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细胞色素还原酶与脂质代谢及健康寿命的调控

Cytochrome reductase and the control of lipid metabolism and healthspan.

作者信息

Martin-Montalvo Alejandro, Sun Yaning, Diaz-Ruiz Alberto, Ali Ahmed, Gutierrez Vincent, Palacios Hector H, Curtis Jessica, Siendones Emilio, Ariza Julia, Abulwerdi Gelareh A, Sun Xiaoping, Wang Annie X, Pearson Kevin J, Fishbein Kenneth W, Spencer Richard G, Wang Miao, Han Xianlin, Scheibye-Knudsen Morten, Baur Joe A, Shertzer Howard G, Navas Placido, Villalba Jose Manuel, Zou Sige, Bernier Michel, de Cabo Rafael

机构信息

Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.

Centro Andaluz de Biología del Desarrollo, and CIBERER, Instituto de Salud Carlos III, Universidad Pablo de Olavide-CSIC, Sevilla, Spain.

出版信息

NPJ Aging Mech Dis. 2016 May 12;2:16006. doi: 10.1038/npjamd.2016.6. eCollection 2016.

Abstract

Cytochrome reductases (CYB5R) are required for the elongation and desaturation of fatty acids, cholesterol synthesis and mono-oxygenation of cytochrome P450 enzymes, all of which are associated with protection against metabolic disorders. However, the physiological role of CYB5R in the context of metabolism, healthspan and aging remains ill-defined. We generated CYB5R-overexpressing flies (CYB5R-OE) and created a transgenic mouse line overexpressing CYB5R3 (CYB5R3-Tg) in the C57BL/6J background to investigate the function of this class of enzymes as regulators of metabolism and age-associated pathologies. Gender- and/or stage-specific induction of CYB5R, and pharmacological activation of CYB5R with tetrahydroindenoindole extended fly lifespan. Increased expression of CYB5R3 was associated with significant improvements in several metabolic parameters that resulted in modest lifespan extension in mice. Diethylnitrosamine-induced liver carcinogenesis was reduced in CYB5R3-Tg mice. Accumulation of high levels of long-chain polyunsaturated fatty acids, improvement in mitochondrial function, decrease in oxidative damage and inhibition of chronic pro-inflammatory pathways occurred in the transgenic animals. These results indicate that CYB5R represents a new target in the study of genes that regulate lipid metabolism and healthspan.

摘要

细胞色素还原酶(CYB5R)参与脂肪酸的延长和去饱和、胆固醇合成以及细胞色素P450酶的单加氧作用,所有这些都与预防代谢紊乱有关。然而,CYB5R在代谢、健康寿命和衰老方面的生理作用仍不明确。我们构建了过表达CYB5R的果蝇(CYB5R-OE),并在C57BL/6J背景下创建了过表达CYB5R3的转基因小鼠品系(CYB5R3-Tg),以研究这类酶作为代谢和年龄相关病理调节因子的功能。CYB5R的性别和/或阶段特异性诱导以及用四氢茚并吲哚对CYB5R进行药理学激活可延长果蝇寿命。CYB5R3表达的增加与几个代谢参数的显著改善相关,这导致小鼠寿命适度延长。CYB5R3-Tg小鼠中,二乙基亚硝胺诱导的肝癌发生减少。转基因动物中出现了高水平长链多不饱和脂肪酸的积累、线粒体功能的改善、氧化损伤的减少以及慢性促炎途径的抑制。这些结果表明,CYB5R是调节脂质代谢和健康寿命的基因研究中的一个新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c5/5515006/b01e030eb5d7/npjamd20166-f1.jpg

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