Chemistry:Met-enkephalin

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Met-enkephalin
Skeletal formula of Met-enkphalin
Met-enkephalin ball-and-stick.png
Names
IUPAC name
(2S)-2-[[(2S)-2-[[2-[[2-[[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]acetyl]amino]acetyl]amino]-3-phenylpropanoyl]amino]-4-methylsulfanylbutanoic acid
Other names
[Met]enkephalin; [Met5]enkephalin; L-Tyrosylglycylglycyl-L-phenylalanyl-L-methionine
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
EC Number
  • 261-335-8
KEGG
MeSH Enkephalin,+Methionine
UNII
Properties
C27H35N5O7S
Molar mass 573.67 g·mol−1
log P 0.607
Acidity (pKa) 3.234
Basicity (pKb) 10.763
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Tracking categories (test):

Met-enkephalin, also known as metenkefalin (INN), sometimes referred to as opioid growth factor (OGF),[1] is a naturally occurring, endogenous opioid peptide that has opioid effects of a relatively short duration. It is one of the two forms of enkephalin, the other being leu-enkephalin. The enkephalins are considered to be the primary endogenous ligands of the δ-opioid receptor, due to their high potency and selectivity for the site over the other endogenous opioids.[2]

History

Met-enkephalin was discovered and characterized by John Hughes, Hans Kosterlitz, et al. in 1975 after a search for endogenous ligands of the opioid receptors.[3]

Chemistry

Met-enkephalin is a pentapeptide with the amino acid sequence tyr-gly-gly-phe-met. The tyrosine residue at position 1 is thought to be analogous to the 3-hydroxyl group on morphine.[citation needed]

Biochemistry

Distribution

Met-enkephalin is found mainly in the adrenal medulla and throughout the central nervous system (CNS), including in the striatum, cerebral cortex, olfactory tubercle, hippocampus, septum, thalamus, and periaqueductal gray, as well as the dorsal horn of the spinal cord.[2] It is also present in the periphery, notably in some primary afferent fibers that innervate the pelvic viscera.[2]

Biosynthesis

Met-enkephalin is synthesized from proenkephalin via proteolytic cleavage[4] in two metabolic steps. Proenkephalin A is first reduced by either one of two trypsin-like endopeptidase enzymes, prohormone convertase 1 (PC1) or prohormone convertase 2 (PC2); then, the resulting intermediates are further reduced by the enzyme carboxypeptidase E (CPE; previously known as enkephalin convertase (EC)).[5][6] Proenkephalin A contains four sequences of met-enkephalin (at the following positions: 100–104; 107–111; 136–140; 210–214), and as a result, its cleavage generates four copies of met-enkephalin peptides at once.[4] In addition, anabolism of proenkephalin A results in the production of one copy each of two C-terminal-extended met-enkephalin derivatives, the heptapeptide met-enkephalin-arg-phe (261–267), and the octapeptide met-enkephalin-arg-gly-leu (186–193),[4] though whether they affect the opioid receptors in a similar manner as met-enkephalin is not entirely clear.[7]

Clearance

Met- and leu-enkephalin are metabolized by a variety of different enzymes, including aminopeptidase N (APN),[8] neutral endopeptidase (NEP),[8] dipeptidyl peptidase 3 (DPP3),[8] carboxypeptidase A6 (CPA6),[9] and angiotensin-converting enzyme (ACE).[10] These enzymes are sometimes referred to as enkephalinases.

Biological activity

Met-enkephalin is a potent agonist of the δ-opioid receptor, and to a lesser extent the μ-opioid receptor, with little to no effect on the κ-opioid receptor. It is through these receptors that met-enkephalin produces its opioid effects, such as analgesia and antidepressant-like effects.

It is also the endogenous ligand of the opioid growth factor receptor (OGFR; formerly known as the ζ-opioid receptor), which plays a role in the regulation of tissue growth and regeneration; hence why met-enkephalin is sometimes called OGF instead.

Pharmacokinetics

Met-enkephalin has low bioavailability, is rapidly metabolized, and has a very short half-life (minutes).[3][11] These properties are considered undesirable in pharmaceuticals as large doses would need to be administered multiple times an hour to maintain a therapeutically relevant effect, making it unlikely that met-enkephalin will ever be used as a medicine.

