山西医药杂志
山西醫藥雜誌
산서의약잡지
SHANXI MEDICAL JOURNAL
2014年
1期
24-26
,共3页
王昆鹏%朱宏%王键%蔡大升%汤如荣
王昆鵬%硃宏%王鍵%蔡大升%湯如榮
왕곤붕%주굉%왕건%채대승%탕여영
缺氧缺血 ,脑%小鼠%肿瘤坏死因子α
缺氧缺血 ,腦%小鼠%腫瘤壞死因子α
결양결혈 ,뇌%소서%종류배사인자α
Hypoxia-ischemia,brain%Mouse%Tumor necrosis factor-alpha
目的:研究γ-促分泌酶抑制剂 MW167阻断Notch信号对脑缺血再灌注小鼠海马肿瘤坏死因子-α(TNF-α)表达的影响。方法72只昆明小鼠分为假手术组(Sham ,8只)、γ-促分泌酶抑制剂组(MW167,32只)、缺血再灌注组(I/R ,32只)。γ-促分泌酶抑制剂组和I/R组依据缺血后再灌注的不同时间点再细分为1、3、7、14 d 4个亚组。应用免疫组织化学法、蛋白印迹法检测各组小鼠海马TNF-α蛋白的表达。结果免疫组织化学和蛋白印迹法结果发现,缺血处理后的各个时间点,TNF-α表达持续增高,与假手术组相比差异有统计学意义(P<0.01);与相同时间点的缺血组比较,MW167组的 TNF-α蛋白阳性表达明显降低(P<0.05)。结论调节炎性因子TNF-α蛋白的表达可能是Notch信号通路参与脑缺血再灌注损伤的机制之一。
目的:研究γ-促分泌酶抑製劑 MW167阻斷Notch信號對腦缺血再灌註小鼠海馬腫瘤壞死因子-α(TNF-α)錶達的影響。方法72隻昆明小鼠分為假手術組(Sham ,8隻)、γ-促分泌酶抑製劑組(MW167,32隻)、缺血再灌註組(I/R ,32隻)。γ-促分泌酶抑製劑組和I/R組依據缺血後再灌註的不同時間點再細分為1、3、7、14 d 4箇亞組。應用免疫組織化學法、蛋白印跡法檢測各組小鼠海馬TNF-α蛋白的錶達。結果免疫組織化學和蛋白印跡法結果髮現,缺血處理後的各箇時間點,TNF-α錶達持續增高,與假手術組相比差異有統計學意義(P<0.01);與相同時間點的缺血組比較,MW167組的 TNF-α蛋白暘性錶達明顯降低(P<0.05)。結論調節炎性因子TNF-α蛋白的錶達可能是Notch信號通路參與腦缺血再灌註損傷的機製之一。
목적:연구γ-촉분비매억제제 MW167조단Notch신호대뇌결혈재관주소서해마종류배사인자-α(TNF-α)표체적영향。방법72지곤명소서분위가수술조(Sham ,8지)、γ-촉분비매억제제조(MW167,32지)、결혈재관주조(I/R ,32지)。γ-촉분비매억제제조화I/R조의거결혈후재관주적불동시간점재세분위1、3、7、14 d 4개아조。응용면역조직화학법、단백인적법검측각조소서해마TNF-α단백적표체。결과면역조직화학화단백인적법결과발현,결혈처리후적각개시간점,TNF-α표체지속증고,여가수술조상비차이유통계학의의(P<0.01);여상동시간점적결혈조비교,MW167조적 TNF-α단백양성표체명현강저(P<0.05)。결론조절염성인자TNF-α단백적표체가능시Notch신호통로삼여뇌결혈재관주손상적궤제지일。
Objective To investigate the effect of the blockage of Notch pathway by γ-secretase inhibitor MW167 on the expression of tumor necrosis factor-α (TNF-α) in hippocampus of cerebral ischemia-reperfusion mice .Methods Seventy-two kunming mice were randomly divided into the sham group (Sham ,n= 8) ,γ-se-crataseinhibitorgroup (MW167,n= 32) and ischemia-reperfusion group (I/R,n= 32).Animals from the MW167 and I/R groups were divided into subgroups based on their execution time after reperfusion (1 ,3 ,7 ,14 d) .The expression of TNF-αin hippocampus of all groups was examined by immunochemistry and Western Blot-ting .Results Compared to sham group ,the expression of TNF-αin hippocampus in MW167 and I/R group in-creased significantly at all time points after ischemia (P<0.01);at the same time point after ischemia ,the expres-sion of TNF-αin MW167 group was significantly lower than that of I/R group (P<0.05) .Conclusion One of the mechanisms of cerebral ischemia-reperfusion injury in which Notch signaling pathway was involved might be regulating the expression of TNF-α.