Citrulline

{{chembox

| Verifiedfields = changed

| Watchedfields = changed

| verifiedrevid = 443676645

| ImageFile = L-Citrullin2.svg

| ImageSize = 230

| ImageFile_Ref = {{chemboximage|correct|??}}

| ImageFile1 = L-Citrulline zwitterion ball from xtal.png

| ImageSize1 = 230

| ImageName1 = Ball and stick model of zwitterionic citrulline

| IUPACName = 2-Amino-5-(carbamoylamino)pentanoic acid{{cite web|title=Citrulline - Compound Summary|url=https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=833&loc=ec_rcs#x291|work=PubChem Compound|publisher=National Center for Biotechnology Information|access-date=1 May 2012|location=USA|date=16 September 2004|at=Identification}}

|Section1={{Chembox Identifiers

| CASNo = 627-77-0

| CASNo_Ref = {{cascite|correct|CAS}}

| CASNo1 = 13594-51-9

| CASNo1_Ref = {{cascite|correct|CAS}}

| CASNo1_Comment = (D)

| CASNo2 = 372-75-8

| CASNo2_Ref = {{cascite|correct|CAS}}

| CASNo2_Comment = (L)

| PubChem = 833

| PubChem1 = 637599

| PubChem1_Comment = D

| PubChem2 = 9750

| PubChem2_Comment = L

| ChemSpiderID = 810

| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}

| ChemSpiderID1 = 553200

| ChemSpiderID1_Ref = {{chemspidercite|changed|chemspider}}

| ChemSpiderID1_Comment = D

| ChemSpiderID2 = 9367

| ChemSpiderID2_Ref = {{chemspidercite|changed|chemspider}}

| ChemSpiderID2_Comment = L

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = 1OYO2NV4NM

| UNII1_Ref = {{fdacite|correct|FDA}}

| UNII1 = KNS2VUH6P2

| UNII1_Comment = (D)

| UNII2_Ref = {{fdacite|correct|FDA}}

| UNII2 = 29VT07BGDA

| UNII2_Comment = (L)

| EINECS = 211-012-2

| DrugBank = DB00155

| DrugBank_Ref = {{drugbankcite|correct|drugbank}}

| KEGG = D07706

| KEGG_Ref = {{keggcite|correct|kegg}}

| MeSHName = Citrulline

| ChEBI = 18211

| ChEBI_Ref = {{ebicite|changed|EBI}}

| ChEMBL = 444814

| ChEMBL_Ref = {{ebicite|correct|EBI}}

| IUPHAR_ligand = 722

| Beilstein = 1725417, 1725415 D, 1725416 L

| Gmelin = 774677 L

| 3DMet = B01217

| SMILES = NC(CCCNC(N)=O)C(O)=O

| StdInChI = 1S/C6H13N3O3/c7-4(5(10)11)2-1-3-9-6(8)12/h4H,1-3,7H2,(H,10,11)(H3,8,9,12)

| StdInChI_Ref = {{stdinchicite|changed|chemspider}}

| StdInChIKey = RHGKLRLOHDJJDR-UHFFFAOYSA-N

| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}

}}

|Section2={{Chembox Properties

| C=6 | H=13 | N=3 | O=3

| Appearance = White crystals

| Odor = Odourless

| LogP = −1.373

| pKa = 2.508

| pKb = 11.489

}}

|Section3={{Chembox Thermochemistry

| Entropy = 254.4 J K−1 mol−1

| HeatCapacity = 232.80 J K−1 mol−1

}}

|Section4={{Chembox Related

| OtherFunction_label = alkanoic acids

| OtherFunction = {{unbulleted list|N-Acetylaspartic acid|Aceglutamide|N-Acetylglutamic acid|Pivagabine}}

| OtherCompounds = {{unbulleted list|Bromisoval|Carbromal}}

}}

}}

The organic compound citrulline is an α-amino acid.{{Citation|last=Banerjee|first=Aryamitra|title=Chapter 15 - Gastrointestinal toxicity biomarkers|date=2014-01-01|url=http://www.sciencedirect.com/science/article/pii/B9780124046306000154|work=Biomarkers in Toxicology|pages=269–277|editor-last=Gupta|editor-first=Ramesh C.|place=Boston|publisher=Academic Press|language=en|doi=10.1016/b978-0-12-404630-6.00015-4|isbn=978-0-12-404630-6|s2cid=88798984 |access-date=2020-11-10|url-access=subscription}} Its name is derived from citrullus, the Latin word for watermelon. Although named and described by gastroenterologists since the late 19th century, it was first isolated from watermelon in 1914 by Japanese researchers Yatarō Koga (古賀彌太郎) and Ryō Ōtake (大嶽了){{cite journal

