NS-398,一种新型非甾体抗炎药,具有有效的镇痛和解热作用,对胃的损害最小。

N Futaki, K Yoshikawa, Y Hamasaka, I Arai, S Higuchi, H Iizuka, S Otomo
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引用次数: 346

摘要

1. NS-398 (N-[2-环己氧基-4-硝基苯基]甲磺酰胺)是一种具有镇痛解热作用的新型非甾体类抗炎药。2. NS-398对大鼠卡拉胶性水肿的抗炎效力与吲哚美辛相当,是双氯芬酸的8倍。在大鼠佐剂性关节炎中,NS-398显示出与loxoprofen相当的治疗效果,但低于吲哚美辛和双氯芬酸。3.NS-398对大鼠佐剂性关节炎疼痛的镇痛效力与吲哚美辛相当,比双氯芬酸和loxoprofen高约3-5倍。在Randall-Selitto法中,NS-398对大鼠的药效是loxoprofen、双氯芬酸和吲哚美辛的2 ~ 7倍。在醋酸致小鼠扭体实验中,NS-398对吲哚美辛和双氯芬酸具有同等效力。4. NS-398对lps致大鼠发热的效力是loxoprofen和indomethacin的1.5-4.5倍,但低于双氯芬酸。5. NS-398在高达1000mg /kg的剂量下产生很少的胃溃疡,而对照药物在10- 30mg /kg的剂量下产生明显的胃损伤。6. NS-398对绵羊精囊微粒体中前列腺素(PG)内过氧化物合成酶的抑制作用低于布洛芬。
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NS-398, a novel non-steroidal anti-inflammatory drug with potent analgesic and antipyretic effects, which causes minimal stomach lesions.

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.

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