4.5 Article

Qingda granule exerts neuroprotective effects against ischemia/reperfusion-induced cerebral injury via lncRNA GAS5/miR-137 signaling pathway

期刊

INTERNATIONAL JOURNAL OF MEDICAL SCIENCES
卷 18, 期 7, 页码 1687-1698

出版社

IVYSPRING INT PUBL
DOI: 10.7150/ijms.53603

关键词

Qingda granule; ischemic stroke; lncRNA GAS5; miR-137; neuronal apoptosis

资金

  1. National Natural Science Foundation of China [81774135]
  2. Fujian Province Natural Science Foundation [2019J01357, 2018J01886]
  3. Science and Technology Major Project of Fujian Province [2019YZ014004]
  4. Science and technology platform construction project of Fujian science and Technology Department [2015Y2001]

向作者/读者索取更多资源

The study demonstrates that Qingda granule has a significant neuroprotective effect on ischemic stroke, improving neurobehavioral deficits, reducing neuron loss, and inhibiting apoptosis. Furthermore, Qingda granule acts through modulating the lncRNA GAS5/miR-137 signaling pathway.
Background: Ischemic stroke is the second leading cause of death and disability worldwide, which needs to develop new pharmaceuticals for its prevention and treatment. Qingda granule (QDG), a traditional Chinese medicine formulation, could improve angiotensin II-induced brain injury and decrease systemic inflammation. In this study, we aimed to evaluate the neuroprotective effect of QDG against ischemia/reperfusion-induced cerebral injury and illustrate the potential mechanisms. Methods: The middle cerebral artery occlusion/reperfusion (MCAO/R) surgery in vivo and oxygen-glucose deprivation/reoxygenation (OGD/R) in vitro models were established. Ischemic infarct volume was quantified using magnetic resonance imaging (MRI). Neurobehavioral deficits were assessed using a five-point scale. Cerebral histopathology was determined by hematoxylin-eosin (HE) staining. Neuronal apoptosis was evaluated by TUNEL and immunostaining with NeuN antibodies. The protective effect of QDG on OGD/R-injured HT22 cells was determined by MTT assay and Hoechst 33258 staining. The expression of lncRNA GASS, miR-137 and apoptosis-related proteins were investigated in MCAO/R-injured rats and in OGD/R-injured HT22 cells using RT-qPCR and western blot analysis. Results: QDG significantly reduced the ischemic infarct volume, which was accompanied with improvements in neurobehavioral deficits. Additionally, QDG significantly ameliorated cerebral histopathological changes and reduced neuron loss in MCAO/R-injured rats. Moreover, QDG improved growth and inhibited apoptosis of HT22 cells injured by OGD/R in vitro. Finally, QDG significantly decreased the expression of lncRNA GASS, Bax and cleaved caspase3, whereas it increased miR-137 and BcI-2 expression in MCAO/R-injured rats and in OGD/R-injured HT22 cells. Conclusion: QDG plays a neuroprotective role in ischemic stroke via regulation of the lncRNA GAS5/miR-137 signaling pathway.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据