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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Suppressive effect of nobiletin, a citrus polymethoxyflavonoid that downregulates thioredoxin-interacting protein expression, on tunicamycin-induced apoptosis in SK-N-SH human neuroblastoma cells
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Suppressive effect of nobiletin, a citrus polymethoxyflavonoid that downregulates thioredoxin-interacting protein expression, on tunicamycin-induced apoptosis in SK-N-SH human neuroblastoma cells

机译:Nobiletin是一种柑橘类多甲氧基类黄酮,能下调与硫氧还蛋白相互作用的蛋白表达,对衣霉素诱导的SK-N-SH人神经母细胞瘤细胞凋亡具有抑制作用。

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摘要

Increased expression of thioredoxin-interacting protein (TXNIP) has recently been proved to be a crucial event for irremediable endoplasmic reticulum (ER) stress resulting in the programmed cell death (apoptosis) of pancreatic β-cells. The present study demonstrated that treatment with 1-10. μg/ml tunicamycin, a potent revulsant of ER stress, drastically induced TXNIP expression accompanied by the generation of cleaved caspase-3 as an indicator of apoptosis in SK-N-SH human neuroblastoma cells. This result substantiated that TXNIP is also involved in neurodegeneration triggered by ER stress. Moreover, we evaluated the effects of nobiletin, a citrus polymethoxyflavonoid, on tunicamycin-induced apoptosis and TXNIP expression in SK-N-SH cells, because we reported previously that this flavonoid might be able to reduce TXNIP expression. Co-treatment of SK-N-SH cells with 100. μM nobiletin and 1. μg/ml tunicamycin for 24. h strongly suppressed apoptosis and increased TXNIP expression induced by 1. μg/ml tunicamycin treatment alone. In addition, we proved that the ability of 100. μM nobiletin treatment to reduce TXNIP expression is exerted from 3. h after the onset of treatment. Therefore, the protective and ameliorative effects of nobiletin on neuronal degeneration and impaired memory, which several studies using animal models have demonstrated, might arise in part from nobiletin's ability to repress TXNIP expression.
机译:最近已证明,与硫氧还蛋白相互作用蛋白(TXNIP)的表达增加是导致无法修复的内质网(ER)应激导致胰腺β细胞程序性死亡(细胞凋亡)的关键事件。本研究证明用1-10进行治疗。 μg/ ml衣霉素,一种有效的内质网应激调节剂,可大幅度诱导TXNIP表达,并产生裂解的caspase-3,作为SK-N-SH人成神经细胞瘤细胞凋亡的指标。该结果证实了TXNIP也参与由ER应激触发的神经变性。此外,我们评估了Nobiletin(一种柑橘类聚甲氧基黄酮类化合物)对衣霉素诱导的SK-N-SH细胞凋亡和TXNIP表达的影响,因为我们以前曾报道过这种类黄酮可能能够降低TXNIP表达。将SK-N-SH细胞与100.μM的Nobiletin和1.μg/ ml的衣霉素共同处理24. h,可强烈抑制单独用1.μg/ ml的衣霉素处理诱导的细胞凋亡并增加TXNIP表达。此外,我们证明了从治疗开始后的3. h开始发挥100.μMNobiletin处理降低TXNIP表达的能力。因此,使用动物模型的多项研究表明,诺比列汀对神经元变性和受损记忆的保护和改善作用可能部分源于诺比列汀抑制TXNIP表达的能力。

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