ornithine oxoglurate

WordNet

an amino acid that does not occur in proteins but is important in the formation of urea

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/11/23 10:30:03」(JST)

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1. 成人における肝性脳症：治療 hepatic encephalopathy in adults treatment
2. 尿素サイクル障害：臨床的特徴および診断 urea cycle disorders clinical features and diagnosis
3. 尿素サイクル障害：管理 urea cycle disorders management
4. 先天性代謝異常：個々の障害の発見 inborn errors of metabolism identifying the specific disorder
5. 肝細胞移植 hepatocyte transplantation

Glutamine and ornithine alpha-ketoglutarate supplementation on malate dehydrogenases expression in hepatectomized rats.

Guimarães Filho A1, Cunha RM2, Vasconcelos PR3, Guimarães SB3.
Acta cirúrgica brasileira / Sociedade Brasileira para Desenvolvimento Pesquisa em Cirurgia.Acta Cir Bras.2014 Jun;29(6):365-70.
PURPOSE: To evaluate the relative gene expression (RGE) of cytosolic (MDH1) and mitochondrial (MDH2) malate dehydrogenases enzymes in partially hepatectomized rats after glutamine (GLN) or ornithine alpha-ketoglutarate (OKG) suplementation.METHODS: One-hundred and eight male Wistar rats were randoml
PMID 24919044

Alpha-ketoglutarate (AKG) inhibits proliferation of colon adenocarcinoma cells in normoxic conditions.

Rzeski W1, Walczak K, Juszczak M, Langner E, Pożarowski P, Kandefer-Szerszeń M, Pierzynowski SG.
Scandinavian journal of gastroenterology.Scand J Gastroenterol.2012 May;47(5):565-71. doi: 10.3109/00365521.2012.660539.
BACKGROUND AND OBJECTIVE: Alpha-ketoglutarate (AKG), a key intermediate in Krebs cycle, is an important biological compound involved in the formation of amino acids, nitrogen transport, and oxidation reactions. AKG is already commercially available as a dietary supplement and its supplementation wit
PMID 22486188

Advances and challenges in the treatment of branched-chain amino/keto acid metabolic defects.

Knerr I1, Weinhold N, Vockley J, Gibson KM.
Journal of inherited metabolic disease.J Inherit Metab Dis.2012 Jan;35(1):29-40. doi: 10.1007/s10545-010-9269-1. Epub 2011 Feb 3.
Disorders of branched-chain amino/keto acid metabolism encompass diverse entities, including maple syrup urine disease (MSUD), the 'classical' organic acidurias isovaleric acidemia (IVA), propionic acidemia (PA), methylmalonic acidemia (MMA) and, among others, rarely described disorders such as 2-me
PMID 21290185