Chinese herbal medicine formula Tao Hong Si Wu decoction protects against cerebral ischemia-reperfusion injury via PI3K/Akt and the Nrf2 signaling pathway

被引:70
作者
Li, Li [1 ]
Yang, Na [2 ,3 ]
Nin, Ling [1 ]
Zhao, Zhilong [2 ,3 ]
Chen, Lu [1 ]
Yu, Jie [1 ]
Jiang, Zhuyun [1 ]
Zhong, Zhendong [2 ,3 ]
Zeng, Daiwen [2 ,3 ]
Qi, Hongyi [1 ]
Xu, Xiaoyu [1 ]
机构
[1] Southwest Univ, Coll Pharmaceut Sci, Chongqing 400716, Peoples R China
[2] Sichuan Acad Med Sci, Inst Lab Anim, Chengdu 610212, Sichuan, Peoples R China
[3] Sichuan Prov Peoples Hosp, Chengdu 610212, Sichuan, Peoples R China
关键词
Tao Hong Si Wu decoction; NF-E2-related factor 2; Phosphatidylinositol; 3-kinase/Akt; Neuroprotection; Ischemia-reperfusion; OXIDATIVE STRESS; Z-LIGUSTILIDE; RADICALS; HORMESIS; OXYGEN;
D O I
10.1007/s11418-014-0865-5
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The Chinese herbal medicine formula Tao Hong Si Wu decoction (THSWD) is traditionally used for the prevention and treatment of ischemic stroke. Transcription factor NF-E2-related factor 2 (Nrf2) regulates a battery of phase II enzymes and is known as the major mechanism of cellular defense against oxidative stress. The present study aimed to explore the potential effect of THSWD on the Nrf2 signaling pathway and the consequent effect during cerebral ischemia-reperfusion (I/R) injury. We found that THSWD reduced infarct volume and improved neurological function in a rat stroke model induced by middle cerebral artery occlusion (MCAO). Additionally, heme oxygenase 1 (HO-1), a key endogenous antioxidant enzyme regulated by Nrf2, was significantly further induced by THSWD in this in vivo model. In neuronal-like PC12 cells, THSWD remarkably up-regulated HO-1 expression and promoted Nrf2 nuclear translocation. Furthermore, phosphatidylinositol 3-kinase (PI3K)/Akt kinase was found to be involved in the upstream of Nrf2 regulation. In an in vitro oxygen-glucose deprivation/reperfusion (OGD-Rep) model, THSWD treatment significantly reduced cell death induced by OGD-Rep insult. Importantly, the protective action was attenuated while PI3K activity was inhibited by a specific inhibitor, LY294002, and the Nrf2 signaling pathway was blocked by antioxidant response element (ARE) decoy oligonucleotides. Collectively, these results demonstrated that THSWD exhibited notable neuroprotective properties in vitro and in vivo and activation of PI3K/Akt and the Nrf2 signaling pathway may be, at least in part, responsible for the protection. This study provides a better understanding of the molecular mechanism underlying the traditional use of the Chinese herbal medicine formula THSWD.
引用
收藏
页码:76 / 85
页数:10
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