NS-398, A NEW ANTIINFLAMMATORY AGENT, SELECTIVELY INHIBITS PROSTAGLANDIN-G H SYNTHASE CYCLOOXYGENASE (COX-2) ACTIVITY IN-VITRO/

NS-398 is a novel anti-inflammatory and analgesic agent which produces much fewer gastrointestinal lesions in rats. Recently, two forms of c yclooxygenase have been identified: a COX-1 first purified from ram se minal vesicles and a newly discovered mitogen-inducible form (COX-2). Effects of NS-398 on activities of these two distinct forms of COX wer e investigated. COX-1 purified from ram seminal vesicles and COX-2 iso lated from sheep placenta (purity was 70%) were used. The COX-1 activi ty was completely unaffected by 10(4 ) NS-398, whereas the COX-2 activ ity was concentration-dependently inhibited, the IC50 value being 3.8 x 10(-6) M. Indomethacin inhibited both COX-1 and COX-2 activity to th e same degree, the IC50 values being 7.4 x 10(-7) M and 9.7 x 10(-7) M , respectively. The anti-inflammatory and analgesic effects of NS-398 were almost as potent as indomethacin, the effective dose range being 0.3-5 mg/kg in rats. The gastrointestinal lesions related to NS-398 we re not significant following a dose of 1000 mg/kg given orally. NS-398 is the first documented agent to have selective inhibition for COX-2, which may result in the less gastrointestinal toxicity.