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Abstract
In two independent studies, ibuprofen and naproxen sodium were found to be equi-effective
in alleviating dysmenorrheic symptoms. However, the effects of these drugs on menstrual
PG release were found to be dissimilar. Ibuprofen primarily inhibited menstrual PGF2α release with little effect on PGE release, whereas, naproxen sodium inhibited both
PGF2α and PGE2 release equally. To verify these results, we determined the inhibitory potency, IC
50' of ibuprofen and naproxen sodium on PGF2α and PGE2 synthesis in the rat uterine homogenate system. The preferential PGF2a inhibitory
activity of ibuprofen was confirmed.
These findings suggest that ibuprofen may, in addition to inhibiting fatty acid cyclooxygenase,
also inhibit PGF2α reductase, or some other PG metabolic pathways which affect PGF a and PGE2 synthesis differently. The significance of this differential PG synthesis inhibitory
effect in dysmenorrheic therapy is discussed.
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References
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Article info
Footnotes
☆This work was supported by research grants from NICHHD (HD-13064) and the NIGMS (GM-07547).
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Copyright
© 1984 Published by Elsevier Inc.