暨南大学学报(自然科学与医学版)
暨南大學學報(自然科學與醫學版)
기남대학학보(자연과학여의학판)
Journal of Jinan University (Natural Science & Medicine Edition)
2015年
5期
410-416
,共7页
齐俊冶%宋燕燕%周卓妍%蔡岳鞠%陈美苑%肖旭文%王兰秀
齊俊冶%宋燕燕%週卓妍%蔡嶽鞠%陳美苑%肖旭文%王蘭秀
제준야%송연연%주탁연%채악국%진미원%초욱문%왕란수
重组促红细胞生成素%脑室周围白质软化%胶质纤维酸性蛋白%缺血缺氧
重組促紅細胞生成素%腦室週圍白質軟化%膠質纖維痠性蛋白%缺血缺氧
중조촉홍세포생성소%뇌실주위백질연화%효질섬유산성단백%결혈결양
erythropoietin%white matter damage%glial fibrillary acidic protein%hypoxia-ische-mia
目的:探讨重组人促红细胞生成素(rhEPO)对3日龄大鼠缺氧缺血性脑白质损伤的胶质纤维酸性蛋白(GFAP)表达的影响.方法:150只3日龄(P3)SD 大鼠随机分为对照组,脑室周围白质软化(PVL)组和 rEPO 治疗组.于造模后1、7、21 d 对各组大鼠脑质量损伤百分比进行检测,造模后3、7、14、21 d 用免疫组织化学方法观察脑组织 GFAP 表达情况等来研究 EPO 对3日龄大鼠缺血缺氧性脑白质损伤的保护作用.结果:PVL 组和 rEPO 组的脑质量损伤%在各取样时间点均明显大于对照组(P <0.05),且 rEPO 组明显小于 PVL 组(P <0.05).HE 染色示 PVL组术后7 d 胼胝体结构疏松,术后21 d 可见侧脑室扩大明显;rEPO 组术后7 d 胼胝体结构基本正常,术后21 d 侧脑室仅稍微扩大.术后3 d PVL 组 GFAP 阳性表达增多(P <0.05),术后7 d rEPO 组和 PVL 组 GFAP 阳性表达均明显增多(P <0.05),且 PVL 组增多更为明显(P <0.05);术后14 d rEPO 组与 PVL 组 GFAP 阳性表达开始回落,但仍多于对照组(P <0.05),PVL 组阳性表达数仍然比 rEPO 组多(P <0.05),术后21 d 各组 GFAP 阳性表达数基本回落至正常水平.结论:脑白质损伤时 GFAP 阳性表达增加,rEPO 能减少脑白质损伤后 GFAP 阳性表达.
目的:探討重組人促紅細胞生成素(rhEPO)對3日齡大鼠缺氧缺血性腦白質損傷的膠質纖維痠性蛋白(GFAP)錶達的影響.方法:150隻3日齡(P3)SD 大鼠隨機分為對照組,腦室週圍白質軟化(PVL)組和 rEPO 治療組.于造模後1、7、21 d 對各組大鼠腦質量損傷百分比進行檢測,造模後3、7、14、21 d 用免疫組織化學方法觀察腦組織 GFAP 錶達情況等來研究 EPO 對3日齡大鼠缺血缺氧性腦白質損傷的保護作用.結果:PVL 組和 rEPO 組的腦質量損傷%在各取樣時間點均明顯大于對照組(P <0.05),且 rEPO 組明顯小于 PVL 組(P <0.05).HE 染色示 PVL組術後7 d 胼胝體結構疏鬆,術後21 d 可見側腦室擴大明顯;rEPO 組術後7 d 胼胝體結構基本正常,術後21 d 側腦室僅稍微擴大.術後3 d PVL 組 GFAP 暘性錶達增多(P <0.05),術後7 d rEPO 組和 PVL 組 GFAP 暘性錶達均明顯增多(P <0.05),且 PVL 組增多更為明顯(P <0.05);術後14 d rEPO 組與 PVL 組 GFAP 暘性錶達開始迴落,但仍多于對照組(P <0.05),PVL 組暘性錶達數仍然比 rEPO 組多(P <0.05),術後21 d 各組 GFAP 暘性錶達數基本迴落至正常水平.結論:腦白質損傷時 GFAP 暘性錶達增加,rEPO 能減少腦白質損傷後 GFAP 暘性錶達.
목적:탐토중조인촉홍세포생성소(rhEPO)대3일령대서결양결혈성뇌백질손상적효질섬유산성단백(GFAP)표체적영향.방법:150지3일령(P3)SD 대서수궤분위대조조,뇌실주위백질연화(PVL)조화 rEPO 치료조.우조모후1、7、21 d 대각조대서뇌질량손상백분비진행검측,조모후3、7、14、21 d 용면역조직화학방법관찰뇌조직 GFAP 표체정황등래연구 EPO 대3일령대서결혈결양성뇌백질손상적보호작용.결과:PVL 조화 rEPO 조적뇌질량손상%재각취양시간점균명현대우대조조(P <0.05),차 rEPO 조명현소우 PVL 조(P <0.05).HE 염색시 PVL조술후7 d 변지체결구소송,술후21 d 가견측뇌실확대명현;rEPO 조술후7 d 변지체결구기본정상,술후21 d 측뇌실부초미확대.술후3 d PVL 조 GFAP 양성표체증다(P <0.05),술후7 d rEPO 조화 PVL 조 GFAP 양성표체균명현증다(P <0.05),차 PVL 조증다경위명현(P <0.05);술후14 d rEPO 조여 PVL 조 GFAP 양성표체개시회락,단잉다우대조조(P <0.05),PVL 조양성표체수잉연비 rEPO 조다(P <0.05),술후21 d 각조 GFAP 양성표체수기본회락지정상수평.결론:뇌백질손상시 GFAP 양성표체증가,rEPO 능감소뇌백질손상후 GFAP 양성표체.
Aim:To explore the neuroprotection effects of recombinant human erythropoietin(rEPO) on 3 day-old neonatal rats with white matter damage.Methods:150 three day-old Sprague-Dawley(SD) rats were randomly divided into control,periventricular leukomalacia(PVL)and rEPO treatment groups (each group n =50).The brain weight and percentage of the brain damage were recorded at 1 d、7 d and 21 d post operation.Immunohistochemistry method was used to determine the changes of GFAP expres-sion levels in the brain at 3 d、7 d 、14 d and 21 d.Results:The percentage of brain damage in the rEPO and PVL groups was found to be significantly increased compared to the control group(P <0.05)at each sampling time point,but that of rEPO group was less than PVL group(P <0.05);Compared to the con-trol group,HE staining showed that in the rEPO group the structure of callosum was basically normal at 7 d post-operation but the lateral ventricles became mildly expanded at 21 d post-operation.However,a loose callosum structure and dilated lateral ventricles were observed at the same sampling time point in PVL group;The expression of GFAP in PVL group was found to be increased at 3 d post-operation(P <0.05).The expression of GFAP in both rEPO and PVL groups increased significantly compared to that of the control group 7 d after modeling,especially in PVL group(P <0.05).The expression of GFAP in both rEPO and PVL groups increased slightly but still higher than that of the control group(P <0.05),and GFAP expression level in PVL group was higher than that of rEPO group(P <0.05)14 d after modeling. At 21 d post-operation,the expression of GFAP in each group recovered to normal levels.Conclusion:The expression of GFAP increased after damage of the white matter.rEPO treatment can significantly re-duce the expression level of GFAP after the white matter damage.