Prebiotic Effect of Fructooligosaccharides from Morinda officinalis on Alzheimer’s Disease in Rodent Models by Targeting the Microbiota-Gut-Brain Axis
Open accessAbstract
Gut microbiota influences the central nervous system disorders such as Alzheimer’s disease (AD). The prebiotics and probiotics can improve the host cognition. A previous study demonstrated that fructooligosaccharides from Morinda officinalis (OMO) exert effective memory improvements in AD-like animals, thereby considered as potential prebiotics; however, the underlying mechanism still remains enigma. Thus, the present study investigated whether OMO is effective in alleviating AD by targeting the microbiota-gut-brain axis. OMO was administered in rats with AD-like symptoms (D-galactose- and Aβ 1-42-induced deficient rats). Significant and systematic deterioration in AD-like animals were identified, including learning and memory abilities, histological changes, production of cytokines, and microbial community shifts. Behavioral experiments demonstrated that OMO administration can ameliorate the learning and memory abilities in both AD-like animals significantly. AD parameters showed that OMO administration cannot only improve oxidative stress and inflammation disorder, but also regulate the synthesis and secretion of neurotransmitter. Histological changes indicated that OMO administration ameliorates the swelling of brain tissues, neuronal apoptosis, and down-regulation of the expression of AD intracellular markers (Tau and Aβ 1-42). 16S rRNA sequencing of gut microbiota indicated that OMO administration maintains the diversity and stability of the microbial community. In addition, OMO regulated the composition and metabolism of gut microbiota in inflammatory bowel disease (IBD) mice model treated by overdosed antibiotics and thus showed the prebiotic potential. Moreover, gut microbiota plays a major role in neurodevelopment, leading to alterations in gene expression in critical brain and intestinal regions, thereby resulting in perturbation to the programming of normal cognitive behaviors. Taken together, our findings suggest that the therapeutic effect of the traditional medicine, M. officinalis, on various neurological diseases such as AD, is at least partially contributed by its naturally occurring chemical constituent, OMO, via modulating the interaction between gut ecology and brain physiology.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Probiotic L. plantarum MTCC1325 and prebiotic FOS from Morinda officinalis restore acetylcholine levels in brains of D-galactose-induced Alzheimer's disease rats by reducing acetylcholinesterase activity.
“Notably, the administration of probiotic L plantarum MTCC1325 restored the levels of acetylcholine in the brains of D-galactose-induced AD rats by reducing AChE activity.532 Similarly, another study found that prebiotic FOS from Morinda officinalis was effective in restoring acetylcholine in the brains of d-galactose-induced AD rats by reducing AChE levels.533”
From Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases (2024) · cites this paper as [533]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
DEGseq: an R package for identifying differentially expressed genes from RNA-seq data
Wang, L., Feng, Z., Wang, X., Wang, X., & Zhang, X. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btp612 · Cited by 4,553 · see citing works
Indigenous bacteria from the gut microbiota regulate host serotonin biosynthesis
Yano, J. M., Yu, K., Donaldson, G. P., Shastri, G. G., Ann, P., Ma, L., Nagler, C. R., Ismagilov, R. F., Mazmanian, S. K., & Hsiao, E. Y. (2015) · Cell · doi:10.1016/j.cell.2015.02.047 · Cited by 3,614 · see citing works
Differential analysis of gene regulation at transcript resolution with RNA-seq
Trapnell, C., Hendrickson, D. G., Sauvageau, M., Goff, L., Rinn, J. L., & Pachter, L. (2013) · Nature Biotechnology · doi:10.1038/nbt.2450 · Cited by 3,492 · see citing works
Cabili, M. N., Trapnell, C., Goff, L. A., Koziol, M. J., Tazón‐Vega, B., Regev, A., & Rinn, J. L. (2011) · Genes & Development · doi:10.1101/gad.17446611 · Cited by 3,473 · see citing works
Hsiao, E. Y., McBride, S. W., Hsien, S., Sharon, G., Hyde, E. R., McCue, T., Codelli, J. A., Chow, J., Reisman, S. E., Petrosino, J. F., et al. (2013) · Cell · doi:10.1016/j.cell.2013.11.024 · Cited by 3,283 · see citing works
Utilizing sequence intrinsic composition to classify protein-coding and long non-coding transcripts
Sun, L. D., Luo, H., Bu, D., Zhao, G., Yu, K., Zhang, C., Liu, Y., Chen, R., & Zhao, Y. C. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt646 · Cited by 2,110 · see citing works
Principles and clinical implications of the brain-gut-enteric microbiota axis
Rhee, S. H., Pothoulakis, C., & Mayer, E. A. (2009) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2009.35 · Cited by 1,342 · cited 1× · see citing works
“The hypothesis that the microbiota-gut-brain axis (Rhee et al., 2009) plays a critical role in health and disease, including neuropsychiatric disorders (Liu et al., 2017), is rapidly progressing.”
Antagonistic activities of lactobacilli and bifidobacteria against microbial pathogens
Servin, A. L. (2004) · FEMS Microbiology Reviews · doi:10.1016/j.femsre.2004.01.003 · Cited by 1,234 · see citing works
The microbiome-gut-brain axis in health and disease
Dinan, T. G., & Cryan, J. F. (2017) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2016.09.007 · Cited by 1,111 · see citing works
Akkermansia muciniphila and its role in regulating host functions
Derrien, M., Belzer, C., & de Vos, W. M. (2017) · Microbial Pathogenesis · doi:10.1016/j.micpath.2016.02.005 · Cited by 1,044 · cited 2× · see citing works
“is positively correlated with a lean phenotype, reduced body weight gain, amelioration of metabolic responses, and restoration of gut barrier function is effectuated by the modulation of mucus layer thickness (Bland, 2016; Derrien et al., 2016; Greer et al., 2016; Henning et al., 2017; Van Herreweghen et al., 2017).”
