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Reduction of coenzyme Q10 content: A possible effect of isoproterenol on heart failure and myocardial infarction in rat

机译:降低辅酶Q10含量:异丙肾上腺素对大鼠心力衰竭和心肌梗塞的可能作用

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Background: Myocardial infarction (MI) was induced by subcutaneous injection of isoproterenol (ISO) to investigate the effect of ISO on Coenzyme Q10 (CoQ10) content of myocardium and subsequent effects on lipid peroxidation, electrocardiogram pattern and hemodynamic parameters of the rat's heart. Method: 36 male Wistar rats were divided randomly into 6 groups. To induce heart failure (HF) and MI, 10 and 100mg/kg of ISO was administered subcutaneously for 10 and 2 consecutive days, respectively. The effects of ISO on myocardium CoQ10 content, concentration of malondialdehyde, ECG pattern and hemodynamic parameters of heart were analyzed. Results: ISO-treated rats showed significant alteration in heart hemodynamic parameters such as reduction of left-ventricular systolic pressure, maximum and minimum rate of developed left ventricular pressure, besides increase of left ventricular end-diastolic pressure. Significant depletion of heart CoQ10 content (from 4.57 and 4.55μg/100mg tissue in control groups to 2.85 and 2.89μg/100mg tissue in ISO-induced HF and MI groups respectively) and increase in tissue levels of malondialdehyde (47.1 and 53.8nmol/100mg tissue in ISO-induced HF and MI groups, respectively) were also observed in ISO-treated animals compared with the normal animals (17.4 and 18.8nmol/100mg tissue in control groups, respectively). Additionally CoQ10 improved ISO effects on hemodynamic parameters and ECG pattern in ISO-induced HF and myocardial injury. Conclusion: The present findings have demonstrated that the cardiotoxic effects of ISO such as oxidative damage and hemodynamic declination might be related to depletion of CoQ10 concentration.
机译:背景:皮下注射异丙肾上腺素(ISO)诱发心肌梗死(MI),以研究ISO对心肌辅酶Q10(CoQ10)含量的影响以及对脂质过氧化,心电图模式和大鼠心脏血流动力学参数的影响。方法:将36只Wistar雄性大鼠随机分为6组。为了诱发心力衰竭(HF)和MI,分别连续10天和2天皮下注射10和100mg / kg的ISO。分析了ISO对心肌CoQ10含量,丙二醛浓度,心电图和心脏血液动力学参数的影响。结果:用ISO治疗的大鼠显示出心脏血液动力学参数的显着改变,例如左心室收缩压降低,左心室压力发展的最大和最小速率以及左心室舒张末期压力升高。心脏CoQ10含量显着减少(从对照组的4.57和4.55μg/ 100mg组织减少到ISO诱导的HF和MI组的2.85和2.89μg/ 100mg组织),丙二醛的组织水平增加(47.1和53.8nmol / 100mg与正常动物相比(在对照组中分别为17.4和18.8nmol / 100mg组织),在用ISO治疗的动物中也观察到了分别在ISO诱导的HF和MI组中的组织(分别为17.4和18.8nmol / 100mg组织)。此外,辅酶Q10改善了ISO对ISO诱发的心衰和心肌损伤中血液动力学参数和ECG模式的影响。结论:本研究结果表明,ISO的心脏毒性作用,例如氧化损伤和血流动力学下降可能与CoQ10浓度的降低有关。

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