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首页> 外文期刊>The FASEB Journal >A hydrogen sulfide-releasing cyclooxygenase inhibitor markedly accelerates recovery from experimental spinal cord injury.
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A hydrogen sulfide-releasing cyclooxygenase inhibitor markedly accelerates recovery from experimental spinal cord injury.

机译:硫化氢释放环氧合酶抑制剂可显著加速实验性脊髓损伤的恢复。

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摘要

Spinal cord trauma causes loss of motor function that is in part due to the ensuing inflammatory response. Hydrogen sulfide (H2S) is a potent, endogenous anti-inflammatory and neuroprotective substance that has been explored for use in the design of novel nonsteroidal anti-inflammatory drugs. In the current study, we evaluated the potential beneficial effects of ATB-346 2-(6-methoxynapthalen- 2-yl)-propionic acid 4-thiocarbamoyl-phenyl ester, an H2S-releasing derivative of naproxen, in a murine model of spinal cord injury (SCI). SCI was induced in mice by spinal cord compression, produced through the application of vascular clips to the dura via a T5 to T8 laminectomy. ATB-346, naproxen (both at 30 μmol/kg), or vehicle was orally administered to the mice 1 and 6 h after SCI and once daily thereafter for 10 d. Motor function Basso Mouse Scale (BMS) of locomotion improved gradually in the mice treated with naproxen. However, those treated with ATB-346 exhibited a significantly more rapid and sustained recovery of motor function, achieving greater than double the increase in locomotion score of the naproxen group by the 10th day of treatment. ATB-346 also significantly reduced the severity of inflammation (proinflammatory cytokines, apoptosis of neural tissue, and nitrosative stress) that characterized the secondary effects of SCI. Again, the effects of ATB-346 were superior to those of naproxen for several parameters. These results showed marked beneficial effects of an H2S-releasing derivative of naproxen in an animal model of SCI, significantly enhancing recovery of motor function, possibly by reducing the secondary inflammation and tissue injury that characterizes this model. The combination of inhibition of cyclooxygenase and delivery of H2S may offer a promising alternative to existing therapies for traumatic injury.-Campolo, M., Esposito, E., Ahmad, A., Di Paola, R., Wallace, J. L., Cuzzocrea, A. Hydrogen sulfide-releasing cyclooxygenase inhibitor markedly accelerates recovery from experimental spinal cord injury.
机译:脊髓创伤会导致运动功能丧失,部分原因是随之而来的炎症反应。硫化氢 (H2S) 是一种有效的内源性抗炎和神经保护物质,已被探索用于新型非甾体抗炎药的设计。在目前的研究中,我们评估了萘普生的 H2S 释放衍生物 ATB-346 [2-(6-甲氧基萘-2-基)-丙酸 4-硫代氨基甲酰基苯基酯] 在脊髓损伤 (SCI) 小鼠模型中的潜在有益作用。脊髓压迫在小鼠中诱导 SCI,通过 T5 至 T8 椎板切除术将血管夹应用于硬脑膜而产生。在SCI后1小时和6小时口服ATB-346,萘普生(均为30μmol / kg)或载体,此后每天一次,持续10天。运动功能[运动巴索小鼠量表(BMS)]在用萘普生治疗的小鼠中逐渐改善。然而,接受 ATB-346 治疗的患者表现出明显更快和更持续的运动功能恢复,在治疗第 10 天时,萘普生组的运动评分增加了一倍以上。ATB-346 还显着降低了炎症(促炎细胞因子、神经组织凋亡和亚硝化应激)的严重程度,这是 SCI 的次要效应的特征。同样,ATB-346在几个参数上的效果优于萘普生。这些结果表明,萘普生的H2S释放衍生物在SCI动物模型中具有显着的有益作用,可能通过减少该模型的继发性炎症和组织损伤来显着增强运动功能的恢复。-Campolo, M., Esposito, E., Ahmad, A., Di Paola, R., Wallace, J. L., Cuzzocrea, A. 硫化氢释放环氧合酶抑制剂显著加速实验性脊髓损伤的恢复。

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