止痛药
药理学
医学
伤害
炎症
六烯酸
敏化
非甾体
机制(生物学)
多不饱和脂肪酸
药品
类阿片
作用机理
消炎药
对乙酰氨基酚
神经科学
慢性疼痛
人体研究
中枢敏化
生物信息学
更安全的
药物发现
痛觉过敏
伤害感受器
作者
Geovana Martelossi-Cebinelli,Tiago H. Zaninelli,Rúbia Casagrande,Sérgio M. Borghi,Waldiceu A. Verri
出处
期刊:Current reviews in clinical and experimental pharmacology
[Bentham Science]
日期:2026-03-11
卷期号:21
标识
DOI:10.2174/0127724328436999251223054038
摘要
Pain is a protective mechanism of the body that is intensified during inflammatory processes through the sensitization of nociceptive neurons. Although current drugs, such as nonsteroidal anti-inflammatory drugs (NSAIDs), glucocorticoids, and opioids, are effective, their side effects reinforce the search for safer alternatives. In this context, studies investigating the analgesic effects of specialized pro-resolving mediators (SPMs), derived from polyunsaturated fatty acids, stand out. Resolvin D1 (RvD1), derived from the omega-3 fatty acid docosahexaenoic acid, acts in a multimodal manner to modulate pain and inflammation by regulating immunological, neuronal, and glial responses. Thus, RvD1 is a promising molecule for resolving inflammatory and painful processes. Herein, we address the main analgesic mechanisms of RvD1 in different preclinical models.
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