Кишечный микробиом и болезнь Альцгеймера

Авторы

  • Sh. Askarova
  • A. Kushugulova
  • A. Kaiyrlykyzy
  • A. Tsoy
  • A. Masoud
  • F. Olzhayev

DOI:

https://doi.org/10.26577/eb-2018-4-1365
        276 78

Аннотация

Болезнь Альцгеймера является хроническим неизлечимым нейродегенеративным заболеванием и наиболее распространенной формой возрастной деменции. На развитие этой патологии у пожилых людей влияют различные факторы, такие как образ жизни, уровень стресса, генетическая предрасположенность, хронические заболевания, а также факторы окружающей среды. Одним из факторов, влияющих на состояние здоровья человека, и привлекающим все большее внимание ученых за последние 15 лет является кишечный микробиом. Микробиом кишечника - это сообщество микроорганизмов, колонизирующих желудочно-кишечный тракт и оказывающих огромное влияние на физиологию человека в норме и патологии. В последние годы накоплена значительная информация о том, что состав кишечной микрофлоры изменяется при различных патологических состояниях организма человека, включая нейродегенеративные заболевания. В связи с вышесказанным, в настоящей обзорной статье обсуждается связь кишечного микробиома и головного мозга и роль микроорганизмов, населяющих гастроэнтеральный тракт в развитии болезни Альцгеймера. 

Ключевые слова: головной мозг, нейродегенерация, болезнь Альцгеймера, бета-амилоид, кишечник, кишечный микробиом.

Библиографические ссылки

1 Prince M., Ali G.-C., Guerchet M., Prina A.M., Albanese E., Wu Y.-T. Recent global trends in the prevalence and incidence of dementia, and survival with dementia // Alzheimer's Research & Therapy. -2016. -Vol. 8. - P. 23.
2 Alzheimer's disease facts and figures // Alzheimer's Association annual report. -2018.
3 Panegyres P.K., Chen H.Y. Differences between early and late onset Alzheimer's disease // Am J Neurodegener Dis. -2013. -Vol. 2, № 4. - P. 300-306.
4 Panegyres P.K., Chen H.Y. Early-onset Alzheimer's disease: a global cross-sectional analysis // Eur J Neurol. -2014.
5 Prince M. A.E., Guerchet M., Prina M. World Alzheimer Report 2014. Dementia and Risk Reduction - London : Alzheimer's Disease International, 2014. URL: http://www.alz.co.uk/research/WorldAlzheimerReport2014.pdf.
6 Huttenhower C. G.D., Knight R., Abubucker S., Badger J.H., Chinwalla A.T., et al., and White O. Structure, function and diversity of the healthy human microbiome // Nature. -2012. -Vol. 486, № 7402. - P. 207-214.
7 Qin J., Li R., Raes J., Arumugam M., Burgdorf K.S., Manichanh C., Nielsen T., Pons N., Levenez F., Yamada T., Mende D.R., Li J., Xu J., Li S., Li D., Cao J., Wang B., Liang H., Zheng H., Xie Y., Tap J., Lepage P., Bertalan M., Batto J.M., Hansen T., Le Paslier D., Linneberg A., Nielsen H.B., Pelletier E., Renault P., Sicheritz-Ponten T., Turner K., Zhu H., Yu C., Li S., Jian M., Zhou Y., Li Y., Zhang X., Li S., Qin N., Yang H., Wang J., Brunak S., Dore J., Guarner F., Kristiansen K., Pedersen O., Parkhill J., Weissenbach J., Bork P., Ehrlich S.D., Wang J. A human gut microbial gene catalogue established by metagenomic sequencing // Nature. -2010. -Vol. 464, № 7285. - P. 59-65.
8 Westfall S., Lomis N., Kahouli I., Dia S.Y., Singh S.P., Prakash S. Microbiome, probiotics and neurodegenerative diseases: deciphering the gut brain axis // Cell Mol Life Sci. -2017. -Vol. 74, № 20. - P. 3769-3787.
9 Cani P.D. Human gut microbiome: hopes, threats and promises // Gut. -2018. -Vol. 67, № 9. - P. 1716-1725.
10 Zhu X., Han Y., Du J., Liu R., Jin K., Yi W. Microbiota-gut-brain axis and the central nervous system // Oncotarget. -2017. -Vol. 8, № 32. - P. 53829-53838.
11 Larroya-Garcia A., Navas-Carrillo D., Orenes-Pinero E. Impact of gut microbiota on neurological diseases: Diet composition and novel treatments // Crit Rev Food Sci Nutr. -2018. - P. 1-15.
12 LaFerla F.M., Green K.N., Oddo S. Intracellular amyloid-beta in Alzheimer's disease // Nat Rev Neurosci. -2007. -Vol. 8, № 7. - P. 499-509.
13 William C.M., Andermann M.L., Goldey G.J., Roumis D.K., Reid R.C., Shatz C.J., Albers M.W., Frosch M.P., Hyman B.T. Synaptic plasticity defect following visual deprivation in Alzheimer's disease model transgenic mice // J Neurosci. -2012. -Vol. 32, № 23. - P. 8004-8011.
