Opiorphin

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Opiorphin[1]
Opiorphin.png
Identifiers
CAS number 864084-88-8 YesY
ChemSpider 28296048 N
ChEMBL CHEMBL2022225 N
Jmol-3D images Image 1
Properties
Molecular formula C29H48N12O8
Molar mass 692.77 g mol−1
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 N (verify) (what is: YesY/N?)
Infobox references

Opiorphin is an endogenous chemical compound first isolated from human saliva. Initial research with mice shows the compound has a painkilling effect greater than that of morphine.[2] It works by stopping the normal breakup of enkephalins, natural pain-killing opioids in the spinal cord. It is a relatively simple molecule consisting of a five-amino acid polypeptide, Gln-Arg-Phe-Ser-Arg.[3][4][5][6][7][8][9][10]

Opiorphin pentapeptide originates from the N-terminal region of the protein PROL1 (proline-rich, lacrimal 1).[3] Opiorphin inhibits three proteases: neutral ecto-endopeptidase (MME), ecto-aminopeptidase N (ANPEP)[3] and perhaps also a dipeptidyl peptidase DPP3.[8] Such action extends the duration of enkephalin effect where the natural pain killers are released physiologically in response to specific potentially painful stimuli, in contrast with administration of narcotics, which floods the entire body and causes many undesirable adverse reactions, including addiction liability and constipation.[11][12] In addition, opiorphin may exert anti-depressive action.[13][14]

Therapeutic application of opiorphin in humans would require modifying the molecule to avoid its rapid degradation in the intestine and its poor penetration of the blood–brain barrier.[11][12]

See also[edit]

References[edit]

  1. ^ Opiorphin at Sigma-Aldrich
  2. ^ Rougeot C, Robert F, Menz L, Bisson JF, Messaoudi M (August 2010). "Systemically active human opiorphin is a potent yet non-addictive analgesic without drug tolerance effects". J. Physiol. Pharmacol. 61 (4): 483–90. PMID 20814077. 
  3. ^ a b c Dickinson DP, Thiesse M (April 1996). "cDNA cloning of an abundant human lacrimal gland mRNA encoding a novel tear protein". Curr. Eye Res. 15 (4): 377–86. doi:10.3109/02713689608995828. PMID 8670737. 
  4. ^ Andy Coghlan (November 13, 2006). "Natural-born painkiller found in human saliva". New Scientist. 
  5. ^ "Natural chemical 'beats morphine'". BBC News. November 14, 2006. 
  6. ^ Mary Beckman (November 13, 2006). "Prolonging Painkillers". ScienceNOW. 
  7. ^ Stanović S, Boranić M, Petrovecki M, et al. (2000). "Thiorphan, an inhibitor of neutral endopeptidase/enkephalinase (CD10/CALLA) enhances cell proliferation in bone marrow cultures of patients with acute leukemia in remission". Haematologia (Budap) 30 (1): 1–10. doi:10.1163/15685590051129814. PMID 10841318. 
  8. ^ a b Thanawala V, Kadam VJ, Ghosh R (October 2008). "Enkephalinase inhibitors: potential agents for the management of pain". Curr Drug Targets 9 (10): 887–94. doi:10.2174/138945008785909356. PMID 18855623. 
  9. ^ Davies KP (March 2009). "The role of opiorphins (endogenous neutral endopeptidase inhibitors) in urogenital smooth muscle biology". J Sex Med. 6 Suppl 3: 286–91. doi:10.1111/j.1743-6109.2008.01186.x. PMC 2864530. PMID 19267851. 
  10. ^ Tian XZ, Chen J, Xiong W, He T, Chen Q (July 2009). "Effects and underlying mechanisms of human opiorphin on colonic motility and nociception in mice". Peptides 30 (7): 1348–54. doi:10.1016/j.peptides.2009.04.002. PMID 19442408. 
  11. ^ a b Rougeot C, Robert F, Menz L, Bisson JF, Messaoudi M (August 2010). "Systemically active human opiorphin is a potent yet non-addictive analgesic without drug tolerance effects". J. Physiol. Pharmacol. 61 (4): 483–90. PMID 20814077. 
  12. ^ a b Popik P, Kamysz E, Kreczko J, Wróbel M (November 2010). "Human opiorphin: the lack of physiological dependence, tolerance to antinociceptive effects and abuse liability in laboratory mice". Behav. Brain Res. 213 (1): 88–93. doi:10.1016/j.bbr.2010.04.045. PMID 20438769. 
  13. ^ Javelot H, Messaoudi M, Garnier S, Rougeot C (June 2010). "Human opiorphin is a naturally occurring antidepressant acting selectively on enkephalin-dependent delta-opioid pathways". J. Physiol. Pharmacol. 61 (3): 355–62. PMID 20610867. 
  14. ^ Yang QZ, Lu SS, Tian XZ, Yang AM, Ge WW, Chen Q (February 2011). "The antidepressant-like effect of human opiorphin via opioid-dependent pathways in mice". Neurosci. Lett. 489 (2): 131–5. doi:10.1016/j.neulet.2010.12.002. PMID 21145938.