Prostaglandin D2

Prostaglandin D2
Names
IUPAC name
9α,15S-dihydroxy-11-oxo-prosta-5Z,13E-dien-1-oic acid
Identifiers
41598-07-6 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:15555 N
ChemSpider 395250 N
ECHA InfoCard 100.164.741
1881
1891
KEGG C00696 N
MeSH Prostaglandin+D2
PubChem 448457
Properties
C20H32O5
Molar mass 352.465 g/mol
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

Prostaglandin D2 (or PGD2) is a prostaglandin that binds to the receptor PTGDR (DP1), as well as CRTH2 (DP2).[1][2] It is a major prostaglandin produced by mast cells – recruits Th2 cells, eosinophils, and basophils. In mammalian organs, large amounts of PGD2 are found only in the brain and in mast cells. It is critical to development of allergic diseases such as asthma.

Research carried out in 1989[3] found PGD2 is the primary mediator of vasodilation (the "niacin flush") after ingestion of niacin (nicotinic acid).

A 2012 research paper indicates a causal link between elevated levels of localized PGD2 and hair growth inhibition.[4] Applied topically, the researchers found PGD2 prevents hair growth, and mice that were genetically inclined to produce higher levels of PGD2 had inhibited hair growth. The researchers also found PGD2 levels were much higher in balding scalp tissue than nonbalding scalp tissue, through increased levels of prostaglandin D2 synthase. The paper suggested that inhibition of hair growth involved binding of PGD2 to a receptor called GPR44, and that GPR44 therefore would be a therapeutic target for androgenic alopecia in both men and women with hair loss and thinning.[5] Because PGD2's relation to asthma has been known for several years, several drugs that seek to reduce the effect of PGD2 through blocking the GPR44 are already in clinical trials.[5]

Production

Effects

Latest Research

In August 2012, Scientists at the University of Pennsylvania announced that they had discovered PGD2 was present on the scalp of balding men at far higher levels than normal, preventing hair follicles from maturing and therefore stopping them from working and growing hair. Dr. George Cotsarelis and his dermatological team at the University say that they are in talks with several pharmaceutical companies about developing treatments which could be available in two years.[8][9][10]

See also

References

  1. Saito S, Tsuda H, Michimata T (May 2002). "Prostaglandin D2 and reproduction". American Journal of Reproductive Immunology (New York, N.Y. : 1989). 47 (5): 295–302. doi:10.1034/j.1600-0897.2002.01113.x. PMID 12148545. Retrieved 2011-04-09.
  2. Pettipher R, Hansel TT (2008). "Antagonists of the prostaglandin D2 receptor CRTH2". Drug News & Perspectives. 21 (6): 317–22. doi:10.1358/dnp.2008.21.6.1246831. PMID 18836589. Retrieved 2011-04-09.
  3. Morrow, JD; Parsons Wg, 3rd; Roberts Lj, 2nd (August 1989). "Release of markedly increased quantities of prostaglandin D2 in vivo in humans following the administration of nicotinic acid". Prostaglandins. 38 (2): 263–74. doi:10.1016/0090-6980(89)90088-9. PMID 2475889.
  4. 1 2 Garza, Luis A.,; et al. (2012-03-21). "Prostaglandin D2 Inhibits Hair Growth and Is Elevated in Bald Scalp of Men with Androgenetic Alopecia". Science Translational Medicine. 4 (126): 126ra34–126ra34. doi:10.1126/scitranslmed.3003122. ISSN 1946-6234. PMC 3319975Freely accessible. PMID 22440736. Retrieved 2012-03-22.
  5. 1 2 "Clues to the cause of male pattern baldness". Nature magazine (News and Comments).
  6. Onoe, H.,; et al. (2012-05-21). "Prostaglandin D2, a cerebral sleep-inducing substance in monkeys". Proceedings of the National Academy of Sciences of the United States of America. 85 (11): 4082–4086. doi:10.1073/pnas.85.11.4082. PMC 280366Freely accessible. PMID 3163802.
  7. Moniot, Brigitte; Declosmenil, Faustine; Barrionuevo, Francisco; Scherer, Gerd; Aritake, Kosuke; Malki, Safia; Marzi, Laetitia; Cohen-Solal, Ann; Georg, Ina; Klattig, Jürgen; Englert, Christoph; Kim, Yuna; Capel, Blanche; Eguchi, Naomi; Urade, Yoshihiro; Boizet-Bonhoure, Brigitte; Poulat, Francis (2009). "The PGD2 pathway, independently of FGF9, amplifies SOX9 activity in Sertoli cells during male sexual differentiation". Development. 136 (11): 1813–1821. doi:10.1242/dev.032631. PMID 19429785.
  8. http://www.dailymail.co.uk/news/article-2190544/Baldness-cure-reverses-genetics-market-years.html
  9. http://www.telegraph.co.uk/health/healthnews/9485807/Baldness-cure-could-be-on-shelves-in-two-years.html
  10. http://www.nytimes.com/2012/07/29/business/baldness-battle-fought-in-the-follicle.html
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