戊四氮点燃慢性癫痫大鼠脑组织TrkB及GLT-1的表达分析
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四川省科技攻关项目(05SG022013)


Analysis of the expressions of TrkB and GLT-1 in the brain of pentylenetetrazol kindling model of chronic epilepsy in rats
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    摘要:

    【摘要】 目的 分析戊四氮(PTZ)点燃慢性癫痫模型SD大鼠脑组织酪氨酸激酶受体B(TrKB)及谷氨酸转运体1(GLT-1)的表达变化,为进一步研究胶质细胞BDNF/TrkB信号通路与GLT-1的相关性提供实验依据,为癫痫的防治提供靶位线索。方法 SD大鼠40只随机分成模型组(30只)及对照组(10只),采用PTZ点燃法制作慢性癫痫大鼠模型。运用Western技术分析SD大鼠PTZ点燃后7天海马及颞叶皮层TrkB和GLT-1的蛋白表达、采用免疫荧光双标法分析SD大鼠PTZ点燃后7天海马及颞叶皮层GFAP/TrkB双标阳性细胞的表达,并与对照组进行比较。结果 SD大鼠慢性癫痫发作后,海马及颞叶皮层TrkB和GLT-1蛋白的表达均明显上调、GFAP/TrkB双标阳性细胞平均光密度值较对照组明显增高(P<0.05)。结论 PTZ点燃慢性癫痫SD大鼠海马及颞叶皮层脑组织TrkB表达上调与GLT-1表达异常之间可能存在内在联系,BDNF/TrkB信号通路可能通过改变PTZ点燃慢性癫痫SD大鼠胶质细胞中GLT-1的生物效应来影响或参与癫痫过程。

    Abstract:

    【Abstract】 Objective To analyze the expressions of TrkB and GLT-1 in the brain of pentylenetetrazol (PTZ) kindling model of chronic epilepsy in rats, and provide evidence for correlation between the BDNF/TrkB pathway and GLT-1 and clues for the prevention and treatment targets of epilepsy.Methods 40 SpragueDawley (SD) rats were randomly classified as model (30) and control (10) groups, respectively. Western blotting was used for analyzing the expression of TrkB and GLT-1, and double immunofluorescence staining was used for detecting the cells positive for both glial fibrillary acidic protein (GFAP) and TrkB in the hippocampus and temporal cortex 7 days after establishing the kindling modelResults Compared with the control group, protein level expression of TrkB and GLT-1, and mean optical density (OD) value of the cells positive for both GFAP and TrkB in the hippocampus and temporal cortex were significantly increased after the onset of epilepsy (P<0.05). Conclusion The BDNF/TrkB pathway may participate in epileptogenesis through modulating the biological effect of GLT-1 in the glial cells of PTZ kindling rats, though the specific mechanism requires further investigation.

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  • 在线发布日期: 2017-06-20
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