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姜黄素的神经保护作用与脑缺血再灌注损伤中自噬和低氧诱导因子-1α之间相互作用的调节有关。

The neuroprotective effects of curcumin are associated with the regulation of the reciprocal function between autophagy and HIF-1α in cerebral ischemia-reperfusion injury.

作者信息

Hou Yang, Wang Jue, Feng Juan

机构信息

Department of Neurology, Shengjing Hospital of China Medical University, Shenyang, Liaoning 110004, People's Republic of China,

出版信息

Drug Des Devel Ther. 2019 Apr 9;13:1135-1144. doi: 10.2147/DDDT.S194182. eCollection 2019.

DOI:10.2147/DDDT.S194182
PMID:31040648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6461000/
Abstract

PURPOSE

The beneficial, neuroprotective effects of curcumin against ischemia-reperfusion injury have been demonstrated. In the present study, whether curcumin exerts neuroprotective effects associated with the inhibition of autophagy and hypoxia inducible factor-1α (HIF-1α) was investigated.

MATERIALS AND METHODS

PC12 cellular model of oxygen glucose deprivation/reperfusion (OGD/R) has been developed to mimic cerebral ischemia-reperfusion injury. Cell viability was evaluated using the CellTiter 96 AQueous One Solution Cell Proliferation Assay. Apoptosis was assessed using flow cytometry. The expression levels of HIF-1α and autophagy-associated proteins, LC3 and P62, were examined using Western blot. The autophagy flux was quantitatively estimated based on the number of autophagic compartments using fluorescence microscopy. In addition, 3-methyladenine (3-MA) was administered to PC12 cells to investigate how autophagy affects HIF-1α. Moreover, the inhibitory effects of HIF-1α on autophagy activation level were examined.

RESULTS

In this study, curcumin decreased the death and apoptosis of cells, and inhibited autophagy and HIF-1α under OGD/R conditions, consistent with 3-MA treatment or HIF-1α downregulation. Moreover, inhibition of autophagy caused a decrease in HIF-1α, and the attenuation of HIF-1α induced autophagy suppression under OGD/R conditions.

CONCLUSION

The results of this study showed that curcumin exerts neuroprotective effects against ischemia-reperfusion, which is associated with the regulation of the reciprocal function between autophagy and HIF-1α.

摘要

目的

姜黄素对缺血再灌注损伤的有益神经保护作用已得到证实。在本研究中,探讨了姜黄素是否通过抑制自噬和缺氧诱导因子-1α(HIF-1α)发挥神经保护作用。

材料与方法

建立氧糖剥夺/再灌注(OGD/R)的PC12细胞模型以模拟脑缺血再灌注损伤。使用CellTiter 96 AQueous One Solution细胞增殖检测试剂盒评估细胞活力。采用流式细胞术评估细胞凋亡。使用蛋白质免疫印迹法检测HIF-1α和自噬相关蛋白LC3及P62的表达水平。基于荧光显微镜下自噬区室的数量对自噬通量进行定量评估。此外,向PC12细胞中加入3-甲基腺嘌呤(3-MA)以研究自噬如何影响HIF-1α。此外,还检测了HIF-1α对自噬激活水平的抑制作用。

结果

在本研究中,姜黄素在OGD/R条件下可降低细胞死亡和凋亡,并抑制自噬和HIF-1α,这与3-MA处理或HIF-1α下调一致。此外,抑制自噬会导致HIF-1α减少,且在OGD/R条件下HIF-1α诱导的自噬抑制减弱。

结论

本研究结果表明,姜黄素对缺血再灌注具有神经保护作用,这与自噬和HIF-1α之间相互作用的调节有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/d37367507f36/dddt-13-1135Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/3d5472bcbd00/dddt-13-1135Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/eae45f7c7979/dddt-13-1135Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/16f5fab8dfee/dddt-13-1135Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/d1f3714e0202/dddt-13-1135Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/d37367507f36/dddt-13-1135Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/3d5472bcbd00/dddt-13-1135Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/eae45f7c7979/dddt-13-1135Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/16f5fab8dfee/dddt-13-1135Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/d1f3714e0202/dddt-13-1135Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/6461000/d37367507f36/dddt-13-1135Fig5.jpg

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