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氯喹对大鼠脑缺血再灌注自噬相关蛋白的影响
引用本文:肖学进,李丹丹,梁佳,李霞,秦书俭,包翠芬. 氯喹对大鼠脑缺血再灌注自噬相关蛋白的影响[J]. 中国临床解剖学杂志, 2017, 35(4): 402-408. DOI: 10.13418/j.issn.1001-165x.2017.04.010
作者姓名:肖学进  李丹丹  梁佳  李霞  秦书俭  包翠芬
作者单位:锦州医科大学 1.细胞生物学教研室, 2.生命科学院, 3.附属第一医院口腔科,
4.解剖学教研室, 5.基础医学实验教学中心, 辽宁 锦州 121001
基金项目:国家自然科学基金(81202783);省科技厅计划项目(2015020696,20170540378)
摘    要:目的 探讨氯喹对大鼠脑缺血再灌注自噬相关蛋白的影响及其机制。 方法 取75只大鼠随机分为假手术组(Sham),模型组(Model),氯喹(CQ)20、40、60 mg/kg组,每组15只。应用线栓法使右脑中动脉栓塞(MCAO),栓塞2 h。3个药物组于栓塞后立即腹腔注射CQ 20、40、60 mg/kg,其余各组注射2 ml 0.9%氯化钠。再灌注24 h后,采用神经功能缺损评分、TTC染色判断模型是否制作成功,采用免疫荧光和免疫印迹法检测大鼠脑自噬相关蛋白的表达。 结果 ① Sham组, Model组, CQ 20、40、60 mg/kg组神经功能缺损评分,分别为0、2.67±0.49、2.93±0.26、2.40±0.51及1.93±0.70。通过TTC染色与Model组比较梗死面积,CQ 20 mg/kg组增大,CQ 40 mg/kg组无明显变化,CQ 60 mg/kg组减小。②免疫荧光和免疫印迹结果显示各组均有蛋白(Atg5、Atg7、Beclin1、Atg12)表达,与Model组比较,其中Sham组仅有极少量表达(P<0.05),CQ 20 mg/kg组表达量无明显差异,CQ 60 mg/kg组的表达量明显减少(P<0.05)。 结论 氯喹对大鼠脑缺血再灌注损伤有双重作用,低剂量20 mg/kg加重损伤,高剂量60 mg/kg减轻损伤。其机制可能与某些脑自噬相关蛋白表达的量有关。

关 键 词:脑缺血再灌注   氯喹   自噬  
收稿时间:2017-03-27

Effects of chloroquine on the expressions of autophagy related proteins after focal cerebral ischemia-reperfusion in rats
XIAO Xue-jin,LI Dan-dan,LIANG Jia,LI Xia,QIN Shu-Jian,BAO Cui-fen. Effects of chloroquine on the expressions of autophagy related proteins after focal cerebral ischemia-reperfusion in rats[J]. Chinese Journal of Clinical Anatomy, 2017, 35(4): 402-408. DOI: 10.13418/j.issn.1001-165x.2017.04.010
Authors:XIAO Xue-jin  LI Dan-dan  LIANG Jia  LI Xia  QIN Shu-Jian  BAO Cui-fen
Affiliation:1.Department of Cell Biology; 2.College of Life Sciences; 3.Department of Stomatology, First Affiliated Hospital; 4.department of human anatomy; 5.Basic Medical Experimental Teaching Center, Jinzhou Medical University, Jinzhou 121001,China
Abstract:Objective To investigate the effects of chloroquine on the expressions of autophagy related proteins after focal cerebral ischemia-reperfusion in adult rats. Methods A total of 75 healthy SD rats were randomly allocated to sham-operation, model and chloroquine(CQ) 20,40 and 60 mg/kg groups. A model of middle cerebral artery occlusion (MCAO) for 2 h was induced by suture method. The CQ 20,40 and 60 mg/kg groups were injected intraperitoneally immediately following MCAO in the 3 medication groups. Neurological deficit scores and TTC staining were evaluated, and then the expressions of autophagy related proteins in area of cerebral ischemia-reperfusion were analyzed by immunofluorescence and Western blot technique at 24 h after reperfusion. Results ①Neurological deficit scores in the sham-operation, model, CQ 20, 40 and 60 mg/kg groups were 0, 2.67±0.49, 2.93±0.26, 2.40±0.51 and 1.93±0.7 respectively. Compared with the infarction area of the model group by TTC staining, the CQ 20 mg/kg group was significantly increased, the CQ 40 mg/kg group was almost like the model group,the CQ 60 mg/kg group was significantly decreased. ② Compared with the model group, the results of immunofluorescence and Western blot technique showed only a trace expressions of proteins(Atg5, Atg7, Beclin1 and Atg12 ) in the sham operation group (P<0.05), and the same pattern of expressions were observed in the CQ 20 mg/kg group. However there was significantly reduced expressions in the CQ 60 mg/kg group (P<0.05). Conclusion The CQ have has two fold effects, i.e., the CQ 20 mg/kg group can aggravate the damage, whereas the CQ 60 mg/kg can alleviatereduce the damage. The mechanism of CQ in the prevention and treatment of cerebral ischemia-reperfusion injury in rats may be associated with the dose of the expressions of some autophagy related proteins.
Keywords:Cerebral ischemia-reperfusion     ,Chloroquine    ,Autophagy,
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