Protection of Alzheimer's disease progression by a human-origin probiotics cocktail

被引:6
作者
Prajapati, Santosh Kumar [1 ,2 ]
Wang, Shaohua [1 ,2 ,4 ]
Mishra, Sidharth P. [1 ,2 ]
Jain, Shalini [1 ,2 ]
Yadav, Hariom [1 ,2 ,3 ]
机构
[1] Univ S Florida, Microbiomes Inst, USF Ctr Microbiome Res, Morsani Coll Med, Tampa, FL 33612 USA
[2] Univ S Florida, Morsani Coll Med, Ctr Excellence Aging & Brain Repair, Dept Neurosurg & Brain Repair, Tampa, FL 33612 USA
[3] Univ S Florida, Morsani Coll Med, Dept Internal Med Digest Dis & Nutr, Tampa, FL 33612 USA
[4] Ohio Univ, Infect & Trop Dis Inst, Heritage Coll Osteopath Med, Dept Biomed Sci, Athens, OH USA
关键词
Microbiome; Alzheimer's disease; Probiotics; Gut; Permeability; Inflammation; Dementia; Cognition; BLOOD-BRAIN-BARRIER; TRANSGENIC MOUSE MODEL; GUT MICROBIOTA; SYSTEMIC INFLAMMATION; COGNITIVE DEFICITS; SEX-DIFFERENCES; A-BETA; NEUROINFLAMMATION; PATHOLOGY; MONOCYTES;
D O I
10.1038/s41598-024-84780-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Microbiome abnormalities (dysbiosis) significantly contribute to the progression of Alzheimer's disease (AD). However, the therapeutic efficacy of microbiome modulators in protecting against these ailments remains poorly studied. Herein, we tested a cocktail of unique probiotics, including 5 Lactobacillus and 5 Enterococcus strains isolated from infant gut with proven microbiome modulating capabilities. We aimed to determine the probiotics cocktail's efficacy in ameliorating AD pathology in a humanized AD mouse model of APP/PS1 strains. Remarkably, feeding mice with 1 x 1011 CFU per day in drinking water for 16 weeks significantly reduced cognitive decline (measured by the Morris Water Maze test) and AD pathology markers, such as A beta aggregation, microglia activation, neuroinflammation, and preserved blood-brain barrier (BBB) tight junctions. The beneficial effects were linked to a reduced inflammatory microbiome, leading to decreased gut permeability and inflammation in both systemic circulation and the brain. Although both male and female mice showed overall improvements in cognition and biological markers, females did not exhibit improvements in specific markers related to inflammation and barrier permeability, suggesting that the underlying mechanisms may differ depending on sex. In conclusion, our results suggest that this unique probiotics cocktail could serve as a prophylactic agent to reduce the progression of cognitive decline and AD pathology. This is achieved by beneficially modulating the microbiome, improving intestinal tight junction proteins, reducing permeability in both gut and BBB, and decreasing inflammation in the gut, blood circulation, and brain, ultimately mitigating AD pathology and cognitive decline.
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页数:15
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共 87 条
[1]   Inflammatory mediators and modulation of blood-brain barrier permeability [J].
Abbott, NJ .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2000, 20 (02) :131-147
[2]   A human-origin probiotic cocktail ameliorates aging-related leaky gut and inflammation via modulating the microbiota/taurine/tight junction axis [J].
Ahmadi, Shokouh ;
Wang, Shaohua ;
Nagpal, Ravinder ;
Wang, Bo ;
Jain, Shalini ;
Razazan, Atefeh ;
Mishra, Sidharth P. ;
Zhu, Xuewei ;
Wang, Zhan ;
Kavanagh, Kylie ;
Yadav, Hariom .
JCI INSIGHT, 2020, 5 (09)
[3]   Inflammation and Alzheimer's disease [J].
