Indoles as essential mediators in the gut-brain axis. Their role in Alzheimer's disease

被引:72
作者
Pappolla, Miguel A. [1 ]
Perry, George [2 ]
Fang, Xiang [1 ]
Zagorski, Michael [3 ]
Sambamurti, Kumar [4 ]
Poeggeler, Burkhard [5 ]
机构
[1] Univ Texas Med Branch, Dept Neurol, Galveston, TX USA
[2] Univ Texas San Antonio, Dept Biol, San Antonio, TX USA
[3] Case Western Reserve Univ, Dept Chem, Cleveland, OH USA
[4] Med Univ South Carolina, Dept Neurobiol, Charleston, SC USA
[5] Quiris Hlth, Gutersloh, Germany
关键词
ARYL-HYDROCARBON RECEPTOR; MILD-COGNITIVE-IMPAIRMENT; AGE-RELATED-CHANGES; OXIDATIVE STRESS; AH RECEPTOR; TRYPTOPHAN-METABOLITES; MOLECULAR-MECHANISMS; BINDING-SITES; DOUBLE-BLIND; MOUSE MODEL;
D O I
10.1016/j.nbd.2021.105403
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sporadic late-onset Alzheimer's disease (AD) is the most frequent cause of dementia associated with aging. Due to the progressive aging of the population, AD is becoming a healthcare burden of unprecedented proportions. Twenty years ago, it was reported that some indole molecules produced by the gut microbiota possess essential biological activities, including neuroprotection and antioxidant properties. Since then, research has cemented additional characteristics of these substances, including anti-inflammatory, immunoregulatory, and amyloid anti-aggregation features. Herein, we summarize the evidence supporting an integrated hypothesis that some of these substances can influence the age of onset and progression of AD and are central to the symbiotic relationship between intestinal microbes and the brain. Studies have shown that some of these substances' activities result from interactions with biologically conserved pathways and with genetic risk factors for AD. By targeting multiple pathologic mechanisms simultaneously, certain indoles may be excellent candidates to ameliorate neurodegeneration. We propose that management of the microbiota to induce a higher production of neuroprotective indoles (e.g., indole propionic acid) will promote brain health during aging. This area of research represents a new therapeutic paradigm that could add functional years of life to individuals who would otherwise develop dementia.
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页数:11
相关论文
共 157 条
[51]   Indole and Tryptophan Metabolism: Endogenous and Dietary Routes to Ah Receptor Activation [J].
Hubbard, Troy D. ;
Murray, Iain A. ;
Perdew, Gary H. .
DRUG METABOLISM AND DISPOSITION, 2015, 43 (10) :1522-1535
[52]   Postmenopausal hormone therapy and Alzheimer disease A prospective cohort study [J].
Imtiaz, Bushra ;
Tuppurainen, Marjo ;
Rikkonen, Toni ;
Kivipelto, Miia ;
Soininen, Hilkka ;
Kroger, Heikki ;
Tolppanen, Anna-Maija .
NEUROLOGY, 2017, 88 (11) :1062-1068
[53]   Microbes and Alzheimer's Disease [J].
Itzhaki, Ruth F. ;
Lathe, Richard ;
Balin, Brian J. ;
Ball, Melvyn J. ;
Bearer, Elaine L. ;
Braak, Heiko ;
Bullido, Maria J. ;
Carter, Chris ;
Clerici, Mario ;
Cosby, S. Louise ;
Del Tredici, Kelly ;
Field, Hugh ;
Fulop, Tamas ;
Grassi, Claudio ;
Griffin, W. Sue T. ;
Haas, Jurgen ;
Hudson, Alan P. ;
Kamer, Angela R. ;
Kell, Douglas B. ;
Licastro, Federico ;
Letenneur, Luc ;
Lovheim, Hugo ;
Mancuso, Roberta ;
Miklossy, Judith ;
Otth, Carola ;
Palamara, Anna Teresa ;
Perry, George ;
Preston, Christopher ;
Pretorius, Etheresia ;
Strandberg, Timo ;
Tabet, Naji ;
Taylor-Robinson, Simon D. ;
Whittum-Hudson, Judith A. .
JOURNAL OF ALZHEIMERS DISEASE, 2016, 51 (04) :979-984
[54]   Prediction of AD with MRI-based hippocampal volume in mild cognitive impairment [J].
Jack, CR ;
Petersen, RC ;
Xu, YC ;
O'Brien, PC ;
Smith, GE ;
Ivnik, RJ ;
Boeve, BF ;
Waring, SC ;
Tangalos, EG ;
Kokmen, E .
NEUROLOGY, 1999, 52 (07) :1397-1403
[55]   Microbiome-Derived Tryptophan Metabolites and Their Aryl Hydrocarbon Receptor-Dependent Agonist and Antagonist Activities [J].
Jin, Un-Ho ;
Lee, Syng-Ook ;
Sridharan, Gautham ;
Lee, Kyongbum ;
Davidson, Laurie A. ;
Jayaraman, Arul ;
Chapkin, Robert S. ;
Alaniz, Robert ;
Safe, Stephen .
MOLECULAR PHARMACOLOGY, 2014, 85 (05) :777-788
[56]   Early Postmenopausal Transdermal 17β-Estradiol Therapy and Amyloid-β Deposition [J].
Kantarci, Kejal ;
Lowe, Val J. ;
Lesnick, Timothy G. ;
Tosakulwong, Nirubol ;
Bailey, Kent R. ;
Fields, Julie A. ;
Shuster, Lynne T. ;
Zuk, Samantha M. ;
Senjem, Matthew L. ;
Mielke, Michelle M. ;
Gleason, Carey ;
Jack, Clifford R., Jr. ;
Rocca, Walter A. ;
Miller, Virginia M. .
JOURNAL OF ALZHEIMERS DISEASE, 2016, 53 (02) :547-556
[57]   The amyloid cascade hypothesis: are we poised for success or failure? [J].
Karran, Eric ;
De Strooper, Bart .
JOURNAL OF NEUROCHEMISTRY, 2016, 139 :237-252
[58]   Analytical method for β-amyloid fibrils using CE-laser induced fluorescence and its application to screening for inhibitors of β-amyloid protein aggregation [J].
Kato, Masaru ;
Kinoshita, Hiroyuki ;
Enokita, Mitsue ;
Hori, Yukiko ;
Hashimoto, Tadafumi ;
Iwatsubo, Takeshi ;
Toyo'oka, Toshimasa .
ANALYTICAL CHEMISTRY, 2007, 79 (13) :4887-4891
[59]  
Katz Ella, 2018, F1000Res, V7, DOI 10.12688/f1000research.14127.1
[60]   The aryl hydrocarbon receptor: a multifunctional chemical sensor for host defense and homeostatic maintenance [J].
Kawajiri, Kaname ;
Fujii-Kuriyama, Yoshiaki .
EXPERIMENTAL ANIMALS, 2017, 66 (02) :75-89