Jonzon Bror, Bjarnason Ingvar, Hawkey Chris, Jones John, Goddard Andrew, Fagerholm Urban, Karlsson Pär
Experimental Medicine, AstraZeneca R&D Södertälje, S-151 85 Södertälje, Sweden.
Inflammopharmacology. 2003;11(4):437-44. doi: 10.1163/156856003322699618.
COX-inhibiting nitric oxide donators (CINODs) are a new class of drugs in development for the treatment of acute and chronic pain. They comprise a COX-inhibiting moiety linked to a nitric-oxide-donating component and are designed to provide an innovative mechanism of action of balanced COX inhibition and controlled nitric oxide donation. Through these pathways, CINODs should provide analgesic and anti-inflammatory efficacy, while offering gastrointestinal safety through the tissue-protective effects of nitric oxide donation. AZD3582 [4-(nitrooxy)butyl-(2S)-2-(6-methoxy-2-naphthyl)propanoate] is the first agent in the CINOD class to enter extensive clinical development. Pre-clinical studies demonstrate that AZD3582 has a superior gastrointestinal safety profile to naproxen, while demonstrating analgesic and anti-inflammatory efficacy. In healthy human volunteers, AZD3582 caused little gastrointestinal damage compared with equimolar doses of naproxen. Studies to evaluate the longer-term gastrointestinal safety of AZD3582, alongside its efficacy in alleviating chronic and acute pain, are ongoing.
环氧化酶抑制性一氧化氮供体(CINODs)是一类正在研发用于治疗急慢性疼痛的新型药物。它们由与一氧化氮供体成分相连的环氧化酶抑制部分组成,旨在提供一种平衡环氧化酶抑制和可控一氧化氮释放的创新作用机制。通过这些途径,CINODs应能提供镇痛和抗炎功效,同时通过一氧化氮释放的组织保护作用确保胃肠道安全性。AZD3582 [4-(硝基氧基)丁基-(2S)-2-(6-甲氧基-2-萘基)丙酸酯] 是首个进入广泛临床研发阶段的CINOD类药物。临床前研究表明,AZD3582的胃肠道安全性优于萘普生,同时具有镇痛和抗炎功效。在健康人类志愿者中,与等摩尔剂量的萘普生相比,AZD3582对胃肠道造成的损伤较小。评估AZD3582长期胃肠道安全性及其缓解急慢性疼痛疗效的研究正在进行中。