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首页> 外文期刊>Brain research >Morphological and functional changes of blood-brain barrier in kindled rats with cortical dysplasia.
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Morphological and functional changes of blood-brain barrier in kindled rats with cortical dysplasia.

机译:点燃的皮质发育异常大鼠血脑屏障的形态和功能变化。

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Cortical dysplasia (CD) is one of the major causes contributing to epileptogenesis associated with blood-brain-barrier (BBB) disturbances. The current study investigated the functional and ultrastructural changes of BBB in pentylenetetrazole (PTZ)-kindled rats with CD. Pregnant rats on E17 were exposed to 145 cGy of gamma-irradiation and offspring were used for experiments. The rats were given PTZ three times per week to induce kindling. The permeability of BBB was determined by using sodium fluorescein (NaFlu). Immunohistochemistry for occludin, GFAP and c-fos, western-blot analysis for occludin and electron microscopy for the ultrastructural alterations in BBB were performed. The brain level of NaFlu did not increase in rats with CD and/or kindling. Following administration of a convulsive dose of PTZ, a significant increase in BBB permeability was observed in kindled rats with CD. Occludin immunoreactivity and expression remained essentially unchanged in all groups. Slightly enhanced immunoreactivity for GFAP was observed in all groups except control. c-fos immunoreactivity in brain sections of kindled rats with CD displayed a striking increase by convulsive PTZ challenge. Tight junctions were ultrastructurally intact, whereas markedly increased number of pinocytotic vesicles was noted in brain endothelium of kindled rats with CD by convulsive dose of PTZ. The present study showed that epileptic seizures induced by convulsive PTZ challenge during kindling-mediated epileptogenesis in the presence of CD changed both functional and ultrastructural properties of the BBB and considerably enhanced transendothelial vesicular transport, while paracellular pathway was apparently not involved in this setting.
机译:皮质发育异常(CD)是导致与血脑屏障(BBB)障碍相关的癫痫发生的主要原因之一。目前的研究调查了戊二烯四唑(PTZ)点燃的CD大鼠BBB的功能和超微结构变化。 E17的怀胎大鼠接受145 cGy的γ射线照射,后代用于实验。每周给大鼠3次PTZ诱导点燃。使用荧光素钠(NaFlu)测定血脑屏障的通透性。进行了免疫球蛋白对occludin,GFAP和c-fos的免疫印迹分析,occludin的western印迹分析和电子显微镜观察BBB的超微结构改变。在患有CD和/或点燃的大鼠中,NaFlu的脑水平并未增加。服用惊厥剂量的PTZ后,在点燃的CD大鼠中观察到BBB渗透性显着增加。在所有组中,闭合蛋白的免疫反应性和表达基本上保持不变。除对照组外,其他各组均观察到GFAP的免疫反应性略有增强。惊厥性PTZ攻击引起CD点燃的大鼠脑部c-fos免疫反应性显着增加。紧密连接是超微结构完整的,而在抽搐剂量的PTZ刺激下,患有CD的成年大鼠脑内皮细胞中的胞吞小泡数量明显增加。本研究表明,在存在CD的情况下,由惊厥性PTZ激发引起的癫痫性发作改变了BBB的功能和超微结构,并显着增强了跨膜囊泡运输,而细胞旁通路显然不参与这种情况。

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