经鼻导入rhG-CSF后脑梗死大鼠内源性神经干细胞的增殖与迁移  被引量:3

Proliferation and migration of neural stem cells in SVZ after cerebral infarction in rats given rhG-CSF intranasally

在线阅读下载全文

作  者:何美清 刘喜梅 孙保亮[2] 

机构地区:[1]山东省泰山慢性病医院,山东泰安271000 [2]泰山医学院附属医院

出  处:《山东医药》2009年第8期21-23,共3页Shandong Medical Journal

基  金:国家自然科学基金资助项目(30770759);泰安市科技发展计划项目(20064019)

摘  要:目的探讨人重组粒细胞集落刺激因子(rhG-CSF)经鼻靶向中枢给药对脑梗死大鼠内源性神经干细胞增殖与迁移的调节作用。方法线栓法制作大脑中动脉阻塞模型(MCAO),皮下或鼻腔给予rhG-CSF(60μg/kg)。运用5-溴脱氧尿苷嘧啶(BrdU)标记及免疫组织化学法检测局灶性脑梗死大鼠室管膜及脑室下层(SVZ)神经干细胞的增殖。结果正常组及假手术对照组大鼠SVZ区域散在少量BrdU阳性细胞;术后7 d和14d,脑梗死组大鼠SVZ区BrdU阳性细胞数明显增加;rhG-CSF组BrdU阳性细胞数进一步增加;经鼻给药组的BrdU阳性细胞数明显高于相应时间点的皮下用药组(P<0.01)。结论rhG-CSF鼻腔给药可以促进脑梗死后大鼠内源性神经干细胞的增殖和靶向迁移。Objective To investigate the proliferation and transference of endogenous neural stem cells (NSCs) in subependymal and subventricular zone (SVZ) in cerebral infarct (CI) rats given rhG-CSF intranasally. Methods Middle cerebral artery occlusion (MCAO) animal model was established by nylon strand, followed by reperfusion 2 hours later. rhG-CSF was used via subcutaneous or intranasal pathway. Rats were sacrificed at the 7th and 14th day after MCAO. Bromodeoxyuridine (BrdU) labeling method and immunohistochemical staining was used to identify the proliferation of neuronal stem cells. The processes of transference of NSCs in SVZ were observed under light microscope, and the data was analyzed statistically. Results Few BrdU cells had survived in SVZ in normal and sham group. The number of BrdU cells obviously increased after MCAO, up-regulated further after given rhG-CSF, and intranasal group 〉 subcutaneous group 〉 MCAO group (P 〈 0.01 ). Conclusion rhG-CSF given intranasally stimulates the proliferation of endogenous NSCs in SVZ in CI rats. And the proliferative cells trend to migrate from the proliferative zone to the target area.

关 键 词:粒细胞集落刺激因子 重组 梗塞 大脑中动脉 干细胞 投药 鼻内 

分 类 号:R743[医药卫生—神经病学与精神病学]

 

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