Orhan Nurcan, Ugur Yilmaz Canan, Ekizoglu Oguzhan, Ahishali Bulent, Arican Nadir, Kucuk Mutlu, Elmas Imdat, Gürses Candan, Kalayci Rivaze, Kaya Mehmet
Department of Neurosciences, The Institute of Experimental Medicine, Istanbul University, 34093 Fatih, Istanbul, Turkey.
Department of Laboratory Animal Biology and Biomedical Application Techniques, The Institute of Experimental Medicine, Istanbul University, 34093 Fatih, Istanbul, Turkey.
Brain Res. 2014 May 14;1563:91-102. doi: 10.1016/j.brainres.2014.03.029. Epub 2014 Mar 25.
We investigated the effects of a cell-permeable superoxide dismutase mimetic, manganese(III) tetrakis(1-methyl-4-pyridyl)porphyrin (MnTMPyP) on blood-brain barrier (BBB) integrity following pentylenetetrazole (PTZ)-induced seizures in experimental preeclampsia symptoms induced by N(omega)-nitro-l-arginine methyl ester (l-NAME) in pregnant rats. To show the functional and morphological alterations in BBB integrity, quantitative analysis of sodium fluorescein (NaFlu) extravasation, immunohistochemistry and electron microscopic assessment of horseradish peroxidase (HRP) permeability were performed. Varying degrees of proteinuria were seen and arterial blood pressure increased in l-NAME-treated pregnant rats (p<0.01). MnTMPyP pretreatment and convulsive PTZ challenge significantly decreased the immunoreactivity of occludin in hippocampal capillaries in l-NAME-treated pregnant rats (p<0.01). BBB permeability to NaFlu significantly increased in pregnant rats treated with l-NAME plus PTZ (p<0.01), but MnTMPyP pretreatment did not significantly decrease NaFlu penetration into the brain parenchyma in these animals. Ultrastructurally, frequent vesicles containing HRP reaction products were observed in the capillary endothelial cells in the cerebral cortex and hippocampus of pregnant rats treated with l-NAME and l-NAME plus PTZ with the abundance being more in the latter group. MnTMPyP pretreatment caused a marked reduction in the frequency of HRP reaction product containing vesicles in both experimental settings. In conclusion, the results of the present study provide evidence that MnTMPyP plays an important role in limiting the enhanced vesicle-mediated transcellular transport in BBB endothelium in a rat model of preeclampsia and the differences in the way of transports of NaFlu and HRP might be responsible for the different effects of MnTMPyP on the BBB permeability to these two tracers.
我们研究了一种可穿透细胞的超氧化物歧化酶模拟物——四(1-甲基-4-吡啶基)锰卟啉(MnTMPyP)对实验性先兆子痫症状的妊娠大鼠在戊四氮(PTZ)诱导癫痫发作后血脑屏障(BBB)完整性的影响。实验性先兆子痫症状由N(ω)-硝基-L-精氨酸甲酯(L-NAME)诱导产生。为了显示BBB完整性的功能和形态学改变,我们进行了荧光素钠(NaFlu)外渗的定量分析、免疫组织化学以及辣根过氧化物酶(HRP)通透性的电子显微镜评估。L-NAME处理的妊娠大鼠出现了不同程度的蛋白尿,且动脉血压升高(p<0.01)。MnTMPyP预处理和惊厥性PTZ激发显著降低了L-NAME处理的妊娠大鼠海马毛细血管中闭合蛋白的免疫反应性(p<0.01)。L-NAME加PTZ处理的妊娠大鼠中,BBB对NaFlu的通透性显著增加(p<0.01),但MnTMPyP预处理并未显著降低这些动物中NaFlu向脑实质的渗透。超微结构上,在L-NAME处理以及L-NAME加PTZ处理的妊娠大鼠的大脑皮质和海马的毛细血管内皮细胞中观察到频繁出现含有HRP反应产物的囊泡,后一组中囊泡数量更多。在两种实验情况下,MnTMPyP预处理均使含有HRP反应产物的囊泡频率显著降低。总之,本研究结果提供了证据,表明MnTMPyP在先兆子痫大鼠模型中限制血脑屏障内皮细胞中增强的囊泡介导的跨细胞转运方面发挥重要作用,并且NaFlu和HRP转运方式的差异可能是MnTMPyP对血脑屏障对这两种示踪剂通透性产生不同影响的原因。