Title : Inhibition of microsomal prostaglandin E-synthase-1 (mPGES-1) selectively suppresses PGE2 in an in vitro equine inflammation model.

Pub. Date : 2017 Oct

PMID : 29042013






6 Functional Relationships(s)
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1 Inhibition of microsomal prostaglandin E-synthase-1 (mPGES-1) selectively suppresses PGE2 in an in vitro equine inflammation model. Dinoprostone prostaglandin E synthase Mus musculus
2 One potential target is microsomal prostaglandin E-synthase-1 (mPGES-1), which is the terminal enzyme downstream of COX-2 in the inducible PGE2 synthesis cascade. Dinoprostone prostaglandin E synthase Mus musculus
3 The objective of this study was to determine if mPGES-1 is a PGE2-selective anti-inflammatory target in equine leukocytes. Dinoprostone prostaglandin E synthase Mus musculus
4 mPGES-1 inhibition also preserved higher basal levels of PGE2 production when compared to either COX inhibitor, which might be beneficial in a clinical setting. Dinoprostone prostaglandin E synthase Mus musculus
5 In conclusion, this work identifies mPGES-1 as a key regulator of PGE2 production and a PGE2-selective target in equine leukocytes. Dinoprostone prostaglandin E synthase Mus musculus
6 In conclusion, this work identifies mPGES-1 as a key regulator of PGE2 production and a PGE2-selective target in equine leukocytes. Dinoprostone prostaglandin E synthase Mus musculus