14 Westmark C.J. What's hAPPening at synapses? The role of amyloid beta-protein precursor and beta-amyloid in neurological disorders // Mol Psychiatry. -2013. -Vol. 18, № 4. - P. 425-434.
15 Cole S.L., Vassar R. The Alzheimer's disease beta-secretase enzyme, BACE1 // Molecular neurodegeneration. -2007. -Vol. 2. - P. 22.
16 Carabotti M., Scirocco A., Maselli M.A., Severi C. The gut-brain axis: interactions between enteric microbiota, central and enteric nervous systems // Ann Gastroenterol. -2015. -Vol. 28, № 2. - P. 203-209.
17 Moloney R.D., Johnson A.C., O'Mahony S.M., Dinan T.G., Greenwood-Van Meerveld B., Cryan J.F. Stress and the Microbiota-Gut-Brain Axis in Visceral Pain: Relevance to Irritable Bowel Syndrome // CNS Neurosci Ther. -2016. -Vol. 22, № 2. - P. 102-117.
18 Petra A.I., Panagiotidou S., Hatziagelaki E., Stewart J.M., Conti P., Theoharides T.C. Gut-Microbiota-Brain Axis and Its Effect on Neuropsychiatric Disorders With Suspected Immune Dysregulation // Clin Ther. -2015. -Vol. 37, № 5. - P. 984-995.
19 Burokas A., Moloney R.D., Dinan T.G., Cryan J.F. Microbiota regulation of the Mammalian gut-brain axis // Adv Appl Microbiol. -2015. -Vol. 91. - P. 1-62.
20 Gareau M.G. Microbiota-gut-brain axis and cognitive function // Adv Exp Med Biol. -2014. -Vol. 817. - P. 357-371.
21 Jiang C., Li G., Huang P., Liu Z., Zhao B. The Gut Microbiota and Alzheimer's Disease // J Alzheimers Dis. -2017. -Vol. 58, № 1. - P. 1-15.
22 Gareau M.G., Wine E., Rodrigues D.M., Cho J.H., Whary M.T., Philpott D.J., Macqueen G., Sherman P.M. Bacterial infection causes stress-induced memory dysfunction in mice // Gut. -2011. -Vol. 60, № 3. - P. 307-317.
23 Michalski B., Corrada M.M., Kawas C.H., Fahnestock M. Brain-derived neurotrophic factor and TrkB expression in the "oldest-old," the 90+ Study: correlation with cognitive status and levels of soluble amyloid-beta // Neurobiol Aging. -2015. -Vol. 36, № 12. - P. 3130-3139.
24 Neufeld K.M., Kang N., Bienenstock J., Foster J.A. Reduced anxiety-like behavior and central neurochemical change in germ-free mice // Neurogastroenterol Motil. -2011. -Vol. 23, № 3. - P. 255-264, e119.
25 Wang T., Hu X., Liang S., Li W., Wu X., Wang L., Jin F. Lactobacillus fermentum NS9 restores the antibiotic induced physiological and psychological abnormalities in rats // Benef Microbes. -2015. -Vol. 6, № 5. - P. 707-717.
26 Liang S., Wang T., Hu X., Luo J., Li W., Wu X., Duan Y., Jin F. Administration of Lactobacillus helveticus NS8 improves behavioral, cognitive, and biochemical aberrations caused by chronic restraint stress // Neuroscience. -2015. -Vol. 310. - P. 561-577.
27 Luo J., Wang T., Liang S., Hu X., Li W., Jin F. Ingestion of Lactobacillus strain reduces anxiety and improves cognitive function in the hyperammonemia rat // Sci China Life Sci. -2014. -Vol. 57, № 3. - P. 327-335.
28 Ohsawa K., Uchida N., Ohki K., Nakamura Y., Yokogoshi H. Lactobacillus helveticus-fermented milk improves learning and memory in mice // Nutr Neurosci. -2015. -Vol. 18, № 5. - P. 232-240.
29 Savignac H.M., Tramullas M., Kiely B., Dinan T.G., Cryan J.F. Bifidobacteria modulate cognitive processes in an anxious mouse strain // Behav Brain Res. -2015. -Vol. 287. - P. 59-72.
30 Harach T., Marungruang N., Duthilleul N., Cheatham V., Mc Coy K.D., Frisoni G., Neher J.J., Fak F., Jucker M., Lasser T., Bolmont T. Reduction of Abeta amyloid pathology in APPPS1 transgenic mice in the absence of gut microbiota // Sci Rep. -2017. -Vol. 7. - P. 41802.
31 Cattaneo A., Cattane N., Galluzzi S., Provasi S., Lopizzo N., Festari C., Ferrari C., Guerra U.P., Paghera B., Muscio C., Bianchetti A., Volta G.D., Turla M., Cotelli M.S., Gennuso M., Prelle A., Zanetti O., Lussignoli G., Mirabile D., Bellandi D., Gentile S., Belotti G., Villani D., Harach T., Bolmont T., Padovani A., Boccardi M., Frisoni G.B. Association of brain amyloidosis with pro-inflammatory gut bacterial taxa and peripheral inflammation markers in cognitively impaired elderly // Neurobiology of Aging. -2017. -Vol. 49. - P. 60-68.
