Prostaglandin E2

Prostaglandin E2 (PGE2), also known as dinoprostone, is a naturally occurring prostaglandin which is used as a medication.[1] As a medication it is used in labor induction, bleeding after delivery, termination of pregnancy, and in newborn babies to keep the ductus arteriosus open.[1][2] In babies it is used in those with congenital heart defects until surgery can be carried out.[2] It may be used within the vagina or by injection into a vein.[1][3]

Prostaglandin E2
Clinical data
Trade namesPGE2, Cervidil, Propess, others
Other names(5Z,11α,13E,15S)-11,15-Dihydroxy-9-oxo-prosta-5,13-dien-1-oic acid
AHFS/Drugs.comMonograph
MedlinePlusa682512
Pregnancy
category
  • US: C (Risk not ruled out)
    Routes of
    administration
    intravaginal, IV
    ATC code
    Identifiers
    CAS Number
    PubChem CID
    IUPHAR/BPS
    DrugBank
    ChemSpider
    ChEBI
    ChEMBL
    CompTox Dashboard (EPA)
    ECHA InfoCard100.006.052
    Chemical and physical data
    FormulaC20H32O5
    Molar mass352.465 g/mol g·mol−1
    3D model (JSmol)
     NY (what is this?)  (verify)

    Common side effects include vomiting, fever, diarrhea, and excessive uterine contraction.[1] In babies there may be decreased breathing and low blood pressure.[2] Care should be taken in people with asthma or glaucoma and it is not recommended in those who have had a prior C-section.[4] Prostaglandin E2 is in the oxytocics family of medications. It works by binding and activating the prostaglandin E2 receptor which results in the opening and softening of the cervix and dilation of blood vessels.[1][2]

    Prostaglandin E2 was first made in 1970 and approved for medical use in the United States in 1977.[2][1] It is on the World Health Organization's List of Essential Medicines, the most effective and safe medicines needed in a health system.[5] In the United Kingdom a dose costs the NHS about 8.50 to 30.00 pounds.[3][6] In the United States a course of treatment costs more than US$200.[4] Prostaglandin E2 works as well as prostaglandin E1 in babies; however, it is much less expensive.[2]

    Physiological effects

    It has important effects in labour (softening the cervix and causing uterine contraction) and also stimulates osteoblasts to release factors that stimulate bone resorption by osteoclasts.

    PGE2 is also the prostaglandin that ultimately induces fever. The set point temperature of the body will remain elevated until PGE2 is no longer present. PGE2 acts on neurons in the preoptic area (POA) through the prostaglandin E receptor 3 (EP3). EP3-expressing neurons in the POA innervate the dorsomedial hypothalamus (DMH), the rostral raphe pallidus nucleus in the medulla oblongata (rRPa), and the paraventricular nucleus (PVN) of the hypothalamus . Fever signals sent to the DMH and rRPa lead to stimulation of the sympathetic output system, which evokes non-shivering thermogenesis to produce body heat and skin vasoconstriction to decrease heat loss from the body surface. It is presumed that the innervation from the POA to the PVN mediates the neuroendocrine effects of fever through the pathway involving pituitary gland and various endocrine organs.

    It is also implicated in duct-dependent congenital heart diseases and is used in infusion in order to open the duct although PGE1 is more commonly used.

    It is a direct vasodilator, relaxing smooth muscles, and it inhibits the release of noradrenaline from sympathetic nerve terminals. It does not inhibit platelet aggregation, where PGI2 does.

    PGE2 also suppresses T cell receptor signaling and may play a role in resolution of inflammation.[7] Up-regulation of PGE2 has been implicated as a possible cause of nail clubbing. Furthermore, its postpartal synthesis in newborns is considered as one cause of patent ductus arteriosus.[8]

    Side effects

    Common side effects include vomiting, fever, diarrhea, and excessive uterine contraction.[1] In babies there may be decreased breathing and low blood pressure.[2] Care should be taken in people with asthma or glaucoma and it is not recommended in those who have had a prior C-section.[4]

    Mechanism of action

    PGE2 is a potent activator of the Wnt signaling pathway. It has been implicated in regulating the developmental specification and regeneration of hematopoietic stem cells through cAMP/PKA activity.[9]

    History

    It was discovered by Bunting, Gryglewski, Moncada and Vane in 1976.

    Society and culture

    It is sold under the trade name of Cervidil(US) and Propess (by Ferring Pharmaceuticals). This is a controlled release vaginal insert. Prostin E2 (by Pfizer Inc.), and Glandin (by Nabiqasim Pharmaceuticals Pakistan) as a vaginal suppository, to prepare the cervix for labour; it is used to induce labour.

    References

    1. "Dinoprostone". The American Society of Health-System Pharmacists. Archived from the original on 16 January 2017. Retrieved 8 January 2017.
    2. Northern Neonatal Network (208). Neonatal Formulary: Drug Use in Pregnancy and the First Year of Life (5 ed.). John Wiley & Sons. p. 2010. ISBN 9780470750353. Archived from the original on 2017-01-13.
    3. British national formulary : BNF 69 (69 ed.). British Medical Association. 2015. pp. 538–540. ISBN 9780857111562.
    4. Hamilton, Richart (2015). Tarascon Pocket Pharmacopoeia 2015 Deluxe Lab-Coat Edition. Jones & Bartlett Learning. p. 361. ISBN 9781284057560.
    5. "WHO Model List of Essential Medicines (19th List)" (PDF). World Health Organization. April 2015. Archived (PDF) from the original on 13 December 2016. Retrieved 8 December 2016.
    6. Ainsworth, Sean B. (2014). Neonatal Formulary: Drug Use in Pregnancy and the First Year of Life. John Wiley & Sons. p. 436. ISBN 9781118819593. Archived from the original on 2017-01-13.
    7. Wiemer, AJ; Hegde, S; Gumperz, JE; Huttenlocher, A (1 October 2011). "A live imaging cell motility screen identifies prostaglandin E2 as a T cell stop signal antagonist". Journal of Immunology. 187 (7): 3663–70. doi:10.4049/jimmunol.1100103. PMC 3178752. PMID 21900181.
    8. Textbook of Pathology 7th Edition © 2015, Harsh Mohan; ISBN 978-93-5152-369-7; p. 404
    9. Goessling, Wolfram; North, Trista E.; Loewer, Sabine; Lord, Allegra M.; Lee, Sang; Stoick-Cooper, Cristi L.; Weidinger, Gilbert; Puder, Mark; Daley, George Q. (2009-03-20). "Genetic interaction of PGE2 and Wnt signaling regulates developmental specification of stem cells and regeneration". Cell. 136 (6): 1136–1147. doi:10.1016/j.cell.2009.01.015. ISSN 1097-4172. PMC 2692708. PMID 19303855.
    This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.