Gut microbes and the brain: paradigm shift in neuroscience
Mayer, E. A., Knight, R., Mazmanian, S. K., Cryan, J. F., & Tillisch, K. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3299-14.2014 · Cited by 1,033 · see citing works
Burokas, A., Arboleya, S., Moloney, R. D., Peterson, V. L., Murphy, K., Clarke, G., Stanton, C., Dinan, T. G., & Cryan, J. F. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.12.031 · Cited by 952 · see citing works
Akbari, E., Asemi, Z., Daneshvar Kakhaki, R., Bahmani, F., Kouchaki, E., Tamtaji, O. R., Hamidi, G. A., & Salami, M. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00256 · Cited by 946 · see citing works
Reduction of Abeta amyloid pathology in APPPS1 transgenic mice in the absence of gut microbiota
Harach, T., Marungruang, N., Duthilleul, N., Cheatham, V., Mc Coy, K. D., Frisoni, G., Neher, J. J., Fåk, F., Jucker, M., Lasser, T., et al. (2017) · Scientific Reports · doi:10.1038/srep41802 · Cited by 901 · see citing works
The Gut Microbiota and Alzheimer’s Disease
Jiang, C., Li, G., Huang, P., Liu, Z., & Zhao, B. (2017) · Journal of Alzheimer's Disease · doi:10.3233/jad-161141 · Cited by 852 · see citing works
Minter, M. R., Zhang, C., Leone, V., Ringus, D. L., Zhang, X., Oyler-Castrillo, P., Musch, M. W., Liao, F., Ward, J. F., Holtzman, D. M., et al. (2016) · Scientific Reports · doi:10.1038/srep30028 · Cited by 655 · see citing works
Petra, A. I., Panagiotidou, S., Hatziagelaki, E., Stewart, J. M., Conti, P., & Theoharides, T. C. (2015) · Clinical Therapeutics · doi:10.1016/j.clinthera.2015.04.002 · Cited by 592 · see citing works
The microbiome and host behavior
Vuong, H. E., Yano, J. M., Fung, T. C., & Hsiao, E. Y. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031347 · Cited by 537 · see citing works
Allen, A. P., Hutch, W., Borre, Y. E., Kennedy, P. J., Temko, A., Boylan, G., Murphy, E., Cryan, J. F., Dinan, T. G., & Clarke, G. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.191 · Cited by 513 · see citing works
Role of gut microbiota and nutrients in amyloid formation and pathogenesis of Alzheimer disease
Pistollato, F., Sumalla Cano, S., Elio, I., Masias Vergara, M., Giampieri, F., & Battino, M. (2016) · Nutrition Reviews · doi:10.1093/nutrit/nuw023 · Cited by 496 · see citing works
Health Benefits of Kimchi (Korean Fermented Vegetables) as a Probiotic Food
Park, K., Jeong, J., Lee, Y.-E., & Daily, J. W. (2014) · Journal of Medicinal Food · doi:10.1089/jmf.2013.3083 · Cited by 471 · see citing works
Bifidobacterium longum with Fructo-Oligosaccharides in Patients with Non Alcoholic Steatohepatitis
Malaguarnera, M., Vacante, M., Antic, T., Giordano, M., Chisari, G., Acquaviva, R., Mastrojeni, S., Malaguarnera, G., Mistretta, A., Volti, G. L., et al. (2011) · Digestive Diseases and Sciences · doi:10.1007/s10620-011-1887-4 · Cited by 456 · see citing works
Intestinal Microbiota Development in Preterm Neonates and Effect of Perinatal Antibiotics
Arboleya, S., Sánchez, B., Milani, C., Duranti, S., Sánchez, G. S., Fernández, N., Reyes‐Gavilán, C. G. D. L., Ventura, M., Margollés, A., & Gueimonde, M. (2014) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2014.09.041 · Cited by 434 · see citing works
Microbes and mental health: A review
Rieder, R., Wisniewski, P. J., Alderman, B. L., & Campbell, S. C. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.01.016 · Cited by 429 · see citing works
The dormant blood microbiome in chronic, inflammatory diseases
Potgieter, M., Bester, J., Kell, D. B., & Pretorius, E. (2015) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuv013 · Cited by 377 · see citing works
Alzheimer’s disease and gut microbiota
Hu, X., Wang, T., & Jin, F. (2016) · Science China Life Sciences · doi:10.1007/s11427-016-5083-9 · Cited by 371 · see citing works
Bacterial Neuroactive Compounds Produced by Psychobiotics
Wall, R., Cryan, J. F., Ross, R. P., Fitzgerald, G. F., Dinan, T. G., & Stanton, C. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-0897-4_10 · Cited by 362 · see citing works
Benjamin, J. L., Hedin, C. R. H., Koutsoumpas, A., Ng, S. C., McCarthy, N. E., Hart, A. L., Kamm, M. A., Sanderson, J. D., Knight, S. C., Forbes, A., et al. (2011) · Gut · doi:10.1136/gut.2010.232025 · Cited by 361 · see citing works
Human gut microbiota: the links with dementia development
Alkasir, R., Li, J., Li, X., Jin, M., & Zhu, B. (2016) · Protein & Cell · doi:10.1007/s13238-016-0338-6 · Cited by 283 · see citing works
Akkermansia muciniphila mediates negative effects of IFNγ on glucose metabolism
Greer, R. L., Dong, X., de Moraes, A. C. F., Zielke, R. A., Fernandes, G. D. R., Peremyslova, E., Vasquez‐Perez, S., Schoenborn, A. A., Gomes, E. P., Pereira, A. C., et al. (2016) · Nature Communications · doi:10.1038/ncomms13329 · Cited by 277 · see citing works
Vanegas, S. M., Meydani, M., Barnett, J. B., Goldin, B., Kane, A., Rasmussen, H., Brown, C., Vangay, P., Knights, D., Jonnalagadda, S., et al. (2017) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.116.146928 · Cited by 277 · see citing works
Dementia: A problem for our age
Abbott, A. (2011) · Nature · doi:10.1038/475s2a · Cited by 243 · see citing works
Structural basis for nutrient acquisition by dominant members of the human gut microbiota
