Nonsteroid drug selectivities for cyclo-oxygenase-1 rather than cyclo-oxygenase-2 are associated with human gastrointestinal toxicity: a full in vitro analysis - PubMed (original) (raw)
Nonsteroid drug selectivities for cyclo-oxygenase-1 rather than cyclo-oxygenase-2 are associated with human gastrointestinal toxicity: a full in vitro analysis
T D Warner et al. Proc Natl Acad Sci U S A. 1999.
Erratum in
- Proc Natl Acad Sci U S A 1999 Aug 17;96(17):9666
Abstract
The beneficial actions of nonsteroid anti-inflammatory drugs (NSAID) can be associated with inhibition of cyclo-oxygenase (COX)-2 whereas their harmful side effects are associated with inhibition of COX-1. Here we report data from two related assay systems, the human whole blood assay and a modified human whole blood assay (using human A549 cells as a source of COX-2). This assay we refer to as the William Harvey Modified Assay. Our aim was to make meaningful comparisons of both classical NSAIDs and newer COX-2-selective compounds. These comparisons of the actions of >40 NSAIDs and novel COX-2-selective agents, including celecoxib, rofecoxib and diisopropyl fluorophosphate, demonstrate a distribution of compound selectivities toward COX-1 that aligns with the risk of serious gastrointestinal complications. In conclusion, this full in vitro analysis of COX-1/2 selectivities in human tissues clearly supports the theory that inhibition of COX-1 underlies the gastrointestinal toxicity of NSAIDs in man.
Figures
Figure 1
The effects of celecoxib (A), diclofenac (B), etodolac (C), ibuprofen (D), meloxicam (E), and nimesulide (F) on the activity of COX-1 (solid line), WBA-COX-2 (short dashed line), and WHMA-COX-2 (long dashed line). Results are expressed as percent of control and are represented as mean ± SEM. (n = 5–8).
Figure 2
The effects of diisopropyl fluorophosphate (A), L-745,337 (B), NS398 (C), and rofecoxib (D) on the activity of COX-1 (solid line), WBA-COX-2 (short dashed line), and WHMA-COX-2 (long dashed line). Results are expressed as percent of control and are represented as mean ± SEM. (n = 5–8).
Figure 3
Determinable log [IC80 ratio (WBA-COX-2/COX-1)] for all agents assayed (see Table 1). The “0 line” indicates equipotency, i.e., an IC80 ratio of 1. Italics indicate compounds with very low potency.
Figure 4
Analysis of the percent inhibition of COX-1 seen when COX-2 (WHMA) is inhibited by 80%. The dotted line indicates equiactivity, i.e., an 80% inhibition of COX-1.
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References
- Vane J R. Nat New Biol. 1971;231:232–239. - PubMed
- Vane J R, Bakhle Y S, Botting R M. Annu Rev Pharmacol Toxicol. 1998;38:97–120. - PubMed
- Patrignani P, Panara M R, Greco A, Fusco O, Natoli C, Iacobelli S, Cipollone F, Ganci A, Créminon, Maclouf J, et al. J Pharmacol Exp Ther. 1994;271:1705–1712. - PubMed
- Brideau C, Kargman S, Liu S, Dallob A L, Ehrich E W, Rodger I W, Chan C-C. Inflamm Res. 1996;45:68–74. - PubMed
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