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NS-398,一种新型非甾体抗炎药,具有强效镇痛和解热作用,对胃部造成的损伤极小。

NS-398, a novel non-steroidal anti-inflammatory drug with potent analgesic and antipyretic effects, which causes minimal stomach lesions.

作者信息

Futaki N, Yoshikawa K, Hamasaka Y, Arai I, Higuchi S, Iizuka H, Otomo S

机构信息

Research Center, Taisho Pharmaceutical Co. Ltd., Saitama, Japan.

出版信息

Gen Pharmacol. 1993 Jan;24(1):105-10. doi: 10.1016/0306-3623(93)90018-s.

Abstract
  1. NS-398 (N-[2-cyclohexyloxy-4-nitrophenyl] methanesulfonamide) is a new non-steroidal anti-inflammatory drug (NSAID) with analgesic and antipyretic effects. 2. The anti-inflammatory potency of NS-398 in rat carrageenin-induced edema was as potent as that of indomethacin and 8 times more potent than diclofenac. In rat adjuvant arthritis, NS-398 showed a therapeutic effect comparable to that seen with loxoprofen but less than that seen with indomethacin and diclofenac. 3. The analgesic potency of NS-398 in rat adjuvant arthritic pain was much the same as that of indomethacin, and was about 3-5 times higher than that of diclofenac and loxoprofen. In the Randall-Selitto method in rats, NS-398 was 2-7 times as potent as loxoprofen, diclofenac and indomethacin. In acetic acid-induced writhing in mice, NS-398 was equipotent to indomethacin and diclofenac. 4. In LPS-induced fever in rats, NS-398 was 1.5-4.5 times as potent as loxoprofen and indomethacin, but less potent than diclofenac. 5. NS-398 produced little gastric ulceration in doses of up to 1000 mg/kg, while reference drugs produced distinct stomach lesions in doses of 10-30 mg/kg. 6. NS-398 inhibited prostaglandin (PG) endoperoxide synthase from sheep seminal vesicle microsomes less potent than that of ibuprofen.
摘要
  1. NS - 398(N - [2 - 环己氧基 - 4 - 硝基苯基]甲磺酰胺)是一种新型非甾体抗炎药(NSAID),具有镇痛和解热作用。2. NS - 398对大鼠角叉菜胶诱导的水肿的抗炎效力与吲哚美辛相当,比双氯芬酸强8倍。在大鼠佐剂性关节炎中,NS - 398显示出与洛索洛芬相当的治疗效果,但低于吲哚美辛和双氯芬酸。3. NS - 398对大鼠佐剂性关节疼痛的镇痛效力与吲哚美辛大致相同,比双氯芬酸和洛索洛芬高约3 - 5倍。在大鼠的Randall - Selitto法中,NS - 398的效力是洛索洛芬、双氯芬酸和吲哚美辛的2 - 7倍。在小鼠醋酸诱导的扭体实验中,NS - 398与吲哚美辛和双氯芬酸等效。4. 在大鼠脂多糖诱导的发热中,NS - 398的效力是洛索洛芬和吲哚美辛的1.5 - 4.5倍,但低于双氯芬酸。5. NS - 398在高达1000 mg/kg的剂量下几乎不产生胃溃疡,而参比药物在10 - 30 mg/kg的剂量下产生明显的胃部损伤。6. NS - 398对绵羊精囊微粒体中前列腺素(PG)内过氧化物合酶的抑制作用比布洛芬弱。

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