Glenwright, A. J., Pothula, K. R., Bhamidimarri, S. P., Chorev, D. S., Baslé, A., Firbank, S. J., Zheng, H., Robinson, C. V., Winterhalter, M., Kleinekathöfer, U., et al. (2017) · Nature · doi:10.1038/nature20828 · Cited by 227 · see citing works
Gut-brain Axis: Role of Lipids in the Regulation of Inflammation, Pain and CNS Diseases
Russo, R., Cristiano, C., Avagliano, C., Caro, C. D., Rana, G. L., Raso, G. M., Canani, R. B., Meli, R., & Calignano, A. (2017) · Current Medicinal Chemistry · doi:10.2174/0929867324666170216113756 · Cited by 213 · see citing works
Revisiting Metchnikoff: Age-related alterations in microbiota-gut-brain axis in the mouse
Scott, K. A., Ida, M., Peterson, V. L., Prenderville, J. A., Moloney, G. M., Izumo, T., Murphy, K., Murphy, A., Ross, R. P., Stanton, C., et al. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2017.02.004 · Cited by 202 · see citing works
Microbiota-gut-brain axis and cognitive function
Gareau, M. G. (2014) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-0897-4_16 · Cited by 189 · see citing works
Davis, D. J., Doerr, H. M., Grzelak, A. K., Busi, S. B., Jašarević, E., Ericsson, A. C., & Bryda, E. C. (2016) · Scientific Reports · doi:10.1038/srep33726 · Cited by 159 · see citing works
Ling, Z., Liu, X., Jia, X., Cheng, Y., Luo, Y., Yuan, L., Wang, Y., Zhao, C., Guo, S., Li, L., et al. (2014) · Scientific Reports · doi:10.1038/srep07485 · Cited by 158 · see citing works
Woo, J.-Y., Gu, W., Kim, K., Jang, S., Han, M. J., & Kim, D. (2014) · Anaerobe · doi:10.1016/j.anaerobe.2014.03.003 · Cited by 155 · see citing works
Gao, J., Zhou, R., You, X., Luo, F., He, H., Chang, X., Zhu, L., Ding, X., & Yan, T. (2016) · Metabolic Brain Disease · doi:10.1007/s11011-016-9813-2 · Cited by 127 · see citing works
Anderson, G., Seo, M., Berk, M., Carvalho, A., & Maes, M. (2016) · Current Pharmaceutical Design · doi:10.2174/1381612822666160906161513 · Cited by 103 · see citing works
Herreweghen, F. V., den Abbeele, P. V., Mulder, T. D., Weirdt, R. D., Geirnaert, A., Hernandez‐Sanabria, E., Vilchez‐Vargas, R., Jáuregui, R., Pieper, D. H., Belzer, C., et al. (2016) · Beneficial Microbes · doi:10.3920/bm2016.0013 · Cited by 95 · see citing works
Zeng, G., Zhang, Z., Lü, L., Xiao, D.-Q., Zong, S., & He, J.-M. (2013) · Rejuvenation Research · doi:10.1089/rej.2012.1389 · Cited by 94 · see citing works
Gut Microbiota: A Modulator of Brain Plasticity and Cognitive Function in Ageing
Leung, K., & Thuret, S. (2015) · Healthcare · doi:10.3390/healthcare3040898 · Cited by 92 · see citing works
Vandenplas, Y., Ludwig, T. G., Bouritius, H., Alliet, P. L., Forde, D., Peeters, S., Huet, F., & Hourihane, J. O. (2017) · Acta Paediatrica · doi:10.1111/apa.13844 · Cited by 87 · see citing works
Pomegranate ellagitannins stimulate the growth of Akkermansia muciniphila in vivo
Henning, S. M., Summanen, P. H., Lee, R., Yang, J., Finegold, S. M., Heber, D., & Li, Z. (2016) · Anaerobe · doi:10.1016/j.anaerobe.2016.12.003 · Cited by 85 · see citing works
Self-citationSage, F. L., Meilhac, O., & Gonthier, M. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2017.02.022 · Cited by 85 · see citing works
High salt diet stimulates gut Th17 response and exacerbates TNBS-induced colitis in mice
Wei, Y., Lu, C., Chen, J., Cui, G., Wang, L., Yu, T., Yang, Y. J., Wu, W., Ding, Y., Li, L., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.13783 · Cited by 83 · see citing works
García-Mazcorro, J. F., Barcenas-Walls, J. R., Suchodolski, J. S., & Steiner, J. M. (2017) · PeerJ · doi:10.7717/peerj.3184 · Cited by 78 · see citing works
Lactobacillus pentosusvar.plantarumC29 protects scopolamine-induced memory deficit in mice
Jung, I.-H., Jung, M., Kim, E.-J., Han, M. J., & Kim, D.-H. (2012) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2012.05437.x · Cited by 77 · see citing works
Lopes, S. M. S., Grigio, F. M., Higashi, B., de Almeida, R. T. R., Krausová, G., Pilau, E. J., Gonçalves, J. E., Gonçalves, R. A. C., & de Oliveira, A. J. B. (2016) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2016.07.043 · Cited by 74 · see citing works
Li, Y., Liu, Y., Yang, M., Wang, H., Huang, W.-C., Zhao, Y., & Luo, Z.-P. (2004) · Life Sciences · doi:10.1016/j.lfs.2004.02.029 · Cited by 72 · see citing works
Valdés-Varela, L., Ruas‐Madiedo, P., & Gueimonde, M. (2016) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2016.11.011 · Cited by 71 · see citing works
Erdman, S. E., & Poutahidis, T. (2016) · International review of neurobiology · doi:10.1016/bs.irn.2016.07.004 · Cited by 67 · see citing works
Jeong, J.-J., Woo, J.-Y., Kim, K.-A., Han, M. J., & Kim, D.-H. (2015) · Letters in Applied Microbiology · doi:10.1111/lam.12393 · Cited by 63 · see citing works
Huang, H., Zheng, B.-W., Guo, Y., Zhao, J., Zhao, J., Ma, X., & Jiang, Z.-F. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-150872 · Cited by 57 · see citing works
Chen, D., Li, N., Li, L., Long, H., Lin, H., Chen, J., He-Ming, Z., Zeng, C., & Liu, S. (2014) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2014.01.021 · Cited by 46 · see citing works
Self-citationAntistress effect of oligosaccharides extracted from Morinda officinalis in mice and rats.
