黄芩苷
TLR2型
肿瘤坏死因子α
小胶质细胞
缺血
炎症
体内
药理学
海马体
神经元
受体
TLR4型
Toll样受体
下调和上调
白细胞介素-1受体
医学
脑缺血
细胞因子
化学
内科学
生物
白细胞介素
神经科学
生物化学
高效液相色谱法
生物技术
色谱法
基因
先天免疫系统
作者
Li Hy,Yuan Zy,Yuegang Wang,Wan Hj,Jian Hu,Chai Ys,Fumin Lei,Xing Dm,Du Lj
出处
期刊:PubMed
日期:2012-05-01
卷期号:125 (9): 1586-93
被引量:43
摘要
Baicalin has a significant anti-inflammation effect and is widely used in the clinical treatment of stroke. Most of the studies of Toll-like receptor 2/4 (TLR2/4) during cerebral ischemia had defined their specific expressions in microglia in hippocampus tissue. To explore the targets of baicalin in stroke, we detected the expressions of TLR2/4 in vitro/vivo.By constructing a cerebral ischemia-reperfusion model in vivo and glucose oxygen deprivation model, we successfully induced neuron damage, then added baicalin and detected expressions of TLR2/4, nuclear factor-kB (NF-kB), tumor necrosis factor-alpha (TNFα), and interleukin-1β (IL-1β) in mRNA level and protein level.We found distinct upregulations of TLR2/4 and TNFα in both mRNA level and protein level in PC12 cells and primary neurons. Moreover, TLR2/4 and TNFα expressions were significantly higher in mice hippocampus treated with cerebral ischemia-reperfusion. Baicalin could downregulate the expressions of TLR2/4 and TNFα in the damaged cells and mice hippocampus effectively.Neurons could respond to the damage and activate the related signal pathway directly. TLR2/4 responsed to the damage and sent the signal to downstream factor TNFα through activating NF-kB. Baicalin could inhibit the inflammatory reaction in neuron damage and TLR might be its targets, which explained why baicalin could widely be used in the clinical treatment of stroke.
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