酪氨酸激酶Fyn在大鼠腦出血后炎癥反應和細胞凋亡中的作用及機制研究
發(fā)布時間:2022-01-02 23:17
背景:細胞凋亡和炎癥反應是造成腦出血后繼發(fā)性腦損傷的重要因素,酪氨酸激酶Fyn介導的細胞凋亡和炎癥反應參與多種神經(jīng)系統(tǒng)疾病的實驗模型,如帕金森病、阿爾茨海默、抑郁癥等,但其在腦出血中的作用仍未可知。目的:探討酪氨酸激酶Fyn在大鼠腦出血后炎癥反應和細胞凋亡的作用及其潛在機制。方法:(1)基底節(jié)注入50μl自體血構建大鼠腦出血(intracerebral hemorrhage,ICH)模型。Western blot檢測酪氨酸激酶Fyn在大鼠腦出血后3h、6h、12h、24h、48h、72h的表達時間分布。(2)通過術前24h側腦室注射小干擾片段的方法抑制Fyn的表達并觀察小干擾片段抑制Fyn后對大鼠腦出血后神經(jīng)功能(Modified Neurological Severity Score,mNss)、腦水腫(腦水含量法)、腦組織形態(tài)學染色(H&E染色)結果及血腦屏障通透性(Evans Blue法)的影響。(3)Western blot檢測抑制Fyn后對大鼠ICH后腦組織中炎癥相關蛋白TNF-α、NF-κB、Caspase1、IL-1β和IL-18的影響;免疫熒光顯微鏡檢測髓過氧化...
【文章來源】:重慶醫(yī)科大學重慶市
【文章頁數(shù)】:60 頁
【學位級別】:碩士
【部分圖文】:
ICH后大鼠腦組織中Fyn的時間分布
重慶醫(yī)科大學碩士研究生學位論文22圖2-1驗證小干擾片段抑制Fyn表達的效果Figure2-1VerifytheeffectofsmallinterferingfragmentsonFynexpression.(A)WesternblotanalysisshowinglevelsofFynandP-FynproteinweredecreasedbyFynsiRNA.(B)Fynexpressionlevelsatdifferenttimepoints.Proteinlevelswerenormalizedtoβ-actin.(C)P-Fynexpressionlevelsatdifferenttimepoints.ProteinlevelswerenormalizedtoFyn.Errorbarsrepresentmean±SD(NS,notsignificantlydifferentcomparedtoICHgroup;*P<0.05,comparedtoShamgroup;#P<0.05,comparedtoICH+NCgroup.n=6/group).ICH,intracerebralhemorrhage;NC,negativecontrolsiRNA;SiRNA-Fyn(Si-Fyn),Fyn-specificsmallinterferingRNA.3.2抑制Fyn后可減輕ICH大鼠的腦水腫ICH后24h和72h,與各自Sham組相比,ICH組腦水含量增加;與各自NC組相比,ICH+Si-Fyn組腦水含量明顯減低(圖1)。圖2-2抑制Fyn后ICH大鼠的腦水腫和神經(jīng)功能評分
重慶醫(yī)科大學碩士研究生學位論文22圖2-1驗證小干擾片段抑制Fyn表達的效果Figure2-1VerifytheeffectofsmallinterferingfragmentsonFynexpression.(A)WesternblotanalysisshowinglevelsofFynandP-FynproteinweredecreasedbyFynsiRNA.(B)Fynexpressionlevelsatdifferenttimepoints.Proteinlevelswerenormalizedtoβ-actin.(C)P-Fynexpressionlevelsatdifferenttimepoints.ProteinlevelswerenormalizedtoFyn.Errorbarsrepresentmean±SD(NS,notsignificantlydifferentcomparedtoICHgroup;*P<0.05,comparedtoShamgroup;#P<0.05,comparedtoICH+NCgroup.n=6/group).ICH,intracerebralhemorrhage;NC,negativecontrolsiRNA;SiRNA-Fyn(Si-Fyn),Fyn-specificsmallinterferingRNA.3.2抑制Fyn后可減輕ICH大鼠的腦水腫ICH后24h和72h,與各自Sham組相比,ICH組腦水含量增加;與各自NC組相比,ICH+Si-Fyn組腦水含量明顯減低(圖1)。圖2-2抑制Fyn后ICH大鼠的腦水腫和神經(jīng)功能評分
【參考文獻】:
期刊論文
[1]抑制Fyn可激活Nrf2信號通路減輕大鼠腦出血后氧化應激損傷[J]. 張莉,王露,肖涵,甘薈,陳輝,鄭淑月,翟瑄,趙敬,梁平. 第三軍醫(yī)大學學報. 2019(21)
