中国组织工程研究与临床康复
中國組織工程研究與臨床康複
중국조직공정연구여림상강복
JOURNAL OF CLINICAL REHABILITATIVE TISSUE ENGINEERING RESEARCH
2010年
36期
6837-6840
,共4页
姜红%许锋%周春清%李向红%舒志荣
薑紅%許鋒%週春清%李嚮紅%舒誌榮
강홍%허봉%주춘청%리향홍%서지영
促红细胞生成素%缺氧缺血性脑损伤%神经干细胞%巢蛋白%新生大鼠
促紅細胞生成素%缺氧缺血性腦損傷%神經榦細胞%巢蛋白%新生大鼠
촉홍세포생성소%결양결혈성뇌손상%신경간세포%소단백%신생대서
背景:巢蛋白是一种存在于神经干细胞的特异性抗原,在神经系统发生病变或损伤引起再生时广泛表达,因此巢蛋白表达常用作判定神经系统发生病变或损伤后能否促进神经再生的一种手段.目的:从神经再生和神经干细胞激活的角度,探讨外源性促红细胞生成素对新生鼠缺氧缺血性脑损伤后神经干细胞巢蛋白表达的影响.方法:结扎大鼠右侧颈总动脉和8%低氧暴露2 h制备新生大鼠缺氧缺血性脑损伤模型.对照组仅游离右侧颈总动脉,不予结扎和缺氧处理.干预组大鼠缺氧缺血后立即腹腔注射重组人促红细胞生成素5 000 IU/kg,1次/d,连用3 d.缺氧缺血性脑损伤组大鼠缺氧缺血后连续腹腔注射等量生理盐水溶液3d.每组随机取8只分别于术后4,7,14d处死.应用免疫组化方法和计算机图像分析技术检测不同时点海马齿状回巢蛋白标记阳性细胞的变化.结果与结论:各时点缺氧缺血性脑损伤组巢蛋白阳性细胞数较对照组增加(P<0.05);各时点干预组巢蛋白阳性细胞较对照组和缺氧缺血性脑损伤组均增加(P<0.05).3组大鼠海马齿状回区巢蛋白阳性细胞数均于术后7 d达高峰.结果提示早期给予重组入促红细胞生成素可促使新生鼠缺氧缺血性脑损伤后海马齿状回区巢蛋白表达增加,促进神经干细胞的增殖再生,在缺氧缺血性脑损伤后神经再生、修复中发挥一定的保护作用.
揹景:巢蛋白是一種存在于神經榦細胞的特異性抗原,在神經繫統髮生病變或損傷引起再生時廣汎錶達,因此巢蛋白錶達常用作判定神經繫統髮生病變或損傷後能否促進神經再生的一種手段.目的:從神經再生和神經榦細胞激活的角度,探討外源性促紅細胞生成素對新生鼠缺氧缺血性腦損傷後神經榦細胞巢蛋白錶達的影響.方法:結扎大鼠右側頸總動脈和8%低氧暴露2 h製備新生大鼠缺氧缺血性腦損傷模型.對照組僅遊離右側頸總動脈,不予結扎和缺氧處理.榦預組大鼠缺氧缺血後立即腹腔註射重組人促紅細胞生成素5 000 IU/kg,1次/d,連用3 d.缺氧缺血性腦損傷組大鼠缺氧缺血後連續腹腔註射等量生理鹽水溶液3d.每組隨機取8隻分彆于術後4,7,14d處死.應用免疫組化方法和計算機圖像分析技術檢測不同時點海馬齒狀迴巢蛋白標記暘性細胞的變化.結果與結論:各時點缺氧缺血性腦損傷組巢蛋白暘性細胞數較對照組增加(P<0.05);各時點榦預組巢蛋白暘性細胞較對照組和缺氧缺血性腦損傷組均增加(P<0.05).3組大鼠海馬齒狀迴區巢蛋白暘性細胞數均于術後7 d達高峰.結果提示早期給予重組入促紅細胞生成素可促使新生鼠缺氧缺血性腦損傷後海馬齒狀迴區巢蛋白錶達增加,促進神經榦細胞的增殖再生,在缺氧缺血性腦損傷後神經再生、脩複中髮揮一定的保護作用.
배경:소단백시일충존재우신경간세포적특이성항원,재신경계통발생병변혹손상인기재생시엄범표체,인차소단백표체상용작판정신경계통발생병변혹손상후능부촉진신경재생적일충수단.목적:종신경재생화신경간세포격활적각도,탐토외원성촉홍세포생성소대신생서결양결혈성뇌손상후신경간세포소단백표체적영향.방법:결찰대서우측경총동맥화8%저양폭로2 h제비신생대서결양결혈성뇌손상모형.대조조부유리우측경총동맥,불여결찰화결양처리.간예조대서결양결혈후립즉복강주사중조인촉홍세포생성소5 000 IU/kg,1차/d,련용3 d.결양결혈성뇌손상조대서결양결혈후련속복강주사등량생리염수용액3d.매조수궤취8지분별우술후4,7,14d처사.응용면역조화방법화계산궤도상분석기술검측불동시점해마치상회소단백표기양성세포적변화.결과여결론:각시점결양결혈성뇌손상조소단백양성세포수교대조조증가(P<0.05);각시점간예조소단백양성세포교대조조화결양결혈성뇌손상조균증가(P<0.05).3조대서해마치상회구소단백양성세포수균우술후7 d체고봉.결과제시조기급여중조입촉홍세포생성소가촉사신생서결양결혈성뇌손상후해마치상회구소단백표체증가,촉진신경간세포적증식재생,재결양결혈성뇌손상후신경재생、수복중발휘일정적보호작용.
BACKGROUND: Nestin is a specific antigen of neural stem cells which widely expressed in lesion of nervous system and brain regeneration.Thus,nestin expression is commonly used to assess whether lesion or damage of the nervous system can promote neural regeneration.OBJECTIVE: To investigate the effects of erythropoietin(EPO)on nestin expression in neural stem cells after hypoxia-ischemia brain damage(HIBD)in neonatal rats from the angles of neural regeneration and activation of neural stem cells.METHODS: HIBD model was established by ligation of the right common carotid artery along with 2-hour 8% hypoxia exposure in neonatal rats.The control group was not subjected to hypoxia-ischemia,and the right common carotid artery was dissociated.The treatment group received an intraperitoneal injection of recombinant human erythropoietin(rh-Epo,5 000 IU/kg)once a day for three days after hypoxia/ischemia,while the two other groups intraperitoneally received normal saline at the same time.In each group,rats were randomly executed immediately,at 4,7,14 days after operation(n = 8).The nestin expression in hippocampal dentate gyrus region was examined by immunohistochemical staining and image quantitative analysis respectively.RESULTS AND CONCLUSION: The number of nestin-positive cells was significantly increased in HIBD group compared to control group at all time points(P < 0.05),and it was also significantly increased in treatment group than the other two groups at all time points(P < 0.05).The numbers of nestin-positive cells in hippocampal dentate gyrus region were significantly increased,and peaked on day 7 after operation in the three groups.The results showed that exogenous rh-Epo could enhance the expression of nestin in hippocampal dentate gyrus region of neonatal rats with HIBD,and promote the proliferation of neural stem cells,rh-Epo plays an important role in the regeneration and repair of neurocytes damaged by hypoxia-ischemia.