COX-1 and COX-2 inhibition in horse blood by phenylbutazone, flunixin, carprofen and meloxicam: an in vitro analysis.

Article Details

Citation

Beretta C, Garavaglia G, Cavalli M

COX-1 and COX-2 inhibition in horse blood by phenylbutazone, flunixin, carprofen and meloxicam: an in vitro analysis.

Pharmacol Res. 2005 Oct;52(4):302-6.

PubMed ID
15939622 [ View in PubMed
]
Abstract

We report on the inhibitory activity of the NSAIDs meloxicam, carprofen, phenylbutazone and flunixin, on blood cyclooxygenases in the horse using in vitro enzyme-linked assays. As expected, comparison of IC50 indicated that meloxicam and carprofen are more selective inhibitors of COX-2 than phenylbutazone and flunixin; meloxicam was the most advantageous for horses of four NSAIDs examined. However at IC80, phenylbutazone (+134.4%) and flunixin (+29.7%) had greater COX-2 selectivity than at IC50, and meloxicam (-41.2%) and carprofen (-12.9%) had lower COX-2 selectivity than at IC50. We therefore propose that the selectivity of NSAIDs should be assessed at the 80% as well as 50% inhibition level.

DrugBank Data that Cites this Article

Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
CarprofenProstaglandin G/H synthase 1ProteinHumans
Unknown
Inhibitor
Details
CarprofenProstaglandin G/H synthase 2ProteinHumans
Yes
Inhibitor
Details
PhenylbutazoneProstaglandin G/H synthase 1ProteinHumans
Yes
Inhibitor
Details
PhenylbutazoneProstaglandin G/H synthase 2ProteinHumans
Yes
Inhibitor
Details