The therapeutic potential of dietary intervention: based on the mechanism of a tryptophan derivative-indole propionic acid on metabolic disorders

被引:29
作者
Niu, Ben [1 ,2 ]
Pan, Tong [1 ,2 ]
Xiao, Yue [1 ,2 ]
Wang, Hongchao [1 ,2 ]
Zhu, Jinlin [1 ,2 ]
Tian, Fengwei [1 ,2 ]
Lu, Wenwei [1 ,2 ,3 ]
Chen, Wei [1 ,2 ,3 ]
机构
[1] Jiangnan Univ, State Key Lab Food Sci & Resources, Wuxi, Peoples R China
[2] Jiangnan Univ, Sch Food Sci & Technol, Wuxi, Peoples R China
[3] Jiangnan Univ, Natl Engn Res Ctr Funct Food, Wuxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Diet intervention; gut microbiota pathway; indole propionic acid (IPA); metabolic disorders; tryptophan mechanism; ARYL-HYDROCARBON RECEPTOR; AROMATIC-AMINO-ACIDS; GUT MICROBIOTA; INDOLE-3-PROPIONIC ACID; KYNURENINE PATHWAY; LIPID-PEROXIDATION; IL-10; RECEPTOR; BRAIN; AVAILABILITY; SEROTONIN;
D O I
10.1080/10408398.2023.2299744
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Tryptophan (TRP) contributes to individual immune homeostasis and good condition via three complex metabolism pathways (5-hydroxytryptamine (5-HT), kynurenine (KP), and gut microbiota pathway). Indole propionic acid (IPA), one of the TRP derivatives of the microbiota pathway, has raised more attention because of its impact on metabolic disorders. Here, we retrospect increasing evidence that TRP metabolites/IPA derived from its proteolysis impact host health and disease. IPA can activate the immune system through aryl hydrocarbon receptor (AHR) and/or Pregnane X receptor (PXR) as a vital mediator among diet-caused host and microbe cross-talk. Different levels of IPA in systemic circulation can predict the risk of NAFLD, T2DM, and CVD. IPA is suggested to alleviate cognitive impairment from oxidative damage, reduce gut inflammation, inhibit lipid accumulation and attenuate the symptoms of NAFLD, putatively enhance the intestinal epithelial barrier, and maintain intestinal homeostasis. Now, we provide a general description of the relationships between IPA and various physiological and pathological processes, which support an opportunity for diet intervention for metabolic diseases.
引用
收藏
页码:1729 / 1748
页数:20
相关论文
共 206 条
[1]   The microbial metabolite indole-3-propionic acid improves glucose metabolism in rats, but does not affect behaviour [J].
Abildgaard, Anders ;
Elfving, Betina ;
Hokland, Marianne ;
Wegener, Gregers ;
Lund, Sten .
ARCHIVES OF PHYSIOLOGY AND BIOCHEMISTRY, 2018, 124 (04) :306-312
[2]   Gut Microbiota Regulation of Tryptophan Metabolism in Health and Disease [J].
Agus, Allison ;
Planchais, Julien ;
Sokol, Harry .
CELL HOST & MICROBE, 2018, 23 (06) :716-724
[3]   Targeted Regulation of PI3K/Akt/mTOR/NF-κB Signaling by Indole Compounds and their Derivatives: Mechanistic Details and Biological Implications for Cancer Therapy [J].
Ahmad, Aamir ;
Biersack, Bernhard ;
Li, Yiwei ;
Kong, Dejuan ;
Bao, Bin ;
Schobert, Rainer ;
Padhye, Subhash B. ;
Sarkar, Fazlul H. .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2013, 13 (07) :1002-1013
[4]   Analysis of gut microbiota of obese individuals with type 2 diabetes and healthy individuals [J].
Ahmad, Aftab ;
Yang, Wanwei ;
Chen, Guofang ;
Shafiq, Muhammad ;
Javed, Sundus ;
Zaidi, Syed Shujaat Ali ;
Shahid, Ramla ;
Liu, Chao ;
Bokhari, Habib .
PLOS ONE, 2019, 14 (12)
[5]   Microbiota-Derived Indole Metabolites Promote Human and Murine Intestinal Homeostasis through Regulation of Interleukin-10 Receptor [J].
Alexeev, Erica E. ;
Lanis, Jordi M. ;
Kao, Daniel J. ;
Campbell, Eric L. ;
Kelly, Caleb J. ;
Battista, Kayla D. ;
Gerich, Mark E. ;
Jenkins, Brittany R. ;
Walk, Seth T. ;
Kominsky, Douglas J. ;
Colgan, Sean P. .
AMERICAN JOURNAL OF PATHOLOGY, 2018, 188 (05) :1183-1194
[6]   Biosynthetic Manipulation of Tryptophan in Bacteria: Pathways and Mechanisms [J].
Alkhalaf, Lona M. ;
Ryan, Katherine S. .
CHEMISTRY & BIOLOGY, 2015, 22 (03) :317-328
[7]   Food processing for the improvement of plant proteins digestibility [J].
Almeida Sa, Amanda Gomes ;
Franco Moreno, Yara Maria ;
Mattar Carciofi, Bruno Augusto .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 2020, 60 (20) :3367-3386
[8]   MONOCLONAL IMMUNOGLOBULIN A ANTIBODIES DIRECTED AGAINST CHOLERA-TOXIN PREVENT THE TOXIN-INDUCED CHLORIDE SECRETORY RESPONSE AND BLOCK TOXIN BINDING TO INTESTINAL EPITHELIAL-CELLS IN-VITRO [J].
APTER, FM ;
LENCER, WI ;
FINKELSTEIN, RA ;
MEKALANOS, JJ ;
NEUTRA, MR .
INFECTION AND IMMUNITY, 1993, 61 (12) :5271-5278
[9]   The Densely O-Glycosylated MUC2 Mucin Protects the Intestine and Provides Food for the Commensal Bacteria [J].
Arike, Liisa ;
Hansson, Gunnar C. .
JOURNAL OF MOLECULAR BIOLOGY, 2016, 428 (16) :3221-3229
[10]   Tryptophan availability for kynurenine pathway metabolism across the life span: Control mechanisms and focus on aging, exercise, diet and nutritional supplements [J].
Badawy, Abdulla A-B. .
NEUROPHARMACOLOGY, 2017, 112 :248-263