Akiyama, H ;
Barger, S ;
Barnum, S ;
Bradt, B ;
Bauer, J ;
Cole, GM ;
Cooper, NR ;
Eikelenboom, P ;
Emmerling, M ;
Fiebich, BL ;
Finch, CE ;
Frautschy, S ;
Griffin, WST ;
Hampel, H ;
Hull, M ;
Landreth, G ;
Lue, LF ;
Mrak, R ;
Mackenzie, IR ;
McGeer, PL ;
O'Banion, MK ;
Pachter, J ;
Pasinetti, G ;
Plata-Salaman, C ;
Rogers, J ;
Rydel, R ;
Shen, Y ;
Streit, W ;
Strohmeyer, R ;
Tooyoma, I ;
Van Muiswinkel, FL ;
Veerhuis, R ;
Walker, D ;
Webster, S ;
Wegrzyniak, B ;
Wenk, G ;
Wyss-Coray, T .
NEUROBIOLOGY OF AGING, 2000, 21 (03) :383-421
[4]   Epigallocatechin-3-gallate Alleviates Cognitive Deficits in APP/PS1 Mice [J].
Bao, Jian ;
Liu, Wei ;
Zhou, Hong-yan ;
Gui, Yu-ran ;
Yang, You-hua ;
Wu, Meng-juan ;
Xiao, Yi-fan ;
Shang, Jin-ting ;
Long, Gui-feng ;
Shu, Xi-ji .
CURRENT MEDICAL SCIENCE, 2020, 40 (01) :18-27
[5]   Gut microbiome of multiple sclerosis patients and paired household healthy controls reveal associations with disease risk and course [J].
Baranzini, Sergio E. ;
iMSMS Consortium .
CELL, 2022, 185 (19) :3467-+
[6]   Accelerated microglial pathology is associated with Aβ plaques in mouse models of Alzheimer's disease [J].
Baron, Rona ;
Babcock, Alicia A. ;
Nemirovsky, Anna ;
Finsen, Bente ;
Monsonego, Alon .
AGING CELL, 2014, 13 (04) :584-595
[7]   Gut microbiota from multiple sclerosis patients enables spontaneous autoimmune encephalomyelitis in mice [J].
Berer, Kerstin ;
Gerdes, Lisa Ann ;
Cekanaviciute, Egle ;
Jia, Xiaoming ;
Xiao, Liang ;
Xia, Zhongkui ;
Liu, Chuan ;
Klotz, Luisa ;
Stauffer, Uta ;
Baranzini, Sergio E. ;
Kuempfel, Tania ;
Hohlfeld, Reinhard ;
Krishnamoorthy, Gurumoorthy ;
Wekerle, Hartmut .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (40) :10719-10724
[8]   Intestinal Microbiota Signatures Associated with Inflammation History in Mice Experiencing Recurring Colitis [J].
Berry, David ;
Kuzyk, Orest ;
Rauch, Isabella ;
Heider, Susanne ;
Schwab, Clarissa ;
Hainzl, Eva ;
Decker, Thomas ;
Muller, Mathias ;
Strobl, Birgit ;
Schleper, Christa ;
Urich, Tim ;
Wagner, Michael ;
Kenner, Lukas ;
Loy, Alexander .
FRONTIERS IN MICROBIOLOGY, 2015, 6
[9]   GATA Factors Regulate Proliferation, Differentiation, and Gene Expression in Small Intestine of Mature Mice [J].
Beuling, Eva ;
Baffour-Awuah, Nana Yaa A. ;
Stapleton, Kelly A. ;
Aronson, Boaz E. ;
Noah, Taeko K. ;
Shroyer, Noah F. ;
Duncan, Stephen A. ;
Fleet, James C. ;
Krasinski, Stephen D. .
GASTROENTEROLOGY, 2011, 140 (04) :1219-+
[10]   What Are the Key Gut Microbiota Involved in Neurological Diseases? A Systematic Review [J].
Bonnechere, Bruno ;
Amin, Najaf ;
van Duijn, Cornelia .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (22)