糖尿病性心肌病大鼠3-nt和tgf-β1的表达及氮氧自由基化合物tempol对其干预研究-expression of 3 - nt and tgf - β 1 in diabetic cardiomyopathy rats and intervention of nitroxide free radical compound tempo.docxVIP
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糖尿病性心肌病大鼠3-nt和tgf-β1的表达及氮氧自由基化合物tempol对其干预研究-expression of 3 - nt and tgf - β 1 in diabetic cardiomyopathy rats and intervention of nitroxide free radical compound tempo
摘要结论:1、通过腹腔注射STZ法诱导建立DC大鼠模型后,长期的高血糖状态可引起大鼠心肌不同程度的损伤。2、DC高糖状态下氧化应激产生的3-NT及TGF-β1可引起心肌细胞坏死、纤维化,3-NT及TGF-β1可能参与了DCM的发生发展。3、2,2,6,6-四甲基-4-哌啶醇(Tempol)对正常大鼠心肌无明显影响,且Tempol可能通过抑制氧化应激反应,下调大鼠心肌及血清3-NT、TGF-β1的表达来减轻DCM大鼠心肌的损伤,发挥对DCM大鼠心肌的保护作用。关键词:糖尿病性心肌病;3硝基酪氨酸;转化因子β1;氮氧自由基化合物ABSTRACTObjective:Thediabeticcardiomyopathyratsmodlewasestablishedbyintravenousinjecionofstreptozocin.DCMratsweretreatedbyTempol.ToexploretheeffectionandpossiblemechanismofTempolondiabeticcardiomyopathyratsbyobservingtheexpressionof3-NTandTGF-β1.Methods:42SDrats(male,200-250g)werefedadaptivelyfor1week.16ofthemwererandomlyelectedasnormalgloup,whiletherestwereelectedasdiabetegroupthatmadebyinjectingSTZ(STZ,55mg/kg).4weekslater,2ratsofdiabetegroupwerekilledrandomly,thenthechangeofmyocardialstructurewereobserdbyHEstainingandMassontrichromestaning.IftheresultsofHEstainingandMassontrichromestaningshowthatthemyocardialstructureof2ratshaddifferentdegreesofdegenerationandnecrosis,interstitialfibrosiscells,anddisorderedmyocardialtissuewereincreased.Wecanconsiderthatdiabeticcardiomyopathymodlehasbeenmadesuccessfully.The16normalratsandtherestof24modleratswererandomlydividedintodifferentgroups.Thegroupingandprocessingmethodisasfollows:(1)Control+salinegroup:normalnondiabeticratsreceivedthenormaldiet,andreceivedthesamevolumeofthesolventfor8weeks.(2)Control+Tempolgroup:ratstreatedwithtempolinadoseof18mg/kg/ddissolvedinsalinebygavagefor8weeksandreceivedthenormaldiet.(3)Diabeticgroup:diabeticratswerejustreceivedthenormaldiet,andreceivedthesamevolumeofthesolventfor8weeks.(4)Diabetic+Tempolgroup:diabeticratswerereatedwithtempolinadoseof18mg/kg.ddissolvedinsalinebygavagefor8weeksandreceivedthenormaldiet.8weekslater,thechangeofmyocardialstructurewereobserdbyHEstainingandMassontrichromestaning,theexpressionof3-NTandTGF-β1inratserumweredetectedbyenzymelinkedimmunosorbentassay(ELISA),theexpressionof3-NTandTGF-β1inratmyocardialwereanalyzedbyimmunohistochemistry.Results:Thediabeticcardiomyopathyratsmodlewassuccessfullyestablishedby
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