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Ligustilide treatment promotes functional recovery in a rat model of spinal cord injury via preventing ROS production

机译:gust本内酯治疗可通过防止ROS产生促进大鼠脊髓损伤模型中的功能恢复

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摘要

Ligustilide from traditional Chinese medicine extract, angelica sinensis is one of the main active components, and has many pharmacological activities related to the effectiveness. This study sought to determine whether neuro-protection of ligustilide promotes functional recovery in a rat model of spinal cord injury (SCI) via preventing ROS production. Male Sprague-Dawley (SD) rats were induced using operation for model SCI. Furthermore, Basso, Beattie, Bresnahan (BBB) scale and footprint analysis of gait was used to assess the neuro-protection of ligustilide on SCI. The intracellular reactive oxygen species (iROS), prostaglandin E(2) (PGE(2)), interleukin-1β (IL-1β) and tumor necrosis factor (TNF)-α production levels were measured by monoclonal enzyme immunoassay kit. Inducible nitric oxide synthase (iNOS) gene expression, activator protein-1 (AP-1) and c-Jun N-terminal kinase (JNK) protein expressions were detected using Quantitative real-time reverse transcription polymerase chain reaction (Q-PCR) and western blot analyses, respectively. Interestingly, treatment with ligustilide significantly increased BBB scale and reduced recovery of coordination in SCI rats. After SCI, the iROS, PGE(2), IL-1β, TNF-α production levels and iNOS gene expression were significantly suppressed in SCI rats. These results suggest that the neuro-protection of ligustilide promotes functional recovery in a rat model of spinal cord injury via preventing ROS production.
机译:当归中的extract本内酯是当归的主要活性成分之一,并具有许多与功效有关的药理活性。这项研究试图确定在保护脊髓损伤(SCI)的大鼠模型中,通过预防ROS的产生,对gust本内酯的神经保护是否促进了功能恢复。使用针对模型SCI的手术诱导雄性Sprague-Dawley(SD)大鼠。此外,Basso,Beattie,Bresnahan(BBB)量表和步态足迹分析用于评估li本内酯对SCI的神经保护作用。用单克隆酶免疫测定试剂盒测定细胞内活性氧(iROS),前列腺素E(2)(PGE(2)),白介素1β(IL-1β)和肿瘤坏死因子(TNF)-α的产生水平。使用定量实时逆转录聚合酶链反应(Q-PCR)检测诱导型一氧化氮合酶(iNOS)基因表达,激活蛋白1(AP-1)和c-Jun N端激酶(JNK)蛋白表达。蛋白质印迹分析。有趣的是,用川gust嗪治疗可显着增加SCI大鼠的BBB规模并降低协调性恢复。 SCI后,SCI大鼠的iROS,PGE(2),IL-1β,TNF-α产生水平和iNOS基因表达被显着抑制。这些结果表明,在预防脊髓损伤的大鼠模型中,li本内酯的神经保护作用可促进ROS的产生,从而促进功能恢复。

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