Department of Anatomy with Radiology, Faculty of Medical and Health Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.
Neurosci Res. 2013 Mar;75(3):256-67. doi: 10.1016/j.neures.2013.01.004. Epub 2013 Feb 8.
Connexin43 (Cx43) is a gap junction protein up-regulated after spinal cord injury and is involved in the on-going spread of secondary tissue damage. To test whether a connexin43 mimetic peptide (Peptide5) reduces inflammation and tissue damage and improves function in an in vivo model of spinal cord injury, rats were subjected to a 10g, 12.5mm weight drop injury at the vertebral level T10 using a MASCIS impactor. Vehicle or connexin43 mimetic peptide was delivered directly to the lesion via intrathecal catheter and osmotic mini-pump for up to 24h after injury. Treatment with Peptide5 led to significant improvements in hindlimb function as assessed using the Basso-Beattie-Bresnahan scale. Peptide5 caused a reduction in Cx43 protein, increased Cx43 phosphorylation and decreased levels of TNF-α and IL-1β as assessed by Western blotting. Immunohistochemistry of tissue sections 5 weeks after injury showed reductions in astrocytosis and activated microglia as well as an increase in motor neuron survival. These results show that administration of a connexin mimetic peptide reduces secondary tissue damage after spinal cord injury by reducing gliosis and cytokine release and indicate the clinical potential for mimetic peptides in the treatment of spinal cord patients.
间隙连接蛋白 43(Cx43)在脊髓损伤后上调,并参与持续的继发性组织损伤扩散。为了测试连接蛋白 43 模拟肽(Peptide5)是否能减少炎症和组织损伤并改善脊髓损伤的体内模型中的功能,研究人员使用 MASCIS 撞击器在 T10 椎体水平对大鼠进行了 10g、12.5mm 重量下降损伤。在损伤后通过鞘内导管和渗透微型泵将载体或连接蛋白模拟肽直接输送到损伤部位长达 24 小时。使用 Basso-Beattie-Bresnahan 量表评估后,Peptide5 治疗导致后肢功能显著改善。Western blot 分析表明,Peptide5 导致 Cx43 蛋白减少,Cx43 磷酸化增加,TNF-α 和 IL-1β 水平降低。损伤后 5 周的组织切片免疫组织化学显示星形胶质细胞和活化的小胶质细胞减少,运动神经元存活增加。这些结果表明,模拟肽的给药通过减少神经胶质增生和细胞因子释放,减少了脊髓损伤后的继发性组织损伤,并表明模拟肽在脊髓损伤患者治疗中的临床潜力。