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Neuropeptide Y induces cardiomyocyte hypertrophy via calcineurin signaling in rats.

机译:神经肽Y通过钙调神经磷酸酶在大鼠中诱导心肌肥大。

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摘要

Neuropeptide Y (NPY) has been shown to participate in cardiac hypertrophy. However, the mechanisms by which NPY induces cardiomyocyte hypertrophy are poorly understood. This study tested the hypothesis that NPY induces cardiomyocyte hypertrophy through Ca(2+)/CaM-dependent calcineurin (CaN) pathway in cultured neonatal rat cardiomyocytes. After 24-h treatment, NPY (100 nM) significantly increased (3)H-leucine incorporation and c-Jun mRNA expression, concomitant with augment of CaN activity and protein level in cardiomyocytes compared to those cells without NPY treatment. The enhancement of (3)H-leucine incorporation and c-Jun mRNA expression in cardiomyocytes treated with NPY were markedly inhibited by cyclosporine A (CsA), a selective inhibitor of CaN. We also investigated the effect of NPY on intracellular Ca(2+) level in cardiomyocytes. There were no obvious changes in intracellular Ca(2+) level of cytoplasm and nucleus in cardiomyocytes treated with NPY (100 nM) for 10 min. However, NPY significantly increased intracellular Ca(2+) level of cytoplasm and nucleus in cardiomyocytes after 24-h treatment. The result suggested that NPY could induce hypertrophy of cardiomyocytes via Ca(2+)/CaM-dependent CaN signal pathway. The enhancement of [Ca(2+)](i) caused by NPY may activate CaN signal pathways to mediate cardiac hypertrophy.
机译:神经肽Y(NPY)已显示参与心脏肥大。但是,NPY诱导心肌肥大的机制了解甚少。这项研究检验了假说NPY通过Ca(2 +)/ CaM依赖性钙调神经磷酸酶(CaN)途径在培养的新生大鼠心肌细胞中诱导心肌肥大。处理24小时后,与未进行NPY处理的细胞相比,NPY(100 nM)显着增加(3)H-亮氨酸的掺入和c-Jun mRNA的表达,同时增加了心肌细胞CaN活性和蛋白质水平。 NPY处理的心肌细胞中(3)H-亮氨酸掺入和c-Jun mRNA表达的增强被CaN的选择性抑制剂环孢霉素A(CsA)显着抑制。我们还调查了NPY对心肌细胞内Ca(2+)水平的影响。 NPY(100 nM)处理10分钟的心肌细胞的细胞内Ca(2+)细胞质和细胞核水平无明显变化。但是,NPY显着增加了24小时治疗后心肌细胞的胞内Ca(2+)水平的细胞质和细胞核。结果表明,NPY可以通过Ca(2 +)/ CaM依赖性CaN信号途径诱导心肌肥大。由NPY引起的[Ca(2 +)](i)增强可能激活CaN信号通路来介导心脏肥大。

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