Weber Michael A
Downstate College of Medicine, State University of New York, Brooklyn, New York 10022, USA.
Am J Med. 2009 May;122(5 Suppl):S16-22. doi: 10.1016/j.amjmed.2009.03.004.
Arthritis pain often occurs concurrently with hypertension and other cardiovascular risk factors. Treating patients with hypertension who have arthritis and other painful conditions can be a challenge because of potential risks associated with the agents commonly used to treat pain and inflammation. Hypertension is associated with endothelial dysfunction and decreased bioavailability of nitric oxide (NO). Naproxcinod, an investigational drug, is the first in a new class of agents called cyclooxygenase-inhibiting NO donators. They differ from traditional nonsteroidal anti-inflammatory drugs in their ability to donate NO, a signaling molecule known to have potentially beneficial effects on the vasculature and the gastrointestinal tract. Naproxcinod, by donating NO, offers a therapeutic option that might mitigate the negative blood pressure effects and adverse gastrointestinal effects associated with traditional arthritis therapies. This article reviews some preliminary preclinical and clinical studies of key safety data of an investigational new NO-donating anti-inflammatory agent.
关节炎疼痛常与高血压及其他心血管危险因素同时出现。由于常用于治疗疼痛和炎症的药物存在潜在风险,治疗患有关节炎及其他疼痛病症的高血压患者可能具有挑战性。高血压与内皮功能障碍及一氧化氮(NO)生物利用度降低有关。萘普生诺德是一种研究性药物,是一类名为环氧化酶抑制性NO供体的新型药物中的首个药物。它们与传统非甾体抗炎药的不同之处在于能够释放NO,NO是一种已知对血管系统和胃肠道具有潜在有益作用的信号分子。萘普生诺德通过释放NO,提供了一种治疗选择,可能减轻与传统关节炎疗法相关的血压负面影响和胃肠道不良反应。本文综述了一种新型NO供体抗炎药关键安全性数据的一些初步临床前和临床研究。