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小鼠肝脏中的热量限制、应激与泛素依赖性途径

Calorie restriction, stress and the ubiquitin-dependent pathway in mouse livers.

作者信息

Scrofano M M, Shang F, Nowell T R, Gong X, Smith D E, Kelliher M, Dunning J, Mura C V, Taylor A

机构信息

Laboratory for Nutrition and Vision Research, Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA 02111, USA.

出版信息

Mech Ageing Dev. 1998 Nov 16;105(3):273-90. doi: 10.1016/s0047-6374(98)00097-9.

Abstract

Calorie restriction (R) is the only known method to delay the aging process and extend mean and maximal lifespan in rodents. R has been shown to delay the age-related accumulation of damaged proteins and to protect organisms from various stresses which can produce damaged proteins. Such stresses include irradiation, heat shock, and oxidative stress. The ubiquitin- and ATP-dependent proteolytic pathway (UPP) has been associated with the degradation of abnormal and/or damaged proteins. We examined the effect of diet and oxidative stress on activities of the UPP in supernatants from livers taken from 23-month-old Emory mice which had been exposed to an in-vivo injection of paraquat. Paraquat induces oxidative stress by generating superoxide radicals. In livers from non-stressed animals, steady-state levels of endogenous ubiquitin conjugates, de novo conjugate formation, and E1 and E2 activities were significantly lower in R animals than in control (C) animals. However, after exposure to paraquat, levels of endogenous ubiquitin conjugates were significantly higher in R versus C animals, and de novo conjugate formation and E1 and E2 activities in R animals rose to levels which were indistinguishable from levels of these activities noted in C animals. R was associated with an increased ability to degrade beta-lactoglobulin by the UPP after an oxidative stress was imposed. Ability to degrade beta-lactoglobulin by the C or R livers in non-stressed animals was not significantly different. Taken together, these data indicate that oxidative stress in R animals is associated with enhanced levels of ubiquitin conjugates and that this enhancement may be due to an increase in UPP activity. These data also indicate that the ability to form ubiquitin conjugates and the UPP system does not change with oxidative stress in C animals. The latter is consistent with prior reports that suggests that older C animals may already be in a state of enhanced oxidative stress and that activities of the UPP provide a sensitive indicator of levels of cellular redox status.

摘要

热量限制(R)是目前已知的唯一能延缓衰老过程并延长啮齿动物平均寿命和最大寿命的方法。研究表明,R可延缓与年龄相关的受损蛋白质积累,并保护生物体免受各种可产生受损蛋白质的应激影响。这些应激包括辐射、热休克和氧化应激。泛素和ATP依赖的蛋白水解途径(UPP)与异常和/或受损蛋白质的降解有关。我们研究了饮食和氧化应激对23月龄埃默里小鼠肝脏上清液中UPP活性的影响,这些小鼠已接受体内百草枯注射。百草枯通过产生超氧自由基诱导氧化应激。在未受应激动物的肝脏中,R组动物内源性泛素缀合物的稳态水平、从头缀合物形成以及E1和E2活性显著低于对照组(C)动物。然而,在接触百草枯后,R组动物内源性泛素缀合物水平显著高于C组动物,且R组动物的从头缀合物形成以及E1和E2活性升至与C组动物这些活性水平无显著差异的水平。在施加氧化应激后,R组动物通过UPP降解β-乳球蛋白的能力增强。在未受应激的动物中,C组或R组肝脏降解β-乳球蛋白的能力无显著差异。综上所述,这些数据表明R组动物的氧化应激与泛素缀合物水平升高有关,这种升高可能是由于UPP活性增加所致。这些数据还表明,C组动物形成泛素缀合物的能力和UPP系统不会随氧化应激而改变。后者与先前的报道一致,即表明年龄较大的C组动物可能已经处于氧化应激增强的状态,且UPP的活性是细胞氧化还原状态水平的敏感指标。

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