Park Kellie A, Vasko Michael R
Department of Pharmacology and Toxicology, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN 46202-5126, USA.
Trends Pharmacol Sci. 2005 Nov;26(11):571-7. doi: 10.1016/j.tips.2005.09.010. Epub 2005 Sep 26.
Growing evidence implicates an increasing number of novel lipids, including eicosanoids, diacylglycerols, lysophosphatidic acids and ceramides, in augmenting the sensitivity of sensory neurons and enhancing pain perception. Many of these lipids are second messengers in signaling pathways that are associated with increasing the sensitivity of sensory neurons, whereas others are putative inflammatory mediators that activate either surface receptors or ion channels in these neurons. Based on the studies we review, it is clear that lipid-derived inflammatory mediators are a novel group of targets for therapeutics to treat inflammation and chronic pain states. However, much work remains to define the roles of these lipids in inflammation and the cellular mechanisms by which they alter the sensitivity of sensory neurons.
越来越多的证据表明,包括类花生酸、二酰基甘油、溶血磷脂酸和神经酰胺在内的越来越多的新型脂质,在增强感觉神经元的敏感性和加剧疼痛感知方面发挥着作用。这些脂质中的许多是信号通路中的第二信使,与感觉神经元敏感性增加相关,而其他一些则是假定的炎症介质,可激活这些神经元中的表面受体或离子通道。基于我们所综述的研究,很明显,脂质衍生的炎症介质是治疗炎症和慢性疼痛状态的新型治疗靶点。然而,仍有许多工作有待完成,以确定这些脂质在炎症中的作用以及它们改变感觉神经元敏感性的细胞机制。