缺血后处理联合水蛭注射液对脑缺血损伤大鼠PI3K表达的影响

被引:13
作者
胡跃强 [1 ]
兰鹏 [2 ]
秦红玲 [1 ]
苏锦勋 [2 ]
覃琴 [1 ]
机构
[1] 广西中医药大学第一附属医院
[2] 广西南宁市中医医院
关键词
脑缺后损伤; 缺血后处理; 水蛭注射液; 磷脂酸肌醇-3激酶;
D O I
暂无
中图分类号
R285.5 [中药实验药理];
学科分类号
100806 [中药药理学];
摘要
目的观察缺血后处理(IPOC)联合水蛭注射液对脑缺血损伤大鼠磷脂酸肌醇-3激酶(PI3K)mRNA及其蛋白表达和脑梗死体积的影响。方法 SD大鼠40只,随机分为假手术组(SO组)、缺血再灌注(MCAO)组、缺血后处理组(IPOC组)、缺血后处理+水蛭注射液后处理组(P-L组)4组。采用线栓法制备大鼠IPOC和MCAO模型,采用TTC染色法计算脑梗死体积,实时荧光定量PCR和Western blot技术检测PI3K mRNA及其蛋白的表达变化。结果大鼠脑缺血再灌注后24h,IPOC组较MCAO组梗死体积明显减小,P-L组脑梗死体积较IPOC组进一步缩小(P<0.05)。SO组的PI3K mRNA及其蛋白的表达量较少,MCAO组的PI3K表达明显增高(P<0.01);IPOC组、P-L组的PI3K表达水平较MCAO组升高(P<0.01);P-L组PI3K表达较IPOC组升高(P<0.05)。结论脑缺血损伤;脑缺血后处理具有神经保护作用,其机制可能与其诱导PI3K的表达有关,水蛭注液可进一步促进其表达而发挥神经保护作用。
引用
收藏
页码:158 / 161
页数:4
相关论文
共 18 条
[1]
Role of phosphoinositide 3-kinase IA (PI3K-IA) activation in cardioprotection induced by ouabain preconditioning.[J].Qiming Duan;Namrata D. Madan;Jian Wu;Jennifer Kalisz;Krunal Y. Doshi;Saptarsi M. Haldar;Lijun Liu;Sandrine V. Pierre.Journal of Molecular and Cellular Cardiology.2015,
[2]
Neuroprotection induced by sevoflurane-delayed post-conditioning is attributable to increased phosphorylation of mitochondrial GSK-3β through the PI3K/Akt survival pathway [J].
Ye, Zhi ;
Xia, Pingping ;
Cheng, Zhi-gang ;
Guo, Qulian .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2015, 348 (1-2) :216-225
[3]
Effect of Sevoflurane postconditioning on gene expression in brain tissue of the middle cerebral artery occlusion rat model [J].
Liu, Hai-Gen ;
Hua, Zhen ;
Zhang, Yan ;
Wang, Ya-Xin ;
Meng, Chun ;
Liang, Yu ;
Tian, Shou-Yuan ;
Ma, Yi-Ping ;
Wang, Liang ;
Wang, Wen-Sheng .
MOLECULAR BIOLOGY REPORTS, 2012, 39 (12) :10505-10513
[4]
Delayed ischemic postconditioning protects hippocampal CA1 neurons by preserving mitochondrial integrity via Akt/GSK3β signaling [J].
Zhou, Caifeng ;
Tu, Jingyi ;
Zhang, Quanguang ;
Lu, Dongshuang ;
Zhu, Ying ;
Zhang, Wenli ;
Yang, Fang ;
Brann, Darrell W. ;
Wang, Ruimin .
NEUROCHEMISTRY INTERNATIONAL, 2011, 59 (06) :749-758
[5]
Reperfusion injury salvage kinase signalling: taking a RISK for cardioprotection.[J].Derek J. Hausenloy;Derek M. Yellon.Heart Failure Reviews.2007, 3
[6]
Preconditioning and postconditioning: United at reperfusion [J].
Hausenloy, Derek J. ;
Yellon, Derek M. .
PHARMACOLOGY & THERAPEUTICS, 2007, 116 (02) :173-191
[7]
Interrupting reperfusion as a stroke therapy: ischemic postconditioning reduces infarct size after focal ischemia in rats [J].
Zhao, Heng ;
Sapolsky, Robert M. ;
Steinberg, Gary K. .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2006, 26 (09) :1114-1121
[8]
Postconditioning: A Form of “Modified Reperfusion” Protects the Myocardium by Activating the Phosphatidylinositol 3-Kinase–Akt Pathway.[J].Andrew Tsang;Derek J. Hausenloy;Mihaela M. Mocanu;Derek M. Yellon.Circulation Research.2004, 3
[9]
脂联素后处理对大鼠心肌缺血/再灌注损伤的影响及ADP/PI3K/Akt信号通路的作用.[J].赵林静;崔柳苏;张金盈;王永玲;.中国应用生理学杂志.2017, 04
[10]
芹黄素联合缺血后处理对大鼠肾缺血再灌注损伤的影响.[J].刘洋;刘修恒;王磊;杜洋;汪志顺;陈志远;郭佳;.中国医药导报.2017, 15