Chien Li-Ying, Cheng Jen-Kun, Chu Dachen, Cheng Chau-Fu, Tsaur Meei-Ling
Institute of Neuroscience, National Yang-Ming University, Taipei, Taiwan.
J Neurosci. 2007 Sep 12;27(37):9855-65. doi: 10.1523/JNEUROSCI.0604-07.2007.
A-type K+ channels (A-channels) are crucial in controlling neuronal excitability, and their downregulation in pain-sensing neurons may increase pain sensation. To test this hypothesis, we first characterized the expression of two A-channels, Kv3.4 and Kv4.3, in rat dorsal root ganglion (DRG) neurons. Kv3.4 was expressed mainly in the nociceptive DRG neurons, in their somata, axons, and nerve terminals innervating the dorsal horn of spinal cord. In contrast, Kv4.3 appeared selectively in the somata of a subset of nonpeptidergic nociceptive DRG neurons. Most Kv4.3(+) DRG neurons also expressed Kv3.4. In a neuropathic pain model induced by spinal nerve ligation in rats, the protein levels of Kv3.4 and Kv4.3 in the DRG neurons were greatly reduced. After Kv3.4 or Kv4.3 expression in lumbar DRG neurons was suppressed by intrathecal injections of antisense oligodeoxynucleotides, mechanical but not thermal hypersensitivity developed. Together, our data suggest that reduced expression of A-channels in pain-sensing neurons may induce mechanical hypersensitivity, a major symptom of neuropathic pain.
A型钾通道(A通道)在控制神经元兴奋性方面至关重要,其在痛觉感受神经元中的下调可能会增强疼痛感。为了验证这一假设,我们首先对大鼠背根神经节(DRG)神经元中两种A通道Kv3.4和Kv4.3的表达进行了表征。Kv3.4主要表达于伤害性DRG神经元及其胞体、轴突以及支配脊髓背角的神经末梢。相比之下,Kv4.3选择性地出现在一部分非肽能伤害性DRG神经元的胞体中。大多数Kv4.3(+) DRG神经元也表达Kv3.4。在大鼠脊髓神经结扎诱导的神经病理性疼痛模型中,DRG神经元中Kv3.4和Kv4.3的蛋白水平大幅降低。鞘内注射反义寡脱氧核苷酸抑制腰段DRG神经元中Kv3.4或Kv4.3的表达后,出现了机械性超敏反应,但热超敏反应未出现。总之,我们的数据表明,痛觉感受神经元中A通道表达的降低可能会诱发机械性超敏反应,这是神经病理性疼痛的主要症状。