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DNA结合肽对衰老过程中一些改变的代谢途径的调节活性。

Regulatory activity of DNA-binding peptides on some metabolic pathways altered in aging.

作者信息

Amici D, Maraldi N, Marsili G, Palatroni P, Gianfranceschi G L

出版信息

Mech Ageing Dev. 1983 Nov-Dec;23(3-4):215-34. doi: 10.1016/0047-6374(83)90022-2.

Abstract

The Smith theory, which describes aging as a consequence of damage at DNA transcription level, suggested to us the opportunity of studying the possible action of DNA-binding peptides from calf thymus on old rats. We previously demonstrated that this peptidic fraction exerts a regulative control on transcriptional activities of DNA in cell and cell-free systems. In order to verify the possible action of these low molecular weight peptides we chose a large range of metabolic and structural parameters which are altered in aging. The results obtained indicate the following conclusions. Lipids. The lipid levels of old rat liver and serum are altered compared with those of young rats; the administration of peptidic fraction to old rats reverses the lipid alterations observed. Glucides. In old rat liver the presence of glycogen is very scanty or completely absent; the animals treated with the peptides show an amount and distribution of glycogen similar to that of adult normal rats. ATP. The peptidic fraction causes in the old rats a marked increase of blood ATP, bringing the level in the range of values determined in young rats. DNA, RNA, proteins. The total synthesis rate of DNA, RNA and proteins in old rat liver is not influenced by the DNA-binding peptides. Vice versa the nucleic acids from liver nuclei of old rats given peptidic fraction contain a greater RNA component compared to control old rats. This result is confirmed by the strong increase of transcriptional activity of DNA for RNA polymerase caused by administration of peptidic fraction to old rats. This increased DNA transcription can be interpreted as a partial recovery of DNA transcriptional capacity which evidently might imply a restoration of impaired metabolic systems. The histochemical and stereological analyses of liver cell compartments confirm the biochemical data.

摘要

史密斯理论将衰老描述为DNA转录水平损伤的结果,这为我们提供了研究来自小牛胸腺的DNA结合肽对老年大鼠可能作用的机会。我们之前证明,这种肽段在细胞和无细胞系统中对DNA的转录活性发挥调节作用。为了验证这些低分子量肽的可能作用,我们选择了一系列在衰老过程中发生改变的代谢和结构参数。所得结果表明以下结论。脂质。与年轻大鼠相比,老年大鼠肝脏和血清中的脂质水平发生了改变;给老年大鼠施用肽段可逆转所观察到的脂质改变。糖类。老年大鼠肝脏中糖原的含量非常少或完全不存在;用这些肽处理的动物显示出糖原的数量和分布与成年正常大鼠相似。三磷酸腺苷(ATP)。肽段使老年大鼠血液中的ATP显著增加,使其水平处于年轻大鼠所测定的值范围内。DNA、RNA、蛋白质。老年大鼠肝脏中DNA、RNA和蛋白质的总合成速率不受DNA结合肽的影响。相反,与对照老年大鼠相比,接受肽段处理的老年大鼠肝细胞核中的核酸含有更大比例的RNA成分。给老年大鼠施用肽段导致RNA聚合酶对DNA的转录活性大幅增加,这证实了这一结果。这种DNA转录增加可被解释为DNA转录能力的部分恢复,这显然可能意味着受损代谢系统的恢复。肝细胞区室的组织化学和体视学分析证实了生化数据。

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