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COX-2选择性抑制剂L-745,337对佐剂性关节炎大鼠炎症及器官前列腺素E2(PGE2)水平的影响。

Effect of the COX-2 selective inhibitor l-745,337 on inflammation and organ prostaglandin E2 (PGE2) levels in adjuvant arthritic rats.

作者信息

Turull N, Queralt J

机构信息

Departament de Fisiologia, Facultat de Farmàcia, Universitat de Barcelona, Spain.

出版信息

Inflammation. 2000 Dec;24(6):533-45. doi: 10.1023/a:1007025423232.

Abstract

The anti-inflammatory activity of the cyclooxygenase-2 inhibitor, L-745,337, was assessed in adjuvant arthritic rats (AA). The relationship between PGE2 organ levels and drug activity or adverse effects was determined. Arthritic rats were orally treated for two weeks with L-745,337 (0.1, 1 and 5 mg/kg/day), indomethacin (1 mg/kg/day) or vehicle and paw swelling was determined. At the end of the study, samples from paw, stomach (wall and mucosa) and kidney were obtained from rats with or without treatment at high doses of L-745,337 or indomethacin and PGE2 levels were determined. The L-745,337 anti-inflammatory effective-dose-50 was 0.4 mg/kg. Maximal anti-inflammation was obtained with L-745,337 or indomethacin at doses of 5 and 1 mg/kg respectively. L-745,337 showed anti-arthritic activity. No stomach ulcers appeared in either untreated or treated arthritic and healthy control rats. In AA rats, PGE2 increased in paw, stomach wall, gastric mucosa and kidney. These levels were lower in all organs after both drugs but not below PGE2 control levels.

摘要

在佐剂性关节炎大鼠(AA)中评估了环氧化酶-2抑制剂L-745,337的抗炎活性。确定了前列腺素E2(PGE2)的器官水平与药物活性或不良反应之间的关系。用L-745,337(0.1、1和5毫克/千克/天)、吲哚美辛(1毫克/千克/天)或赋形剂对关节炎大鼠进行为期两周的口服治疗,并测定爪肿胀情况。在研究结束时,从接受或未接受高剂量L-745,337或吲哚美辛治疗的大鼠中获取爪、胃(胃壁和胃黏膜)和肾脏的样本,并测定PGE2水平。L-745,337的抗炎半数有效剂量为0.4毫克/千克。分别以5毫克/千克和1毫克/千克的剂量给予L-745,337或吲哚美辛可获得最大抗炎效果。L-745,337显示出抗关节炎活性。未治疗和治疗后的关节炎大鼠及健康对照大鼠均未出现胃溃疡。在AA大鼠中,爪、胃壁、胃黏膜和肾脏中的PGE2水平升高。两种药物治疗后,所有器官中的这些水平均降低,但未低于PGE2对照水平。

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