| last1 = Koga

| first1 = Yatarō

| last2 = Ōtake

| first2 = Ryō

| title = Study report on the constituents of squeezed watermelon

| journal = Tokyo Kagaku Kaishi [Journal of the Tokyo Chemical Society]

| volume = 35

| number = 5

| pages = 519–528

| doi = 10.1246/nikkashi1880.35.519

| year = 1914

}}{{cite journal

|last1 = Fragkos

|first1 = Konstantinos C.

|last2 = Forbes

|first2 = Alastair

| title = Was citrulline first a laxative substance? The truth about modern citrulline and its isolation

| journal = Nihon Ishigaku Zasshi [Journal of the Japanese Society for the History of Medicine]

| volume = 57

| number = 3

| pages = 275–292

| url = http://jshm.or.jp/journal/57-3/57-3_275.pdf

| pmid = 22397107

| year = 2011

}} and further codified by Mitsunori Wada of Tokyo Imperial University in 1930.{{cite journal

| last = Wada

| first = Mitsunori

| title = On the occurrence of a new amino acid in watermelon. Citrullus vulgaris, Schrad.

| journal = Proceedings of the Imperial Academy

| volume = 6

| number = 1

| pages = 15–17

| doi = 10.2183/pjab1912.6.15

| year = 1930

}}{{cite journal

| last = Wada

| first = Mitsunori

| title = On the occurrence of a new amino acid in watermelon, Citrullus vulgaris, Schrad.

| journal = Bulletin of the Agricultural Chemical Society of Japan

| volume = 6

| number = 1–5

| pages = 32–34

| doi = 10.1271/bbb1924.6.32

| year = 1930

}}{{cite journal

| author = Wada, Mitsunori

| title = Über Citrullin, eine neue Aminosäure im Preßsaft der Wassermelone, Citrullus vulgaris, Schrad.

| journal = Biochemische Zeitschrift

| volume = 224

| pages = 420–429

| year = 1930

| language = de

}}

It has the formula H2NC(O)NH(CH2)3CH(NH2)CO2H. It is a key intermediate in the urea cycle, the pathway by which mammals excrete ammonia by converting it into urea. Citrulline is also produced as a byproduct of the enzymatic production of nitric oxide from the amino acid arginine, catalyzed by nitric oxide synthase.{{cite web|title=Nos2 - Nitric Oxide Synthase|url=https://www.uniprot.org/uniprot/P29477|website=Uniprot.org|publisher=Uniprot Consortium|access-date=10 February 2015}}

Biosynthesis

Citrulline can be derived from:

Citrulline is made from ornithine and carbamoyl phosphate in one of the central reactions in the urea cycle. It is also produced from arginine as a byproduct of the reaction catalyzed by NOS family (NOS; [https://enzyme.expasy.org/EC/1.14.13.39 EC 1.14.13.39]).{{cite book |vauthors=Cox M, Lehninger AL, Nelson DR |title=Lehninger principles of biochemistry |publisher=Worth Publishers |location=New York |year=2000 |page= [https://archive.org/details/lehningerprincip01lehn/page/449 449] |isbn=978-1-57259-153-0 |edition=3rd |access-date= 13 March 2020 |url=https://archive.org/details/lehningerprincip01lehn }} It is also prevalent in trichohyalin at the inner root sheath and medulla of hair follicles, where it is synthesized from arginine.{{Cite journal

| last1 = Rogers | first1 = G. E.

| last2 = Rothnagel | first2 = J. A.

| title = A sensitive assay for the enzyme activity in hair follicles and epidermis that catalyses the peptidyl-arginine-citrulline post-translational modification

| journal = Current Problems in Dermatology

| volume = 11

| pages = 171–184

| year = 1983

| pmid = 6653155

| doi = 10.1159/000408673

| isbn = 978-3-8055-3752-0

}} Arginine is first oxidized into N-hydroxyl-arginine, which is then further oxidized to citrulline concomitant with release of nitric oxide.

