Reduced expression of A-type potassium channels in primary sensory neurons induces mechanical hypersensitivity

LY Chien, JK Cheng, D Chu, CF Cheng… - Journal of …, 2007 - Soc Neuroscience
LY Chien, JK Cheng, D Chu, CF Cheng, ML Tsaur
Journal of Neuroscience, 2007Soc Neuroscience
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 …
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.
Soc Neuroscience