クレアチンリン酸、ホスホクレアチン
WordNet
- an organic compound of creatine and phosphoric acid; found in the muscles of vertebrates where its hydrolysis releases energy for muscular contraction (同)creatine_phosphate, creatine phosphoric acid
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/02/26 04:57:47」(JST)
[Wiki en表示]
Phosphocreatine |
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IUPAC name
N-Methyl-N-(phosphonocarbamimidoyl)glycine
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Other names
Creatine phosphate; phosphorylcreatine; creatine-P; phosphagen; fosfocreatine
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Identifiers |
Abbreviations |
PCr |
CAS number |
67-07-2 Y |
PubChem |
587 |
UNII |
020IUV4N33 Y |
EC number |
200-643-9 |
ATC code |
C01EB06 |
Jmol-3D images |
Image 1 |
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OC(CN(C)C(N)=NP(O)(O)=O)=O
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InChI=1/C4H10N3O5P/c1-7(2-3(8)9)4(5)6-13(10,11)12/h2H2,1H3,(H,8,9)(H4,5,6,10,11,12)/f/h8,10-11H,5H2/b6-4+
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Properties |
Molecular formula |
C4H10N3O5P |
Molar mass |
211.11 g mol−1 |
Y (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
Infobox references |
Phosphocreatine, also known as creatine phosphate (CP) or PCr (Pcr), is a phosphorylated creatine molecule that serves as a rapidly mobilizable reserve of high-energy phosphates in skeletal muscle and the brain.
Contents
- 1 Chemistry
- 2 Function
- 3 History
- 4 References
- 5 External links
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Chemistry
Phosphocreatine is formed from parts of three amino acids: arginine (Arg), glycine (Gly), and methionine (Met). It can be synthesized by formation of guanidinoacetate from Arg and Gly (in kidney) followed by methylation (S-adenosyl methionine is required) to creatine (in liver), and phosphorylation by creatine kinase (ATP is required) to phosphocreatine (in muscle); catabolism: dehydration to form the cyclic Schiff base creatinine. Phosphocreatine is synthesized in the liver and transported to the muscle cells, via the bloodstream, for storage.
The creatine phosphate shuttle facilitates transport of high energy phosphate from mitochondria.
Function
Phosphocreatine can anaerobically donate a phosphate group to ADP to form ATP during the first 2 to 7 seconds following an intense muscular or neuronal effort. Conversely, excess ATP can be used during a period of low effort to convert creatine to phosphocreatine. The reversible phosphorylation of creatine (i.e., both the forward and backward reaction) is catalyzed by several creatine kinases. The presence of creatine kinase (CK-MB, MB for muscle/brain) in Blood plasma is indicative of tissue damage and is used in the diagnosis of myocardial infarction.[1] The cell's ability to generate phosphocreatine from excess ATP during rest, as well as its use of phosphocreatine for quick regeneration of ATP during intense activity, provides a spatial and temporal buffer of ATP concentration. In other words, phosphocreatine acts as high-energy reserve in a coupled reaction; the energy given off from donating the phosphate group is used to regenerate the other compound - in this case, ATP. Phosphocreatine plays a particularly important role in tissues that have high, fluctuating energy demands such as muscle and brain.
History
The discovery of phosphocreatine[2][3] was reported by Grace and Philip Eggleton of the University of Cambridge[4] and separately by Cyrus Fiske and Yellapragada Subbarow of the Harvard Medical School[5] in 1927. A few years later David Nachmansohn, working under Meyerhof at the Kaiser Wilhelm Institute in Dahlem, Berlin, contributed to the understanding of the phosphocreatine's role in the cell.[3]
References
- ^ Schlattner, U.; Tokarska-Schlattner, M., and Wallimann, T. (2006). "Mitochondrial creatine kinase in human health and disease". Biochimica et Biophysica Acta - Molecular Basis of Disease 1762 (2): 164–180. doi:10.1016/j.bbadis.2005.09.004. PMID 16236486.
- ^ Saks, Valdur (2007). Molecular system bioenergetics: energy for life. Weinheim: Wiley-VCH. p. 2. ISBN 978-3-527-31787-5.
