Suppr超能文献

小鼠年龄很重要:年龄如何影响小鼠血浆代谢组。

Mouse Age Matters: How Age Affects the Murine Plasma Metabolome.

作者信息

Pann Patrick, de Angelis Martin Hrabě, Prehn Cornelia, Adamski Jerzy

机构信息

Research Unit Molecular Endocrinology and Metabolism, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), 85764 Neuherberg, Germany.

German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), 85764 Neuherberg, Germany.

出版信息

Metabolites. 2020 Nov 19;10(11):472. doi: 10.3390/metabo10110472.

Abstract

A large part of metabolomics research relies on experiments involving mouse models, which are usually 6 to 20 weeks of age. However, in this age range mice undergo dramatic developmental changes. Even small age differences may lead to different metabolomes, which in turn could increase inter-sample variability and impair the reproducibility and comparability of metabolomics results. In order to learn more about the variability of the murine plasma metabolome, we analyzed male and female C57BL/6J, C57BL/6NTac, 129S1/SvImJ, and C3HeB/FeJ mice at 6, 10, 14, and 20 weeks of age, using targeted metabolomics (BIOCRATES Absolute™ p150 Kit). Our analysis revealed high variability of the murine plasma metabolome during adolescence and early adulthood. A general age range with minimal variability, and thus a stable metabolome, could not be identified. Age-related metabolomic changes as well as the metabolite profiles at specific ages differed markedly between mouse strains. This observation illustrates the fact that the developmental timing in mice is strain specific. We therefore stress the importance of deliberate strain choice, as well as consistency and precise documentation of animal age, in metabolomics studies.

摘要

代谢组学研究的很大一部分依赖于涉及小鼠模型的实验,这些小鼠通常为6至20周龄。然而,在这个年龄范围内,小鼠会经历显著的发育变化。即使是很小的年龄差异也可能导致不同的代谢组,进而增加样本间的变异性,并损害代谢组学结果的可重复性和可比性。为了更多地了解小鼠血浆代谢组的变异性,我们使用靶向代谢组学(BIOCRATES Absolute™ p150试剂盒)对6、10、14和20周龄的雄性和雌性C57BL/6J、C57BL/6NTac、129S1/SvImJ和C3HeB/FeJ小鼠进行了分析。我们的分析揭示了青春期和成年早期小鼠血浆代谢组的高度变异性。无法确定一个变异性最小、代谢组稳定的一般年龄范围。不同小鼠品系之间,与年龄相关的代谢组学变化以及特定年龄的代谢物谱存在显著差异。这一观察结果说明了小鼠的发育时间具有品系特异性这一事实。因此,我们强调在代谢组学研究中,慎重选择品系以及对动物年龄进行一致且精确记录的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df3e/7699431/0131861bd761/metabolites-10-00472-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验