32 Vogt N.M., Kerby R.L., Dill-McFarland K.A., Harding S.J., Merluzzi A.P., Johnson S.C., Carlsson C.M., Asthana S., Zetterberg H., Blennow K., Bendlin B.B., Rey F.E. Gut microbiome alterations in Alzheimer’s disease // Scientific Reports. -2017. -Vol. 7, № 1. - P. 13537.
33 Zhuang Z.Q., Shen L.L., Li W.W., Fu X., Zeng F., Gui L., Lu Y., Cai M., Zhu C., Tan Y.L., Zheng P., Li H.Y., Zhu J., Zhou H.D., Bu X.L., Wang Y.J. Gut Microbiota is Altered in Patients with Alzheimer's Disease // J Alzheimers Dis. -2018. -Vol. 63, № 4. - P. 1337-1346.
34 Tasnim N., Abulizi N., Pither J., Hart M.M., Gibson D.L. Linking the Gut Microbial Ecosystem with the Environment: Does Gut Health Depend on Where We Live? // Frontiers in Microbiology. -2017. -Vol. 8. - P. 1935.
35 Salazar N., Valdes-Varela L., Gonzalez S., Gueimonde M., de Los Reyes-Gavilan C.G. Nutrition and the gut microbiome in the elderly // Gut Microbes. -2017. -Vol. 8, № 2. - P. 82-97.
36 Nagpal R., Mainali R., Ahmadi S., Wang S., Singh R., Kavanagh K., Kitzman D.W., Kushugulova A., Marotta F., Yadav H. Gut microbiome and aging: Physiological and mechanistic insights // Nutrition and Healthy Aging. -2018. -Vol. 4, № 4. - P. 267-285.
37 Mariat D., Firmesse O., Levenez F., Guimaraes V., Sokol H., Dore J., Corthier G., Furet J.P. The Firmicutes/Bacteroidetes ratio of the human microbiota changes with age // BMC Microbiol. -2009. -Vol. 9. - P. 123.
38 Satokari R., Rantanen R., Pitka l., Salminen S. Probiotics and prebiotics in the elderly individuals // Handbook of prebiotics and probiotics incredients – Health benefits and food applications Cho S., Finocchiaro E. - Taylor and Francis : CRC Press, Boca Raton 2010. - P. 341–353.
39 Hopkins M.J., Macfarlane G.T. Changes in predominant bacterial populations in human faeces with age and with Clostridium difficile infection // J Med Microbiol. -2002. -Vol. 51, № 5. - P. 448-454.
40 Gavini F., Cayuela C., Antoine J.-M., Lecoq C., Lefebvre B., J-M M., Neut C. Differences in the distribution of bifidobacterial and enterobacterial species in human faecal microflora of three different (children, adults, elderly) age groups // Microb Ecol Health Dis. -2001. -Vol. 13, № 1. - P. 40-45.
41 He F., Ouwehand A.C., Isolauri E., Hosoda M., Benno Y., Salminen S. Differences in composition and mucosal adhesion of bifidobacteria isolated from healthy adults and healthy seniors // Curr Microbiol. -2001. -Vol. 43, № 5. - P. 351-354.
42 Strandwitz P. Neurotransmitter modulation by the gut microbiota // Brain Research. -2018. -Vol. 1693. - P. 128-133.
43 Junges V.M., Closs V.E., Nogueira G.M., Gottlieb M.G.V. Crosstalk Between Gut Microbiota and the Central Nervous System: A Focus for Alzheimer's Disease // Curr Alzheimer Res. -2018.
44 Bartosch S., Fite A., Macfarlane G.T., McMurdo M.E.T. Characterization of Bacterial Communities in Feces from Healthy Elderly Volunteers and Hospitalized Elderly Patients by Using Real-Time PCR and Effects of Antibiotic Treatment on the Fecal Microbiota // Applied and Environmental Microbiology. -2004. -Vol. 70, № 6. - P. 3575-3581.
45 Layton A., McKay L., Williams D., Garrett V., Gentry R., Sayler G. Development of Bacteroides 16S rRNA gene TaqMan-based real-time PCR assays for estimation of total, human, and bovine fecal pollution in water // Appl Environ Microbiol. -2006. -Vol. 72, № 6. - P. 4214-4224.
46 van Tongeren S.P., Slaets J.P., Harmsen H.J., Welling G.W. Fecal microbiota composition and frailty // Appl Environ Microbiol. -2005. -Vol. 71, № 10. - P. 6438-6442.
47 Woodmansey E.J., McMurdo M.E., Macfarlane G.T., Macfarlane S. Comparison of compositions and metabolic activities of fecal microbiotas in young adults and in antibiotic-treated and non-antibiotic-treated elderly subjects // Appl Environ Microbiol. -2004. -Vol. 70, № 10. - P. 6113-6122.
