Regulation of blood brain barrier integrity by microbiome-associated methylamines and cognition by trimethylamine N-oxide

被引:126
作者
Hoyles, Lesley [1 ]
Pontifex, Matthew G. [2 ]
Rodriguez-Ramiro, Ildefonso [2 ,3 ]
Anis-Alavi, M. Areeb [4 ]
Jelane, Khadija S. [4 ]
Snelling, Tom [5 ]
Solito, Egle [6 ,7 ]
Fonseca, Sonia [8 ]
Carvalho, Ana L. [8 ]
Carding, Simon R. [2 ,8 ]
Muller, Michael [2 ]
Glen, Robert C. [5 ,9 ]
Vauzour, David [2 ]
McArthur, Simon [4 ]
机构
[1] Nottingham Trent Univ, Sch Sci & Technol, Dept Biosci, Nottingham, England
[2] Univ East Anglia, Norwich Med Sch, Norwich, Norfolk, England
[3] Madrid Inst Adv Studies IMDEA Food, Metab Syndrome Grp, E-28049 Madrid, Spain
[4] Queen Mary Univ London, Fac Med & Dent, Inst Dent, London, England
[5] Imperial Coll London, Fac Med, Dept Metab Digest & Reprod, London, England
[6] Queen Mary Univ London, Fac Med & Dent, William Harvey Res Inst, London, England
[7] Univ Naples Federico II, Dipartimento Med Mol & Biotecnol Med, Naples, Italy
[8] Quadram Inst, Gut Microbes & Hlth Res Programme, Norwich Res Pk, Norwich, Norfolk, England
[9] Univ Cambridge, Ctr Mol Informat, Dept Chem, Cambridge, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Trimethylamine N-oxide; Trimethylamine; Blood-brain barrier; Cognition; ANNEXIN A1; TRANSGENIC MICE; DIETARY CHOLINE; FATTY-ACIDS; PERFORMANCE; DISRUPTION; METABOLITE; IDENTIFICATION; ACCUMULATION; INVOLVEMENT;
D O I
10.1186/s40168-021-01181-z
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Communication between the gut microbiota and the brain is primarily mediated via soluble microbe-derived metabolites, but the details of this pathway remain poorly defined. Methylamines produced by microbial metabolism of dietary choline and L-carnitine have received attention due to their proposed association with vascular disease, but their effects upon the cerebrovascular circulation have hitherto not been studied. Results: Here, we use an integrated in vitro/in vivo approach to show that physiologically relevant concentrations of the dietary methylamine trimethylamine N-oxide (TMAO) enhanced blood-brain barrier (BBB) integrity and protected it from inflammatory insult, acting through the tight junction regulator annexin Al. In contrast, the TMAO precursor trimethylamine (TMA) impaired BBB function and disrupted tight junction integrity. Moreover, we show that long-term exposure to TMAO protects murine cognitive function from inflammatory challenge, acting to limit astrocyte and microglial reactivity in a brain region-specific manner. Conclusion: Our findings demonstrate the mechanisms through which microbiome-associated methylamines directly interact with the mammalian BBB, with consequences for cerebrovascular and cognitive function.
引用
收藏
页数:21
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