Institute of Biomedical Science, National Chung-Hsing University, Taichung 40244, Taiwan.
Department of Neurosurgery, Taichung Veterans General Hospital, Taichung 40754, Taiwan.
Int J Mol Sci. 2018 Aug 16;19(8):2421. doi: 10.3390/ijms19082421.
Dual leucine zipper kinase (DLK) is a member of mitogen-activated protein kinase kinase kinase (MAP3K) family mainly involved in neuronal degeneration. However, the role of DLK signaling in the neuropathic pain has not yet been fully determined. Chronic constrictive injury (CCI) was conducted by four 3-0 chromic gut ligatures loosely ligated around the sciatic nerve. Escalated DLK expression over the dorsal root ganglion was observed from one to four rings of CCI. Remarkable expression of DLK was observed in primary dorsal root ganglion cells culture subjected to electrical stimulation and attenuated by DLK short hairpin RNA (shRNA) treatment. Intrathecal injection of DLK shRNA attenuates the expression of DLK over the dorsal root ganglion and hippocampus neurons and increased the threshold of mechanical allodynia and decreased thermal hyperalgesia. In CatWalk gait analysis, significant decreases of print area, maximum contact maximum intensity, stand phase, single stance, and regular index by CCI were alleviated by the DLK shRNA administration. In conclusion, the expression of DLK was up-regulated in chronic constrictive injury and attenuated by the administration of DLK shRNA, which paralleled the improvement of neurobehavior of neuropathic pain. The modulation of DLK expression is a potential clinic treatment option for neuropathic pain.
双亮氨酸拉链激酶 (DLK) 是丝裂原活化蛋白激酶激酶激酶 (MAP3K) 家族的成员,主要参与神经元变性。然而,DLK 信号在神经病理性疼痛中的作用尚未完全确定。慢性缩窄性损伤 (CCI) 通过四个 3-0 铬制肠线松散地结扎在坐骨神经周围进行。在 CCI 的一到四环上观察到背根神经节中 DLK 表达的增加。在电刺激下,初级背根神经节细胞培养中观察到明显的 DLK 表达,并通过 DLK 短发夹 RNA (shRNA) 处理减弱。鞘内注射 DLK shRNA 可减弱背根神经节和海马神经元中 DLK 的表达,增加机械性痛觉过敏的阈值,并降低热痛觉过敏。在 CatWalk 步态分析中,CCI 引起的印迹面积、最大接触最大强度、站立阶段、单腿支撑和规则指数显著减少,DLK shRNA 给药可缓解这些症状。总之,DLK 的表达在慢性缩窄性损伤中上调,通过给予 DLK shRNA 可减弱其表达,这与神经病理性疼痛的神经行为改善相平行。DLK 表达的调节可能是治疗神经病理性疼痛的一种潜在临床选择。