Suppr超能文献

塞来昔布用于治疗疼痛和炎症:临床前及临床研究结果

Celecoxib for the treatment of pain and inflammation: the preclinical and clinical results.

作者信息

Tindall E

机构信息

Portland Medical Associates, Ore., USA.

出版信息

J Am Osteopath Assoc. 1999 Nov;99(11 Suppl):S13-7.

Abstract

Inflammation and pain, the principal signs and symptoms of arthritis along with swelling and stiffness, are routinely controlled by treatment with a nonsteroidal anti-inflammatory drug (NSAID). Celecoxib, an anti-inflammatory and analgesic agent indicated for the treatment of osteoarthritis and rheumatoid arthritis, is the first cyclooxygenase (COX) inhibitor with well-defined cyclooxygenase-2 (COX-2) specificity. Preclinical studies of celecoxib in vitro and in vivo support the COX-2 hypothesis that the therapeutic effects of NSAIDs are due to the inhibition of COX-2, and the adverse events associated with NSAID therapy are due to the inhibition of cyclooxygenase-1 (COX-1), the constitutively expressed isoform of COX. Clinical trials in patients with osteoarthritis or rheumatoid arthritis found that the efficacy of celecoxib is superior to that of placebo and comparable to that of naproxen, a conventional NSAID. Clinical studies also found celecoxib to be safe and well tolerated, with no evidence of alteration in platelet aggregation or gastrointestinal ulceration.

摘要

炎症和疼痛是关节炎的主要体征和症状,常伴有肿胀和僵硬,通常用非甾体抗炎药(NSAID)进行治疗。塞来昔布是一种用于治疗骨关节炎和类风湿性关节炎的抗炎镇痛药,是首个具有明确的环氧化酶-2(COX-2)特异性的环氧化酶(COX)抑制剂。塞来昔布的临床前体外和体内研究支持COX-2假说,即NSAIDs的治疗作用是由于抑制COX-2,而与NSAID治疗相关的不良事件是由于抑制环氧化酶-1(COX-1),即COX的组成型表达同工型。在骨关节炎或类风湿性关节炎患者中进行的临床试验发现,塞来昔布的疗效优于安慰剂,且与传统NSAID萘普生相当。临床研究还发现塞来昔布安全且耐受性良好,没有血小板聚集改变或胃肠道溃疡的证据。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验