Coggeshall Richard E, Tate Simon, Carlton Susan M
Department of Anatomy and Neurosciences, Marine Biomedical Institute, University of Texas Medical Branch, Galveston, TX 77555-1069, USA.
Neurosci Lett. 2004 Jan 23;355(1-2):45-8. doi: 10.1016/j.neulet.2003.10.023.
In an attempt to understand mechanisms underlying peripheral sensitization of primary afferent fibers, we investigated the presence of the tetrodotoxin-resistant Na+ channel subunits Nav1.8 (SNS) and Nav1.9 (SNS2) on axons in digital nerves of normal and inflamed rat hindpaws. In normal animals, 14.3% of the unmyelinated and 10.7% of the myelinated axons labeled for the Nav1.8 subunit. These percentages significantly increased in 48 h inflamed animals to 22.0% (1.5-fold increase) and 57.5% (6-fold increase) for unmyelinated and myelinated axons, respectively. In normal animals, Nav1.9 labeled 9.9% of the unmyelinated and 2.1% of the myelinated axons and following inflammation, the proportion of Nav1.9-labeled unmyelinated axons significantly decreased to 3.0% with no change in the proportion of labeled myelinated axons. These data indicate that Nav1.8 and Nav1.9 subunits are transported to the periphery in normal animals and are differentially regulated during inflammation. The massive increase in Nav1.8 expression in myelinated axons suggests that these may contribute to peripheral sensitization and inflammatory hyperalgesia.
为了了解初级传入纤维外周敏化的潜在机制,我们研究了正常和炎症状态下大鼠后爪趾神经轴突上对河豚毒素耐受的Na⁺通道亚基Nav1.8(SNS)和Nav1.9(SNS2)的存在情况。在正常动物中,14.3%的无髓轴突和10.7%的有髓轴突标记有Nav1.8亚基。在炎症48小时的动物中,这些百分比分别显著增加到无髓轴突的22.0%(增加1.5倍)和有髓轴突的57.5%(增加6倍)。在正常动物中,Nav1.9标记了9.9%的无髓轴突和2.1%的有髓轴突,炎症后,Nav1.9标记的无髓轴突比例显著降至3.0%,而标记的有髓轴突比例没有变化。这些数据表明,Nav1.8和Nav1.9亚基在正常动物中被转运到外周,并在炎症期间受到不同的调节。有髓轴突中Nav1.8表达的大量增加表明,这些轴突可能导致外周敏化和炎症性痛觉过敏。