Graduate Program in Physical Therapy and Rehabilitation Science, 1-242 Medical Education Building, University of Iowa, Iowa City, IA 52242, USA.
Neuroscience. 2010 Oct 27;170(3):893-900. doi: 10.1016/j.neuroscience.2010.08.003. Epub 2010 Aug 5.
Acid sensing ion channels (ASIC) are found in sensory neurons, including those that innervate muscle tissue. After peripheral inflammation there is an increase in proton concentration in the inflamed tissue, which likely activates ASICs. Previous studies from our laboratory in an animal model of muscle inflammation show that hyperalgesia does not occur in ASIC3 and ASIC1 knockout mice. Therefore, in the present study we investigated if pH activated currents in sensory neurons innervating muscle are altered after induction of muscle inflammation. Sensory neurons innervating mouse (C57/Bl6) muscle were retrogradely labeled with 1,1-dioctadecyl-3,3,3,3 tetramethylindocarbocyanine perchlorate (DiI). Two weeks after injection of DiI, mice were injected with 3% carrageenan to induce inflammation (n=8; 74 neurons) or pH 7.2 saline (n=5; 40 neurons, control) into the gastrocnemius muscle. 24 h later sensory neurons from L4-L6 dorsal root ganglia (DRG) were isolated and cultured. The following day the DRG neuron cultures were tested for responses to pH by whole-cell patch-clamp technique. Approximately 40% of neurons responded to pH 5 with an inward rapidly desensitizing current consistent with ASIC channels in both groups. The mean pH-evoked current amplitudes were significantly increased in muscle sensory neurons from inflamed mice (pH 5.0, 3602 ± 470 pA) in comparison to the controls (pH 7.4, 1964 ± 370 pA). In addition, the biophysical properties of ASIC-like currents were altered after inflammation. Changes in ASIC channels result in enhanced responsiveness to decreases in pH, and likely contribute to the increased hyperalgesia observed after muscle inflammation.
酸敏离子通道(ASIC)存在于感觉神经元中,包括那些支配肌肉组织的神经元。外周炎症后,炎症组织中质子浓度增加,可能会激活 ASIC。我们实验室之前在肌肉炎症的动物模型中的研究表明,ASIC3 和 ASIC1 基因敲除小鼠不会出现痛觉过敏。因此,在本研究中,我们研究了肌肉炎症诱导后,支配肌肉的感觉神经元中 pH 激活电流是否发生改变。使用 1,1-二辛基-3,3,3,3-四甲基吲哚碳菁高氯酸盐(DiI)逆行标记支配小鼠(C57/Bl6)肌肉的感觉神经元。DiI 注射后两周,将 3%角叉菜胶注入小鼠的比目鱼肌中以诱导炎症(n=8;74 个神经元)或 pH 7.2 生理盐水(n=5;40 个神经元,对照组)。24 小时后,从 L4-L6 背根神经节(DRG)分离和培养感觉神经元。次日,通过全细胞膜片钳技术测试 DRG 神经元培养物对 pH 的反应。在两组中,约 40%的神经元对 pH 5 有反应,表现为快速脱敏的内向电流,与 ASIC 通道一致。与对照组(pH 7.4,1964±370 pA)相比,来自炎症小鼠的肌肉感觉神经元中 pH 诱发电流幅度显著增加(pH 5.0,3602±470 pA)。此外,炎症后 ASIC 样电流的生物物理特性发生改变。ASIC 通道的变化导致对 pH 值降低的反应增强,可能导致肌肉炎症后观察到的痛觉过敏增加。