中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2010年
9期
869-872
,共4页
王艺东%施晓耕%黎祥喷%谢芬%彭英
王藝東%施曉耕%黎祥噴%謝芬%彭英
왕예동%시효경%려상분%사분%팽영
脑梗死%肾性高血压%基因芯片
腦梗死%腎性高血壓%基因芯片
뇌경사%신성고혈압%기인심편
Cerebral infarction%Renovascular hypertension%Gene chip
目的 利用基因芯片技术研究肾性高血压大鼠脑梗死后期梗死灶边缘区皮层基因表达谱的改变及其意义.方法 利用双肾双夹法复制肾性高血压大鼠模型,再采用线栓法复制成大脑中动脉闭塞模型,并设置假手术组,术后7 d取梗死灶边缘区域脑皮层,提取RNA,经过荧光标记后与含5705个基因的oligo芯片进行杂交、扫描,采集图像,经数据分析筛选出差异表达的基因.结果 差异表达基因共197个(包括表达序列标签12个),其中表达上调174个,下调23个.12类功能分组的基因均有上调,下调的基因仅包括运输、转录调控、信号、应激反应、代谢和细胞粘附组的基因.12类功能分组中有17个差异表达基因尚未有文献报道与脑缺血/梗死相关.结论 脑梗死后期基因表达仍然非常活跃,预示着损伤与修复的分子机制和可能的治疗靶点.
目的 利用基因芯片技術研究腎性高血壓大鼠腦梗死後期梗死竈邊緣區皮層基因錶達譜的改變及其意義.方法 利用雙腎雙夾法複製腎性高血壓大鼠模型,再採用線栓法複製成大腦中動脈閉塞模型,併設置假手術組,術後7 d取梗死竈邊緣區域腦皮層,提取RNA,經過熒光標記後與含5705箇基因的oligo芯片進行雜交、掃描,採集圖像,經數據分析篩選齣差異錶達的基因.結果 差異錶達基因共197箇(包括錶達序列標籤12箇),其中錶達上調174箇,下調23箇.12類功能分組的基因均有上調,下調的基因僅包括運輸、轉錄調控、信號、應激反應、代謝和細胞粘附組的基因.12類功能分組中有17箇差異錶達基因尚未有文獻報道與腦缺血/梗死相關.結論 腦梗死後期基因錶達仍然非常活躍,預示著損傷與脩複的分子機製和可能的治療靶點.
목적 이용기인심편기술연구신성고혈압대서뇌경사후기경사조변연구피층기인표체보적개변급기의의.방법 이용쌍신쌍협법복제신성고혈압대서모형,재채용선전법복제성대뇌중동맥폐새모형,병설치가수술조,술후7 d취경사조변연구역뇌피층,제취RNA,경과형광표기후여함5705개기인적oligo심편진행잡교、소묘,채집도상,경수거분석사선출차이표체적기인.결과 차이표체기인공197개(포괄표체서렬표첨12개),기중표체상조174개,하조23개.12류공능분조적기인균유상조,하조적기인부포괄운수、전록조공、신호、응격반응、대사화세포점부조적기인.12류공능분조중유17개차이표체기인상미유문헌보도여뇌결혈/경사상관.결론 뇌경사후기기인표체잉연비상활약,예시착손상여수복적분자궤제화가능적치료파점.
Objective To analyze the gene expression profiling in the periinfarct cortex in the late stage after stroke onset in renovascular hypertensive rats (RHRs) with gene chip technology.Methods RHRs were induced by the method of Goldblatt's 2k2c operation. Cerebral infarction was also induced by permanent middle cerebral artery occlusion (pMCAO) in RHRs. Sham-operated group was established as controls. Total RNA was extracted from the perinfarct cerebral cortex in injured hemisphere 7 d after pMCAO, and the RNA was performed fluorescence labeling, followed by hybridization with 5705 oligo chips. And then, scanning was performed; the data was collected and chosen for microarray analysis using oligonucleotide arrays. Resuits In total, 197 genes were expressed differentially, including 174 genes up-regulated expression and 23 genes down-regulated expression. The up-regulated genes were distributed among all 12 functional categories; the down-regulated genes were distributed only in the categories of transport, transcription regulator, signal,response to stress, metabolism and cell adhesion. Among the 12 functional categories, only 17differentially expressed genes were not previously reported to be associated with brain ischemia/infarction. Conelusion Active gene expression at late stage of cerebral infarction may imply the molecular mechanisms of injury or repair, being the targets of therapeutic intervention.