Klinik und Poliklinik für Anaesthesiologie, Universitätsklinikum Würzburg, Germany.
Ann N Y Acad Sci. 2012 Jun;1257:199-206. doi: 10.1111/j.1749-6632.2012.06499.x.
Peripheral neurons are surrounded by the perineurium that forms the blood-nerve barrier and protects the nerve. Although the barrier serves as protection, it also hampers drug delivery of analgesic drugs to the peripheral nerve. We previously showed that opening of the barrier using hypertonic solutions facilitates drug delivery, for example, of hydrophilic opioids, which selectively target nociceptors. The perineurial barrier is formed by tight junction proteins, including claudin-1, claudin-5, and occludin. Under pathophysiological conditions such as nerve crush injury, the perineurial barrier is opened and tight junction proteins are no longer present. After several days, tight junction proteins reappear and the barrier reseals. Similarly, perineurial injection of hypertonic saline transiently opens the barrier, claudin-1 disappears, and hydrophilic analgesic drugs are effective. In the future, these findings could be used to reseal the barrier breakdown and could be applied to other barriers like the blood-brain or the intestinal mucosal barrier.
周围神经被神经外膜环绕,神经外膜形成血神经屏障并保护神经。尽管该屏障起到保护作用,但也阻碍了镇痛药物向周围神经的递药。我们之前的研究表明,使用高渗溶液打开屏障可以促进药物输送,例如亲水性阿片类药物,这些药物可以选择性地靶向伤害感受器。神经外膜屏障由紧密连接蛋白形成,包括 Claudin-1、Claudin-5 和 Occludin。在神经挤压损伤等病理生理条件下,神经外膜屏障会打开,紧密连接蛋白不再存在。几天后,紧密连接蛋白重新出现,屏障重新密封。同样,神经外膜注射高渗盐水会短暂打开屏障,Claudin-1 消失,亲水性镇痛药有效。将来,这些发现可用于重新封闭屏障破裂,并可应用于其他屏障,如血脑或肠黏膜屏障。