双COX-2/5-LOX抑制剂抗炎研究进展综述

IF 3.3 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Neetu Agrawal
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引用次数: 0

摘要

慢性疼痛和炎症是普遍存在的临床问题,严重影响患者的生活质量,通常与关节炎、癌症和心血管疾病等严重疾病有关。因此,有效管理炎症是一项重要的公共卫生优先事项。目前的抗炎治疗——包括非甾体抗炎药(NSAIDs)、皮质类固醇、改善疾病的抗风湿药(DMARDs)和生物制剂——可以缓解症状,但经常受到副作用的限制,如胃肠道毒性、免疫抑制或心血管风险。此外,大多数这些疗法仅针对炎症级联中的单一途径。COX-2和5-LOX的双重抑制剂已成为一种有前景的治疗类,因为它们同时阻断前列腺素和白三烯合成的两种关键酶。这种双重作用方法提供了增强的功效,并可能减少与选择性或非选择性COX抑制相关的不良反应。本文讨论了炎症的潜在机制,评估了目前的治疗方案,并强调了双COX-2/5-LOX抑制剂作为下一代炎症管理策略的药理学优势和发展现状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Comprehensive Review on the Advancements of Dual COX-2/5-LOX Inhibitors as Anti-Inflammatory Drugs

A Comprehensive Review on the Advancements of Dual COX-2/5-LOX Inhibitors as Anti-Inflammatory Drugs

Chronic pain and inflammation are widespread clinical issues that significantly affect patients' quality of life and are often associated with serious conditions such as arthritis, cancer, and cardiovascular disease. Effective management of inflammation is therefore a major public health priority. Current anti-inflammatory treatments—including non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids, disease-modifying antirheumatic drugs (DMARDs), and biologics—offer symptomatic relief but are frequently limited by side effects such as gastrointestinal toxicity, immunosuppression, or cardiovascular risks. Moreover, most of these therapies target only a single pathway in the inflammatory cascade. Dual inhibitors of COX-2 and 5-LOX have emerged as a promising therapeutic class, as they simultaneously block two key enzymes involved in prostaglandin and leukotriene synthesis. This dual-action approach offers enhanced efficacy and may reduce adverse effects linked to selective or non-selective COX inhibition. This review discusses the underlying mechanisms of inflammation, evaluates current treatment options, and highlights the pharmacological advantages and development status of dual COX-2/5-LOX inhibitors as a next-generation strategy for inflammation management.

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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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