Tabata-Imai Ayako, Inoue Ran, Mori Hisashi
Department of Molecular Neuroscience, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
PLoS One. 2014 Aug 18;9(8):e105282. doi: 10.1371/journal.pone.0105282. eCollection 2014.
D-Serine, an endogenous coagonist of the N-methyl-D-aspartate receptor (NMDAR), is widely distributed in the central nervous system and is synthesized from L-serine by serine racemase (SR). NMDAR plays an important role in pain processing including central sensitization that eventually causes hyperalgesia. To elucidate the roles of D-serine and SR in pain transmission, we evaluated the behavioral changes and spinal nociceptive processing induced by formalin using SR knock-out (KO) mice. We found that SR is mainly distributed in lamina II of the dorsal horn of the spinal cord in wild-type (WT) mice. Although the formalin injected subcutaneously induced the biphasic pain response of licking in SR-KO and WT mice, the time spent on licking was significantly longer in the SR-KO mice during the second phase of the formalin test. The number of neurons immunopositive for c-Fos and phosphorylated extracellular signal-regulated kinase (p-ERK), which are molecular pain markers, in laminae I-II of the ipsilateral dorsal horn was significantly larger in the SR-KO mice. Immunohistochemical staining revealed that the distribution of SR changed from being broad to being concentrated in cell bodies after the formalin injection. On the other hand, the expression level of the cytosolic SR in the ipsilateral dorsal horn significantly decreased. Oral administration of 10 mM D-serine in drinking water for one week cancelled the difference in pain behaviors between WT and SR-KO mice in phase 2 of the formalin test. These findings demonstrate that the SR-KO mice showed increased sensitivity to inflammatory pain and the WT mice showed translocation of SR and decreased SR expression levels after the formalin injection, which suggest a novel antinociceptive mechanism via SR indicating an important role of D-serine in pain transmission.
D-丝氨酸是N-甲基-D-天冬氨酸受体(NMDAR)的内源性协同激动剂,广泛分布于中枢神经系统,由丝氨酸消旋酶(SR)从L-丝氨酸合成。NMDAR在疼痛处理中起重要作用,包括最终导致痛觉过敏的中枢敏化。为阐明D-丝氨酸和SR在疼痛传递中的作用,我们使用SR基因敲除(KO)小鼠评估了福尔马林诱导的行为变化和脊髓伤害性处理。我们发现SR主要分布于野生型(WT)小鼠脊髓背角的Ⅱ层。虽然皮下注射福尔马林在SR-KO小鼠和WT小鼠中均诱导了舔舐的双相疼痛反应,但在福尔马林试验的第二阶段,SR-KO小鼠的舔舐时间明显更长。同侧背角Ⅰ-Ⅱ层中对c-Fos和磷酸化细胞外信号调节激酶(p-ERK)免疫阳性的神经元数量,在SR-KO小鼠中显著更多,c-Fos和p-ERK是分子疼痛标志物。免疫组织化学染色显示,福尔马林注射后,SR的分布从广泛变为集中在细胞体中。另一方面,同侧背角中胞质SR的表达水平显著降低。在饮水中口服10 mM D-丝氨酸一周消除了福尔马林试验第2阶段WT小鼠和SR-KO小鼠之间疼痛行为的差异。这些发现表明,SR-KO小鼠对炎性疼痛的敏感性增加,福尔马林注射后WT小鼠出现SR易位和SR表达水平降低,这提示了一种通过SR的新型抗伤害感受机制,表明D-丝氨酸在疼痛传递中起重要作用。