神经损伤与功能重建
神經損傷與功能重建
신경손상여공능중건
NEURAL INJURY AND FUNCTIONAL RECONSTRUCTION
2014年
2期
87-91
,共5页
王倩%熊永洁%张苏明%甘莉%李珍
王倩%熊永潔%張囌明%甘莉%李珍
왕천%웅영길%장소명%감리%리진
神经干细胞%细胞活性%氧糖剥夺%模型
神經榦細胞%細胞活性%氧糖剝奪%模型
신경간세포%세포활성%양당박탈%모형
neural stem cells%cell viability%oxygen glucose deprivation%model
目的:建立离体神经干细胞(NSCs)氧糖剥夺(OGD)模型,并观察缺氧、缺糖等不同培养条件对NSCs存活和增殖的影响。方法:体外培养小鼠NSCs,制备OGD模型。将NSCs分为OGD组和正常组,每组分别干预2、4、6、8、10 h。采用MTT法检测OGD干预不同时间对NSCs活性的影响。通过MTT法观察正常培养、单独缺氧、单独缺糖、缺氧缺糖、高糖各组干预8 h对NSCs活性的影响。结果:OGD组干预8、10 h的NSCs OD值低于相应时点的正常组,差异有统计学意义(<0.05)。单独缺氧、单独缺糖、缺氧缺糖、高糖培养组的NSCs OD值均低于正常对照组(<0.05)。单独缺糖、高糖培养组与氧糖剥夺组的NSCs OD值比较,差异无统计学意义。结论:OGD≥8 h对NSCs造成明显的损伤。缺糖是OGD模型造成NSCs损伤的主要因素。葡萄糖浓度是影响NSCs存活和增殖的关键培养条件。
目的:建立離體神經榦細胞(NSCs)氧糖剝奪(OGD)模型,併觀察缺氧、缺糖等不同培養條件對NSCs存活和增殖的影響。方法:體外培養小鼠NSCs,製備OGD模型。將NSCs分為OGD組和正常組,每組分彆榦預2、4、6、8、10 h。採用MTT法檢測OGD榦預不同時間對NSCs活性的影響。通過MTT法觀察正常培養、單獨缺氧、單獨缺糖、缺氧缺糖、高糖各組榦預8 h對NSCs活性的影響。結果:OGD組榦預8、10 h的NSCs OD值低于相應時點的正常組,差異有統計學意義(<0.05)。單獨缺氧、單獨缺糖、缺氧缺糖、高糖培養組的NSCs OD值均低于正常對照組(<0.05)。單獨缺糖、高糖培養組與氧糖剝奪組的NSCs OD值比較,差異無統計學意義。結論:OGD≥8 h對NSCs造成明顯的損傷。缺糖是OGD模型造成NSCs損傷的主要因素。葡萄糖濃度是影響NSCs存活和增殖的關鍵培養條件。
목적:건립리체신경간세포(NSCs)양당박탈(OGD)모형,병관찰결양、결당등불동배양조건대NSCs존활화증식적영향。방법:체외배양소서NSCs,제비OGD모형。장NSCs분위OGD조화정상조,매조분별간예2、4、6、8、10 h。채용MTT법검측OGD간예불동시간대NSCs활성적영향。통과MTT법관찰정상배양、단독결양、단독결당、결양결당、고당각조간예8 h대NSCs활성적영향。결과:OGD조간예8、10 h적NSCs OD치저우상응시점적정상조,차이유통계학의의(<0.05)。단독결양、단독결당、결양결당、고당배양조적NSCs OD치균저우정상대조조(<0.05)。단독결당、고당배양조여양당박탈조적NSCs OD치비교,차이무통계학의의。결론:OGD≥8 h대NSCs조성명현적손상。결당시OGD모형조성NSCs손상적주요인소。포도당농도시영향NSCs존활화증식적관건배양조건。
ObjectiveTo establish a oxygen-glucose deprivation (OGD) model of neural stem cells (NSCs) and to investigate the effects of oxygen deprivation, glucose deprivation, OGD and high glucose on the survival and proliferation of NSCs culture respectively. Methods:The NSCs were separated from cortices of fetal mice and i-dentified. For the establishment of OGD, the NSCs were cultured in glucose-free DMEM and placed in a modular anaerobic chamber. The NSCs incubated in a normal condition were used as a control group. Both the cells in the control and OGD groups were incubated for different time durations (2 h, 4 h, 6 h, 8 h, 10 h). MTT assay was used to detect the effects of OGD on the survival and proliferation of NSCs. Besides, the NSCs were randomly as-signed into the control 8h group, oxygen deprivation 8 h group, glucose deprivation 8 h group, OGD 8 h group and high glucose 8 h group, and the cell viabilities were measured with MTT assay. Results:Compared to the nor-mal condition, the cell viabilities of OGD group were decreased at the time points of 8 h and 10 h significantly ( <0.05). The cell viabilities of oxygen deprivation 8h group, glucose deprivation 8h group and high glucose 8 h group were decreased when compared to control 8h group(all <0.05). There was no significant difference among glucose deprivation 8 h group, OGD 8 h group and high glucose 8 h group. Conclusion:The growth of NSCs was decreased significantly with OGD for 8 h or longer. In the model of OGD, low glucose concentrations might be the major detrimental factor for NSCs and the glucose concentration play an important role in the survival and proliferation of NSCs.