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本文引用的文献

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Impact of caloric restriction on health and survival in rhesus monkeys from the NIA study.热量限制对 NIA 研究中恒河猴健康和存活的影响。
Nature. 2012 Sep 13;489(7415):318-21. doi: 10.1038/nature11432.
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SIRT3 protein deacetylates isocitrate dehydrogenase 2 (IDH2) and regulates mitochondrial redox status.SIRT3 蛋白使异柠檬酸脱氢酶 2(IDH2)去乙酰化,调节线粒体氧化还原状态。
J Biol Chem. 2012 Apr 20;287(17):14078-86. doi: 10.1074/jbc.M112.355206. Epub 2012 Mar 13.
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Calorie restriction reduces oxidative stress by SIRT3-mediated SOD2 activation.热量限制通过 SIRT3 介导的 SOD2 激活减少氧化应激。
Cell Metab. 2010 Dec 1;12(6):662-7. doi: 10.1016/j.cmet.2010.11.015.
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Cell. 2010 Nov 24;143(5):802-12. doi: 10.1016/j.cell.2010.10.002.
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Mitochondrial SIRT3 and heart disease.线粒体 SIRT3 与心脏病。
Cardiovasc Res. 2010 Nov 1;88(2):250-6. doi: 10.1093/cvr/cvq250. Epub 2010 Aug 4.
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Mitochondrial oxidative damage and apoptosis in age-related hearing loss.年龄相关性听力损失中的线粒体氧化损伤和细胞凋亡。
Mech Ageing Dev. 2010 Jul-Aug;131(7-8):480-6. doi: 10.1016/j.mad.2010.04.006. Epub 2010 Apr 29.
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Extending healthy life span--from yeast to humans.延长健康寿命——从酵母到人类。
Science. 2010 Apr 16;328(5976):321-6. doi: 10.1126/science.1172539.
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SIRT3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation.SIRT3 通过可逆酶去乙酰化作用调节线粒体脂肪酸氧化。
Nature. 2010 Mar 4;464(7285):121-5. doi: 10.1038/nature08778.
9
Age-related hearing loss in C57BL/6J mice is mediated by Bak-dependent mitochondrial apoptosis.C57BL/6J小鼠与年龄相关的听力损失是由Bak依赖性线粒体凋亡介导的。
Proc Natl Acad Sci U S A. 2009 Nov 17;106(46):19432-7. doi: 10.1073/pnas.0908786106. Epub 2009 Nov 9.
10
Recent progress in the biology and physiology of sirtuins.沉默调节蛋白生物学与生理学的最新进展。
Nature. 2009 Jul 30;460(7255):587-91. doi: 10.1038/nature08197.

保持良好听力:热量限制、Sirt3 和谷胱甘肽。

Maintaining good hearing: calorie restriction, Sirt3, and glutathione.

机构信息

Department of Aging and Geriatric Research, University of Florida, Gainesville, FL 32610, USA.

出版信息

Exp Gerontol. 2013 Oct;48(10):1091-5. doi: 10.1016/j.exger.2013.02.014. Epub 2013 Feb 20.

DOI:10.1016/j.exger.2013.02.014
PMID:23454634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3759555/
Abstract

Reducing calorie intake extends the lifespan of a variety of experimental models and delays progression of age-related hearing loss (AHL). AHL is a common feature of aging and is characterized by age-related decline of hearing associated with loss of sensory hair cells, spiral ganglion neurons, and/or stria vascularis degeneration in the cochlea. Sirtuins are a family of NAD(+)-dependent enzymes that regulate lifespan in lower organisms and have emerged as broad regulators of cellular fate. Our recent study indicated that mitochondrial Sirt3, a member of the sirtuin family, mediates the anti-aging effects of calorie restriction (CR) on AHL in mice. Interestingly, we also found that weight loss alone may not be sufficient for maintaining normal hearing. How does CR slow the progression of AHL through regulation of Sirt3? Here we review the evidence that during CR, Sirt3 slows the progression of AHL by promoting the glutathione-mediated mitochondrial antioxidant defense system in mice. A significant reduction in food consumption in one's daily life may not be a desirable and realistic option for most people. Therefore, identification/discovery of compounds that induce the activation of SIRT3 or glutathione reductase, or that increase mitochondrial glutathione levels has potential for maintaining good hearing through mimicking the anti-aging effects of CR in human inner ear cells.

摘要

减少热量摄入可以延长多种实验模型的寿命,并延缓与年龄相关的听力损失 (AHL) 的进展。AHL 是衰老的一个常见特征,其特征是与感觉毛细胞、螺旋神经节神经元和/或耳蜗中的血管纹退化相关的听力随年龄下降。Sirtuins 是一类依赖 NAD(+)的酶,可调节低等生物的寿命,并且已成为细胞命运的广泛调节剂。我们最近的研究表明,线粒体 Sirt3(Sirtuins 家族的一员)介导了热量限制 (CR) 对小鼠 AHL 的抗衰老作用。有趣的是,我们还发现,单独减轻体重可能不足以维持正常听力。CR 通过调节 Sirt3 如何减缓 AHL 的进展?在这里,我们回顾了证据,即 CR 期间,Sirt3 通过促进谷胱甘肽介导的线粒体抗氧化防御系统来减缓 AHL 的进展。在日常生活中显著减少食物摄入可能不是大多数人理想和现实的选择。因此,鉴定/发现可诱导 SIRT3 或谷胱甘肽还原酶激活或增加线粒体谷胱甘肽水平的化合物,通过模拟 CR 对人内耳细胞的抗衰老作用,具有维持良好听力的潜力。