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Influences of HIF-l?± on Bax/Bcl-2 and VEGF expressions in rats with spinal cord injury

机译:HIF-1α±对脊髓损伤大鼠Bax / Bcl-2和VEGF表达的影响

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Hypoxia-inducible factor 1-alpha (HIF-1α) is a subunit of HIF-l and thought to be able to protect hypoxic cells from apoptosis or necrosis under ischemic and anoxic conditions. This study aimed to investigated whether recombinant adenovirus vector over-expressing HIF-lα could affect apoptosis-related proteins (Bcl-2 and Bax) and vascular endothelial growth factor (VEGF) in a rat spinal cord injury (SCI) model. A total of 60 male SD rats were divided into 4 groups: Sham, Control, Ad-Blank and Ad-HIF-1α groups. 1, 3, 7, 14, 28 days after surgery, the behavioral recovery was evaluated with BBB scales. Then, rats were sacrificed and the spinal cord was collected for detection of Bcl-2, Bax and VEGF expressions by immunohistochemistry. Results showed the Bcl-2, Bax, VEGF and HIF-lα expressions increased in animals with SCI, but the increase in Bcl-2, VEGF and HIF-lα expressions were higher in Ad-HIF-1α group when compared with other groups, but Bax expression decreased significantly. In addition, administration of Ad-HIF-1α significantly reduced apoptotic cells and promoted the recovery of neurological function. In conclusion, administration of Ad-HIF-1α after SCI could ameliorate neuronal apoptosis and promote angiogenesis in rats. Our study provides a basis for further exploration of the relationship between HIF1α and SCI.
机译:缺氧诱导因子1-α(HIF-1α)是HIF-1的一个亚基,被认为能够在缺血和缺氧条件下保护低氧细胞免于凋亡或坏死。这项研究旨在调查在大鼠脊髓损伤(SCI)模型中过量表达HIF-1α的重组腺病毒载体是否会影响凋亡相关蛋白(Bcl-2和Bax)和血管内皮生长因子(VEGF)。将60只雄性SD大鼠分为4组:假手术,对照组,Ad-Blank和Ad-HIF-1α组。术后1、3、7、14、28天,用BBB量表评估行为恢复。然后,处死大鼠并收集脊髓以通过免疫组织化学检测Bcl-2,Bax和VEGF的表达。结果显示,SCI动物中Bcl-2,Bax,VEGF和HIF-1α的表达增加,而Ad-HIF-1α组中Bcl-2,VEGF和HIF-1α的表达高于其他组,但是Bax表达明显下降。另外,Ad-HIF-1α的施用显着减少了凋亡细胞并促进了神经功能的恢复。总之,在脊髓损伤后给予Ad-HIF-1α可以改善大鼠神经元的凋亡并促进血管新生。我们的研究为进一步探索HIF1α和SCI之间的关系提供了基础。

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