首页> 外文期刊>Journal of inherited metabolic disease >Long-term exposure of human proximal tubule cells to hydroxycobalamin(c-lactam) as a possible model to study renal disease in methylmalonic acidurias.
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Long-term exposure of human proximal tubule cells to hydroxycobalamin(c-lactam) as a possible model to study renal disease in methylmalonic acidurias.

机译:人类近端肾小管细胞长期暴露于羟钴胺(c-内酰胺)作为研究甲基丙二酸尿症肾脏疾病的可能模型。

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摘要

Dysfunction of proximal tubules resulting in tubulointerstitial nephritis and chronic renal failure is a frequent long-term complication of methylmalonic acidurias. However, the underlying pathomechanisms have not yet been extensively studied owing to the lack of suitable in vitro and in vivo models. Application of hydroxycobalamin[c-lactam] has been shown to inhibit the metabolism of hydroxycobalamin and, thereby, to induce methylmalonic aciduria in rats, oligodendrocytes, and rat hepatocytes. Our study characterizes the biochemical and bioenergetic effects of long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam], aiming to establish a novel in vitro model for the renal pathogenesis of methylmalonic acidurias. Incubation of human proximal tubule cells with hydroxycobalamin[c-lactam] and propionic acid resulted in a strong, time-dependent intra- and extracellular accumulation of methylmalonic acid. Bioenergetic studies of respiratory chain enzyme complexes revealed an increase of complex II-IV activity after 2 weeks and an increase of complex I and IV activity as well as a decrease of complex II and III activity after 3 weeks of incubation. In addition, human proximal tubule cells displayed reduced glutathione content after the exposure to hydroxycobalamin[c-lactam] and propionic acid.
机译:导致肾小管间质性肾炎和慢性肾功能衰竭的近端肾小管功能障碍是甲基丙二酸尿症的长期长期并发症。然而,由于缺乏合适的体外和体内模型,尚未对潜在的致病机理进行广泛的研究。已显示出应用羟基钴胺素[c-内酰胺]抑制羟基钴胺素的代谢,从而在大鼠,少突胶质细胞和大鼠肝细胞中诱导甲基丙二酸尿症。我们的研究表征了人类近端肾小管细胞长期暴露于羟基钴胺素[c-内酰胺]的生化和生物能效应,旨在建立甲基丙二酸尿症肾脏发病的新型体外模型。用羟基钴胺素[c-内酰胺]和丙酸孵育人近端肾小管细胞导致甲基丙二酸强烈,时间依赖性地在细胞内和细胞外积累。呼吸链酶复合物的生物能研究表明,孵育2周后复合物II-IV活性增加,复合物I和IV活性增加,复合物II和III活性降低。另外,人类近端小管细胞暴露于羟基钴胺素[c-内酰胺]和丙酸后显示出降低的谷胱甘肽含量。

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