首页> 外文期刊>Chemical research in toxicology >Leucoisoprenochrome-o-semiquinone Formation in Freshly Isolated Adult Rat Cardiomyocytes.
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Leucoisoprenochrome-o-semiquinone Formation in Freshly Isolated Adult Rat Cardiomyocytes.

机译:新鲜分离的成年大鼠心肌细胞中的亮白异戊二烯氧基-o-半醌形成。

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Sustained high levels of circulating catecholamines can lead to cardiotoxicity. There is increasing evidence that this process may result from metal-catalyzed catecholamine oxidation into semiquinones, quinones, and aminochromes. We have previously shown that Cu(2+)-induced oxidation of isoproterenol into isoprenochrome induces toxic effects in isolated cardiomyocytes. The aim of this study was to characterize the isoproterenol oxidation process and to locate the formation of semiquinone radicals in cardiomyocyte suspensions. Freshly isolated rat cardiomyocytes were incubated with 1 or 10 mM isoproterenol and 20 muM Cu(2+) for 4 h. The formation of an isoproterenol oxidation radical was detected in the extracellular medium, cells, membranes, and heavy organelles by electron spin resonance spectroscopy. An electron spin resonance signal assigned to leucoisoprenochrome-o-semiquinone increased in a time-dependent manner in the extracellular medium. A second electron spin resonance signal, characteristic of an immobilized radical, was also found in the cardiomyocytes. The latter was attributed to leucoisoprenochrome-o-semiquinone immobilized on cellular components such as membranes, cytoskeleton, nucleus, and heavy organelles. In addition, the levels of leucoisoprenochrome-o-semiquinone decreased in the presence of glutathione. Computer simulations of the experimental spectra indicate the formation of two distinct isomeric leucoisoprenochrome-o-semiquinone radicals during isoproterenol oxidation. The present study shows that the isoproterenol oxidation in isolated rat cardiomyocytes correlates with the formation of leucoisoprenochrome-o-semiquinone in the cells and in the extracellular medium, suggesting that it might be involved in cardiotoxicity induced by the oxidation of catecholamines.
机译:持续高水平的循环儿茶酚胺可导致心脏毒性。越来越多的证据表明,此过程可能是由于金属催化的儿茶酚胺氧化成半醌,醌和氨基色素而导致的。我们以前已经表明,Cu(2+)诱导的异丙基肾上腺素氧化为异戊二烯色素在分离的心肌细胞中诱导毒性作用。这项研究的目的是表征异丙肾上腺素的氧化过程,并定位心肌细胞悬液中半醌自由基的形成。将新鲜分离的大鼠心肌细胞与1或10 mM异丙肾上腺素和20μMCu(2+)孵育4小时。通过电子自旋共振光谱在细胞外介质,细胞,膜和重细胞器中检测到异丙肾上腺素氧化自由基的形成。分配给白细胞异戊二烯酸-邻-半醌的电子自旋共振信号在细胞外培养基中以时间依赖性方式增加。在心肌细胞中还发现了第二个电子自旋共振信号,该信号具有固定化自由基的特征。后者归因于固定在细胞成分(如膜,细胞骨架,细胞核和重细胞器)上的隐异戊二烯酸-邻-半醌。另外,在谷胱甘肽存在下,白细胞异戊二烯色素-o-半醌的水平降低。实验光谱的计算机模拟表明在异丙肾上腺素氧化过程中形成了两个不同的异构异色异戊二烯-邻半醌基团。本研究表明,离体大鼠心肌细胞中异丙肾上腺素的氧化与细胞和细胞外培养基中白细胞异戊二烯色素-o-半醌的形成有关,表明它可能与儿茶酚胺氧化引起的心脏毒性有关。

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