ERK2和PI-3K在小柴胡汤抗大鼠肝纤维化中的表达  被引量:9

Xiaochaihu Decoction treats liver fibrosis in rats by regulating expression of ERK2 and PI-3K

在线阅读下载全文

作  者:李晋[1] 徐尚福[2] 罗果[1] 白国辉[1] 

机构地区:[1]遵义医学院医学与生物学研究中心,贵州遵义563000 [2]遵义医学院基础药理省部共建教育部重点实验室/药理学教研室,贵州遵义563000

出  处:《中成药》2014年第11期2238-2242,共5页Chinese Traditional Patent Medicine

基  金:国家自然科学基金(81360661);贵州省科学技术基金(黔科合J字LKZ[2010]43号)

摘  要:目的观察小柴胡汤对肝纤维化大鼠肝组织细胞外信号调节激酶2(ERK2)、磷酸肌醇-3激酶(PI-3K)表达的影响,探讨小柴胡汤治疗肝纤维化的分子机制。方法皮下注射10%四氯化碳制备大鼠肝纤维化模型,第9周开始四氯化碳给药同时给予小柴胡汤灌胃治疗6周。通过血清生化检测反映肝脏功能;HE染色法观察肝组织病理学变化;免疫组织化学方法观察肝组织α-平滑肌肌动蛋白(α-smooth muscle actin,α-SMA)的表达,以反映肝星状细胞的活化情况;Real time RT-PCR观察ERK2、PI-3K mRNA的表达。结果与模型组相比,小柴胡汤中、高剂量组在血清学和组织学上均有明显改善,肝组织ERK2、PI-3K mRNA的表达明显减少,具有统计学意义。结论小柴胡汤抗四氯化碳诱导大鼠肝纤维化作用可能与干预Ras/ERK和PI-3K信号通路有关。AIM To observe the effect of Xiaochaihu Decoction on the expression of extracellular signal-regulated kinase 2 (ERK2) and phosphoinositide-3 kinase (PI-3 K) in rat with hepatic fibrosis and to explore their molecular mechanism.METHODS Liver fibrosis in rats was induced by subcutaneous injection of 10% CCl4.Rats were then treated with oral Xiaochaihu Decoction for six weeks starting from the ninth week.Liver function was tested by serum biochemical reaction.Liver tissue was analyzed by HE staining.α-smooth muscle actin was observed by immunohistochemistry to reflect the activation of hepatic stellate cells.The expression of ERK2 and PI-3K was measured by real time RT-PCR.RESULTS Compared with the model group,the middle and high dose of Xiaochaihu Decoction groups significantly improved in serology and histology.They obviously reduced the expression of ERK2 and PI-3K with statistical significance.CONCLUSION Xiaochaihu Decoction in the treatment of CCl4-induced liver fibrosis may be related to the intervention in Ras/ERK and PI-3K signaling pathway.

关 键 词:肝纤维化 小柴胡汤 细胞外信号调节激酶2 (ERK2) 磷酸肌醇-3激酶(PI-3K) 

分 类 号:R966[医药卫生—药理学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象