Prostaglandin E receptors.

Article Details

Citation

Sugimoto Y, Narumiya S

Prostaglandin E receptors.

J Biol Chem. 2007 Apr 20;282(16):11613-7. Epub 2007 Feb 28.

PubMed ID
17329241 [ View in PubMed
]
Abstract

Prostaglandin (PG) E(2) exerts its actions by acting on a group of G-protein-coupled receptors (GPCRs). There are four GPCRs responding to PGE(2) designated subtypes EP1, EP2, EP3, and EP4 and multiple splicing isoforms of the subtype EP3. The EP subtypes exhibit differences in signal transduction, tissue localization, and regulation of expression. This molecular and biochemical heterogeneity of PGE receptors leads to PGE(2) being the most versatile prostanoid. Studies on knock-out mice deficient in each EP subtype have defined PGE(2) actions mediated by each subtype and identified the role each EP subtype plays in various physiological and pathophysiological responses. Here we review recent advances in PGE receptor research.

DrugBank Data that Cites this Article

Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
DinoprostoneProstaglandin E2 receptor EP1 subtypeProteinHumans
Yes
Agonist
Details
DinoprostoneProstaglandin E2 receptor EP2 subtypeProteinHumans
Yes
Agonist
Details
DinoprostoneProstaglandin E2 receptor EP3 subtypeProteinHumans
Yes
Agonist
Details
DinoprostoneProstaglandin E2 receptor EP4 subtypeProteinHumans
Yes
Agonist
Details