Li, Y., Li, Y., Xu, Y.-K., Yang, M., Zhao, Y., & Luo, Z.-P. (2001) · PubMed · Cited by 44 · see citing works
Protective Effect of Bajijiasu Against β-Amyloid-Induced Neurotoxicity in PC12 Cells
Chen, D., Zhang, P., Lin, L., Shuai, O., He-Ming, Z., Liu, S., & Wang, J.-Y. (2013) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-013-9950-7 · Cited by 41 · see citing works
Self-citationEffect of Dendrobium officinale on D-galactose-induced aging mice
Liang, C., Liang, Y., Liu, H., Zhu, D., Hou, S., Wu, Y., Huang, S. M., & Lai, X. (2017) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-016-2631-x · Cited by 40 · see citing works
Protective effects of bajijiasu in a rat model of Aβ25-35-induced neurotoxicity
Chen, D., Zhāng, P., Lin, L., Zhang, H.-M., Deng, S., Wu, Z., Shuai, O., Liu, S., & Wang, J.-Y. (2014) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2014.04.004 · Cited by 38 · see citing works
Self-citationChoi, Y. J., Yang, H. S., Jo, J. H., Lee, S. C., Park, T. Y., Choi, B. S., Seo, K., & Huh, C.-K. (2015) · Preventive Nutrition and Food Science · doi:10.3746/pnf.2015.20.2.126 · Cited by 38 · see citing works
Rigo-Adrover, M., Pérez-Berezo, T., Ramos-Romero, S., van Limpt, K., Knipping, K., Garssen, J., Knol, J., Franch, À., Castell, M., & Pérez-Cano, F. J. (2017) · British Journal Of Nutrition · doi:10.1017/s0007114516004566 · Cited by 34 · see citing works
Berberine rescues d-galactose-induced synaptic/memory impairment by regulating the levels of Arc
Zhan, P., Peng, C., & Zhang, L. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.12.006 · Cited by 30 · see citing works
Cerebral mTOR signal and pro-inflammatory cytokines in Alzheimer’s disease rats
Wang, X., Li, G., Hu, H., Ma, C., Ma, D., Liu, X., & Jiang, X. (2016) · Translational Neuroscience · doi:10.1515/tnsci-2016-0022 · Cited by 25 · see citing works
Diling, C., Yong, T., Jian, Y., Chaoqun, Z., Shuai, O., & Yizhen, X. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00219 · Cited by 20 · see citing works
Self-citationTanner, S. A., Lacroix, C., Del’Homme, C., Jans, C., Zihler, A., Bernalier‐Donadille, A., & Chassard, C. (2015) · British Journal Of Nutrition · doi:10.1017/s0007114515002263 · Cited by 17 · see citing works
Qing'E formula alleviates the aging process in D-galactose-induced aging mice
Zhong, L., Huang, F., Shi, H., Wu, H., Zhang, B., Wu, X., Wei, X., & Wang, Z. (2016) · Biomedical Reports · doi:10.3892/br.2016.667 · Cited by 16 · see citing works
Intestinal Microbiome, Akkermansia muciniphila, and Medical Nutrition Therapy.
Bland, J. K. S. (2016) · PubMed Central · Cited by 11 · see citing works
Minocycline ameliorates d-galactose-induced memory deficits and loss of Arc/Arg3.1 expression
Xu, L., Fen, L., Li, W., Xu, J., Sun, X., Qin, L., Zhang, Q.-L., Yao, Y., Yu, Q.-K., & Liang, X. (2016) · Molecular Biology Reports · doi:10.1007/s11033-016-4051-6 · Cited by 6 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases
Loh, J. S., Mak, W. Q., Tan, L. K. S., Ng, C. X., Chan, H. H., Yeow, S. H., Foo, J. B., Ong, Y. S., How, C. W., & Khaw, K. Y. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01743-1 · Cited by 1,193 · see citing works
Chen, Y., Xu, J., & Chen, Y. (2021) · Nutrients · doi:10.3390/nu13062099 · Cited by 917 · see citing works
Gut microbiota and dysbiosis in Alzheimer's disease: Implications for pathogenesis and treatment
Liu, S., Gao, J., Zhu, M., Liu, K., & Zhang, H.-L. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-02073-3 · Cited by 516 · see citing works
Antibiotics, gut microbiota, and Alzheimer’s disease
Angelucci, F., Cechova, K., Amlerova, J., & Hort, J. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1494-4 · Cited by 454 · see citing works
The impact of the microbiota-gut-brain axis on Alzheimer’s disease pathophysiology
Doifode, T., Giridharan, V. V., Generoso, J. S., Bhatti, G., Collodel, A., Schulz, P. E., Forlenza, O. V., & Barichello, T. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2020.105314 · Cited by 347 · see citing works
The Potential Role of Gut Microbiota in Alzheimer’s Disease: From Diagnosis to Treatment
Varesi, A., Pierella, E., Romeo, M., Piccini, G. B., Alfano, C., Bjørklund, G., Oppong, A., Ricevuti, G., Esposito, C., Chirumbolo, S., et al. (2022) · Nutrients · doi:10.3390/nu14030668 · Cited by 225 · see citing works
Gut microbiota, cognitive frailty and dementia in older individuals: A systematic review
Ticinesi, A., Tana, C., Nouvenne, A., Prati, B., Lauretani, F., & Meschi, T. (2018) · Clinical Interventions in Aging · doi:10.2147/cia.s139163 · Cited by 215 · see citing works
Chudzik, A., Orzyłowska, A., Rola, R., & Stanisz, G. J. (2021) · Biomolecules · doi:10.3390/biom11071000 · Cited by 212 · see citing works
The role of gut microbiota in pathogenesis of Alzheimer's disease
Bostancıklıoğlu, M. (2019) · Journal of Applied Microbiology · doi:10.1111/jam.14264 · Cited by 200 · see citing works
He, J., Li, X., Wang, Z., Bennett, S., Chen, K., Xiao, Z., Zhan, J., Chen, S., Hou, Y., Chen, J., et al. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01344 · Cited by 196 · see citing works
