首页> 外文期刊>Molecular biology reports >Protective effect of calpain inhibitor N-acetyl-L-leucyl-L-leucyl-L-norleucinal on acute alcohol consumption related cardiomyopathy
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Protective effect of calpain inhibitor N-acetyl-L-leucyl-L-leucyl-L-norleucinal on acute alcohol consumption related cardiomyopathy

机译:钙蛋白酶抑制剂N-乙酰基-L-亮氨酰-L-亮氨酰-L-净核苷对急性饮酒相关性心肌病的保护作用

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Excessive alcohol consumption and alcoholism cause medical problems with high mortality and morbidity rates. In this study we aimed to decrease the alcohol related tissue damage by inhibiting calpain activation which plays an important role in apoptosis and necrosis, in rats with cardiomyopathy induced by acute alcohol consumption. Male Sprague-Dawley rats were separated into four groups (control, vehicle, alcohol and alcohol + inhibitor) with 10 rats in each. Control group received isocaloric maltose while vehicle group received isocaloric maltose with DMSO, and alcohol group received 8 g/kg absolute ethanol by gavage. Inhibitor group received 20 mg/kg calpain inhibitor 1 intraperitonally prior to alcohol administration. Calpain activities, cathepsin L levels and cytochrome c release rates were significantly increased in alcohol group compared to control group (p < 0.05). Serum CK MB and BNP levels of alcohol group were excessively increased compared to control group (respectively p < 0.001 and p < 0.01). Serum BNP levels of alcohol + inhibitor group were significantly (p < 0.05) decreased compared to alcohol group. In addition to these, histological evaluation of light microscope images and the results of DNA fragmentation and immunohistochemical caspase-3 activity results showed significant improvement of these parameters in alcohol + inhibitor group compared to alcohol group. Results of our biochemical and histological evaluation results revealed that the calpain inhibitor N-acetyl-leu-leu-norleucinal may have an ameliorating effect on acute alcohol consumption related cardiac tissue damage due to its effects on cell death pathways.
机译:过量饮酒和酗酒会导致高死亡率和高发病率的医学问题。在这项研究中,我们旨在通过抑制钙蛋白酶的活化来减少与酒精有关的组织损伤,钙蛋白酶的活化在急性饮酒引起的心肌病大鼠中在凋亡和坏死中起重要作用。将雄性Sprague-Dawley大鼠分为四组(对照组,媒介物,酒精和酒精+抑制剂),每组10只。对照组接受等量麦芽糖,媒介物组采用DMSO接受等量麦芽糖,酒精组通过管饲法接受8 g / kg的无水乙醇。在饮酒之前,抑制剂组腹膜内接受20 mg / kg钙蛋白酶抑制剂1。与对照组相比,酒精组的钙蛋白酶活性,组织蛋白酶L水平和细胞色素c释放速率显着增加(p <0.05)。与对照组相比,酒精组的血清CK MB和BNP水平过高(分别为p <0.001和p <0.01)。与酒精组相比,酒精+抑制剂组的血清BNP水平显着降低(p <0.05)。除此之外,与酒精组相比,酒精+抑制剂组的光学显微镜图像的组织学评估以及DNA片段化结果和免疫组化caspase-3活性结果表明,这些参数有显着改善。我们的生化和组织学评估结果表明,钙蛋白酶抑制剂N-乙酰基-亮氨酸-亮氨酸-正亮氨酸可能由于其对细胞死亡途径的影响而对急性饮酒相关的心脏组织损伤具有改善作用。

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