48 Nagpal R., Mainali R., Ahmadi S., Wang S., Singh R., Kavanagh K., Kitzman D.W., Kushugulova A., Marotta F., Yadav H. Gut microbiome and aging: Physiological and mechanistic insights // Nutr Healthy Aging. -2018. -Vol. 4, № 4. - P. 267-285.
49 Elahy M., Jackaman C., Mamo J.C.L., Lam V., Dhaliwal S.S., Giles C., Nelson D., Takechi R. Blood–brain barrier dysfunction developed during normal aging is associated with inflammation and loss of tight junctions but not with leukocyte recruitment // Immunity & Ageing. -2015. -Vol. 12, № 1. - P. 2.
50 Tran L., Greenwood-Van Meerveld B. Age-Associated Remodeling of the Intestinal Epithelial Barrier // The Journals of Gerontology Series A: Biological Sciences and Medical Sciences. -2013. -Vol. 68, № 9. - P. 1045-1056.
51 Evans M.L., Gichana E., Zhou Y., Chapman M.R. Bacterial Amyloids // Methods Mol Biol. -2018. -Vol. 1779. - P. 267-288.
52 Schwartz K., Boles B.R. Microbial amyloids--functions and interactions within the host // Curr Opin Microbiol. -2013. -Vol. 16, № 1. - P. 93-99.
53 Hufnagel D.A., Tukel C., Chapman M.R. Disease to dirt: the biology of microbial amyloids // PLoS Pathog. -2013. -Vol. 9, № 11. - P. e1003740.
54 Rapsinski G.J., Wynosky-Dolfi M.A., Oppong G.O., Tursi S.A., Wilson R.P., Brodsky I.E., Tukel C. Toll-like receptor 2 and NLRP3 cooperate to recognize a functional bacterial amyloid, curli // Infect Immun. -2015. -Vol. 83, № 2. - P. 693-701.
55 Nishimori J.H., Newman T.N., Oppong G.O., Rapsinski G.J., Yen J.-H., Biesecker S.G., Wilson R.P., Butler B.P., Winter M.G., Tsolis R.M., Ganea D., Tükel Ç. Microbial Amyloids Induce Interleukin 17A (IL-17A) and IL-22 Responses via Toll-Like Receptor 2 Activation in the Intestinal Mucosa // Infection and Immunity. -2012. -Vol. 80, № 12. - P. 4398-4408.
56 Sun J., Zhang S., Zhang X., Zhang X., Dong H., Qian Y. IL-17A is implicated in lipopolysaccharide-induced neuroinflammation and cognitive impairment in aged rats via microglial activation // Journal of Neuroinflammation. -2015. -Vol. 12. - P. 165.
57 Perriard G., Mathias A., Enz L., Canales M., Schluep M., Gentner M., Schaeren-Wiemers N., Du Pasquier R.A. Interleukin-22 is increased in multiple sclerosis patients and targets astrocytes // Journal of Neuroinflammation. -2015. -Vol. 12. - P. 119.
58 Zhan X., Stamova B., Sharp F.R. Lipopolysaccharide Associates with Amyloid Plaques, Neurons and Oligodendrocytes in Alzheimer's Disease Brain: A Review // Front Aging Neurosci. -2018. -Vol. 10. - P. 42.
59 Chen S.G., Stribinskis V., Rane M.J., Demuth D.R., Gozal E., Roberts A.M., Jagadapillai R., Liu R., Choe K., Shivakumar B., Son F., Jin S., Kerber R., Adame A., Masliah E., Friedland R.P. Exposure to the Functional Bacterial Amyloid Protein Curli Enhances Alpha-Synuclein Aggregation in Aged Fischer 344 Rats and Caenorhabditis elegans // Scientific Reports. -2016. -Vol. 6. - P. 34477.
60 Zhang R., Miller R.G., Gascon R., Champion S., Katz J., Lancero M., Narvaez A., Honrada R., Ruvalcaba D., McGrath M.S. Circulating endotoxin and systemic immune activation in sporadic amyotrophic lateral sclerosis (sALS) // J Neuroimmunol. -2009. -Vol. 206, № 1-2. - P. 121-124.
61 Zhao Y., Jaber V., Lukiw W.J. Secretory Products of the Human GI Tract Microbiome and Their Potential Impact on Alzheimer's Disease (AD): Detection of Lipopolysaccharide (LPS) in AD Hippocampus // Frontiers in Cellular and Infection Microbiology. -2017. -Vol. 7. - P. 318.
62 Hauss-Wegrzyniak B., Lynch M.A., Vraniak P.D., Wenk G.L. Chronic brain inflammation results in cell loss in the entorhinal cortex and impaired LTP in perforant path-granule cell synapses // Exp Neurol. -2002. -Vol. 176, № 2. - P. 336-341.