Shabbir, U., Arshad, M. S., Sameen, A., & Oh, D.-H. (2021) · Nutrients · doi:10.3390/nu13020690 · Cited by 191 · see citing works
From Probiotics to Psychobiotics: Live Beneficial Bacteria Which Act on the Brain-Gut Axis
Bermúdez‐Humarán, L. G., Salinas, E., Ortíz, G. G., Ramírez-Jirano, L. J., Morales, J. A., & Bitzer-Quintero, O. K. (2019) · Nutrients · doi:10.3390/nu11040890 · Cited by 172 · see citing works
Ansari, F., Pourjafar, H., Tabrizi, A., & Homayouni, A. (2020) · Current Pharmaceutical Biotechnology · doi:10.2174/1389201021666200107113812 · Cited by 170 · see citing works
Understanding the Gut–Brain Axis and Its Therapeutic Implications for Neurodegenerative Disorders
Zheng, Y., Bonfili, L., Wei, T., & Eleuteri, A. M. (2023) · Nutrients · doi:10.3390/nu15214631 · Cited by 175 · see citing works
Gut microbiota and pro/prebiotics in Alzheimer’s disease
Pluta, R. M., Ułamek-Kozioł, M., Januszewski, S., & Czuczwar, S. J. (2020) · Aging · doi:10.18632/aging.102930 · Cited by 171 · see citing works
The interaction between the gut Microbiota and herbal medicines
An, X., Bao, Q. D., Di, S., Zhao, Y. C., Zhao, S., Zhang, H., Lian, F., & Tong, X. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109252 · Cited by 166 · see citing works
Microbiota influence the development of the brain and behaviors in C57BL/6J mice
Lu, J., Synowiec, S., Lu, L., Yu, Y., Bretherick, T., Takada, S., Yarnykh, V., Caplan, J., Caplan, M., Claud, E. C., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0201829 · Cited by 159 · see citing works
Kim, H. S., Kim, S., Shin, S. J., Park, Y. H., Nam, Y., Lee, K. W., Lee, K. W., Kim, S., Yang, H. D., Yang, H. D., et al. (2021) · Translational Neurodegeneration · doi:10.1186/s40035-021-00273-y · Cited by 161 · see citing works
Sun, J., Liu, S., Ling, Z., Wang, F., Ling, Y., Gong, T., Fang, N., Ye, S., Si, J., & Liu, J. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.8b07313 · Cited by 145 · see citing works
Liu, Y., Liu, W., Li, J., Tang, S., Wang, M., Huang, W., Yao, W., & Gao, X. (2018) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2018.10.041 · Cited by 139 · see citing works
Yang, X.-D., Wang, L.-K., Wu, H.-Y., & Jiao, L. (2018) · BMC Anesthesiology · doi:10.1186/s12871-018-0642-1 · Cited by 129 · see citing works
Self-citationWu, S., Bekhit, A. E. A., Wu, Q., Chen, M., Liao, X., Wang, J., & Ding, Y. (2020) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2020.12.019 · Cited by 123 · see citing works
Self-citationFunctional and nutraceutical properties of fructo-oligosaccharides derivatives: A review
Rahim, M. A., Saeed, F., Khalid, W., Hussain, M., & Anjum, F. M. (2021) · International Journal of Food Properties · doi:10.1080/10942912.2021.1986520 · Cited by 108 · see citing works
Vinuesa, Á., Pomilio, C. J., Gregosa, A., Bentivegna, M., Presa, J., Bellotto, M., Saravia, F., & Beauquis, J. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.653651 · Cited by 111 · see citing works
Yang, X., Diling, C., Yang, J. T., Ting, L., Guoyan, H., Hualun, L., Xiaocui, T., Lai, G., Shuai, O., Chaoqun, Z., et al. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00412 · Cited by 108 · see citing works
Self-citationWang, M., Amakye, W. K., Guo, L., Gong, C., Zhao, Y., Yao, M., & Ren, J. (2019) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201900326 · Cited by 99 · see citing works
Pérez-Escalante, E., Alatorre‐Santamaría, S., Ovando, A. C., Salazar, V., Bautista, M., Cruz-Guerrero, A. E., Flores-Aguilar, J. F., & González-Olivares, L. G. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1813683 · Cited by 98 · see citing works
Murray, E. R., Kemp, M., & Nguyen, T. T. (2022) · Archives of Clinical Neuropsychology · doi:10.1093/arclin/acac008 · Cited by 98 · see citing works
The role of prebiotics in cognition, anxiety, and depression
de Paiva, I. H. R., Duarte-Silva, E. P., & Peixoto, C. A. (2020) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2020.03.006 · Cited by 93 · see citing works
Tang, W., Meng, Z., Li, N., Liu, Y., Li, L., Chen, D., & Yang, Y. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.611014 · Cited by 89 · see citing works
Self-citationBrain modulation by the gut microbiota: From disease to therapy
Mitra, S., Dash, R., Nishan, A. A., Habiba, S. U., & Moon, I. S. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2022.12.001 · Cited by 87 · see citing works
Varesi, A., Campagnoli, L. I. M., Fahmideh, F., Pierella, E., Romeo, M., Ricevuti, G., Nicoletta, M., Chirumbolo, S., & Pascale, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012289 · Cited by 88 · see citing works
Yang, L., Ao, Y., Li, Y., Dai, B., Li, J., Duan, W., Gao, W., Zhao, Z., Han, Z., & Guo, R. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02715-y · Cited by 87 · see citing works
Balancing reactive oxygen species generation by rebooting gut microbiota
Singh, V., Ahlawat, S., Mohan, H., Gill, S. S., & Sharma, K. K. (2022) · Journal of Applied Microbiology · doi:10.1111/jam.15504 · Cited by 83 · see citing works
