Microbial metabolism of dietary components to bioactive metabolites: opportunities for new therapeutic interventions

被引:259
作者
Zhang, Linda S. [1 ,2 ]
Davies, Sean S. [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Div Clin Pharmacol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Vanderbilt Inst Chem Biol, Nashville, TN 37232 USA
来源
GENOME MEDICINE | 2016年 / 8卷
基金
美国国家卫生研究院;
关键词
CHAIN FATTY-ACIDS; CONJUGATED LINOLEIC-ACID; P-CRESYL SULFATE; TRIMETHYLAMINE-N-OXIDE; ARYL-HYDROCARBON RECEPTOR; BOUND UREMIC TOXINS; KAPPA-B ACTIVATION; GUT MICROBIOTA; COLORECTAL-CANCER; INDOXYL SULFATE;
D O I
10.1186/s13073-016-0296-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mass spectrometry- and nuclear magnetic resonance-based metabolomic studies comparing diseased versus healthy individuals have shown that microbial metabolites are often the compounds most markedly altered in the disease state. Recent studies suggest that several of these metabolites that derive from microbial transformation of dietary components have significant effects on physiological processes such as gut and immune homeostasis, energy metabolism, vascular function, and neurological behavior. Here, we review several of the most intriguing diet-dependent metabolites that may impact host physiology and may therefore be appropriate targets for therapeutic interventions, such as short-chain fatty acids, trimethylamine N-oxide, tryptophan and tyrosine derivatives, and oxidized fatty acids. Such interventions will require modulating either bacterial species or the bacterial biosynthetic enzymes required to produce these metabolites, so we briefly describe the current understanding of the bacterial and enzymatic pathways involved in their biosynthesis and summarize their molecular mechanisms of action. We then discuss in more detail the impact of these metabolites on health and disease, and review current strategies to modulate levels of these metabolites to promote human health. We also suggest future studies that are needed to realize the full therapeutic potential of targeting the gut microbiota.
引用
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页数:18
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