63 Zhao Y., Lukiw W.J. Bacteroidetes Neurotoxins and Inflammatory Neurodegeneration // Mol Neurobiol. -2018.
64 Bhattacharjee S., Zhao Y., Dua P., Rogaev E.I., Lukiw W.J. microRNA-34a-Mediated Down-Regulation of the Microglial-Enriched Triggering Receptor and Phagocytosis-Sensor TREM2 in Age-Related Macular Degeneration // PLoS One. -2016. -Vol. 11, № 3. - P. e0150211.
65 Kahn M.S., Kranjac D., Alonzo C.A., Haase J.H., Cedillos R.O., McLinden K.A., Boehm G.W., Chumley M.J. Prolonged elevation in hippocampal Abeta and cognitive deficits following repeated endotoxin exposure in the mouse // Behav Brain Res. -2012. -Vol. 229, № 1. - P. 176-184.
66 Asti A., Gioglio L. Can a bacterial endotoxin be a key factor in the kinetics of amyloid fibril formation? // J Alzheimers Dis. -2014. -Vol. 39, № 1. - P. 169-179.
67 Jaeger L.B., Dohgu S., Sultana R., Lynch J.L., Owen J.B., Erickson M.A., Shah G.N., Price T.O., Fleegal-Demotta M.A., Butterfiled D.A., Banks W.A. Lipopolysaccharide Alters the Blood-brain Barrier Transport of Amyloid Beta Protein: A Mechanism for Inflammation in the Progression of Alzheimer’s Disease // Brain, behavior, and immunity. -2009. -Vol. 23, № 4. - P. 507-517.
68 Hauss-Wegrzyniak B., Wenk G.L. Beta-amyloid deposition in the brains of rats chronically infused with thiorphan or lipopolysaccharide: the role of ascorbic acid in the vehicle // Neurosci Lett. -2002. -Vol. 322, № 2. - P. 75-78.
References
(2018) Alzheimer's disease facts and figures. Alzheimer's Association annual report vol.
Asti A, L Gioglio (2014) Can a bacterial endotoxin be a key factor in the kinetics of amyloid fibril formation? Journal of Alzheimer's disease : JAD vol. 39, pp. 169-179.
Bartosch S, A Fite, GT Macfarlane, MET McMurdo (2004) Characterization of bacterial communities in feces from healthy elderly volunteers and hospitalized elderly patients by using real-time pcr and effects of antibiotic treatment on the fecal microbiota. Applied and environmental microbiology vol. 70, pp. 3575-3581.
Bhattacharjee S, Y Zhao, P Dua, EI Rogaev, WJ Lukiw (2016) Microrna-34a-mediated down-regulation of the microglial-enriched triggering receptor and phagocytosis-sensor trem2 in age-related macular degeneration. PloS one vol. 11, pp. e0150211.
Burokas A, RD Moloney, TG Dinan, JF Cryan (2015) Microbiota regulation of the mammalian gut-brain axis. Advances in applied microbiology vol. 91, pp. 1-62.
Cani PD (2018) Human gut microbiome: Hopes, threats and promises. Gut vol. 67, pp. 1716-1725.
Carabotti M, A Scirocco, MA Maselli, C Severi (2015) The gut-brain axis: Interactions between enteric microbiota, central and enteric nervous systems. Annals of gastroenterology vol. 28, pp. 203-209.
Cattaneo A, N Cattane, S Galluzzi, S Provasi, N Lopizzo, C Festari, C Ferrari, UP Guerra, B Paghera, C Muscio, A Bianchetti, GD Volta, M Turla, MS Cotelli, M Gennuso, A Prelle, O Zanetti, G Lussignoli, D Mirabile, D Bellandi, S Gentile, G Belotti, D Villani, T Harach, T Bolmont, A Padovani, M Boccardi, GB Frisoni (2017) Association of brain amyloidosis with pro-inflammatory gut bacterial taxa and peripheral inflammation markers in cognitively impaired elderly. Neurobiology of Aging vol. 49, pp. 60-68.
Chen SG, V Stribinskis, MJ Rane, DR Demuth, E Gozal, AM Roberts, R Jagadapillai, R Liu, K Choe, B Shivakumar, F Son, S Jin, R Kerber, A Adame, E Masliah, RP Friedland (2016) Exposure to the functional bacterial amyloid protein curli enhances alpha-synuclein aggregation in aged fischer 344 rats and caenorhabditis elegans. Scientific Reports vol. 6, pp. 34477.
Cole SL, R Vassar (2007) The alzheimer's disease beta-secretase enzyme, bace1. Molecular neurodegeneration vol. 2, pp. 22.
Elahy M, C Jackaman, JCL Mamo, V Lam, SS Dhaliwal, C Giles, D Nelson, R Takechi (2015) Blood–brain barrier dysfunction developed during normal aging is associated with inflammation and loss of tight junctions but not with leukocyte recruitment. Immunity & Ageing vol. 12, pp. 2.
Evans ML, E Gichana, Y Zhou, MR Chapman (2018) Bacterial amyloids. Methods in molecular biology (Clifton, NJ) vol. 1779, pp. 267-288.
Gareau MG (2014) Microbiota-gut-brain axis and cognitive function. Advances in experimental medicine and biology vol. 817, pp. 357-371.
