Luo Yunxia, Chen Hansen, Tsoi Bun, Wang Qi, Shen Jiangang
Science and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangzhou, China.
School of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Front Pharmacol. 2021 Apr 15;12:653795. doi: 10.3389/fphar.2021.653795. eCollection 2021.
Danggui-Shayao-San (DSS) is a famous Traditional Chinese Medicine formula that used for treating pain disorders and maintaining neurological health. Recent studies indicate that DSS has neuroprotective effects against ischemic brain damage but its underlining mechanisms remain unclear. Herein, we investigated the neuroprotective mechanisms of DSS for treating ischemic stroke. Adult male Sprague-Dawley (S.D.) rats were subjected to 2 h of middle cerebral artery occlusion (MCAO) plus 22 h of reperfusion. Both ethanol extract and aqueous extract of DSS (12 g/kg) were orally administrated into the rats at 30 min prior to MCAO ischemic onset. We found that 1) ethanol extract of DSS, instead of aqueous extract, reduced infarct sizes and improved neurological deficit scores in the post-ischemic stroke rats; 2) Ethanol extract of DSS down-regulated the expression of the cleaved-caspase 3 and Bax, up-regulated bcl-2 and attenuated apoptotic cell death in the ischemic brains; 3) Ethanol extract of DSS decreased the production of superoxide and peroxynitrite; 4) Ethanol extract of DSS significantly down-regulated the expression of p67 but has no effect on p47 and iNOS statistically. 5) Ethanol extract of DSS significantly up-regulated the expression of SIRT1 in the cortex and striatum of the post-ischemic brains; 6) Co-treatment of EX527, a SIRT1 inhibitor, abolished the DSS's neuroprotective effects. Taken together, DSS could attenuate oxidative/nitrosative stress and inhibit neuronal apoptosis against cerebral ischemic-reperfusion injury via SIRT1-dependent manner.
当归芍药散(DSS)是一种著名的用于治疗疼痛性疾病和维持神经健康的中药方剂。最近的研究表明,DSS对缺血性脑损伤具有神经保护作用,但其潜在机制尚不清楚。在此,我们研究了DSS治疗缺血性中风的神经保护机制。成年雄性Sprague-Dawley(S.D.)大鼠接受2小时的大脑中动脉闭塞(MCAO)加22小时的再灌注。在MCAO缺血发作前30分钟,将DSS的乙醇提取物和水提取物(12克/千克)口服给予大鼠。我们发现:1)DSS的乙醇提取物而非水提取物可减少缺血性中风后大鼠的梗死面积并改善神经功能缺损评分;2)DSS的乙醇提取物下调缺血脑中裂解的半胱天冬酶3和Bax的表达,上调bcl-2并减轻凋亡细胞死亡;3)DSS的乙醇提取物减少超氧化物和过氧亚硝酸盐的产生;4)DSS的乙醇提取物显著下调p67的表达,但对p47和诱导型一氧化氮合酶在统计学上无影响;5)DSS的乙醇提取物显著上调缺血后大脑皮层和纹状体中SIRT1的表达;6)SIRT1抑制剂EX527的联合处理消除了DSS的神经保护作用。综上所述,DSS可通过SIRT1依赖性方式减轻氧化/亚硝化应激并抑制神经元凋亡,以对抗脑缺血再灌注损伤。