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Neuroprotective effects of safranal in a rat model of traumatic injury to the spinal cord by anti-apoptotic, anti-inflammatory and edema-attenuating

机译:藏红素在抗凋亡,消炎和水肿减轻大鼠脊髓损伤模型中的神经保护作用

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Studies on the pathology of spinal cord injury (SCI) have focused on inflammation-associated neuronal apoptosis. The traditional Chinese medicine safranal has been studied extensively and found to have various beneficial health effects. However, study of its potential role in neuroprotection and the underlying mechanism of action in SCI models has been limited. We investigated the effect of safranal on neurologic functions and histopathologic changes after SCI and the mechanism underlying its neuroprotective effects. First, the most effective safranal dose for SCI was evaluated with the Basso, Beattie, and Bresnahan Locomotor Rating Scale and H&E staining: 100 mg/kg was the most effective dose of safranal for SCI. Histopathologic changes were evaluated by performing Nissl staining, which indicated an increased number of neurons after safranal administration. In terms of the mechanism of action, anti-apoptotic effect, downregulation of inflammation, and edema-attenuating effects were detected. TUNEL staining and electron microscopy revealed that safranal treatment inhibited injury-induced apoptosis, and affected the expression of the apoptosis-related genes Bax and Bcl-2, which indicated an anti-apoptotic role after SCI. Safranal treatment suppressed immunoreactivity and expression of the inflammatory cytokines IL-1 beta, TNF-alpha, and p38 MAPK, and increased expression of IL-10 after SCI, suggesting an anti-inflammatory effect. Safranal treatment suppressed expression of AQP-4, which is related to spinal-cord edema, suggesting an edema-attenuating effect. These data suggest that safranal promotes the recovery of neuronal function after SCI in rats, and that this effect is related to its anti-apoptotic, anti-inflammatory, and edema-attenuating effects. (C) 2015 Elsevier Ltd. All rights reserved.
机译:脊髓损伤(SCI)的病理学研究集中在炎症相关的神经元凋亡。对中草药sa进行了广泛的研究,发现其对健康有益。但是,对其在SCI模型中的神经保护作用和潜在作用机制的研究一直很有限。我们调查了SCI后sa对神经功能和组织病理学变化的影响以及其神经保护作用的潜在机制。首先,用Basso,Beattie和Bresnahan Locomotor评定量表和H&E染色评估了SCI的最有效sa剂剂量:100 mg / kg是SCI的最有效of剂剂量。通过进行尼氏染色来评估组织病理学变化,尼氏染色表明在sa治疗后神经元数量增加。就作用机理而言,检测到抗凋亡作用,炎症下调和浮肿减轻作用。 TUNEL染色和电镜观察发现,fra药治疗抑制损伤诱导的凋亡,并影响凋亡相关基因Bax和Bcl-2的表达,表明SCI后具有抗凋亡作用。 Safranal处理抑制免疫反应性和炎症细胞因子IL-1β,TNF-α和p38 MAPK的表达,并在SCI后增加IL-10的表达,表明具有抗炎作用。 Safranal处理抑制了与脊髓水肿有关的AQP-4的表达,表明有减轻水肿的作用。这些数据表明,鼠尾草可促进大鼠SCI后神经元功能的恢复,并且这种作用与其抗凋亡,抗炎和浮肿减轻作用有关。 (C)2015 Elsevier Ltd.保留所有权利。

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