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首页> 外文期刊>Peptides: An International Journal >Neuropeptide Y damages the integrity of mitochondrial structure and disrupts energy metabolism in cultured neonatal rat cardiomyocytes
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Neuropeptide Y damages the integrity of mitochondrial structure and disrupts energy metabolism in cultured neonatal rat cardiomyocytes

机译:神经肽Y破坏了培养的新生大鼠心肌细胞中线粒体结构的完整性并破坏了能量代谢

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摘要

Neuropeptide Y (NPY) plays an important role in cardiovascular diseases including stress cardiomyopathy, hypertrophic cardiomyopathy, heart failure, diabetic cardiomyopathy, hypertension, and so on. However, inconsistent results related to the role of NPY in the different types of cardiomyopathies make the exact involvement of the peptide elusive. Considering these effects are known to be involved in energy balance, as the hearts energy producer, the mitochondria, should be investigated, and not only mitochondrial structure but also its potential. Up to now, the impact of NPY on energy metabolism and mitochondria in cultured neonatal rat cardiomyocytes has not been reported. The main objective of our study was to test the role of NPY in cultured neonatal rat cardiomyocytes. After 24-h stimulation of NPY, the ATP content and activity of the cardiomyocytes were determined by Cell Counting Kit-8 and ATP-dependent bioluminescence assay kit, respectively. To further measure these effects, mitochondrial membrane potential was measured by JC-1 staining, the change of mitochondrial structure was detected by transmission electron microscopy, and the levels of PGC-1 alpha (a marker of mitochondrial energy metabolism) mRNA and protein expression were determined by real-time PCR and Western blotting, respectively. The results showed that after 24-h stimulation of NPY, ATP content and activity in the cardiomyocytes were decreased. Moreover, cardiomyocyte mitochondria were changed in morphology. Further, a decline of mitochondrial membrane potential was induced in a dose-dependent manner and the levels of PGC-1 alpha mRNA and protein expression were up-regulated after being treated by different dose of NPY. The results indicate that energy metabolism is suppressed, mitochondrial structure and membrane potential damaged, and PGC-alpha is changed in cultured neonatal rat cardiomyocytes after being treated by NPY. (C) 2015 Elsevier Inc. All rights reserved.
机译:神经肽Y(NPY)在包括应激性心肌病,肥厚型心肌病,心力衰竭,糖尿病性心肌病,高血压等心血管疾病中起重要作用。但是,与NPY在不同类型的心肌病中的作用有关的不一致结果使得该肽的确切参与难以捉摸。考虑到这些影响与能量平衡有关,因此应该研究心脏能量产生器线粒体,不仅要研究线粒体的结构,还要研究其潜力。迄今为止,尚未报道NPY对培养的新生大鼠心肌细胞能量代谢和线粒体的影响。我们研究的主要目的是测试NPY在培养的新生大鼠心肌细胞中的作用。刺激NPY 24小时后,分别通过Cell Counting Kit-8和ATP依赖性生物发光测定试剂盒测定心肌细胞的ATP含量和活性。为了进一步测量这些效果,通过JC-1染色测量线粒体膜电位,通过透射电镜检测线粒体结构的变化,并检测PGC-1α(线粒体能量代谢的标志物)的mRNA和蛋白质表达。分别通过实时PCR和蛋白质印迹法测定。结果显示,在刺激NPY 24小时后,心肌细胞中ATP含量和活性降低。此外,心肌线粒体的形态发生了变化。此外,线粒体膜电位的下降以剂量依赖性方式引起,并且在用不同剂量的NPY治疗后,PGC-1α的mRNA和蛋白质表达水平被上调。结果表明,NPY处理后,新生大鼠心肌细胞能量代谢受到抑制,线粒体结构和膜电位受损,PGC-α发生改变。 (C)2015 Elsevier Inc.保留所有权利。

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