Liu Ming-Gang, Zhang Fu-Kang, Guo She-Wei, Zhao Lan-Feng, An Yang-Yuan, Cui Xiu-Yu, Chen Jun
Institute for Biomedical Sciences of Pain, Capital Medical University, Beijing 100069, PR China.
Neurosci Lett. 2007 Oct 29;427(1):39-43. doi: 10.1016/j.neulet.2007.09.001. Epub 2007 Sep 8.
The present study was undertaken to investigate whether isoforms of c-Jun N-terminal kinase (JNK 46 kDa and 54 kDa), one component of the mitogen-activated protein kinase (MAPK) family, might show region-related differential activation patterns in both naïve and pain-experiencing rats. In naïve rats, no significant difference was observed in total expression level of the two JNK isoforms between spinal cord and primary somatosensory cortex (S1 area). However, phosphorylated JNK 46 kDa was normally expressed in the S1 area, but not in the spinal cord, while neither of the two structures contained phosphorylated JNK 54 kDa. Subcutaneous bee venom (BV)-induced persistent pain stimulation resulted in a significant increase in the phosphorylation of both JNK isoforms in each area for a long period (lasting at least 48 h). Nevertheless, JNK 46 kDa exhibited a much higher activation than JNK 54 kDa in the spinal cord, whereas the same noxious stimulation elicited evident activation of JNK 54 kDa in the S1 area, leaving JNK 46 kDa less affected. Intraplantar injection of sterile saline solution, causing acute and transient pain, produced almost the same changes in activation profile of the two JNK isoforms as found in the BV-treated rats. These results implicate that individual members of the JNK family may be associated with specific regions of nociceptive processing. Also, the two JNK isoforms are supposed to function differently according to their locations within the rat central nervous system.
本研究旨在调查丝裂原活化蛋白激酶(MAPK)家族成员之一的c-Jun氨基末端激酶(JNK 46 kDa和54 kDa)亚型在未经历疼痛和经历过疼痛的大鼠中是否呈现与区域相关的差异激活模式。在未经历疼痛的大鼠中,脊髓和初级体感皮层(S1区)之间两种JNK亚型的总表达水平未观察到显著差异。然而,磷酸化的JNK 46 kDa在S1区正常表达,但在脊髓中不表达,而这两个结构中均未检测到磷酸化的JNK 54 kDa。皮下注射蜂毒(BV)诱导的持续性疼痛刺激导致每个区域中两种JNK亚型的磷酸化水平在很长一段时间内(至少持续48小时)显著增加。然而,JNK 46 kDa在脊髓中的激活程度远高于JNK 54 kDa,而相同的有害刺激在S1区引发了JNK 54 kDa的明显激活,JNK 46 kDa受影响较小。足底注射无菌盐溶液引起急性和短暂性疼痛,在两种JNK亚型的激活模式上产生了与BV处理大鼠几乎相同的变化。这些结果表明,JNK家族的各个成员可能与伤害性处理的特定区域相关。此外,两种JNK亚型在大鼠中枢神经系统中的功能可能因其位置不同而有所差异。