Gut Microbiota: Implications in Alzheimer’s Disease
He, Y., Li, B., Sun, D., & Chen, S. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9072042 · Cited by 81 · see citing works
Baldi, S., Mundula, T., Nannini, G., & Amedei, A. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i39.6715 · Cited by 85 · see citing works
The intestinal microbiome and its relevance for functionality in older persons
Ticinesi, A., Tana, C., & Nouvenne, A. (2019) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000521 · Cited by 80 · see citing works
An update on the interactions between Alzheimer's disease, autophagy and inflammation
Bostancıklıoğlu, M. (2019) · Gene · doi:10.1016/j.gene.2019.04.040 · Cited by 78 · see citing works
Thompson, R. S., Gaffney, M., Hopkins, S., Kelley, T., González, A., Bowers, S. J., Vitaterna, M. H., Turek, F. W., Foxx, C. L., Lowry, C. A., et al. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.07.006 · Cited by 80 · see citing works
Ghaffari, S., Abbasi, A., Somi, M. H., Moaddab, S. Y., Nikniaz, L., Kafil, H. S., & Leylabadlo, H. E. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2045894 · Cited by 74 · see citing works
Rosário, D., Borén, J., Uhlén, M., Proctor, G., Aarsland, D., Mardinoğlu, A., & Shoaie, S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00716 · Cited by 66 · see citing works
Lei, W., Cheng, Y., Liu, X., Gao, J., Zhu, Z., Ding, W., Xu, X., Li, Y., Ling, Z., Jiang, R., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1582119 · Cited by 68 · see citing works
Cheng, W., Ho, J. Y. S., & Chang, R. C. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101620 · Cited by 67 · see citing works
Memorable Food: Fighting Age-Related Neurodegeneration by Precision Nutrition
Milošević, M. S., Arsić, A., Cvetković, Z., & Vučić, V. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.688086 · Cited by 65 · see citing works
Can We Treat Neuroinflammation in Alzheimer’s Disease?
Sánchez‐Sarasúa, S., Fernández-Pérez, I., Espinosa‐Fernández, V., Sánchez‐Pérez, A. M., & Ledesma, J. C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228751 · Cited by 63 · see citing works
Functional Foods: An Approach to Modulate Molecular Mechanisms of Alzheimer’s Disease
Atlante, A., Amadoro, G., Bobba, A., & Latina, V. (2020) · Cells · doi:10.3390/cells9112347 · Cited by 65 · see citing works
Contribution of Gut Microbiota to Immunological Changes in Alzheimer’s Disease
van Olst, L., Roks, S. J. M., Kamermans, A., Verhaar, B. J. H., van der Geest, A. M., Muller, M., van der Flier, W. M., & de Vries, H. E. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.683068 · Cited by 67 · see citing works
Srivastava, S., Basak, U. O., Naghibi, M., Vijayakumar, V., Parihar, R., Patel, J. A., Jadon, P., Pandit, A., Dargad, R., Khanna, S., et al. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2338322 · Cited by 62 · see citing works
Dietary Regulation of Gut-Brain Axis in Alzheimer’s Disease: Importance of Microbiota Metabolites
Frausto, D. M., Forsyth, C. B., Keshavarzian, A., & Voigt, R. M. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.736814 · Cited by 61 · see citing works
Krishaa, L., Ng, T. K. S., Wee, H. N., & Ching, J. (2023) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2023.111787 · Cited by 60 · see citing works
Gut microbiome: An intermediary to neurotoxicity
Dempsey, J. L., Little, M., & Cui, J. Y. (2019) · NeuroToxicology · doi:10.1016/j.neuro.2019.08.005 · Cited by 62 · see citing works
Lian, Z., Xu, Y., Wang, C., Chen, Y., Li, Y., Liu, Z., Liu, Y., He, P., Cai, Z., & Zhao, J. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106714 · Cited by 60 · see citing works
Target Dysbiosis of Gut Microbes as a Future Therapeutic Manipulation in Alzheimer’s Disease
Zhu, F., Li, C., Chu, F., Tian, X., & Zhu, J. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.544235 · Cited by 58 · see citing works
Shanmugam, H., Ganguly, S., & Priya, B. (2021) · Food Frontiers · doi:10.1002/fft2.125 · Cited by 56 · see citing works
Narisetty, V., Parhi, P., Binoop, M., Hazeena, S. H., Kumar, A. N., Gullón, B., Srivastava, A., Nair, L. M., Alphy, M. P., Sindhu, R., et al. (2021) · Bioresource Technology · doi:10.1016/j.biortech.2021.126590 · Cited by 56 · see citing works
Vitamin K2 Holds Promise for Alzheimer’s Prevention and Treatment
Popescu, A., & German, M. (2021) · Nutrients · doi:10.3390/nu13072206 · Cited by 55 · see citing works
Cutuli, D., Decandia, D., Giacovazzo, G., & Coccurello, R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914686 · Cited by 58 · see citing works
Petracco, G., Faimann, I., & Reichmann, F. (2025) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2025.108831 · Cited by 54 · see citing works
Ruiz‐González, C., Román, P., Rueda‐Ruzafa, L., Rodríguez-Arrastia, M. J., & Cardona, D. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110189 · Cited by 53 · see citing works
Dysbiosis and Alzheimer’s Disease: Cause or Treatment Opportunity?