[D-Ala2]-Met-enkephalinamide (DALA), is a synthetic enkephalin analog which is not susceptible to degradation by brain enzymes and at low doses (5 to 10 micrograms) caused profound, long-lasting, morphine-like analgesia when microinjected into a rat’s brain.[12]

See also

References

  1. ↑ "Preproenkephalin mRNA expression in the developing and adult rat brain". Brain Research. Molecular Brain Research 21 (1–2): 85–98. January 1994. doi:10.1016/0169-328x(94)90381-6. PMID 8164525. 
  2. ↑ 2.0 2.1 2.2 Christoph Stein (1999). Opioids in pain control: basic and clinical aspects. Cambridge University Press. pp. 22–23. ISBN 978-0-521-62269-1. https://books.google.com/books?id=4Rfr8cQayvgC&pg=PA22. Retrieved 25 November 2011. 
  3. ↑ 3.0 3.1 Thomas Carleton Moore (1993). Neurovascular immunology: vasoactive neurotransmitters and modulators in cellular immunity and memory. CRC Press. p. 179. ISBN 978-0-8493-6894-3. https://books.google.com/books?id=dJyJGevjkzQC&pg=PA179. Retrieved 25 November 2011. 
  4. ↑ 4.0 4.1 4.2 Fleur L. Strand (1999). Neuropeptides: regulators of physiological processes. MIT Press. p. 348. ISBN 978-0-262-19407-5. https://archive.org/details/neuropeptidesreg0000stra. Retrieved 25 November 2011. 
  5. ↑ "Opioid peptide biosynthesis: enzymatic selectivity and regulatory mechanisms". The FASEB Journal 1 (1): 16–21. July 1987. doi:10.1096/fasebj.1.1.3111927. PMID 3111927. http://www.fasebj.org/cgi/pmidlookup?view=long&pmid=3111927. 
  6. ↑ "Enkephalin, its precursor, processing enzymes, and receptor as part of a local opioid network throughout the respiratory system of lung cancer patients". Human Pathology 41 (5): 632–42. May 2010. doi:10.1016/j.humpath.2009.08.025. PMID 20040394. 
  7. ↑ "Endogenous peptide: Met-enkephalin-Arg-Phe, differently regulate expression of opioid receptors on chronic treatment". Neuropeptides 43 (5): 355–62. October 2009. doi:10.1016/j.npep.2009.07.003. PMID 19716174. 
  8. ↑ 8.0 8.1 8.2 "Enkephalinase inhibitors: potential agents for the management of pain". Current Drug Targets 9 (10): 887–94. October 2008. doi:10.2174/138945008785909356. PMID 18855623. http://www.bentham-direct.org/pages/content.php?CDT/2008/00000009/00000010/0009J.SGM. 
  9. ↑ "Characterization of carboxypeptidase A6, an extracellular matrix peptidase". The Journal of Biological Chemistry 283 (11): 7054–63. March 2008. doi:10.1074/jbc.M707680200. PMID 18178555. 
  10. ↑ "Separate metabolic pathways for Leu-enkephalin and Met-enkephalin-Arg(6)-Phe(7) degradation by rat striatal synaptosomal membranes". Neurochemistry International 4 (5): 389–96. 1982. doi:10.1016/0197-0186(82)90081-X. PMID 20487892. 
  11. ↑ William J. Kraemer; Alan David Rogol (29 August 2005). The endocrine system in sports and exercise. John Wiley & Sons. pp. 203–. ISBN 978-1-4051-3017-2. https://books.google.com/books?id=TlC5Hfl04sMC&pg=PA203. Retrieved 25 November 2011. 
  12. ↑ Pert, C. B.; Pert, A.; Chang, J. K.; Fong, B. T. (1976-10-15). "(D-Ala2)-Met-enkephalinamide: a potent, long-lasting synthetic pentapeptide analgesic". Science 194 (4262): 330–332. doi:10.1126/science.968485. ISSN 0036-8075. PMID 968485. Bibcode: 1976Sci...194..330P. 



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