Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Sodium butyrate

From Wikipedia, the free encyclopedia
Sodium butyrate
Names
Preferred IUPAC name
Sodium butanoate
Other names
Sodium butyrate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.005.326Edit this at Wikidata
UNII
  • InChI=1S/C4H8O2.Na/c1-2-3-4(5)6;/h2-3H2,1H3,(H,5,6);/q;+1/p-1
  • CCCC(=O)[O-].[Na+]
Properties
C4H7NaO2
Molar mass110.088 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Sodium butyrate is acompound with formula Na(C3H7COO). It is thesodiumsalt ofbutyric acid. It has various effects on cultured mammalian cells including inhibition ofproliferation, induction ofdifferentiation andinduction orrepression of gene expression.[1] As such, it can be used in lab to bring about any of these effects. Specifically, butyrate treatment of cells results in histone hyperacetylation, and butyrate itself inhibits class Ihistone deacetylase (HDAC) activity,[2] specificallyHDAC1,HDAC2,HDAC3, and butyrate can be used in determining histone deacetylene inchromatin structure and function.Inhibition ofHDAC activity is estimated to affect the expression of only 2% of mammalian genes.[3]

In the lab, sodium butyrate is usually found as a white, water-soluble, crystalline solid. The chemical is notable for having a very strong, unpleasant smell that lingers.[4] When working with sodium butyrate, gloves, eye protection and respiratory masks are advised for safety purposes.[5]

The compound is found in human diet, notably produced in large amounts fromdietary fiber in the gut and present in Parmesan cheese and butter.[6] Nevertheless, the most common source of sodium butyrate in the gut is from consumption oflegumes.[7]

See also

[edit]

References

[edit]
  1. ^Kruh, Jacques (1981). "Effects of sodium butyrate, a new pharmacological agent, on cells in culture".Molecular and Cellular Biochemistry.42 (2):65–82.doi:10.1007/BF00222695.PMID 6174854.S2CID 24214720.
  2. ^Candido, E; Reeves, Raymond; Davie, James R. (1978). "Sodium butyrate inhibits histone deacetylation in cultured cells".Cell.14 (1):105–13.doi:10.1016/0092-8674(78)90305-7.PMID 667927.S2CID 33206068.
  3. ^Davie, James R. (2003)."Inhibition of Histone Deacetylase Activity by Butyrate".The Journal of Nutrition.133 (7 Suppl):2485S –2493S.doi:10.1093/jn/133.7.2485s.PMID 12840228.
  4. ^"Sodium butanoate | 156-54-7".Chemicalbook.com. Retrieved2016-05-31.
  5. ^"Sodium butyrate ≥98.5% (GC) | Sigma-Aldrich".Sigmaaldrich.com. Retrieved2016-05-31.
  6. ^Li, Huating; Gao, Zhanguo; Zhang, Jin; Ye, Xin; Xu, Aimin; Ye, Jianping; Jia, Weiping (1 April 2012)."Sodium Butyrate Stimulates Expression of Fibroblast Growth Factor 21 in Liver by Inhibition of Histone Deacetylase 3".Diabetes.61 (4):797–806.doi:10.2337/db11-0846.PMC 3314370.PMID 22338096. Retrieved27 November 2021 – via diabetes.diabetesjournals.org.
  7. ^Buettner, Dan (22 May 2015)."Want Great Longevity and Health? It Takes a Village".Wsj.com. Retrieved27 November 2021.

Further reading

[edit]
  • Govindarajan, Nambirajan; Agis-Balboa, Roberto Carlos; Walter, Jonas; Sananbenesi, Farahnaz; Fischer, André (2011). "Sodium Butyrate Improves Memory Function in an Alzheimer's Disease Mouse Model When Administered at an Advanced Stage of Disease Progression".Journal of Alzheimer's Disease.26 (1):187–97.doi:10.3233/JAD-2011-110080.PMID 21593570.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Sodium_butyrate&oldid=1198581948"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp