Agrawal Neetu
Institute of Pharmaceutical Research, GLA University, Mathura, Uttar Pradesh, India.
Chem Biol Drug Des. 2025 May;105(5):e70114. doi: 10.1111/cbdd.70114.
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.
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,且常常与关节炎、癌症和心血管疾病等严重病症相关。因此,有效控制炎症是公共卫生的一项重大优先事项。目前的抗炎治疗方法,包括非甾体抗炎药(NSAIDs)、皮质类固醇、改善病情抗风湿药(DMARDs)和生物制剂,虽能缓解症状,但常常受到诸如胃肠道毒性、免疫抑制或心血管风险等副作用的限制。此外,这些疗法大多仅针对炎症级联反应中的单一途径。COX-2和5-LOX双重抑制剂已成为一类有前景的治疗药物,因为它们能同时阻断参与前列腺素和白三烯合成的两种关键酶。这种双重作用方法可提高疗效,并可能减少与选择性或非选择性COX抑制相关的不良反应。本综述讨论了炎症的潜在机制,评估了当前的治疗选择,并强调了双重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。