Wang Wei-Wei, Han Jian-Hong, Wang Lin, Bao Tian-Hao
Department of Cardiology, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, PR China; Key Laboratory of Stem Cells and Regenerative Medicine, Institute of Molecular and Clinical Medicine, Kunming Medical University, Kunming, Yunnan, PR China; Department of Anatomy and Development Biology, Monash University, Clayton, vic 3800, Australia.
The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, PR China.
Iran J Basic Med Sci. 2017 Mar;20(3):272-279. doi: 10.22038/IJBMS.2017.8355.
Scutellarin, a flavonoid extracted from the medicinal herb Erigeron breviscapus Hand-Mazz, protects neurons from damage and inhibits glial activation. Here we examined whether scutellarin may also protect neurons from hypoxia-induced damage.
Mice were exposed to hypoxia for 7 days and then administered scutellarin (50 mg/kg/d) or vehicle for 30 days Cognitive impairment in the two groups was assessed using the Morris water maze test, cell proliferation in the hippocampus was compared using 5-bromo-2-deoxyuridine (BrdU) immunohistochemistry, and hippocampal levels of nestin and neuronal class III β-tubulin (Tuj-1) were measured using Western blotting. These results were validated in vitro by treating cultured neural stem cells (NSCs) with scutellarin (30 μM).
Treating mice with scutellarin shortened escape times and increased the number of platform crossings, it increased the number of BrdU-positive proliferating cells in the hippocampus, and it up-regulated expression of nestin and Tuj-1. Treating NSC cultures with scutellarin increased the number of proliferating cells and the proportion of cells differentiating into neurons instead of astrocytes. The increase in NSC proliferation was associated with phosphorylation of extracellular signal-regulated kinase (ERK) 1/2, while neuronal differentiation was associated with altered expression of differentiation-related genes.
Scutellarin may alleviate cognitive impairment in a mouse model of hypoxia by promo-ting proliferation and neuronal differentiation of NSCs.
灯盏花素是从药用植物短葶飞蓬中提取的一种黄酮类化合物,可保护神经元免受损伤并抑制胶质细胞活化。在此,我们研究了灯盏花素是否也能保护神经元免受缺氧诱导的损伤。
将小鼠暴露于缺氧环境7天,然后给予灯盏花素(50毫克/千克/天)或赋形剂,持续30天。使用莫里斯水迷宫试验评估两组小鼠的认知障碍,通过5-溴-2-脱氧尿苷(BrdU)免疫组织化学比较海马体中的细胞增殖情况,并使用蛋白质免疫印迹法测量海马体中巢蛋白和神经元III类β-微管蛋白(Tuj-1)的水平。通过用灯盏花素(30微摩尔)处理培养的神经干细胞(NSCs),在体外验证了这些结果。
用灯盏花素治疗小鼠可缩短逃避时间并增加穿越平台的次数,增加海马体中BrdU阳性增殖细胞的数量,并上调巢蛋白和Tuj-1的表达。用灯盏花素处理NSC培养物可增加增殖细胞的数量以及分化为神经元而非星形胶质细胞的细胞比例。NSC增殖的增加与细胞外信号调节激酶(ERK)1/2的磷酸化有关,而神经元分化与分化相关基因的表达改变有关。
灯盏花素可能通过促进NSCs的增殖和神经元分化来减轻缺氧小鼠模型中的认知障碍。