Genovese Tiziana, Esposito Emanuela, Mazzon Emanuela, Di Paola Rosanna, Meli Rosaria, Caminiti Rocco, Bramanti Placido, Fink Mitchell P, Cuzzocrea Salvatore
IRCCS Centro Neurolesi Bonino-Pulejo, Messina, Italy.
Shock. 2009 Aug;32(2):217-27. doi: 10.1097/SHK.0b013e31818d4073.
The aim of the present study was to evaluate in a mouse model of spinal cord injury (SCI) the effect of the treatment with ethyl pyruvate (EP). Spinal cord injury was induced by the application of vascular clips (force of 24 g) to the dura via a four-level T5-T8 laminectomy in mice. Treatment with EP (75, 25, or 8.5 mg/kg) 1 and 6 h after the SCI significantly decreased (a) the degree of spinal cord inflammation and tissue injury (histological score), (b) neutrophil infiltration (myeloperoxidase activity), (c) nitrotyrosine formation and iNOS expression, (d) proinflammatory cytokines expression, (e) nuclear factor kappaB activation, (f) extracellular signal-regulated kinase 1/2 mitogen-activated protein kinase phosphorylation, and (g) apoptosis (TUNEL staining, Fas ligand, Bax, and Bcl-2 expression). Moreover, EP (75, 25, or 8.5 mg/kg) significantly ameliorated in a dose-dependent manner the loss of limb function (evaluated by motor recovery score). Taken together, our results demonstrate that EP treatment reduces the development of inflammation and tissue injury associated with spinal cord trauma.
本研究的目的是在脊髓损伤(SCI)小鼠模型中评估丙酮酸乙酯(EP)治疗的效果。通过对小鼠进行T5-T8四级椎板切除术并对硬脊膜施加血管夹(24 g力)来诱导脊髓损伤。在脊髓损伤后1小时和6小时用EP(75、25或8.5 mg/kg)治疗可显著降低:(a)脊髓炎症和组织损伤程度(组织学评分);(b)中性粒细胞浸润(髓过氧化物酶活性);(c)硝基酪氨酸形成和诱导型一氧化氮合酶表达;(d)促炎细胞因子表达;(e)核因子κB激活;(f)细胞外信号调节激酶1/2丝裂原活化蛋白激酶磷酸化;以及(g)细胞凋亡(TUNEL染色、Fas配体、Bax和Bcl-2表达)。此外,EP(75、25或8.5 mg/kg)以剂量依赖方式显著改善肢体功能丧失(通过运动恢复评分评估)。综上所述,我们的结果表明,EP治疗可减少与脊髓创伤相关的炎症和组织损伤的发展。