首页> 美国卫生研究院文献>The Journals of Gerontology Series A: Biological Sciences and Medical Sciences >Exposure to High or Low Glucose Levels Accelerates the Appearance of Markers of Endothelial Cell Senescence and Induces Dysregulation of Nitric Oxide Synthase
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Exposure to High or Low Glucose Levels Accelerates the Appearance of Markers of Endothelial Cell Senescence and Induces Dysregulation of Nitric Oxide Synthase

机译:暴露于高或低葡萄糖水平会加速内皮细胞衰老标记的出现并诱导一氧化氮合酶失调。

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摘要

To test the hypothesis that aging impairs endothelial cell response to glucose stress, we utilized a human umbilical vein endothelial cell in vitro model in which clinically relevant concentrations of normal (5.5mM), high (25mM), and low (1.5mM) glucose were tested. With advancing population doubling, exposure to normal glucose gradually decreased endothelial nitric oxide synthase expression and activity, resulting in slow, progressive development of markers of cell senescence (by population doubling level [PDL] 44). High or low glucose treatment accelerated the appearance of markers of senescence (by ~PDL 35) along with declines in endothelial nitric oxide synthase expression and activity. Human umbilical vein endothelial cells exposed to alternating low and high glucose gave even more rapid acceleration in the appearance of markers of senescence (by ~PDL 18) and reduction in endothelial nitric oxide synthase levels. Thus, exposure to low and high glucose induces earlier appearance of markers of endothelial cell senescence and dysregulation of the nitric oxide synthase gene and protein expression and function. These findings will help to elucidate endothelial dysfunction associated with glucose intolerance and improve future therapy for diabetic seniors.
机译:为了检验衰老会损害内皮细胞对葡萄糖应激的假说,我们使用了人脐静脉内皮细胞体外模型,其中临床上相关浓度的正常(5.5mM),高(25mM)和低(1.5mM)葡萄糖为经过测试。随着种群数量的增加,暴露于正常葡萄糖会逐渐降低内皮型一氧化氮合酶的表达和活性,从而导致细胞衰老标记物的缓慢,逐步发展(通过种群数量增加[PDL] 44)。高或低葡萄糖治疗加速了衰老标记的出现(通过〜PDL 35),同时内皮一氧化氮合酶表达和活性下降。暴露于低葡萄糖和高葡萄糖的交替作用的人脐静脉内皮细胞在衰老标记的出现(通过〜PDL 18)和内皮型一氧化氮合酶水平降低方面甚至提供了更快的加速。因此,暴露于低和高葡萄糖会诱导内皮细胞衰老的标志物的早期出现,以及一氧化氮合酶基因,蛋白质表达和功能的失调。这些发现将有助于阐明与葡萄糖耐受不良相关的内皮功能障碍,并改善糖尿病老年人的未来治疗。

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