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吗啡预处理兔心肌MALDI-TOF-MS分析
引用本文:谭嵘,邹定全,常业恬. 吗啡预处理兔心肌MALDI-TOF-MS分析[J]. 中南大学学报(医学版), 2010, 35(6): 607. DOI: 10.3969/j.issn.1672-7347.2010.06.011
作者姓名:谭嵘  邹定全  常业恬
作者单位:中南大学湘雅二医院麻醉科, 长沙 410011
摘    要:目的:对吗啡预处理兔心肌进行基质辅助激光解吸飞行时间质谱(matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, MALDI-TOF-MS)分析。方法:将6只新西兰大白兔随机分为对照组和吗啡预处理组,每组3只。对照组静脉注射生理盐水1 mL/kg, 吗啡预处理组静脉注射吗啡3 mg/kg。用双向凝胶电泳法分离两组24 h后的心肌组织蛋白,图像分析后找出差异蛋白。用MALDI-TOF-MS鉴定部分差异蛋白。结果:两组的差异明显点共有51个,取15个差异蛋白质进行质谱分析,初步鉴定出8个蛋白质,包括应激蛋白(醛糖还原酶、锌指蛋白312)、信号转导蛋白(Src相关的酪氨酸激酶)、代谢相关蛋白(碳酸酐酶12前体、电子转移黄素蛋白β亚单位、甘油醛-3-磷酸脱氢酶)、炎性反应相关蛋白(肿瘤坏死因子配体超家族成员11)和跨膜转运蛋白。结论:这些差异表达的蛋白可能在吗啡对心肌延迟性保护中发挥作用。

关 键 词:吗啡  预适应  延迟相  基质辅助激光解吸飞行时间质谱分析  

Proteomic analysis of morphine rabbit myocardium with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
TAN Rong,ZOU Dingquan,CHANG Yetian. Proteomic analysis of morphine rabbit myocardium with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry[J]. Journal of Central South University. Medical sciences, 2010, 35(6): 607. DOI: 10.3969/j.issn.1672-7347.2010.06.011
Authors:TAN Rong  ZOU Dingquan  CHANG Yetian
Affiliation:Department of Anesthesiology, Second Xiangya Hospital, Central South University, Changsha 410011, China
Abstract:ObjectiveTo analyze the morphine rabbit myocardium with matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry(MALDI-TOF-MS).MethodsSix New Zealand white rabbits were randomly assigned to a control group (Group C) and a morphine group(Group M). Group C were pretreated with bolus injection of saline 1mL/kg.Group M were pretreated with bolus injection of morphine 3 mg/kg. The myocardium tissue proteins of the rabbits 24 hours after the injection of morphine or saline preconditioned were extracted and separated by two dimensional gel electrophoresis(2-DE), and the images were analyzed and different proteins were found. Some of the different proteins were determined with MALDI-TOF-MS.ResultsThere were 51 protein spots that displaied quantitive changes in expression(P<0.05), 15 protein spots were choosen for MS analysis, and 8 proteins were preliminarily identified.They were aldose reductase,zinc finger protein 312,src related tyrosine kinase, carbonic anhydrase 12 precursor,electron transfer flavoprotein beta-subunit,glyceraldehyde-3-phosphate dehydrogenase, tumor necrosis factor ligand superfamily member 11 and transmembrane emp24 domain-containing protein. ConclusionThese proteins may be involved in the cardioprotection of morphine preconditioning.
Keywords:morphine  myocardial preconditioning;late phase;matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry,
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