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Chronic type 2 diabetes reduces the integrity of the blood-brain barrier by reducing tightjunction proteins in the hippocampus

机译:慢性2型糖尿病可通过减少紧绷程度来减少血脑屏障的完整性海马中的连接蛋白

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摘要

In the present study, we investigated the effects of type 2 diabetes-induced hyperglycemia on the integrity of the blood–brain barrier and tight junction markers in the rat hippocampus. Forty-week-old diabetic (Zucker diabetic fatty, ZDF) rats and littermate control (Zucker lean control, ZLC) rats were used in this study. We evaluated the integrity of the blood–brain barrier by measuring sodium fluorescein extravasation and blood vessel ultrastructure. In addition, tight junction markers, such as zona occludens-1, occludin and claudin-5, were quantified by western blot analysis. ZDF rats showed significantly increased sodium fluorescein leakage in the hippocampus. Tight junction markers, such as occludin and claudin-5, were significantly decreased in the hippocampi of ZDF rats compared to those of ZLC rats. In addition, ZDF rats showed ultrastructural changes with phagocytic findings in the blood vessels. These results suggest that chronic untreated diabetes impairs the permeability of the hippocampal blood–brain barrier by down-regulating occludin and claudin-5, indicating that chronic untreated diabetes may cause hippocampus-dependent dysfunction.
机译:在本研究中,我们调查了2型糖尿病诱发的高血糖对大鼠海马中血脑屏障和紧密连接标记完整性的影响。在该研究中使用了四十周龄的糖尿病(Zucker糖尿病性脂肪,ZDF)大鼠和同窝对照(Zucker瘦肉对照,ZLC)大鼠。我们通过测量荧光素钠外渗和血管超微结构评估了血脑屏障的完整性。另外,通过western印迹分析定量了紧密连接标记,例如透明带闭合蛋白-1,闭合蛋白和claudin-5。 ZDF大鼠显示海马中的荧光素钠泄漏明显增加。与ZLC大鼠相比,ZDF大鼠海马中的紧密连接标记物,例如occludin和claudin-5明显减少。此外,ZDF大鼠显示超微结构改变,并在血管中有吞噬现象。这些结果表明,未经治疗的慢性糖尿病会通过下调occludin和claudin-5的表达而损害海马血脑屏障的通透性,表明慢性未经治疗的糖尿病可能会导致海马依赖性功能障碍。

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