Citrulline is also made by enterocytes of the small intestine.{{Citation|last=DeLegge|first=Mark H.|title=Chapter 7 - Enteral Access and Enteral Nutrition in Patients With Short Bowel Syndrome|date=2019-01-01|url=http://www.sciencedirect.com/science/article/pii/B978012814330800007X|work=Adult Short Bowel Syndrome|pages=81–96|editor-last=Corrigan|editor-first=Mandy L.|publisher=Academic Press|language=en|doi=10.1016/b978-0-12-814330-8.00007-x|isbn=978-0-12-814330-8|s2cid=81295089|access-date=2020-11-10|editor2-last=Roberts|editor2-first=Kristen|editor3-last=Steiger|editor3-first=Ezra|url-access=subscription}}

Function

Citrulline is a metabolic intermediate within the urea cycle, which is the pathway by which mammals excrete ammonia by converting it into urea. Citrulline is also produced as a byproduct of the enzymatic production of nitric oxide from the amino acid arginine, catalyzed by nitric oxide synthase. In the yeast species Saccharomyces cerevisiae, citrulline is a metabolic intermediate in the latter, cytosolic half of the arginine biosynthesis pathway.{{cite web | url=https://pathway.yeastgenome.org/YEAST/new-image?object=CITRUL-BIO2-PWY | title=Saccharomyces cerevisiae citrulline biosynthesis }}

Several proteins contain citrulline as a result of a post-translational modification. These citrulline residues are generated by a family of enzymes called peptidylarginine deiminases (PADs), which convert arginine into citrulline in a process called citrullination or deimination with the help of calcium ions. Proteins that normally contain citrulline residues include myelin basic protein (MBP), filaggrin, and several histone proteins, whereas other proteins, such as fibrin and vimentin are susceptible to citrullination during cell death and tissue inflammation.

Circulating citrulline concentration is a biomarker of intestinal functionality.{{Cite journal|last1=Fragkos|first1=Konstantinos C.|last2=Forbes|first2=Alastair|date=2017-10-12|title=Citrulline as a marker of intestinal function and absorption in clinical settings: A systematic review and meta-analysis|journal=United European Gastroenterology Journal|volume=6|issue=2|pages=181–191|language=en|doi=10.1177/2050640617737632|pmid=29511548|pmc=5833233}}{{cite journal | last1 = Crenn | first1 = P. | display-authors = etal | year = 2000 | title = Post-absorptive plasma citrulline concentration is a marker of intestinal failure in short bowel syndrome patients | journal = Gastroenterology | volume = 119 | issue = 6| pages = 1496–505 | doi=10.1053/gast.2000.20227| pmid = 11113071 | doi-access = free }}

Commercial use

L-citrulline is sold as a dietary supplement, usually in powder form. Advocates suggest that since L-citrulline boosts nitric oxide production, helping arterial function and thus blood flow throughout the body, this might be helpful in treating or preventing various ailments.

  • Lowering blood pressure in people with elevated blood pressure.{{cite journal | pmc=6369322 | date=2019 | last1=Barkhidarian | first1=B. | last2=Khorshidi | first2=M. | last3=Shab-Bidar | first3=S. | last4=Hashemi | first4=B. | title=Effects of L-citrulline supplementation on blood pressure: A systematic review and meta-analysis | journal=Avicenna Journal of Phytomedicine | volume=9 | issue=1 | pages=10–20 | pmid=30788274 }}
  • Easing symptoms of mild-to-moderate erectile dysfunction, with fewer risks than Viagra.
  • Ameliorating circulatory problems such as slow wound healing due to diabetes.
  • Raising muscle protein levels, preventing malnourishment in the elderly and possibly improving athletic performance.
  • Treating intestinal problems, including short bowel syndrome, celiac disease and radiation-caused small bowel damage
  • Various genetic disorders and health conditions such as liver disease, Parkinson's disease and certain dementias.

Some of these assertions are based on animal studies, and like most dietary supplement claims have not be endorsed by the Food and Drugs Administration.{{cite web |last1=Miller |first1=Kelli |title=L-citrulline |url=https://www.webmd.com/vitamins-and-supplements/l-citrulline-uses-and-risks |website=WebMD |publisher=WebMD LLC |access-date=16 December 2024}}

L-citrulline is added to certain energy drinks such as Reign and touted for its thermogenic effects.Label on Reign Inferno Watermelon Overlord can; Reign Beverage Company: Los Angeles, 2020

See also

References

{{reflist|20em}}

{{Non-proteinogenic amino acids}}

{{Amino acid metabolism intermediates}}

Category:Alpha-Amino acids

Category:Ureas

Category:Urea cycle

Category:Non-proteinogenic amino acids

Category:Biomarkers