Gut Microbiota in Vascular Disease: Therapeutic Target?

被引:28
作者
Anbazhagan, A. N. [1 ]
Priyamvada, S. [1 ]
Priyadarshini, M. [2 ]
机构
[1] Univ Illinois, Div Gastroenterol & Hepatol, Dept Med, Coll Med, Chicago, IL 60612 USA
[2] Northwestern Univ, Feinberg Sch Med, Div Endocrinol Metab & Mol Med, Chicago, IL 60611 USA
关键词
Cardiovascular disease; carnitine; choline; gut microbiota; trimethylamine; trimethylamine-N-oxide; CHAIN FATTY-ACIDS; PROTEIN-COUPLED RECEPTOR; TRIMETHYLAMINE-N-OXIDE; GLUCOSE-METABOLISM; NERVOUS-SYSTEM; ATHEROSCLEROSIS; OBESITY; DIET; PHOSPHATIDYLCHOLINE; FERMENTATION;
D O I
10.2174/1570161115666170105095834
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Background: Gut microbiota is increasingly recognized as a powerful regulator of host physiology. Most of its effects are mediated through metabolites acting as energy sources, signaling receptor ligands and substrates for host enzymes. Owing to the meta-stability and high amenability of the gut microbiota to modification by diet and environment predicting specific gut microbes or its metabolites responsible for different host metabolic states is often confounded. Methods: The Pubmed was searched for research articles on gut microbiota and cardiovascular disease. Results: The searched articles reported a direct role of gut microbes in cardiovascular disorders (CVD). The interaction among gut microbial metabolism (through breakdown of certain dietary nutrients like choline), host immune system and lipid metabolism generate conditions that promote atherosclerosis development. Importantly, components of this interactive system can be explored to identify points of intervention in the path of disease development. Based on this strategies targeting gut microbial composition and activity are being explored as therapies against CVD. Use of archaebiotics and 3,3-dimethyl-1-butanol aiming to reduce TMA (trimethylamine) conversion to TMAO (trimethylamine-N-oxide) and high fibre diets to reduce TMA precursors while simultaneously selecting for beneficial gut bacteria are attractive anti-atherogenic approaches. Conclusion: Success of these approaches in humans however, requires extensive research.
引用
收藏
页码:291 / 295
页数:5
相关论文
共 66 条
[1]
Effects of antibiotic therapy on outcomes of patients with coronary artery disease - A meta-analysis of randomized controlled trials [J].
Andraws, R ;
Berger, JS ;
Brown, DL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 293 (21) :2641-2647
[2]
Propionate. Anti-obesity and satiety enhancing factor? [J].
Arora, Tulika ;
Sharma, Rajkumar ;
Frost, Gary .
APPETITE, 2011, 56 (02) :511-515
[3]
Male mice that lack the G-protein-coupled receptor GPR41 have low energy expenditure and increased body fat content [J].
Bellahcene, Mohamed ;
O'Dowd, Jacqueline F. ;
Wargent, Ed T. ;
Zaibi, Mohamed S. ;
Hislop, David C. ;
Ngala, Robert A. ;
Smith, David M. ;
Cawthorne, Michael A. ;
Stocker, Claire J. ;
Arch, Jonathan R. S. .
BRITISH JOURNAL OF NUTRITION, 2013, 109 (10) :1755-1764
[4]
Trimethylamine-N-Oxide, a Metabolite Associated with Atherosclerosis, Exhibits Complex Genetic and Dietary Regulation [J].
Bennett, Brian J. ;
Vallim, Thomas Q. de Aguiar ;
Wang, Zeneng ;
Shih, Diana M. ;
Meng, Yonghong ;
Gregory, Jill ;
Allayee, Hooman ;
Lee, Richard ;
Graham, Mark ;
Crooke, Rosanne ;
Edwards, Peter A. ;
Hazen, Stanley L. ;
Lusis, Aldons J. .
CELL METABOLISM, 2013, 17 (01) :49-60
[5]
Short, but Smart: SCFAs Train T Cells in the Gut to Fight Autoimmunity in the Brain [J].
Bhutia, Yangzom D. ;
Ganapathy, Vadivel .
IMMUNITY, 2015, 43 (04) :629-631
[6]
Archaebiotics Proposed therapeutic use of archaea to prevent trimethylaminuria and cardiovascular disease [J].
Brugere, Jean-Francois ;
Borrel, Guillaume ;
Gaci, Nadia ;
Tottey, William ;
O'Toole, Paul W. ;
Malpuech-Brugere, Corinne .
GUT MICROBES, 2014, 5 (01) :5-10
[7]
Short-chain fatty acids in control of body weight and insulin sensitivity [J].
Canfora, Emanuel E. ;
Jocken, Johan W. ;
Blaak, Ellen E. .
NATURE REVIEWS ENDOCRINOLOGY, 2015, 11 (10) :577-591
[8]
Gut microbiota fermentation of prebiotics increases satietogenic and incretin gut peptide production with consequences for appetite sensation and glucose response after a meal [J].
Cani, Patrice D. ;
Lecourt, Elodie ;
Dewulf, Evelyne M. ;
Sohet, Florence M. ;
Pachikian, Barbara D. ;
Naslain, Damien ;
De Backer, Fabienne ;
Neyrinck, Audrey M. ;
Delzenne, Nathalie M. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2009, 90 (05) :1236-1243
[9]
Role of gut microbiota in the modulation of atherosclerosis-associated immune response [J].
Chistiakov, Dmitry A. ;
Bobryshev, Yuri V. ;
Kozarov, Emil ;
Sobenin, Igor A. ;
Orekhov, Alexander N. .
FRONTIERS IN MICROBIOLOGY, 2015, 6
[10]
Cummings J. H., 1995, PHYSL CLIN ASPECTS S