Gareau MG, E Wine, DM Rodrigues, JH Cho, MT Whary, DJ Philpott, G Macqueen, PM Sherman (2011) Bacterial infection causes stress-induced memory dysfunction in mice. Gut vol. 60, pp. 307-317.
Gavini F, C Cayuela, J-M Antoine, C Lecoq, B Lefebvre, M J-M, C Neut (2001) Differences in the distribution of bifidobacterial and enterobacterial species in human faecal microflora of three different (children, adults, elderly) age groups. Microb Ecol Health Dis vol. 13, pp. 40-45.
Harach T, N Marungruang, N Duthilleul, V Cheatham, KD Mc Coy, G Frisoni, JJ Neher, F Fak, M Jucker, T Lasser, T Bolmont (2017) Reduction of abeta amyloid pathology in appps1 transgenic mice in the absence of gut microbiota. Sci Rep vol. 7, pp. 41802.
Hauss-Wegrzyniak B, MA Lynch, PD Vraniak, GL Wenk (2002) Chronic brain inflammation results in cell loss in the entorhinal cortex and impaired ltp in perforant path-granule cell synapses. Experimental neurology vol. 176, pp. 336-341.
Hauss-Wegrzyniak B, GL Wenk (2002) Beta-amyloid deposition in the brains of rats chronically infused with thiorphan or lipopolysaccharide: The role of ascorbic acid in the vehicle. Neuroscience letters vol. 322, pp. 75-78.
He F, AC Ouwehand, E Isolauri, M Hosoda, Y Benno, S Salminen (2001) Differences in composition and mucosal adhesion of bifidobacteria isolated from healthy adults and healthy seniors. Current microbiology vol. 43, pp. 351-354.
Hopkins MJ, GT Macfarlane (2002) Changes in predominant bacterial populations in human faeces with age and with clostridium difficile infection. Journal of medical microbiology vol. 51, pp. 448-454.
Hufnagel DA, C Tukel, MR Chapman (2013) Disease to dirt: The biology of microbial amyloids. PLoS pathogens vol. 9, pp. e1003740.
Huttenhower C. GD, Knight R., Abubucker S., Badger J.H., Chinwalla A.T., et al., and White O. (2012) Structure, function and diversity of the healthy human microbiome. Nature vol. 486, pp. 207-214.
Jaeger LB, S Dohgu, R Sultana, JL Lynch, JB Owen, MA Erickson, GN Shah, TO Price, MA Fleegal-Demotta, DA Butterfiled, WA Banks (2009) Lipopolysaccharide alters the blood-brain barrier transport of amyloid beta protein: A mechanism for inflammation in the progression of alzheimer’s disease. Brain, behavior, and immunity vol. 23, pp. 507-517.
Jiang C, G Li, P Huang, Z Liu, B Zhao (2017) The gut microbiota and alzheimer's disease. Journal of Alzheimer's disease : JAD vol. 58, pp. 1-15.
Junges VM, VE Closs, GM Nogueira, MGV Gottlieb (2018) Crosstalk between gut microbiota and the central nervous system: A focus for alzheimer's disease. Current Alzheimer research vol.
Kahn MS, D Kranjac, CA Alonzo, JH Haase, RO Cedillos, KA McLinden, GW Boehm, MJ Chumley (2012) Prolonged elevation in hippocampal abeta and cognitive deficits following repeated endotoxin exposure in the mouse. Behavioural brain research vol. 229, pp. 176-184.
LaFerla FM, KN Green, S Oddo (2007) Intracellular amyloid-beta in alzheimer's disease. Nat Rev Neurosci vol. 8, pp. 499-509.
Larroya-Garcia A, D Navas-Carrillo, E Orenes-Pinero (2018) Impact of gut microbiota on neurological diseases: Diet composition and novel treatments. Critical reviews in food science and nutrition vol., pp. 1-15.
Layton A, L McKay, D Williams, V Garrett, R Gentry, G Sayler (2006) Development of bacteroides 16s rrna gene taqman-based real-time pcr assays for estimation of total, human, and bovine fecal pollution in water. Applied and environmental microbiology vol. 72, pp. 4214-4224.
Liang S, T Wang, X Hu, J Luo, W Li, X Wu, Y Duan, F Jin (2015) Administration of lactobacillus helveticus ns8 improves behavioral, cognitive, and biochemical aberrations caused by chronic restraint stress. Neuroscience vol. 310, pp. 561-577.
Luo J, T Wang, S Liang, X Hu, W Li, F Jin (2014) Ingestion of lactobacillus strain reduces anxiety and improves cognitive function in the hyperammonemia rat. Science China Life sciences vol. 57, pp. 327-335.
Mariat D, O Firmesse, F Levenez, V Guimaraes, H Sokol, J Dore, G Corthier, JP Furet (2009) The firmicutes/bacteroidetes ratio of the human microbiota changes with age. BMC microbiology vol. 9, pp. 123.
