?map00280+C00356|website=Kyoto Encyclopedia of Genes and Genomes|publisher=Kanehisa Laboratories|date=27 January 2016|accessdate=1 February 2018}} 7. ^1 {{cite web|title=β-D-hydroxybutyric acid: Biological activity|url=http://www.guidetopharmacology.org/GRAC/LigandDisplayForward?tab=biology&ligandId=1593|website=IUPHAR/BPS Guide to Pharmacology|publisher=International Union of Basic and Clinical Pharmacology|accessdate=5 February 2018|quote=}} 8. ^1 2 3 4 5 {{cite journal |vauthors=Sleiman SF, Henry J, Al-Haddad R, El Hayek L, Abou Haidar E, Stringer T, Ulja D, Karuppagounder SS, Holson EB, Ratan RR, Ninan I, Chao MV |title=Exercise promotes the expression of brain derived neurotrophic factor (BDNF) through the action of the ketone body β-hydroxybutyrate |journal=eLife |volume=5 |issue= |pages= |year=2016 |pmid=27253067 |pmc=4915811 |doi=10.7554/eLife.15092 |url=}} 9. ^{{cite journal | vauthors=Gilbert DL, Pyzik PL, Freeman JM | title=The ketogenic diet: seizure control correlates better with serum beta-hydroxybutyrate than with urine ketones | journal= Journal of Child Neurology | volume=15 | issue=3 | pages=787–790 | year=2000 | doi= 10.1177/088307380001501203 | pmid = 11198492 }} 10. ^{{cite journal |author1=Yoshiharu Doi |author2=Masao Kunioka |author3=Yoshiyuki Nakamura |author4=Kazuo Soga | title = Nuclear magnetic resonance studies on unusual bacterial copolyesters of 3-hydroxybutyrate and 4-hydroxybutyrate | journal = Macromolecules | year = 1988 | volume = 21 | issue = 9 | pages = 2722–2727 | doi=10.1021/ma00187a012}} 11. ^Dieter Seebach, Albert K. Beck, Richard Breitschuh, and Kurt Job "Direct Degradation of the Biopolymer Poly[(R)-3-Hydroxybutrric Acid to (R)-3-Hydroxybutanoic Acid and Its Methyl Ester" Org. Synth. 1993, 71, 39. {{DOI|10.15227/orgsyn.071.0039}} References{{Reflist}}{{Cholesterol and steroid intermediates}}{{HDAC inhibitors}}{{DEFAULTSORT:Hydroxybutyric acid, beta-}} 4 : Antidepressants|Beta hydroxy acids|Biomolecules|Histone deacetylase inhibitors |
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