Janeiro, M. H., Ramírez, M. J., & Solas, M. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-01024-9 · Cited by 50 · see citing works
Zhong, S.-R., Kuang, Q., Zhang, F., Chen, B., & Zhong, Z.-G. (2021) · Translational Neuroscience · doi:10.1515/tnsci-2020-0206 · Cited by 54 · see citing works
The Potential Utility of Prebiotics to Modulate Alzheimer’s Disease: A Review of the Evidence
Kang, J. W., & Zivkovic, A. M. (2021) · Microorganisms · doi:10.3390/microorganisms9112310 · Cited by 49 · see citing works
Impact of Microbiome–Brain Communication on Neuroinflammation and Neurodegeneration
Stolzer, I., Scherer, E., Süß, P., Rothhammer, V., Winner, B., Neurath, M. F., & Günther, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914925 · Cited by 47 · see citing works
Microglia and gut microbiota: A double-edged sword in Alzheimer's disease
Bano, N., Khan, S., Ahamad, S., Kanshana, J. S., Dar, N. J., Khan, S. J., Nazir, A., & Bhat, S. A. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102515 · Cited by 49 · see citing works
Functional constituents of plant-based foods boost immunity against acute and chronic disorders
Khalid, W., Arshad, M. S., Ranjha, M. M. A. N., Różańska, M. B., Irfan, S., Shafique, B., Rahim, M. A., Khalid, M. Z., Abdi, G., & Kowalczewski, P. Ł. (2022) · Open Life Sciences · doi:10.1515/biol-2022-0104 · Cited by 50 · see citing works
Gut microbiome and Alzheimer’s disease: What we know and what remains to be explored
Kapoor, B., Biswas, P., Gulati, M., Rani, P., & Gupta, R. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102570 · Cited by 46 · see citing works
The gut microbiome as a target for adjuvant therapy in obstructive sleep apnea
Badran, M., Mashaqi, S., & Gozal, D. (2020) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2020.1841749 · Cited by 45 · see citing works
Fructooligosaccharides production and the health benefits of prebiotics
Nobre, C., Simões, L. S., Gonçalves, D. A., Berni, P. R. D. A., & Teixeira, J. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823506-5.00002-3 · Cited by 45 · see citing works
Role of Gut Microbiota in Combating Oxidative Stress
Dam, B., Misra, A., & Banerjee, S. (2019) · Springer eBooks · doi:10.1007/978-981-13-8763-0_4 · Cited by 45 · see citing works
Gut dysbiosis in stroke and its implications on Alzheimer’s disease‐like cognitive dysfunction
Cho, J., Park, Y. J., Gonzales‐Portillo, B., Saft, M., Cozene, B., Sadanandan, N., & Borlongan, C. V. (2021) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13613 · Cited by 44 · see citing works
The Role of Gut Microbiota—Gut—Brain Axis in Perioperative Neurocognitive Dysfunction
Lu, J. G., Hou, W., Gao, S., Zhang, Y., & Zong, Y. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.879745 · Cited by 42 · see citing works
Qu, L., Li, Y., Liu, F., Fang, Y., He, J., Ma, J., Xu, T., Wang, L., Lei, P., Dong, H., et al. (2023) · Aging and Disease · doi:10.14336/ad.2023.0823-2 · Cited by 46 · see citing works
The fusiform gyrus exhibits an epigenetic signature for Alzheimer’s disease
Ma, D., Fetahu, I. S., Wang, M., Fang, R., Li, J., Liu, H., Gramyk, T., Iwanicki, I. J., Gu, S., Xu, W., et al. (2020) · Clinical Epigenetics · doi:10.1186/s13148-020-00916-3 · Cited by 43 · see citing works
Zhang, S., Lv, S., Li, Y., Wei, D., Zhou, X., Niu, X., Yang, Z., Song, W., Zhang, Z., & Peng, D. (2023) · European Journal of Nutrition · doi:10.1007/s00394-023-03208-7 · Cited by 41 · see citing works
Gut microbiota and its metabolites in Alzheimer’s disease: from pathogenesis to treatment
Zou, X., Zou, G., Zou, X., Wang, K., & Chen, Z. (2024) · PeerJ · doi:10.7717/peerj.17061 · Cited by 40 · see citing works
Ticinesi, A., Mancabelli, L., Carnevali, L., Nouvenne, A., Meschi, T., Rio, D. D., Ventura, M., Sgoifo, A., & Angelino, D. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-215493 · Cited by 40 · see citing works
Hao, X., Ding, N., Zhang, Y., Yang, Y., Zhao, Y., Zhao, J. J., Li, Y., & Li, Z. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.960026 · Cited by 41 · see citing works
Bashir, B., Alam, S., Khandale, N. B., Birla, D., Vishwas, S., Pandey, N. K., Gupta, G., Paudel, K. R., Dureja, H., Kumar, P., et al. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102236 · Cited by 39 · see citing works
Yassin, L. K., Skrabulyte-Barbulescu, J., Alshamsi, S. H., Saeed, S., Alkuwaiti, S. H., Almazrouei, S., Alnuaimi, A., BaniYas, S., Aldhaheri, D., Alderei, M., et al. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1667448 · Cited by 46 · see citing works
Neurodegenerative Microbially-Shaped Diseases: Oxidative Stress Meets Neuroinflammation
Silva, D. F., Empadinhas, N., Cardoso, S. M., & Esteves, A. R. (2022) · Antioxidants · doi:10.3390/antiox11112141 · Cited by 39 · see citing works
Ma, L., Jiang, X., Huang, Q.-Y., Chen, W., Zhang, H., Pei, H., Cao, Y., Wang, H., & Li, H. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115244 · Cited by 38 · see citing works
Systemic inflammation as a central player in the initiation and development of Alzheimer’s disease
Bayraktaroğlu, I., Ortí-Casañ, N., Dam, D. V., Deyn, P. P. D., & Eisel, U. L. M. (2025) · Immunity & Ageing · doi:10.1186/s12979-025-00529-5 · Cited by 42 · see citing works
Impact of Gut Microbiome Manipulation in 5xFAD Mice on Alzheimer’s Disease-Like Pathology
