Inhibition of the Soluble Epoxide Hydrolase as an Analgesic Strategy: A Review of Preclinical Evidence

被引:28
作者
Wang, Yuxin [1 ]
Wagner, Karen M. [1 ]
Morisseau, Christophe [1 ]
Hammock, Bruce D. [1 ]
机构
[1] Univ Calif Davis, UC Davis Comprehens Canc Ctr, Dept Entomol & Nematol, Davis, CA 95616 USA
关键词
epoxy fatty acids; chronic pain; molecular mechanisms; ENDOPLASMIC-RETICULUM STRESS; ACTIVATED-RECEPTOR-GAMMA; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; EPOXYGENATED FATTY-ACIDS; EPOXYEICOSATRIENOIC ACIDS; NEUROPATHIC PAIN; PPAR-GAMMA; THERAPEUTIC TARGET; PHARMACOLOGICAL INHIBITION; MITOCHONDRIAL DYSFUNCTION;
D O I
10.2147/JPR.S241893
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic pain is a complicated condition which causes substantial physical, emotional, and financial impacts on individuals and society. However, due to high cost, lack of efficacy and safety problems, current treatments are insufficient. There is a clear unmet medical need for safe, nonaddictive and effective therapies in the management of pain. Epoxy-fatty acids (EpFAs), which are natural signaling molecules, play key roles in mediation of both inflammatory and neuropathic pain sensation. However, their molecular mechanisms of action remain largely unknown. Soluble epoxide hydrolase (sEH) rapidly converts EpFAs into less bioactive fatty acid diols in vivo; therefore, inhibition of sEH is an emerging therapeutic target to enhance the beneficial effect of natural EpFAs. In this review, we will discuss sEH inhibition as an analgesic strategy for pain management and the underlying molecular mechanisms.
引用
收藏
页码:61 / 72
页数:12
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