Michalski B, MM Corrada, CH Kawas, M Fahnestock (2015) Brain-derived neurotrophic factor and trkb expression in the "oldest-old," the 90+ study: Correlation with cognitive status and levels of soluble amyloid-beta. Neurobiol Aging vol. 36, pp. 3130-3139.
Moloney RD, AC Johnson, SM O'Mahony, TG Dinan, B Greenwood-Van Meerveld, JF Cryan (2016) Stress and the microbiota-gut-brain axis in visceral pain: Relevance to irritable bowel syndrome. CNS neuroscience & therapeutics vol. 22, pp. 102-117.
Nagpal R, R Mainali, S Ahmadi, S Wang, R Singh, K Kavanagh, DW Kitzman, A Kushugulova, F Marotta, H Yadav (2018a) Gut microbiome and aging: Physiological and mechanistic insights. Nutr Healthy Aging vol. 4, pp. 267-285.
Nagpal R, R Mainali, S Ahmadi, S Wang, R Singh, K Kavanagh, DW Kitzman, A Kushugulova, F Marotta, H Yadav (2018b) Gut microbiome and aging: Physiological and mechanistic insights. Nutrition and Healthy Aging vol. 4, pp. 267-285.
Neufeld KM, N Kang, J Bienenstock, JA Foster (2011) Reduced anxiety-like behavior and central neurochemical change in germ-free mice. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society vol. 23, pp. 255-264, e119.
Nishimori JH, TN Newman, GO Oppong, GJ Rapsinski, J-H Yen, SG Biesecker, RP Wilson, BP Butler, MG Winter, RM Tsolis, D Ganea, Ç Tükel (2012) Microbial amyloids induce interleukin 17a (il-17a) and il-22 responses via toll-like receptor 2 activation in the intestinal mucosa. Infection and Immunity vol. 80, pp. 4398-4408.
Ohsawa K, N Uchida, K Ohki, Y Nakamura, H Yokogoshi (2015) Lactobacillus helveticus-fermented milk improves learning and memory in mice. Nutritional neuroscience vol. 18, pp. 232-240.
Panegyres PK, HY Chen (2013) Differences between early and late onset alzheimer's disease. Am J Neurodegener Dis vol. 2, pp. 300-306.
Panegyres PK, HY Chen (2014) Early-onset alzheimer's disease: A global cross-sectional analysis. Eur J Neurol vol.
Perriard G, A Mathias, L Enz, M Canales, M Schluep, M Gentner, N Schaeren-Wiemers, RA Du Pasquier (2015) Interleukin-22 is increased in multiple sclerosis patients and targets astrocytes. Journal of Neuroinflammation vol. 12, pp. 119.
Petra AI, S Panagiotidou, E Hatziagelaki, JM Stewart, P Conti, TC Theoharides (2015) Gut-microbiota-brain axis and its effect on neuropsychiatric disorders with suspected immune dysregulation. Clinical therapeutics vol. 37, pp. 984-995.
Prince M, G-C Ali, M Guerchet, AM Prina, E Albanese, Y-T Wu (2016) Recent global trends in the prevalence and incidence of dementia, and survival with dementia. Alzheimer's Research & Therapy vol. 8, pp. 23.
Prince M. AE, Guerchet M., Prina M. 2014. World alzheimer report 2014. Dementia and risk reduction. Alzheimer's Disease International, London.
Qin J, R Li, J Raes, M Arumugam, KS Burgdorf, C Manichanh, T Nielsen, N Pons, F Levenez, T Yamada, DR Mende, J Li, J Xu, S Li, D Li, J Cao, B Wang, H Liang, H Zheng, Y Xie, J Tap, P Lepage, M Bertalan, JM Batto, T Hansen, D Le Paslier, A Linneberg, HB Nielsen, E Pelletier, P Renault, T Sicheritz-Ponten, K Turner, H Zhu, C Yu, S Li, M Jian, Y Zhou, Y Li, X Zhang, S Li, N Qin, H Yang, J Wang, S Brunak, J Dore, F Guarner, K Kristiansen, O Pedersen, J Parkhill, J Weissenbach, P Bork, SD Ehrlich, J Wang (2010) A human gut microbial gene catalogue established by metagenomic sequencing. Nature vol. 464, pp. 59-65.
Rapsinski GJ, MA Wynosky-Dolfi, GO Oppong, SA Tursi, RP Wilson, IE Brodsky, C Tukel (2015) Toll-like receptor 2 and nlrp3 cooperate to recognize a functional bacterial amyloid, curli. Infect Immun vol. 83, pp. 693-701.
Salazar N, L Valdes-Varela, S Gonzalez, M Gueimonde, CG de Los Reyes-Gavilan (2017) Nutrition and the gut microbiome in the elderly. Gut microbes vol. 8, pp. 82-97.
Satokari R, R Rantanen, l Pitka, S Salminen 2010 Probiotics and prebiotics in the elderly individuals. Pages 341–353 in S Cho, E Finocchiaro eds. Handbook of prebiotics and probiotics incredients – health benefits and food applications CRC Press, Boca Raton Taylor and Francis
Savignac HM, M Tramullas, B Kiely, TG Dinan, JF Cryan (2015) Bifidobacteria modulate cognitive processes in an anxious mouse strain. Behavioural brain research vol. 287, pp. 59-72.
