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多胺在L-精氨酸抑制异丙肾上腺素诱导的大鼠心肌肥厚中的作用
引用本文:林岩,徐长庆,王丽娜,李鸿珠,赵雅君,席玉慧,王国忠.多胺在L-精氨酸抑制异丙肾上腺素诱导的大鼠心肌肥厚中的作用[J].中国病理生理杂志,2009,25(11):2099-2104.
作者姓名:林岩  徐长庆  王丽娜  李鸿珠  赵雅君  席玉慧  王国忠
作者单位:1齐齐哈尔医学院病理生理教研室,黑龙江 齐齐哈尔 161006; 2哈尔滨医科大学病理生理教研室, 3黑龙江生物医药工程重点实验室,黑龙江 哈尔滨 150081
基金项目:国家自然科学基金资助项目,黑龙江省青年科学技术专项基金资助项目,黑龙江省普通高等学校青年学术骨干支持计划资助项目 
摘    要:目的: 研究多胺在L-精氨酸抑制病理性心肌肥厚中的作用及机制。方法:异丙肾上腺素(ISO)皮下注射复制大鼠心肌肥厚模型,L-精氨酸作为干预因素,检测心脏肥大指数,心肌组织胶原染色,心房利钠肽(ANP)的转录水平,观察L-精氨酸对心肌肥大的影响;不同时段,应用高效液相色谱仪(HPLC)测定心肌组织内多胺含量,应用Western blotting结合图像分析系统,检测各组大鼠心肌组织鸟氨酸脱羧酶(ODC)和精眯/精胺乙酰转移酶(SSAT)的蛋白表达水平;检测血清NO含量和NOS活性。结果:皮下注射ISO7d后,心肌肥大指数增加,心肌纤维增粗、排列紊乱,ANP mRNA表达增加;L-精氨酸干预可抑制ISO诱导的心肌肥大,随着L-精氨酸作用时间延长,心肌组织多胺含量减少,血清NOS活性增强,NO含量增加。同时,ODC蛋白表达下调,SSAT蛋白表达上调。结论:L-精氨酸抑制ISO诱导的心肌肥大,其机制可能与下调L-精氨酸/多胺通路、上调L-精氨酸/NO通路有关。

关 键 词:多胺  心肌肥厚  
收稿时间:2008-12-12
修稿时间:2009-3-13

Role of polyamines in L-arginine inhibiting isoproterenol induced cardiac hypertrophy rat
LIN Yan,XU Chang-qing,WANG Li-na,LI Hong-zhu,ZHAO Ya-jun,XI Yu-hui,WANG Guo-zhong.Role of polyamines in L-arginine inhibiting isoproterenol induced cardiac hypertrophy rat[J].Chinese Journal of Pathophysiology,2009,25(11):2099-2104.
Authors:LIN Yan  XU Chang-qing  WANG Li-na  LI Hong-zhu  ZHAO Ya-jun  XI Yu-hui  WANG Guo-zhong
Institution:1Department of Pathophysiology, Qiqihaer Medical College, Qiqihaer 161006, China; 2Department of Pathophysiology, Harbin Medical University, 3Bio-pharmaceutical Key Laboratory of Heilongjiang Province, Harbin 150081, China. E-mail: xucq45@126.com
Abstract:AIM: To explore the role and possible mechanism of polyamine in L-arginine inhibiting cardiac hypertrophy induced by isoproterenol (ISO). METHODS: Hypertrophic model of rats was established using ISO. Pretreated with L-arginine, hypertrophy status of rats was determined by hypertrophy coefficient, collagen content and the expression of ANP mRNA. High performance liquid chromatography (HPLC) was used to measure the concentrations of polyamines. Western blotting was performed to detect the expressions of ornithine decarboxylase (ODC) and spermidine/spermine N1-acetyltransferase (SSAT). The activity and levels of NOS and NO in serum were also observed. RESULTS: Hypertrophy coefficient and expression of ANP mRNA increased significantly after injection of ISO for 7 d. Moreover, cardiac muscle fibres became thick and disorganized. Pretreated with L-arginine, the above index decreased. Meanwhile, the concentration of polyamine was decreased and plasma NO content and NOS activity were increased, the expression of ODC was downregulated and the expression of SSAT was upregulated. CONCLUSION: Exogenous L-arginine inhibits cardiac hypertrophy through downregulating L-arginine/polyamine pathway and upregulating L-arginine/NO pathway.
Keywords:Polyamine  Myocardial hypertrophy  Arginine
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