Padilla Françoise, Couble Marie-Lise, Coste Bertrand, Maingret François, Clerc Nadine, Crest Marcel, Ritter Amy M, Magloire Henry, Delmas Patrick
Laboratoire de Neurophysiologie Cellulaire, CNRS, UMR 6150, Faculté de Médecine, IFR Jean Roche, Bd. Pierre Dramard, 13916 Marseille Cedex 20, France.
Mol Cell Neurosci. 2007 May;35(1):138-52. doi: 10.1016/j.mcn.2007.02.008. Epub 2007 Feb 15.
The Nav1.9 sodium channel is expressed in nociceptive DRG neurons where it contributes to spontaneous pain behavior after peripheral inflammation. Here, we used a newly developed antibody to investigate the distribution of Nav1.9 in rat and mouse trigeminal ganglion (TG) nerve endings and in enteric nervous system (ENS). In TGs, Nav1.9 was expressed in the soma of small- and medium-sized, peripherin-positive neurons. Nav1.9 was present along trigeminal afferent fibers and at terminals in lip skin and dental pulp. In the ENS, Nav1.9 was detected within the soma and proximal axons of sensory, Dogiel type II, myenteric and submucosal neurons. Immunological data were correlated with the detection of persistent TTX-resistant Na(+) currents sharing similar properties in DRG, TG and myenteric neurons. Collectively, our data support a potential role of Nav1.9 in the transmission of trigeminal pain and the regulation of intestinal reflexes. Nav1.9 might therefore constitute a molecular target for therapeutic treatments of orofacial pain and gastrointestinal syndromes.
Nav1.9 钠通道在伤害性背根神经节(DRG)神经元中表达,在外周炎症后它会导致自发疼痛行为。在此,我们使用一种新开发的抗体来研究 Nav1.9 在大鼠和小鼠三叉神经节(TG)神经末梢以及肠神经系统(ENS)中的分布。在三叉神经节中,Nav1.9 在中小型、外周蛋白阳性神经元的胞体中表达。Nav1.9 存在于三叉神经传入纤维以及唇部皮肤和牙髓的终末部位。在肠神经系统中,在感觉性、Dogiel II 型、肌间神经丛和黏膜下神经元的胞体和近端轴突中检测到 Nav1.9。免疫数据与在背根神经节、三叉神经节和肌间神经丛神经元中检测到的具有相似特性的持续性河豚毒素抗性钠电流相关。总体而言,我们的数据支持 Nav1.9 在三叉神经痛传递和肠道反射调节中的潜在作用。因此,Nav1.9 可能构成治疗口面部疼痛和胃肠道综合征的分子靶点。