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缺血后处理对在体大鼠缺血-再灌注心肌细胞色素P450表氧化酶2J3/环氧二十碳三烯酸系统的影响
引用本文:于刚刚,芦玲巧,曾翔俊,王红霞,常静,王晶,张立克.缺血后处理对在体大鼠缺血-再灌注心肌细胞色素P450表氧化酶2J3/环氧二十碳三烯酸系统的影响[J].中国微循环,2009,13(4):231-235.
作者姓名:于刚刚  芦玲巧  曾翔俊  王红霞  常静  王晶  张立克
作者单位:首都医科大学病理生理学教研室,北京,100069
摘    要:目的观察缺血后处理拈抗心肌缺血-再灌注损伤时内源性细胞色素P450表氧化酶2J3/环氧二十碳三烯酸(CYP2J3/EET)系统的变化。方法复制在体大鼠心肌缺血-再灌注损伤及缺血后处理模型。雄性Wistar大鼠(250—300)g随机分为三组:假手术组(Sham)、缺血-再灌注组(I—R)、缺血后处理组(IPo)。动脉插管测定心功能指标,采用TTC染色法测定心肌梗死范围,采用RT—PCR法检测心脏细胞色素P450表氧化酶亚型2J3(CYP2J3)mRNA表达,采用Western blot方法测定心肌组织CYP2J3蛋白水平的变化,高效液相色谱法测定11,12-EET含量。结果与I-R组相比IPo组左室收缩末压(LVESP)、左室内压最大上升/下降速率(±LVdp/dtmax)均显著升高;心肌梗死面积减少20.76%(P〈0.01);与Sham组及I—R组相比IPo组CYP2J3mRNA、CYP2J3蛋白及11,12-EET含量明显升高(P〈0.05)。结论Po可减轻在体心肌I—R损伤同时上调心脏CYP2J3/EET系统;提示CYP2J3/EET系统可能与IPo拮抗心脏I-R损伤作用相关。

关 键 词:缺血后处理  缺血-再灌注损伤  心脏  细胞色素P450表氧化酶2J3  环-二十碳三烯酸

Effect of Ischemic Postconditioning on CYP2J3/EET System in Rat Heart in Vivo
YU Gang-gang,LU Ling-qiao,ZENG Xiang-jun,WANG Hong-xia,CHANG Jing,WANG Jing,ZHANG Li-ke.Effect of Ischemic Postconditioning on CYP2J3/EET System in Rat Heart in Vivo[J].Journal of Chinese Microcirculation,2009,13(4):231-235.
Authors:YU Gang-gang  LU Ling-qiao  ZENG Xiang-jun  WANG Hong-xia  CHANG Jing  WANG Jing  ZHANG Li-ke
Institution:. (Department of Pathophysiology , Capital Medical University, Beijing 100069, China)
Abstract:Objective To observe the variation of endogenous CYP2J3/EET system in rat heart in vivo after ischemic postconditioning( IPo). Methods All Wistar rats were randomly divided into three groups as follows: Sham group, I/R group and IPo group. The myocardial ischemia-reperfusion and the IPo models in vivo were made. Observing the changes of heart rate (HR), left ventricular end-systolic pressure(LVESP) and maximum velocity of increase or decrease of LV pressure(± LVdP/dtmax). Infarction size was measured by triphenyhetrazolium chloride(TTC) staining. The expression of CYP2J3 mRNA was tested by RT-PCR. The expression of CYP2J3 protein was detected by Western blot. 11, 12-epoxyeicosatrienoic acid( 11, 12-EET) was observed by high-performance liquid chromatography( HPLC). Results Compared with I/R group, the levels of LVESP and ± LVdp/dt were all significantly increased. Infarction size was significantly reduced in IPo group compared with I-R group ( P 〈 0.05). CYP2J3 mRNA was increased compared with I/R and Sham groups, consistent with increased expression of CYP2J3 protein and 11, 12-EET. Conclusion These data suggest that IPo protects myocardium against I-R injury which may involve endogenous activation of CYP2J3/ EET system.
Keywords:Postconditioning  Ischemia-reperfusion injury  Heart  CYP2J3  EETs
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