資源描述:
《缺氧缺血性腦損傷后豐富環(huán)境刺激對大鼠海馬ca1區(qū)神經(jīng)元凋亡的影響》由會員上傳分享,免費(fèi)在線閱讀,更多相關(guān)內(nèi)容在工程資料-天天文庫。
1、缺氧缺血性腦損傷后豐富環(huán)境刺激對大鼠海馬CA1區(qū)神經(jīng)元凋亡的影響宋遠(yuǎn)見1,裴冬生1,孫亞峰1,張芳1,張兆成2,劉紅芝1(1徐州醫(yī)學(xué)院基礎(chǔ)學(xué)院,江蘇徐州221004;2徐州市中小學(xué)生衛(wèi)生保健所,徐州221002)提要:目的 觀察豐富環(huán)境刺激對缺氧缺血性腦損傷(hypoxic-ischemicbraindamage,HIBD)新生大鼠海馬CA1區(qū)神經(jīng)元的影響。方法 取健康7日齡SD大鼠90只,隨機(jī)分為3組:①正常對照組:30只,不建立模型,不刺激。②缺氧缺血非刺激組:30只,采用Sale法建立缺氧缺血性腦損傷模型,但不給豐富環(huán)境刺激。③豐富環(huán)境刺激組:30只,建立缺氧缺血性腦損傷模型,術(shù)后豐
2、富環(huán)境刺激(2h/次,1次/d),共20d。分別在缺氧缺血后第3天和20天時各組隨機(jī)選10只,斷頭取腦,分別采用免疫印跡和焦油紫染色的方法檢測大鼠腦缺氧缺血后海馬CA1區(qū)JNK1/2和Bad(ser128)的磷酸化和神經(jīng)元凋亡情況。結(jié)果?、倥c正常對照組比較,缺血非刺激組腦缺氧缺血后第3天腦組織中JNK1/2和Bad(ser128)的磷酸化程度顯著增高(P<0.05);第20天海馬神經(jīng)元損傷非常嚴(yán)重(P<0.05)。②豐富環(huán)境刺激組相對缺血非刺激組JNK1/2和Bad(ser128)磷酸化有所降低(P<0.05);海馬神經(jīng)元損傷明顯減輕(P<0.05)。結(jié)論 豐富環(huán)境刺激可以促進(jìn)缺氧缺血性腦
3、損傷恢復(fù),減少海馬CA1區(qū)神經(jīng)元損傷,降低其中JNK1/2和Bad(ser128)的磷酸化程度是可能的機(jī)制之一。關(guān)鍵詞:缺氧缺血性腦損傷;豐富環(huán)境;海馬;JNK1/2;Bad(ser128)中圖法分類號:R72 文獻(xiàn)標(biāo)識碼:AEffectsofenrichedenvironmentalinterventiononcellsapoptosisofCA1regionduringhypoxia-ischemicbraindamageinrathippocampusSONGYuan-jian1,PEIDong-sheng1,SUNYa-feng1,ZHANGFang1,ZHANGZhao-che
4、ng2,LIUHong-zhi1(1SchoolofBasicMedicalSciencesofXuzhouMedicalCollege,Xuzhou221002,China;2HealthcareagencyofXuzhouprimaryandmiddleschoolstudents,Xuzhou221002,China)Abstract:ObjectiveToobservethetheenrichedenvironmentalinterventiononcellapoptosissinhippocampalCA1regionafterhypoxia-ischemicbraindamag
5、e(HIBD)inneonatalrats.Methods90healthySD7-day-oldratswererandomlydividedintothreegroups:①Controlgroup:30rats,nottobeestablishedhypoxic-ischemicbraininjurymodel,nottobestimulatedbyenrichedenvironment.②Non-stimulatedgroup:30rats,tobeestablishedmodelebutnottobestimulated.③Stimulatedgroup:30rats,tobee
6、stablishedmodelbeforeenrichedenvironmentalstimulation(2h/times,1/d)for20days.10ratswereselectedfromeachgrouponthethird3rddayandthetwentieth20thdayafterHypoxiaischemiaandthenthebrainsoweredecapitatedtodetectedthephosphorylationofJNK1/2andBad(ser128)inCA1regionbyWesternblotandneuronsinjurybyCreslyvi
7、olet-strained.Results①ThephosphorylationlevelofJNK1/2andBad(ser128)onthethird3rddayinnon-stimulatedgroupsignificantlyhigherincreasedthanincomparedwithcontrolgroup(P<0.05);InjuryApoptosisofcellsOrcellloss?inhippoc