Sodium butyrate: Difference between revisions

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{{Chembox
{{Chembox
| Verifiedfields = changed
| ImageFile=sodium butyrate.png
| Watchedfields = changed
| ImageSize=200px
| verifiedrevid = 400838964
| IUPACName = Sodium butanoate
| ImageFile=Sodium butyrate formula V.1.svg
| ImageSize=250px
| PIN = Sodium butanoate
| OtherNames = Sodium butyrate
| OtherNames = Sodium butyrate
| Section1 = {{Chembox Identifiers
| Section1 = {{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 156-54-7
| CASNo = 156-54-7
| UNII = 8RAS91C36W
| UNII_Ref = {{fdacite|correct|FDA}}
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 64103
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 62381
| PubChem = 5222465
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 8727
| InChI = 1S/C4H8O2.Na/c1-2-3-4(5)6;/h2-3H2,1H3,(H,5,6);/q;+1/p-1
| SMILES = CCCC(=O)[O-].[Na+]
}}
}}
| Section2 = {{Chembox Properties
| Section2 = {{Chembox Properties
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'''Sodium butyrate''' is a [[Compound (chemistry)|compound]] with formula Na(C<sub>3</sub>H<sub>7</sub>COO). It is the [[sodium]] [[salt]] of [[butyric acid]]. It has various effects on cultured mammalian cells including inhibition of [[Cell growth|proliferation]], induction of [[Cellular differentiation|differentiation]] and [[Regulation of gene expression|induction]] or [[Repressor|repression]] of gene expression. 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 HDAC activity. Butyrate has been an essential vehicle for determining the role of [[Histone acetylation and deacetylation|histone acetylation]] in [[chromatin]] structure and function. Inhibition of [[HDAC]] activity affects the expression of only 2% of mammalian genes.
'''Sodium butyrate''' is a [[Compound (chemistry)|compound]] with formula Na(C<sub>3</sub>H<sub>7</sub>COO). It is the [[sodium]] [[Salt (chemistry)|salt]] of [[butyric acid]]. It has various effects on cultured mammalian cells including inhibition of [[Cell growth|proliferation]], induction of [[Cellular differentiation|differentiation]] and [[Regulation of gene expression|induction]] or [[Repressor|repression]] of gene expression.<ref name=Kruh>{{cite journal |doi=10.1007/BF00222695 |title=Effects of sodium butyrate, a new pharmacological agent, on cells in culture |year=1981 |last1=Kruh |first1=Jacques |journal=Molecular and Cellular Biochemistry |volume=42 |issue=2 |pmid=6174854 |pages=65–82|s2cid=24214720 }}</ref> 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 I [[histone deacetylase]] (HDAC) activity,<ref name=Candid>{{cite journal |doi=10.1016/0092-8674(78)90305-7 |title=Sodium butyrate inhibits histone deacetylation in cultured cells |year=1978 |last1=Candido |first1=E |journal=Cell |volume=14 |pages=105–13 |pmid=667927 |last2=Reeves |first2=Raymond |last3=Davie |first3=James R. |issue=1|s2cid=33206068 }}</ref> specifically [[HDAC1]], [[HDAC2]], [[HDAC3]], and butyrate can be used in determining histone deacetylene in [[chromatin]] structure and function. [[Histone deacetylase inhibitor|Inhibition]] of [[HDAC]] activity is estimated to affect the expression of only 2% of mammalian genes.<ref>{{cite journal |pmid=12840228 |year=2003 |last1=Davie |first1=James R. |title=Inhibition of Histone Deacetylase Activity by Butyrate |volume=133 |issue=7 Suppl |pages=2485S–2493S |journal=The Journal of Nutrition |url=http://jn.nutrition.org/cgi/pmidlookup?view=long&pmid=12840228|doi=10.1093/jn/133.7.2485s |doi-access=free }}</ref>

<ref>{{cite journal | journal = J. Nutr. | volume = 133 | issue = 7 Suppl | pages = 2485S–2493S | year = 2003 | title = Inhibition of Histone Deacetylase Activity by Butyrate | author = James R. Davie | url = http://jn.nutrition.org/cgi/content/full/133/7/2485S | pmid = 12840228}}</ref>
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.<ref>{{cite web|url=http://www.chemicalbook.com/ChemicalProductProperty_EN_CB7391358.htm|title=Sodium butanoate {{!}} 156-54-7|website=Chemicalbook.com|access-date=2016-05-31}}</ref> When working with sodium butyrate, gloves, eye protection and respiratory masks are advised for safety purposes.<ref>{{cite web|url=http://www.sigmaaldrich.com/catalog/product/sial/b5887?lang=en&region=AU|title=Sodium butyrate ≥98.5% (GC) {{!}} Sigma-Aldrich|website=Sigmaaldrich.com|access-date=2016-05-31}}</ref>

The compound is found in human diet, notably produced in large amounts from [[dietary fiber]] in the gut and present in Parmesan cheese and butter.<ref>{{cite journal|url=https://diabetes.diabetesjournals.org/content/61/4/797|title=Sodium Butyrate Stimulates Expression of Fibroblast Growth Factor 21 in Liver by Inhibition of Histone Deacetylase 3|first1=Huating|last1=Li|first2=Zhanguo|last2=Gao|first3=Jin|last3=Zhang|first4=Xin|last4=Ye|first5=Aimin|last5=Xu|first6=Jianping|last6=Ye|first7=Weiping|last7=Jia|date=1 April 2012|journal=Diabetes|volume=61|issue=4|pages=797–806|access-date=27 November 2021|via=diabetes.diabetesjournals.org|doi=10.2337/db11-0846| pmc=3314370 |pmid=22338096}}</ref> Nevertheless, the most common source of sodium butyrate in the gut is from consumption of [[legumes]].<ref>{{cite web|url=https://www.wsj.com/articles/want-great-longevity-and-health-it-takes-a-village-1432304395|title=Want Great Longevity and Health? It Takes a Village|first=Dan|last=Buettner|date=22 May 2015|access-date=27 November 2021|website=Wsj.com}}</ref>

==See also==
* [[Butyric acid]]


==References==
==References==
{{reflist}}
{{Reflist}}


==Further reading==
[[Category:Butyrates]]
* {{cite journal |pmid=21593570 |year=2011 |last1=Govindarajan |first1=Nambirajan |last2=Agis-Balboa |first2=Roberto Carlos |last3=Walter |first3=Jonas |last4=Sananbenesi |first4=Farahnaz |last5=Fischer |first5=André |title=Sodium Butyrate Improves Memory Function in an Alzheimer's Disease Mouse Model When Administered at an Advanced Stage of Disease Progression |volume=26 |issue=1 |pages=187–97 |doi=10.3233/JAD-2011-110080 |journal=Journal of Alzheimer's Disease}}
[[Category:Sodium compounds]]


{{HDAC inhibitors}}
[[de:Natriumbutyrat]]

[[Category:Butyrates]]
[[Category:GABA analogues]]
[[Category:Organic sodium salts]]
[[Category:Histone deacetylase inhibitors]]
[[Category:Foul-smelling chemicals]]