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肠道微生物组随年龄变化而改变大脑脂质组成。

Age-Related Changes in the Gut Microbiota Modify Brain Lipid Composition.

机构信息

Centre des Sciences du Goût et de l'Alimentation, AgroSup Dijon, CNRS, INRAE, University of Bourgogne Franche-Comté, Eye and Nutrition Research Group, Dijon, France.

Micalis Institute, INRAE, AgroParisTech, University Paris-Saclay, Jouy-en-Josas, France.

出版信息

Front Cell Infect Microbiol. 2020 Jan 14;9:444. doi: 10.3389/fcimb.2019.00444. eCollection 2019.

DOI:10.3389/fcimb.2019.00444
PMID:31993375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6970973/
Abstract

Understanding the molecular mechanisms underlying the changes observed during aging is a prerequisite to design strategies to prevent age-related diseases. Aging is associated with metabolic changes, including alteration in the brain lipid metabolism. These alterations may contribute to the development of pathophysiological conditions. Modifications in the gut microbiota composition are also observed during aging. As communication axes exist between the gut microbiota and the brain and knowing that microbiota influences the host metabolism, we speculated on whether age-associated modifications in the gut microbiota could be involved in the lipid changes observed in aging brain. For that purpose, germ-free mice were colonized by the fecal microbiota of young or old donor mice. Lipid classes and fatty acid profiles were determined in the brain (cortex), plasma and liver by thin-layer chromatography on silica gel-coated quartz rods and gas chromatography. Gut colonization by microbiota of old mice resulted in a significant increase in total monounsaturated fatty acids (MUFA) and a significant decrease in the relative amounts of cholesterol and total polyunsaturated fatty acids (PUFA) in the cortex. Among the eight most represented fatty acids in the cortex, the relative abundances of five (C18:1n-9, C22:6n-3, C20:4n-6, C18:1n-7, and C20:1n-9) were significantly altered in mice inoculated with an aged microbiota. Liquid chromatography analyses revealed that the relative abundance of major species among phosphatidyl and plasmenylcholine (PC 16:0/18:1), phosphatidyl and plasmenylethanolamine (PE 18:0/22:6), lysophosphatidylethanolamine (LPE 22:6) and sphingomyelins (SM d18:1/18:0) were significantly altered in the cortex of mice colonized by the microbiota obtained from aged donors. Transplantation of microbiota from old mice also modified the lipid class and fatty acid content in the liver. Finally, we found that the expression of several genes involved in MUFA and PUFA synthesis (, and ) was dysregulated in mice inoculated with an aged microbiota. In conclusion, our data suggest that changes in gut microbiota that are associated with aging can impact brain and liver lipid metabolisms. Lipid changes induced by an aged microbiota recapitulate some features of aging, thus pointing out the potential role of microbiota alterations in the age-related degradation of the health status.

摘要

了解衰老过程中观察到的变化的分子机制是设计预防与年龄相关疾病的策略的前提。衰老与代谢变化有关,包括大脑脂质代谢的改变。这些改变可能有助于发展生理病理条件。在衰老过程中还观察到肠道微生物组组成的改变。由于肠道微生物组和大脑之间存在通讯轴,并且知道微生物组会影响宿主代谢,我们推测与年龄相关的肠道微生物组的改变是否与衰老大脑中观察到的脂质变化有关。为此,无菌小鼠通过年轻或年老供体小鼠的粪便微生物组定植。通过硅胶涂覆石英棒上的薄层色谱法和气相色谱法,在大脑(皮层)、血浆和肝脏中确定脂质类和脂肪酸谱。用老年小鼠的微生物组定植肠道会导致皮层中总单不饱和脂肪酸(MUFA)显著增加,胆固醇和总多不饱和脂肪酸(PUFA)的相对量显著减少。在皮层中最具代表性的八种脂肪酸中,五种(C18:1n-9、C22:6n-3、C20:4n-6、C18:1n-7 和 C20:1n-9)的相对丰度在接种老化微生物组的小鼠中显著改变。液相色谱分析显示,在磷酸胆碱(PC 16:0/18:1)和磷脂酰乙醇胺(PE 18:0/22:6)、溶血磷脂酰乙醇胺(LPE 22:6)和神经鞘磷脂(SM d18:1/18:0)中的主要物种的相对丰度在由年老供体获得的微生物组定植的小鼠的皮层中发生了显著改变。来自老年供体的微生物组的移植也改变了肝脏的脂质类和脂肪酸含量。最后,我们发现,在接种老化微生物组的小鼠中,几种参与 MUFA 和 PUFA 合成的基因(,和)的表达失调。总之,我们的数据表明,与衰老相关的肠道微生物组的变化会影响大脑和肝脏的脂质代谢。由老化微生物组诱导的脂质变化再现了衰老的一些特征,从而指出了微生物组改变在与年龄相关的健康状态恶化中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d13e/6970973/783982203e7d/fcimb-09-00444-g0007.jpg
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