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首页> 外文期刊>American Journal of Physiology >Cardioprotective effects of nitroparacetamol and paracetamol in acute phase of myocardial infarction in experimental rats.
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Cardioprotective effects of nitroparacetamol and paracetamol in acute phase of myocardial infarction in experimental rats.

机译:硝基对乙酰氨基酚和扑热息痛对大鼠心肌梗死急性期的心脏保护作用。

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We aimed to determine whether nitroparacetamol (NO-paracetamol) and paracetamol exhibit cardioprotective effects. Myocardial infarction (MI) was induced in rats, and drug treatment was started 1 wk before surgery. Mortality rate and infarct size at 2 days after MI were compared. Treatment groups included vehicle (saline), paracetamol (5 mg x kg(-1) x day(-1)) and NO-paracetamol (15 mg x kg(-1) x day(-1)). Mortality rates for vehicle (n = 80), paracetamol (n = 79), and NO-paracetamol (n = 76) groups were 37.5%, 21.5%, and 26.3%, respectively. Infarct size for the vehicle group was 44.8% (+/-6.1%) of the left ventricle (LV). For the paracetamol and NO-paracetamol groups, infarct size was 31.3% (+/-5.6%) and 30.7% (+/-8.1%) of the LV, respectively. Both paracetamol- and NO-paracetamol-treated groups showed increased activities of catalase and SOD compared with the vehicle group. They could attenuate endothelial, inducible, and neuronal nitric oxide synthase and cyclooxygenase-1 and -2 gene expression after MI. The observation indicates the potential clinical significance of the cardioprotective effects of these drugs.
机译:我们旨在确定硝基扑热息痛(NO-扑热息痛)和扑热息痛是否表现出心脏保护作用。在大鼠中诱发心肌梗塞(MI),并在手术前1周开始药物治疗。比较MI后2天的死亡率和梗死面积。治疗组包括媒介物(生理盐水),扑热息痛(5 mg x kg(-1)x天(-1))和一氧化氮扑热息痛(15 mg x kg(-1)x day(-1))。媒介物(n = 80),扑热息痛(n = 79)和NO-扑热息痛(n = 76)组的死亡率分别为37.5%,21.5%和26.3%。媒介物组的梗塞面积为左心室(LV)的44.8%(+/- 6.1%)。对于扑热息痛和NO-扑热息痛组,梗塞面积分别为LV的31.3%(+/- 5.6%)和30.7%(+/- 8.1%)。与媒介物组相比,对乙酰氨基酚和NO-对乙酰氨基酚治疗组均表现出过氧化氢酶和SOD活性增加。它们可以减弱心肌梗死后内皮,可诱导的和神经元一氧化氮合酶以及环氧合酶-1和-2基因的表达。观察结果表明这些药物的心脏保护作用的潜在临床意义。

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