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首页> 外文期刊>Scientific reports. >Real-time in vivo two-photon imaging study reveals decreased cerebro-vascular volume and increased blood-brain barrier permeability in chronically stressed mice
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Real-time in vivo two-photon imaging study reveals decreased cerebro-vascular volume and increased blood-brain barrier permeability in chronically stressed mice

机译:体内实时的双光子成像研究表明,在慢性应激小鼠中降低了脑血管体积和增加的血脑屏障渗透性

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Chronic stress disrupts brain homeostasis and adversely affects the cerebro-vascular system. Even though the effects of chronic stress on brain system have been extensively studied, there are few in vivo dynamic studies on the effects of chronic stress on the cerebro-vascular system. In this study, the effects of chronic stress on cerebral vasculature and BBB permeability were studied using in vivo two-photon (2p) microscopic imaging with an injection of fluorescence-conjugated dextran. Our real-time 2p imaging results showed that chronic stress reduced the vessel diameter and reconstructed vascular volume, regardless of vessel type and branching order. BBB permeability was investigated with two different size of tracers. Stressed animals exhibited a greater BBB permeability to 40-kDa dextran, but not to 70-kDa dextran, which is suggestive of weakened vascular integrity following stress. Molecular analysis revealed significantly higher VEGFa mRNA expression and a reduction in claudin-5. In summary, chronic stress decreases the size of cerebral vessels and increases BBB permeability. These results may suggest that the sustained decrease in cerebro-vascular volume due to chronic stress leads to a hypoxic condition that causes molecular changes such as VEGF and claudin-5, which eventually impairs the function of BBB.
机译:慢性应激破坏脑稳态,对脑血管系统产生不利影响。尽管慢性胁迫对脑体系的影响得到了广泛研究,但体内患有慢性胁迫对脑血管系统的影响的体内动态研究。在该研究中,使用荧光缀合的葡聚糖注射的体内两光子(2P)微观成像研究了慢性胁迫对脑脉管系统和BBB渗透性的影响。我们的实时2P成像结果表明,无论血管类型和支化序列,慢性应激降低了血管直径和重建血管体积。用两种不同的示踪剂调查了BBB渗透性。压力的动物表现出更大的BBB渗透性至40-kda葡聚糖,但不是70-kda葡聚糖,这暗示了应激后血管完整性弱化。分子分析显示出显着更高的VEGFA mRNA表达和克劳丁蛋白-5的还原。总之,慢性应激降低了脑血管的尺寸并增加了BBB渗透性。这些结果可能表明,由于慢性应激引起的脑血管体积持续降低导致缺氧条件,导致VEGF和CLAUDIN-5等分子变化,这最终损害了BBB的功能。

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