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一种中性粒细胞弹性蛋白酶抑制剂(ONO - 5046)可减轻大鼠脊髓损伤后的神经损伤。

A neutrophil elastase inhibitor (ONO-5046) reduces neurologic damage after spinal cord injury in rats.

作者信息

Tonai T, Shiba K, Taketani Y, Ohmoto Y, Murata K, Muraguchi M, Ohsaki H, Takeda E, Nishisho T

机构信息

Department of Orthopedic Surgery and Clinical Research Institute, National Zentsuji Hospital, Kagawa, Japan.

出版信息

J Neurochem. 2001 Sep;78(5):1064-72. doi: 10.1046/j.1471-4159.2001.00488.x.

Abstract

In view of a cytoprotective effect of elastase inhibitor on chemokine-mediated tissue injury, we examined the neuroprotective effect of ONO-5046, a specific inhibitor of neutrophil elastase, in rats with spinal cord injury. Standardized spinal cord compression markedly increased cytokine-induced neutrophil chemo-attractant (CINC)-1 mRNA and protein. Their increases correlated with neurologic severity of injured rats. Immunohistochemically, CINC-1 protein was detected sequentially in vascular endothelial cells at 4 h, in perivascular neutrophils at 8 h, and in neutrophils infiltrating into cord substance at 12 h. Pretreatment with ONO-5046 (50 mg/kg) markedly ameliorated motor disturbance in injured rats, and reduced CINC-1 protein and mRNA expression. ONO-5046 also significantly reduced the increase of neutrophil accumulation or infiltration estimated by myeloperoxidase activity, and the extent of vascular permeability by Evans blue extravasation in the injured cord segment in comparison to control animals receiving vehicle. These results suggest that CINC-1 contributed to inflammation in rat spinal cord injury and ONO-5046 attenuated neurologic damage partly by blocking CINC-1 production of the chemoattractant, preventing neutrophil activation and vascular endothelial cell injury.

摘要

鉴于弹性蛋白酶抑制剂对趋化因子介导的组织损伤具有细胞保护作用,我们研究了中性粒细胞弹性蛋白酶的特异性抑制剂ONO - 5046对脊髓损伤大鼠的神经保护作用。标准化的脊髓压迫显著增加了细胞因子诱导的中性粒细胞趋化因子(CINC)-1的mRNA和蛋白水平。它们的增加与受伤大鼠的神经严重程度相关。免疫组织化学显示,CINC - 1蛋白在4小时时于血管内皮细胞中依次被检测到,8小时时在血管周围的中性粒细胞中被检测到,12小时时在浸润到脊髓实质中的中性粒细胞中被检测到。用ONO - 5046(50毫克/千克)预处理可显著改善受伤大鼠的运动障碍,并降低CINC - 1蛋白和mRNA表达。与接受赋形剂的对照动物相比,ONO - 5046还显著减少了通过髓过氧化物酶活性估计的中性粒细胞积聚或浸润的增加,以及通过伊文思蓝外渗估计的损伤脊髓节段的血管通透性程度。这些结果表明,CINC - 1在大鼠脊髓损伤炎症中起作用,ONO - 5046部分通过阻断趋化因子CINC - 1的产生、防止中性粒细胞活化和血管内皮细胞损伤来减轻神经损伤。

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