Department of Anatomy and Neuroscience, Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo 663-8501, Japan.
Neuroscience. 2010 Sep 1;169(3):994-1006. doi: 10.1016/j.neuroscience.2010.05.058. Epub 2010 May 31.
While the voltage-gated sodium channels (VGSCs) are the key molecules for neuronal activities, the precise distribution of them in spinal cord is not clear in previous studies. We examined the expression of mRNAs for alpha-subunits of VGSC (Navs) in adult rat spinal cord before and 7 days after L5 spinal nerve ligation (SPNL) or complete Freund's adjuvant (CFA)-induced paw inflammation by in situ hybridization histochemistry, reverse transcription-polymerase chain reaction, and immunohistochemistry. Nav1.1 and Nav1.6 mRNAs were present in all laminae, except for lamina II, including the spinothalamic tract neurons in lamina I identified by retrograde tracing of Fluoro-gold. Nav1.2 mRNA was predominantly observed in the superficial layers (laminae I, II), and Nav1.3 mRNA was more restricted to these layers. All these transcripts were expressed by the neurons characterized by immunostaining for neuron-specific nuclear protein. Nav1.7 mRNA was selectively expressed by a half of motoneurons in lamina IX. No signals for Nav1.8 or Nav1.9 mRNAs were detected. Immunohistochemistry for Nav1.1, Nav1.2, Nav1.6, and Nav1.7 proteins verified some of these neuronal distributions. L5 SPNL decreased Nav1.1 and Nav1.6 mRNAs, and increased Nav1.3 and Nav1.7 mRNAs in the axotomized spinal motoneurons, without any changes in other laminae of L4-6 spinal segments. Intradermal injection of CFA did not cause any transcriptional change. Our findings demonstrate that spinal neurons have different compositions of VGSCs according to their location in laminae. Pathophysiological changes of spinal neuronal activity may due to post-transcriptional changes of VGSCs. Comparison with our previous data concerning the subpopulation-specific distribution of Nav transcripts in primary afferent neurons provides potentially specific targets for local analgesics at the peripheral nerve and spinal levels.
虽然电压门控钠离子通道(VGSCs)是神经元活动的关键分子,但它们在脊髓中的精确分布在以前的研究中并不清楚。我们通过原位杂交组织化学、逆转录聚合酶链反应和免疫组织化学检查了 L5 脊神经结扎(SPNL)或完全弗氏佐剂(CFA)诱导的爪炎症后 7 天成年大鼠脊髓中 VGSC(Navs)α亚单位 mRNA 的表达。Nav1.1 和 Nav1.6 mRNA 存在于所有层中,除了 II 层,包括通过 Fluoro-gold 逆行追踪鉴定的 I 层中的脊髓丘脑束神经元。Nav1.2 mRNA 主要观察到在浅层(I、II 层),而 Nav1.3 mRNA 更局限于这些层。所有这些转录本均由神经元特异性核蛋白免疫染色鉴定的神经元表达。Nav1.7 mRNA 选择性地由 I 层中的一半运动神经元表达。未检测到 Nav1.8 或 Nav1.9 mRNA 的信号。Nav1.1、Nav1.2、Nav1.6 和 Nav1.7 蛋白的免疫组织化学验证了其中一些神经元分布。L5 SPNL 减少了轴突切断的脊髓运动神经元中的 Nav1.1 和 Nav1.6 mRNA,并增加了 Nav1.3 和 Nav1.7 mRNA,而 L4-6 脊髓节段的其他层没有任何变化。皮内注射 CFA 不会引起任何转录变化。我们的发现表明,脊髓神经元根据其在层中的位置具有不同的 VGSC 组成。脊髓神经元活动的病理生理变化可能是由于 VGSCs 的转录后变化。与我们以前关于初级传入神经元中 Nav 转录物亚群特异性分布的研究数据进行比较,为外周神经和脊髓水平的局部镇痛药提供了潜在的特异性靶点。