Department of Physiology and Anatomy, Tohoku Pharmaceutical University, 4-4-1 Komatsushima, Aoba-ku, Sendai 981-8558, Japan.
Neurosci Lett. 2011 May 16;495(2):83-7. doi: 10.1016/j.neulet.2011.02.038. Epub 2011 Feb 23.
The involvement of spinal glial cells in the nociceptive behaviors induced by 800 pmol of histamine was determined in mice. Histamine at 800 pmol injected intrathecally (i.t.) produced nociceptive behaviors, consisting of scratching, biting and licking. The nociceptive behaviors induced by histamine were significantly suppressed by i.t. co-administration with tachykinin NK(1) receptor antagonist CP99,994 or competitive antagonist for N-methyl-d-aspartate (NMDA) receptor d-(-)-2-amino-5-phosphonovaleric acid (d-APV). The i.t. pretreatment with the glial cell inhibitor dl-fluorocitric acid or minocycline failed to affect the nociceptive behaviors induced by histamine. However, in mice pretreated i.t. with dl-fluorocitric acid or minocycline, the nociceptive behaviors induced by histamine were significantly suppressed by i.t. co-administration with CP99,994 but not d-APV. In Western blot analysis using lumbar spinal cords, i.t. treatment with 800 pmol of histamine increased the phosphorylation of the NR1 subunit of NMDA receptors. The increased phosphorylation of the NR1 subunit of NMDA receptors by histamine was abolished by i.t. pretreatment with dl-fluorocitric acid or minocycline. The present results suggest that histamine at 800 pmol elicits nociceptive behaviors through activation of the neuronal NK(1) receptor and the NR1 subunit-containing NMDA receptors on glial cells in the spinal cord.
在小鼠中确定了脊髓神经胶质细胞在 800 pmol 组胺诱导的痛觉行为中的作用。鞘内注射 800 pmol 组胺可产生痛觉行为,包括搔抓、咬和舔。鞘内共同给予速激肽 NK(1)受体拮抗剂 CP99,994 或 N-甲基-D-天冬氨酸 (NMDA) 受体竞争性拮抗剂 d-(-)-2-氨基-5-膦戊酸 (d-APV) 可显著抑制组胺诱导的痛觉行为。鞘内预先给予神经胶质细胞抑制剂 dl-氟柠檬酸或米诺环素,不能影响组胺诱导的痛觉行为。然而,在预先鞘内给予 dl-氟柠檬酸或米诺环素的小鼠中,组胺诱导的痛觉行为可被鞘内共同给予 CP99,994 显著抑制,但不能被 d-APV 抑制。在使用腰椎脊髓的 Western blot 分析中,鞘内给予 800 pmol 组胺增加了 NMDA 受体 NR1 亚单位的磷酸化。dl-氟柠檬酸或米诺环素鞘内预处理可消除组胺对 NMDA 受体 NR1 亚单位磷酸化的增加。本研究结果表明,800 pmol 组胺通过激活脊髓神经胶质细胞上的神经元 NK(1)受体和包含 NR1 亚单位的 NMDA 受体引起痛觉行为。