- ^ a b Ochoa, Severo (1989). Sherman, E. J.; National Academy of Sciences. eds. David Nachmansohn. Biographical Memoirs. 58. National Academies Press. pp. 357–404. ISBN 978-0-309-03938-3.
- ^ Eggleton, Philip; Eggleton, Grace Palmer (1927). "The inorganic phosphate and a labile form of organic phosphate in the gastrocnemius of the frog". Biochemical Journal 21 (1): 190–195. PMC 1251888. PMID 16743804. http://www.biochemj.org/bj/021/bj0210190.htm.
- ^ Fiske, Cyrus H.; Subbarao, Yellapragada (1927). "The nature of the 'inorganic phosphate' in voluntary muscle". Science 65 (1686): 401–403. doi:10.1126/science.65.1686.401. PMID 17807679. http://www.sciencemag.org/content/vol65/issue1686/index.dtl#articles.
External links
- Human Metabolome Database at the University of Alberta
UpToDate Contents
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English Journal
- Diagnostic approaches to predict persistent post-traumatic symptoms after mild traumatic brain injury - a literature review.
- Studerus-Germann AM1,2, Thiran JP3, Daducci A3, Gautschi OP4.
- The International journal of neuroscience.Int J Neurosci.2016 Apr;126(4):289-98. doi: 10.3109/00207454.2015.1033620. Epub 2015 Jul 28.
- Mild traumatic brain injury (mTBI) is one of the most frequently diagnosed neurological disorders in emergency departments. Although there are established recommendations for the diagnosis and treatment in the acute stage, there is an on-going debate in which diagnostic methods and risk factors pred
- PMID 26000929
- Metabolic voxel-based analysis of the complete human brain using fast 3D-MRSI: Proof of concept in multiple sclerosis.
- Donadieu M1,2, Le Fur Y1,2, Lecocq A1,2, Maudsley AA3, Gherib S1,2,4, Soulier E1,2, Confort-Gouny S1,2, Pariollaud F1,2,4, Ranjeva MP1,2,4, Pelletier J1,4, Guye M1,2, Zaaraoui W1,2, Audoin B1,4, Ranjeva JP1.
- Journal of magnetic resonance imaging : JMRI.J Magn Reson Imaging.2016 Jan 12. doi: 10.1002/jmri.25139. [Epub ahead of print]
- PURPOSE: To detect local metabolic abnormalities over the complete human brain in multiple sclerosis (MS) patients, we used optimized fast volumic echo planar spectroscopic imaging (3D-EPSI).MATERIALS AND METHODS: Weighted mean combination of two 3D-EPSI covering the whole brain acquired at 3T in AC
- PMID 26756662
- Simple and effective exercise design for assessing in vivo mitochondrial function in clinical applications using (31)P magnetic resonance spectroscopy.
- Sleigh A1,2, Lupson V1, Thankamony A3, Dunger DB3, Savage DB4, Carpenter TA1, Kemp GJ5.
- Scientific reports.Sci Rep.2016 Jan 11;6:19057. doi: 10.1038/srep19057.
- The growing recognition of diseases associated with dysfunction of mitochondria poses an urgent need for simple measures of mitochondrial function. Assessment of the kinetics of replenishment of the phosphocreatine pool after exercise using (31)P magnetic resonance spectroscopy can provide an in viv
- PMID 26751849
Japanese Journal
- Pioglitazone improves whole-body aerobic capacity and skeletal muscle energy metabolism in patients with metabolic syndrome
- Phloridzin inhibits high K<sup>+</sup>-induced contraction via the inhibition of sodium: glucose cotransporter 1 in rat ileum
- Phloridzin inhibits high K<sup>+</sup>-induced contraction via the inhibition of sodium–glucose cotransporter 1 in rat ileum
Related Links
- Phosphocreatine, also known as creatine phosphate (CP) or PCr (Pcr), is a phosphorylated creatine molecule that serves as a rapidly mobilizable reserve of high-energy phosphates in skeletal muscle and the brain.
★リンクテーブル★
[★]
- 英
- phosphocreatine
- 同
- クレアチンリン酸 creatine phosphate