中国实验动物学报
中國實驗動物學報
중국실험동물학보
ACTA LABORATORIUM ANIMALIS SCIENTIA SINICA
2014年
4期
41-46
,共6页
谢宸宸%罗勇%高祥%庞月珊%李满%汶海琪%陈瑞芳
謝宸宸%囉勇%高祥%龐月珊%李滿%汶海琪%陳瑞芳
사신신%라용%고상%방월산%리만%문해기%진서방
局灶脑缺血/再灌注%SDF-1α%血管再生%电针%大鼠
跼竈腦缺血/再灌註%SDF-1α%血管再生%電針%大鼠
국조뇌결혈/재관주%SDF-1α%혈관재생%전침%대서
Focal cerebral ischemia /reperfusion%SDF-1α%Angiogenesis%Electroacupuncture%Rat
目的:探讨电针促进局灶脑缺血/再灌注后缺血海马区血管再生的机制。方法180只雄性SD大鼠随机分为假手术组、模型组、电针组、CXCR4特异性拮抗剂AMD3100药物组、AMD3100+电针组。线栓法制备右侧局灶脑缺血/再灌注模型。取大鼠“百会”穴( GV 20)及左侧“四关”穴(合谷LI 4/太冲LR 3)为电针穴位,刺激时间为30 min/d。采用逆转录聚合酶链反应法( RT-PCR)检测各组缺血海马区SDF-1α、CXCR4 mRNA表达,免疫荧光双标法检测CD34+VEGFR2+EPCs源性血管的表达。结果与假手术组比较,模型组与电针组SDF-1α、CX-CR4 mRNA表达明显增高(P<0.05),其中电针组各时间点相对模型组增高更为显著(P<0.05)。 AMD3100+电针组缺血海马SDF-1α、CXCR4 mRNA表达在再灌注后1 d时明显高于电针组( P<0.05),但后逐渐下降,7 d时明显低于电针组( P<0.01)。与模型组比较,电针组再灌注3 d、7 d海马CD34+VEGFR2+EPCs源性血管表达明显增多( P<0.05)。与电针组比较,AMD3100+电针组再灌注后7 d CD34+VEGFR2+EPCs源性血管表达明显下降( P<0.01)。 CD34+VEGFR2+血管表达变化与SDF-1α的表达变化显著相关(R=0.784,P<0.01)。结论电针可通过上调局灶脑缺血/再灌注大鼠缺血海马区SDF-1α/CXCR4的表达,促进血管再生。
目的:探討電針促進跼竈腦缺血/再灌註後缺血海馬區血管再生的機製。方法180隻雄性SD大鼠隨機分為假手術組、模型組、電針組、CXCR4特異性拮抗劑AMD3100藥物組、AMD3100+電針組。線栓法製備右側跼竈腦缺血/再灌註模型。取大鼠“百會”穴( GV 20)及左側“四關”穴(閤穀LI 4/太遲LR 3)為電針穴位,刺激時間為30 min/d。採用逆轉錄聚閤酶鏈反應法( RT-PCR)檢測各組缺血海馬區SDF-1α、CXCR4 mRNA錶達,免疫熒光雙標法檢測CD34+VEGFR2+EPCs源性血管的錶達。結果與假手術組比較,模型組與電針組SDF-1α、CX-CR4 mRNA錶達明顯增高(P<0.05),其中電針組各時間點相對模型組增高更為顯著(P<0.05)。 AMD3100+電針組缺血海馬SDF-1α、CXCR4 mRNA錶達在再灌註後1 d時明顯高于電針組( P<0.05),但後逐漸下降,7 d時明顯低于電針組( P<0.01)。與模型組比較,電針組再灌註3 d、7 d海馬CD34+VEGFR2+EPCs源性血管錶達明顯增多( P<0.05)。與電針組比較,AMD3100+電針組再灌註後7 d CD34+VEGFR2+EPCs源性血管錶達明顯下降( P<0.01)。 CD34+VEGFR2+血管錶達變化與SDF-1α的錶達變化顯著相關(R=0.784,P<0.01)。結論電針可通過上調跼竈腦缺血/再灌註大鼠缺血海馬區SDF-1α/CXCR4的錶達,促進血管再生。
목적:탐토전침촉진국조뇌결혈/재관주후결혈해마구혈관재생적궤제。방법180지웅성SD대서수궤분위가수술조、모형조、전침조、CXCR4특이성길항제AMD3100약물조、AMD3100+전침조。선전법제비우측국조뇌결혈/재관주모형。취대서“백회”혈( GV 20)급좌측“사관”혈(합곡LI 4/태충LR 3)위전침혈위,자격시간위30 min/d。채용역전록취합매련반응법( RT-PCR)검측각조결혈해마구SDF-1α、CXCR4 mRNA표체,면역형광쌍표법검측CD34+VEGFR2+EPCs원성혈관적표체。결과여가수술조비교,모형조여전침조SDF-1α、CX-CR4 mRNA표체명현증고(P<0.05),기중전침조각시간점상대모형조증고경위현저(P<0.05)。 AMD3100+전침조결혈해마SDF-1α、CXCR4 mRNA표체재재관주후1 d시명현고우전침조( P<0.05),단후축점하강,7 d시명현저우전침조( P<0.01)。여모형조비교,전침조재관주3 d、7 d해마CD34+VEGFR2+EPCs원성혈관표체명현증다( P<0.05)。여전침조비교,AMD3100+전침조재관주후7 d CD34+VEGFR2+EPCs원성혈관표체명현하강( P<0.01)。 CD34+VEGFR2+혈관표체변화여SDF-1α적표체변화현저상관(R=0.784,P<0.01)。결론전침가통과상조국조뇌결혈/재관주대서결혈해마구SDF-1α/CXCR4적표체,촉진혈관재생。
