López-Vales Rubèn, García-Alías Guillermo, Guzmán-Lenis Monica S, Forés Joaquim, Casas Catalina, Navarro Xavier, Verdú Enrique
Group of Neuroplasticity and Regeneration Group, Institute of Neuroscience and Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.
Spine (Phila Pa 1976). 2006 May 1;31(10):1100-6. doi: 10.1097/01.brs.0000216448.61860.1d.
We studied the effects of inhibitors of COX-2 (NS398) and iNOS (aminoguanidine) alone or in combination with olfactory ensheathing cell (OEC) grafts after spinal cord injury in the rat.
To assess the role exerted by COX-2 and iNOS after spinal cord injury and an OEC transplant.
COX-2 and iNOS exert a detrimental effect after spinal cord injury. In contrast, OECs grafted into the injured spinal cord mediate neuroprotection and also promote the up-regulation of COX-2 and iNOS.
Photochemical injury was induced at T8 spinal cord segment. Rats received local injection of OECs (n = 15) or vehicle (DMEM; n = 15). Six subgroups of rats (n = 5 rats each) were given NS398 (DM-NS; OEC-NS), aminoguanidine (DM-AG; OEC-AG), or saline (DM-SS; OEC-SS). Locomotor ability, pain sensibility, tissue sparing, and density of blood vessels were evaluated.
Two weeks following injury, motor skills and nociceptive response were significantly higher in DM-NS and DM-AG than in DM-SS rats. The area of preserved spinal cord parenchyma was higher in treated animals than in those given saline. In contrast, functional outcome, tissue sparing, and density of blood vessels were lower in OEC-NS and OEC-AG than in OEC-SS animals.
These results suggest that, although COX-2 and iNOS exert a detrimental role after spinal cord injury, they may play an important role in the neuroprotective mechanisms induced by OEC grafts after spinal cord injury.
我们研究了环氧化酶-2(COX-2)抑制剂(NS398)和诱导型一氧化氮合酶(iNOS)抑制剂(氨基胍)单独或与嗅鞘细胞(OEC)移植联合应用于大鼠脊髓损伤后的效果。
评估脊髓损伤和OEC移植后COX-2和iNOS所起的作用。
脊髓损伤后COX-2和iNOS发挥有害作用。相比之下,移植到损伤脊髓的OEC介导神经保护作用,并且还促进COX-2和iNOS的上调。
在T8脊髓节段诱导光化学损伤。大鼠接受局部注射OEC(n = 15)或赋形剂(DMEM;n = 15)。将大鼠分为六个亚组(每组n = 5只大鼠),分别给予NS398(DM-NS;OEC-NS)、氨基胍(DM-AG;OEC-AG)或生理盐水(DM-SS;OEC-SS)。评估运动能力、疼痛敏感性、组织保留情况和血管密度。
损伤后两周,DM-NS组和DM-AG组大鼠的运动技能和伤害性反应显著高于DM-SS组大鼠。接受治疗的动物保留的脊髓实质面积高于给予生理盐水的动物。相比之下,OEC-NS组和OEC-AG组的功能结果、组织保留情况和血管密度低于OEC-SS组动物。
这些结果表明,虽然脊髓损伤后COX-2和iNOS发挥有害作用,但它们可能在脊髓损伤后OEC移植诱导的神经保护机制中起重要作用。