The Baker Laboratory of Pharmacology, Department of Pharmacology, Kirksville College of Osteopathic Medicine, AT Still University of Health Sciences, Kirksville, MO 63501, USA.
J Neurophysiol. 2012 Oct;108(8):2230-41. doi: 10.1152/jn.00219.2012. Epub 2012 Aug 1.
Muscle afferents are critical regulators of motor function (Group I and II) and cardiovascular responses to exercise (Group III and IV). However, little is known regarding the expressed voltage-dependent ion channels. We identified muscle afferent neurons in dorsal root ganglia (DRGs), using retrograde labeling to examine voltage-dependent sodium (Na(V)) channels. In patch-clamp recordings, we found that the dominant Na(V) current in the majority of identified neurons was insensitive to tetrodotoxin (TTX-R), with Na(V) current in only a few (14%) neurons showing substantial (>50%) TTX sensitivity (TTX-S). The TTX-R current was sensitive to a Na(V)1.8 channel blocker, A803467. Immunocytochemistry demonstrated labeling of muscle afferent neurons by a Na(V)1.8 antibody, which further supported expression of these channels. A portion of the TTX-R Na(V) current appeared to be noninactivating during our 25-ms voltage steps, which suggested activity of Na(V)1.9 channels. The majority of the noninactivating current was insensitive to A803467 but sensitive to extracellular sodium. Immunocytochemistry showed labeling of muscle afferent neurons by a Na(V)1.9 channel antibody, which supports expression of these channels. Further examination of the muscle afferent neurons showed that functional TTX-S channels were expressed, but were largely inactivated at physiological membrane potentials. Immunocytochemistry showed expression of the TTX-S channels Na(V)1.6 and Na(V)1.7 but not Na(V)1.1. Na(V)1.8 and Na(V)1.9 appear to be the dominant functional sodium channels in small- to medium-diameter muscle afferent neurons. The expression of these channels is consistent with the identification of these neurons as Group III and IV, which mediate the exercise pressor reflex.
肌梭传入神经是运动功能(I 组和 II 组)和心血管对运动反应(III 组和 IV 组)的关键调节者。然而,对于表达的电压依赖性离子通道知之甚少。我们使用逆行标记法鉴定背根神经节 (DRG) 中的肌梭传入神经元,以检查电压依赖性钠 (Na(V)) 通道。在膜片钳记录中,我们发现大多数鉴定神经元中的主导 Na(V)电流对河豚毒素 (TTX)不敏感,只有少数(14%)神经元中的 Na(V)电流对 TTX 有显著(>50%)敏感性(TTX-S)。TTX-R 电流对 Na(V)1.8 通道阻滞剂 A803467 敏感。免疫细胞化学显示 Na(V)1.8 抗体标记肌梭传入神经元,进一步支持这些通道的表达。部分 TTX-R Na(V)电流在我们的 25-ms 电压步骤中似乎是非失活的,这表明 Na(V)1.9 通道的活性。大部分非失活电流对 A803467 不敏感,但对细胞外钠敏感。免疫细胞化学显示 Na(V)1.9 通道抗体标记肌梭传入神经元,支持这些通道的表达。对肌梭传入神经元的进一步检查表明,功能性 TTX-S 通道被表达,但在生理膜电位下大部分被失活。免疫细胞化学显示 TTX-S 通道 Na(V)1.6 和 Na(V)1.7 的表达,但 Na(V)1.1 不表达。Na(V)1.8 和 Na(V)1.9 似乎是中小直径肌梭传入神经元中主导的功能性钠通道。这些通道的表达与这些神经元被鉴定为介导运动加压反射的 III 组和 IV 组一致。