Schwartz K, BR Boles (2013) Microbial amyloids--functions and interactions within the host. Current opinion in microbiology vol. 16, pp. 93-99.
Strandwitz P (2018) Neurotransmitter modulation by the gut microbiota. Brain Research vol. 1693, pp. 128-133.
Sun J, S Zhang, X Zhang, X Zhang, H Dong, Y Qian (2015) Il-17a is implicated in lipopolysaccharide-induced neuroinflammation and cognitive impairment in aged rats via microglial activation. Journal of Neuroinflammation vol. 12, pp. 165.
Tasnim N, N Abulizi, J Pither, MM Hart, DL Gibson (2017) Linking the gut microbial ecosystem with the environment: Does gut health depend on where we live? Frontiers in Microbiology vol. 8, pp. 1935.
Tran L, B Greenwood-Van Meerveld (2013) Age-associated remodeling of the intestinal epithelial barrier. The Journals of Gerontology Series A: Biological Sciences and Medical Sciences vol. 68, pp. 1045-1056.
van Tongeren SP, JP Slaets, HJ Harmsen, GW Welling (2005) Fecal microbiota composition and frailty. Applied and environmental microbiology vol. 71, pp. 6438-6442.
Vogt NM, RL Kerby, KA Dill-McFarland, SJ Harding, AP Merluzzi, SC Johnson, CM Carlsson, S Asthana, H Zetterberg, K Blennow, BB Bendlin, FE Rey (2017) Gut microbiome alterations in alzheimer’s disease. Scientific Reports vol. 7, pp. 13537.
Wang T, X Hu, S Liang, W Li, X Wu, L Wang, F Jin (2015) Lactobacillus fermentum ns9 restores the antibiotic induced physiological and psychological abnormalities in rats. Beneficial microbes vol. 6, pp. 707-717.
Westfall S, N Lomis, I Kahouli, SY Dia, SP Singh, S Prakash (2017) Microbiome, probiotics and neurodegenerative diseases: Deciphering the gut brain axis. Cellular and molecular life sciences : CMLS vol. 74, pp. 3769-3787.
Westmark CJ (2013) What's happening at synapses? The role of amyloid beta-protein precursor and beta-amyloid in neurological disorders. Molecular psychiatry vol. 18, pp. 425-434.
William CM, ML Andermann, GJ Goldey, DK Roumis, RC Reid, CJ Shatz, MW Albers, MP Frosch, BT Hyman (2012) Synaptic plasticity defect following visual deprivation in alzheimer's disease model transgenic mice. J Neurosci vol. 32, pp. 8004-8011.
Woodmansey EJ, ME McMurdo, GT Macfarlane, S Macfarlane (2004) Comparison of compositions and metabolic activities of fecal microbiotas in young adults and in antibiotic-treated and non-antibiotic-treated elderly subjects. Applied and environmental microbiology vol. 70, pp. 6113-6122.
Zhan X, B Stamova, FR Sharp (2018) Lipopolysaccharide associates with amyloid plaques, neurons and oligodendrocytes in alzheimer's disease brain: A review. Frontiers in aging neuroscience vol. 10, pp. 42.
Zhang R, RG Miller, R Gascon, S Champion, J Katz, M Lancero, A Narvaez, R Honrada, D Ruvalcaba, MS McGrath (2009) Circulating endotoxin and systemic immune activation in sporadic amyotrophic lateral sclerosis (sals). J Neuroimmunol vol. 206, pp. 121-124.
Zhao Y, V Jaber, WJ Lukiw (2017) Secretory products of the human gi tract microbiome and their potential impact on alzheimer's disease (ad): Detection of lipopolysaccharide (lps) in ad hippocampus. Frontiers in Cellular and Infection Microbiology vol. 7, pp. 318.
Zhao Y, WJ Lukiw (2018) Bacteroidetes neurotoxins and inflammatory neurodegeneration. Molecular neurobiology vol.
Zhu X, Y Han, J Du, R Liu, K Jin, W Yi (2017) Microbiota-gut-brain axis and the central nervous system. Oncotarget vol. 8, pp. 53829-53838.
Zhuang ZQ, LL Shen, WW Li, X Fu, F Zeng, L Gui, Y Lu, M Cai, C Zhu, YL Tan, P Zheng, HY Li, J Zhu, HD Zhou, XL Bu, YJ Wang (2018) Gut microbiota is altered in patients with alzheimer's disease. Journal of Alzheimer's disease : JAD vol. 63, pp. 1337-1346.

Загрузки

Как цитировать

Askarova, S., Kushugulova, A., Kaiyrlykyzy, A., Tsoy, A., Masoud, A., & Olzhayev, F. (2019). Кишечный микробиом и болезнь Альцгеймера. Вестник КазНУ. Серия биологическая, 77(4), 74–85. https://doi.org/10.26577/eb-2018-4-1365