Ornithine

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L-Ornithine
L-Ornithin2.svg
Ornithine ball-and-stick.png
Names
IUPAC name
L-Ornithine
Other names
(+)-(S)-2,5-Diaminovaleric acid, (+)-(S)-2,5-Diaminopentanoic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
DrugBank
ECHA InfoCard 100.000.665
EC Number 200-731-7
KEGG
MeSH Ornithine
UNII
Properties[1]
C5H12N2O2
Molar mass 132.16 g/mol
Melting point 140 °C (284 °F; 413 K)
soluble
Solubility soluble in ethanol
Acidity (pKa) 1.94
+11.5 (H2O, c = 6.5)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Ornithine is a non-proteinogenic amino acid that plays a role in the urea cycle. Ornithine is abnormally accumulated in the body in ornithine transcarbamylase deficiency. The radical is ornithyl.

Role in urea cycle[edit]

L-Ornithine is one of the products of the action of the enzyme arginase on L-arginine, creating urea. Therefore, ornithine is a central part of the urea cycle, which allows for the disposal of excess nitrogen. Ornithine is recycled and, in a manner, is a catalyst. First, ammonia is converted into carbamoyl phosphate (H
2
NC(O)OPO2−
3
). Ornithine is converted into a urea derivative at the δ (terminal) nitrogen by carbamoyl phosphate synthetase. Another nitrogen is added from aspartate, producing the denitrogenated fumarate, and the resulting arginine (a guanidinium compound) is hydrolysed back to ornithine, producing urea. The nitrogens of urea come from the ammonia and aspartate, and the nitrogen in ornithine remains intact.

Ornithine lactamization

Ornithine is not an amino acid coded for by DNA, that is, not proteinogenic. However, in mammalian non-hepatic tissues, the main use of the urea cycle is in arginine biosynthesis, so, as an intermediate in metabolic processes, ornithine is quite important.[2]

Other reactions[edit]

Ornithine, via the action of ornithine decarboxylase (E.C. 4.1.1.17), is the starting point for the synthesis of polyamines such as putrescine.

In bacteria, such as E. coli, ornithine can be synthesized from L-glutamate.[3]

Research[edit]

Exercise fatigue[edit]

L-Ornithine supplementation attenuated fatigue in subjects in a placebo-controlled study using a cycle ergometer. The results suggested that L-ornithine has an antifatigue effect in increasing the efficiency of energy consumption and promoting the excretion of ammonia.[4][5]

Weightlifting supplement[edit]

Amino acid supplements, including L-ornithine, are frequently marketed to bodybuilders and weightlifters with claims for increasing levels of human growth hormone (HGH), muscle mass and strength. A clinical study reported that L-ornithine at 2 g/d did not increase HGH.[6] A review on the topic concluded "The use of specific amino acids to stimulate GH release by athletes is not recommended."[7]

Cirrhosis[edit]

L-Ornithine L-aspartate (LOLA), a stable salt of ornithine and aspartic acid, has been used in the treatment of cirrhosis.[8]

References[edit]

  1. ^ Weast, Robert C., ed. (1981). CRC Handbook of Chemistry and Physics (62nd ed.). Boca Raton, FL: CRC Press. p. C-408. ISBN 0-8493-0462-8. 
  2. ^ Weber, Arthur L.; Miller, Stanley L. (1981). "Reasons for the Occurrence of the Twenty Coded Protein Amino Acids" (PDF). J. Mol. Evol. 17 (5): 273–284. PMID 7277510. doi:10.1007/BF01795749. 
  3. ^ "Ornithine Biosynthesis". School of Biological and Chemical Sciences, Queen Mary, University of London. Retrieved 2007-08-17. 
  4. ^ Sugino, T.; Shirai, T.; Kajimoto, Y.; Kajimoto, O. (2008). "L-ornithine supplementation attenuates physical fatigue in healthy volunteers by modulating lipid and amino acid metabolism". Nutrition research. 28 (11): 738–43. PMID 19083482. doi:10.1016/j.nutres.2008.08.008. 
  5. ^ Demura, S.; Yamada, T.; Yamaji, S.; Komatsu, M.; Morishita, K. (2010). "The effect of L-ornithine hydrochloride ingestion on performance during incremental exhaustive ergometer bicycle exercise and ammonia metabolism during and after exercise". European journal of clinical nutrition. 64 (10): 1166–71. PMID 20717126. doi:10.1038/ejcn.2010.149. 
  6. ^ Fogelholm, G. M.; Näveri, H. K.; Kiilavuori, K. T.; Härkönen, M. H.; et al. (1993). "Low-dose amino acid supplementation: no effects on serum human growth hormone and insulin in male weightlifters". International Journal of Sport Nutrition. 3 (3): 290–297. PMID 8220394. doi:10.1123/ijsn.3.3.290. 
  7. ^ Chromiak JA, Antonio J (2002). "Use of amino acids as growth hormone-releasing agents by athletes". Nutrition. 18 (7-8): 657–61. PMID 12093449. 
  8. ^ Sikorska, H.; Cianciara, J.; Wiercińska-Drapało, A. (2010). "Physiological functions of L-ornithine and L-aspartate in the body and the efficacy of administration of L-ornithine-L-aspartate in conditions of relative deficiency". Polski merkuriusz lekarski: organ Polskiego Towarzystwa Lekarskiego. 28 (168): 490–5. PMID 20642112. 

External links[edit]