[2]Binding between Prion Protein and Aβ Oligomers Contributes to the Pathogenesis of Alzheimer’s Disease[J]. Chang Kong,Hao Xie,Zhenxing Gao,Ming Shao,Huan Li,Run Shi,Lili Cai,Shanshan Gao,Taolei Sun,Chaoyang Li. Virologica Sinica. 2019(05)
本文編號:3565077
【文章來源】:重慶醫(yī)科大學重慶市
【文章頁數(shù)】:60 頁
【學位級別】:碩士
【部分圖文】:
ICH后大鼠腦組織中Fyn的時間分布
重慶醫(yī)科大學碩士研究生學位論文22圖2-1驗證小干擾片段抑制Fyn表達的效果Figure2-1VerifytheeffectofsmallinterferingfragmentsonFynexpression.(A)WesternblotanalysisshowinglevelsofFynandP-FynproteinweredecreasedbyFynsiRNA.(B)Fynexpressionlevelsatdifferenttimepoints.Proteinlevelswerenormalizedtoβ-actin.(C)P-Fynexpressionlevelsatdifferenttimepoints.ProteinlevelswerenormalizedtoFyn.Errorbarsrepresentmean±SD(NS,notsignificantlydifferentcomparedtoICHgroup;*P<0.05,comparedtoShamgroup;#P<0.05,comparedtoICH+NCgroup.n=6/group).ICH,intracerebralhemorrhage;NC,negativecontrolsiRNA;SiRNA-Fyn(Si-Fyn),Fyn-specificsmallinterferingRNA.3.2抑制Fyn后可減輕ICH大鼠的腦水腫ICH后24h和72h,與各自Sham組相比,ICH組腦水含量增加;與各自NC組相比,ICH+Si-Fyn組腦水含量明顯減低(圖1)。圖2-2抑制Fyn后ICH大鼠的腦水腫和神經(jīng)功能評分
重慶醫(yī)科大學碩士研究生學位論文22圖2-1驗證小干擾片段抑制Fyn表達的效果Figure2-1VerifytheeffectofsmallinterferingfragmentsonFynexpression.(A)WesternblotanalysisshowinglevelsofFynandP-FynproteinweredecreasedbyFynsiRNA.(B)Fynexpressionlevelsatdifferenttimepoints.Proteinlevelswerenormalizedtoβ-actin.(C)P-Fynexpressionlevelsatdifferenttimepoints.ProteinlevelswerenormalizedtoFyn.Errorbarsrepresentmean±SD(NS,notsignificantlydifferentcomparedtoICHgroup;*P<0.05,comparedtoShamgroup;#P<0.05,comparedtoICH+NCgroup.n=6/group).ICH,intracerebralhemorrhage;NC,negativecontrolsiRNA;SiRNA-Fyn(Si-Fyn),Fyn-specificsmallinterferingRNA.3.2抑制Fyn后可減輕ICH大鼠的腦水腫ICH后24h和72h,與各自Sham組相比,ICH組腦水含量增加;與各自NC組相比,ICH+Si-Fyn組腦水含量明顯減低(圖1)。圖2-2抑制Fyn后ICH大鼠的腦水腫和神經(jīng)功能評分
【參考文獻】:
期刊論文
[1]抑制Fyn可激活Nrf2信號通路減輕大鼠腦出血后氧化應激損傷[J]. 張莉,王露,肖涵,甘薈,陳輝,鄭淑月,翟瑄,趙敬,梁平. 第三軍醫(yī)大學學報. 2019(21)
[2]Binding between Prion Protein and Aβ Oligomers Contributes to the Pathogenesis of Alzheimer’s Disease[J]. Chang Kong,Hao Xie,Zhenxing Gao,Ming Shao,Huan Li,Run Shi,Lili Cai,Shanshan Gao,Taolei Sun,Chaoyang Li. Virologica Sinica. 2019(05)
本文編號:3565077
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