Objective To explore the effect of electroacupuncture on CD 34 +VEGFR2 +endothelial progenitor cell (EPC)-derived vessels and stromal cell-derived factor-1α(SDF-1α)/CXCR4, and study its mechanism of promoting an-giogenesis in hippocampus after focal cerebral ischemia /reperfusion .Methods A total of 180 healthy male adult Sprague Dawley (SD) rats were randomly divided into sham operation (sham) group, model (I/R) group, electroacupuncture (I/RE) group, I/RE plus AMD3100 (A specific antagonist of CXCR4) group (I/REA) and AMD3100 (I/RA) group. The rats received filament occlusion of the right middle cerebral artery for 2 hours followed by reperfusion .Electroacupunc-ture was applied to “Baihui” (GV20)/“Siguan” (Hegu LI 4/Taichong LR 3) acupoints for 30 min, once a day.The mR-NA expression of SDF-1αand CXCR4 were detected by reverse transcription-polymerase chain reaction ( RT-PCR) .Double immunofluorescence was used to stain CD 34 +VEGFR2 +EPC-derived vessels.Results Compared with the sham group, the mRNA expressions of SDF-1αand CXCR4 were significantly upregulated in I/R and I/RE group ( P<0.05 ) , but that in I/RE group was more significantly increased than I/R group(P<0.05).In addition, the mRNA expression of SDF-1αand CXCR4 were highly increased on day 1 in the I/REA group than that of I/RE group, but decreased than that of I/RE group on day 7 after reperfusion (P<0.01).CD34 +VEGFR2 +EPCs-derived vessels were obviously increased on 3d and 7d in the I/RE group compared with that of the I/R group, and significantly decreased on 7d in the I/REA group compared with that of the I/RE group ( P<0.01) .Conclusions Electroacupuncture can effectively promote an-giogenesis through upregulating the expression of SDF-1αand CXCR4 in rat ischemic hippocampus after focal cerebral is-chemia/reperfusion.