Guilherme, M. D. S., Nguyen, V. T. T., Reinhardt, C., & Endres, K. (2021) · Microorganisms · doi:10.3390/microorganisms9040815 · Cited by 38 · see citing works
Rahman, Z., Bhale, N. A., Dikundwar, A. G., & Dandekar, M. P. (2023) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-023-10109-y · Cited by 37 · see citing works
Ristori, S., Bertoni, G., Bientinesi, E., & Monti, D. (2025) · Nutrients · doi:10.3390/nu17111837 · Cited by 42 · see citing works
Shen, L., & Ji, H. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-181143 · Cited by 36 · see citing works
Bi, T., Feng, R., Zhan, L., Ren, W., & Lu, X. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.651517 · Cited by 36 · see citing works
Some Candidate Drugs for Pharmacotherapy of Alzheimer’s Disease
Miziak, B., Błaszczyk, B., & Czuczwar, S. J. (2021) · Pharmaceuticals · doi:10.3390/ph14050458 · Cited by 35 · see citing works
Gut-Brain Axis and Neurological Disorders-How Microbiomes Affect our Mental Health
Bhatia, N. Y., Jalgaonkar, M. P., Hargude, A. B., Sherje, A. P., Oza, M. J., & Doshi, G. (2022) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527321666220822172039 · Cited by 37 · see citing works
Uceda, S., Echeverry‐Alzate, V., Reiriz, M., Miguel, E. M., Pérez-Curiel, A., Gómez-Senent, S., & Beltrán-Velasco, A. I. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713294 · Cited by 35 · see citing works
Neuroprotective Potential of Non-Digestible Oligosaccharides: An Overview of Experimental Evidence
Divyashri, G., Sadanandan, B., Murthy, K. N. C., Shetty, K., & Mamta, K. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.712531 · Cited by 34 · see citing works
Role of fructooligosaccharides in promoting beneficial gut bacteria: A Prebiotic perspective
Singh, P., Gupta, S., Kundu, A., Grover, M., & Saha, S. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.105726 · Cited by 32 · see citing works
Taj, T., Kaushik, M., Islam, A., Das, J., Kumar, B., Hussain, M. S., Ramzan, M., Ashique, S., Tariq, M., Sridhar, S. B., et al. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118861 · Cited by 33 · see citing works
Current Alzheimer disease research highlights: evidence for novel risk factors
Brenowitz, W. D., Xiang, Y., McEvoy, C. T., Yang, C., Yaffe, K. S., Le, W., & Leng, Y. (2021) · Chinese Medical Journal · doi:10.1097/cm9.0000000000001706 · Cited by 32 · see citing works
A critical review on the relationship of herbal medicine, Akkermansia muciniphila, and human health
Bu, F., Zhang, S., Duan, Z., Ding, Y., Chen, T., Wang, R., Feng, Z., Shi, G., Zhou, J., & Chen, Y. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110352 · Cited by 31 · see citing works
de Rijke, T. J., Doting, M. H. E., van Hemert, S., Deyn, P. P. D., Munster, B. C. V., Harmsen, H. J. M., & Sommer, I. E. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.879491 · Cited by 32 · see citing works
Chu, Z., Han, S., Luo, Y., Zhou, Y., Zhu, L., & Luo, F. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2222404 · Cited by 32 · see citing works
CircNF1-419 improves the gut microbiome structure and function in AD-like mice
Diling, C., Qi, L., Guo, Y., Liu, Y., Xiaocui, T., Zhu, X., Zeng, M., Li, R., Shuai, O., Dongdong, W., et al. (2020) · Aging · doi:10.18632/aging.102614 · Cited by 30 · see citing works
Self-citationRetractedFongang, B., Satizábal, C. L., Kautz, T. F., Wadop, Y. N., Muhammad, J. A. S., Vasquez, E. L., Mathews, J. J., Gireud, M., Saklad, A. R., Himali, J. J., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-40872-5 · Cited by 29 · see citing works
Unveiling the Health Benefits of Prebiotics: A Comprehensive Review
Kumari, A. R., Rashmi, K. G., Sudhakaran, A., Warrier, A. S., & Singh, N. K. (2024) · Indian Journal of Microbiology · doi:10.1007/s12088-024-01235-4 · Cited by 29 · see citing works
- Authors
- Chen, D., Yang, X., Yang, J., Lai, G., Yong, T., Tang, X., Shuai, O., Zhou, G., Xie, Y., & Wu, Q.
- Affiliations
- Chinese Academy of Sciences (CN)
- Guangzhou Medical University (CN)
- Guangxi University of Chinese Medicine (CN)
- Corresponding author
- Chen, Diling
- Xie, Yizhen
- Venue
- Frontiers in Aging Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2017-12-08
- Volume
- 9
- Pages
- 403-403
- ISSN
- 1663-4365 (ISSN-L)
- PMC
- PMC5727096
- OpenAlex
- W2775686313
- Cited by
- 227
- References
- 70
- Citations by year
- 2026: 16 · 2025: 28 · 2024: 31 · 2023: 29 · 2022: 42 · 2021: 36 · 2020: 23 · 2019: 13 · 2018: 9
- FWCI
- 9.11
- Type
- journal article
- Language
- en
- Update notices
- corrigendum (2025-05-14)
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Aging Neuroscience (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Guangzhou Medical University (2016C28)
- Guangdong Academy of Sciences (2016GDASRC-0102)
- Guangzhou Municipal Science and Technology Project
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Nursing › Nutrition and Dietetics › Microbial Metabolites in Food Biotechnology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Keywords
- fructooligosaccharides, Morinda officinalis, Alzheimer's disease, prebiotics, microbiota-gut-brain axis, gut microbiota, learning and memory, oxidative stress, neuroinflammation, amyloid-beta, tau protein, neuronal apoptosis, antibiotic-induced dysbiosis, inflammatory bowel disease, traditional medicine
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review