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Effect of obesity on early blood?¢????brain barrier disruption following transient focal cerebral ischemia

机译:肥胖对短暂性局灶性脑缺血后早期血脑屏障的影响

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Summary Objective We determined the effect of obesity on early post-ischemic blood?¢????brain barrier (BBB) disruption. Methods Male C57BL/6J mice were fed a high-fat diet (HFD) or standard chow for 16 weeks. Transient focal cerebral ischemia was induced by directly ligating the middle cerebral artery for 2 h. Early BBB disruption was assessed by measuring Evans Blue and sodium fluorescein extravasation at 3 h of reperfusion. Results Obesity produced an increase in cerebral vasodilation/hyperaemia during reperfusion. N(omega)-propyl-L-arginine and 7-nitroindazole (neuronal nitric oxide synthase inhibitors) failed to alter the cerebral vasodilation/hyperaemia in lean mice, but significantly inhibited the cerebral vasodilation/hyperaemia in obese mice. The magnitude of early post-ischemic BBB disruption was significantly greater in obese mice compared with lean mice. Topical treatment with N(omega)-propyl-L-arginine, 7-nitroindazole or N(omega)-propyl-L-arginine, 7-nitroindazole (a non-specific nitric oxide synthase [NOS] inhibitor) completely abolished the BBB disruption in lean mice, but only partially suppressed the BBB disruption in obese mice. Furthermore, a reduced matrix metallopeptidase (MMP)-9 activity and increased endothelial NOS accompanied with unchanged protein expression of tight/adherens junctions were found in cerebral cortex of obese mice. Conclusions Our findings suggest that obesity exacerbates early post-ischemic BBB disruption via a mechanism independent of MMP or NOS.
机译:摘要目的我们确定了肥胖对缺血后早期血脑屏障(BBB)破坏的影响。方法对雄性C57BL / 6J小鼠进行高脂饮食(HFD)或标准食物喂养16周。直接结扎大脑中动脉2 h诱发短暂性局灶性脑缺血。通过在再灌注3 h时测量伊文思蓝和荧光素钠外渗来评估早期的血脑屏障破坏。结果肥胖在再灌注过程中增加了脑血管舒张/血钾过多。 N(ω)-丙基-L-精氨酸和7-硝基吲唑(神经型一氧化氮合酶抑制剂)未能改变瘦小鼠的脑血管舒张/充血,但显着抑制了肥胖小鼠的脑血管舒张/充血。与瘦小鼠相比,肥胖小鼠的早期缺血后血脑屏障破坏的幅度明显更大。用N(ω)-丙基-L-精氨酸,7-硝基吲唑或N(ω)-丙基-L-精氨酸,7-硝基吲唑(非特异性一氧化氮合酶[NOS]抑制剂)进行局部治疗可完全消除BBB破坏。在瘦小鼠中,但是仅部分抑制肥胖小鼠中的BBB破坏。此外,在肥胖小鼠的大脑皮层中发现降低的基质金属肽酶(MMP)-9活性和增加的内皮NOS,同时紧密/粘附连接的蛋白表达未发生变化。结论我们的发现表明,肥胖症通过一种独立于MMP或NOS的机制加剧了缺血性BBB的早期破坏。

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