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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Reduced blood‐brain barrier expression of fatty acid‐binding protein 5 is associated with increased vulnerability of APP/PS1 mice to cognitive deficits from low omega‐3 fatty acid diets
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Reduced blood‐brain barrier expression of fatty acid‐binding protein 5 is associated with increased vulnerability of APP/PS1 mice to cognitive deficits from low omega‐3 fatty acid diets

机译:降低脂肪酸结合蛋白5的血脑屏障表达与应用程序/ ps1小鼠的脆弱性增加有关,从低ω-3脂肪酸饮食中的认知缺陷增加

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摘要

Lower levels of the cognitively beneficial docosahexaenoic acid (DHA) are often observed in Alzheimer's disease (AD) brains. Brain DHA levels are regulated by the blood‐brain barrier (BBB) transport of plasma‐derived DHA, a process facilitated by fatty acid‐binding protein 5 (FABP5). This study reports a 42.1?±?12.6% decrease in the BBB transport of 14 C‐DHA in 8‐month‐old AD transgenic mice (APPswe,PSEN1?E9) relative to wild‐type mice, associated with a 34.5?±?6.7% reduction in FABP5 expression in isolated brain capillaries of AD mice. Furthermore, short‐term spatial and recognition memory deficits were observed in AD mice on a 6‐month n‐3 fatty acid‐depleted diet, but not in AD mice on control diet. This intervention led to a dramatic reduction (41.5?±?11.9%) of brain DHA levels in AD mice. This study demonstrates FABP5 deficiency and impaired DHA transport at the BBB are associated with increased vulnerability to cognitive deficits in mice fed an n‐3 fatty acid‐depleted diet, in line with our previous studies demonstrating a crucial role of FABP5 in BBB transport of DHA and cognitive function.
机译:所述认知有益十二碳六烯酸(DHA)的较低水平在阿尔茨海默氏病(AD)的大脑经常观察到。脑DHA水平通过血浆来源的DHA,通过脂肪酸结合蛋白5(FABP5)促进了过程的血 - 脑屏障(BBB)运输调节。这项研究报告在14 C-DHA的在8月龄AD转基因小鼠中的BBB转运42.1?±?12.6%的降低(APPSWE,PSEN1?E9)相对于野生型小鼠,具有34.5关联?±?在FABP5表达6.7%的减少在AD小鼠的分离的脑毛细血管。此外,在AD小鼠中观察到在6个月的n-3脂肪酸耗竭的饮食短期空间和识别记忆缺失,但没有在对照饮食AD小鼠。这种干预导致脑DHA水平在AD小鼠的显着降低(41.5?±?11.9%)。这项研究表明在BBB FABP5不足和受损的DHA运输与脆弱性增加小鼠的认知缺陷相关喂食的n-3脂肪酸耗竭的饮食,符合我们先前的研究表明其DHA的BBB运输FABP5的重要作用和认知功能。

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