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小白菊内酯通过 Akt/GSK-3β通路减轻 PC12 细胞脑缺血再灌注损伤。

Parthenolide attenuates cerebral ischemia/reperfusion injury via Akt/GSK-3β pathway in PC12 cells.

机构信息

Department of Human Anatomy, Xi'an Medical University, Xi'an 710021, People's Republic of China.

Department of Human Anatomy, Xi'an Medical University, Xi'an 710021, People's Republic of China.

出版信息

Biomed Pharmacother. 2017 May;89:1159-1165. doi: 10.1016/j.biopha.2017.03.009. Epub 2017 Mar 24.

Abstract

Parthenolide (PN), a sesquiterpene lactone isolated from the herbal medicine feverfew (Tanacetum parthenium), was reported to possess neuroprotective activity. However, the neuroprotective effect of PN against cerebral ischemia/reperfusion (I/R) injury remains unclear. Therefore, the aim of the present study was to explore the neuroprotective effects of PN against oxygen-glucose deprivation (OGD)-induced apoptosis in PC12 cells and the underlying mechanisms. Our results demonstrated that PN ameliorated OGD/R-evoked neuronal injury and oxidative stress in PC12 cells. In addition, PN notably decreased HIF-1α expression, as well as inhibited apoptosis in PC12 cells after OGD/R. Furthermore, PN pretreatment significantly enhanced the phosphorylation of Akt and GSK-3β in PC12 cells exposed to OGD/R. In conclusion, the present study demonstrated that PN exhibits a neuroprotective effect against OGD/R through activation of the Akt/GSK-3β signaling pathway. Our findings suggest that PN has the potential to serve as a novel therapeutic agent for cerebral I/R injury.

摘要

小白菊内酯(PN)是从草药小白菊(Tanacetum parthenium)中分离得到的一种倍半萜内酯,具有神经保护活性。然而,PN 对脑缺血/再灌注(I/R)损伤的神经保护作用尚不清楚。因此,本研究旨在探讨 PN 对 PC12 细胞氧葡萄糖剥夺(OGD)诱导的细胞凋亡的神经保护作用及其机制。研究结果表明,PN 可改善 OGD/R 诱导的 PC12 细胞损伤和氧化应激。此外,PN 还显著降低了 OGD/R 后 PC12 细胞中 HIF-1α 的表达,并抑制了细胞凋亡。此外,PN 预处理可显著增强 OGD/R 暴露的 PC12 细胞中 Akt 和 GSK-3β 的磷酸化。综上所述,本研究表明 PN 通过激活 Akt/GSK-3β 信号通路对 OGD/R 发挥神经保护作用。我们的研究结果表明,PN 具有治疗脑 I/R 损伤的潜力。

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