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A perspective for alzheimer disease from gut microbiota-associated NMR-based fecal metabolomics: a study with 5XFAD mice

dc.contributor.authorTekin, Nazlihan
dc.contributor.authorSahin, Furkan
dc.contributor.authorSahin, Betul
dc.contributor.authorKaya, Zelal Zuhal
dc.contributor.authorYilmaz, Ali
dc.contributor.authorGraham, Stewart F.
dc.contributor.authorSerteser, Mustafa
dc.contributor.authorBaykal, Ahmet Tarik
dc.date.accessioned2026-11-05T11:07:19Z
dc.date.issued2026
dc.description.abstractAlzheimer's disease (AD), a neurodegenerative, irreversible, and progressive brain disorder, is characterized by memory loss and cognitive dysfunction. In neurodegeneration, gut microbiota and their metabolites have an impact on behavior and brain function. This study aimed to identify fecal candidate discriminant metabolites in 5XFAD mice assosciated with AD as compared to an age-matched wild-type (WT) healthy mice groups at three different time points (3, 6, and 9 month) using Proton Nuclear Magnetic Resonance (H-1 NMR) spectroscopy. A total of 18 male mice (n = 9 for 5XFAD mice and n = 9 for WT, with three animals per age group) were used to determine the fecal candidate discriminant metabolites. As a result of the study, it was identified a total of 67 metabolites in fecal samples. Among these, 19 metabolites were found significantly up-regulated or down-regulated in 5XFAD mice compared to WT mice during the disease progress. According to the volcano plot analysis (FC >= 1.2 and p-value <= 0.05), the potential candidate discriminant metabolites were fumarate and malate in 3-month-old 5XFAD mice, 3-methylxanthine, glucose, cholate, phenylacetate, and trimethylamine N-oxide (TMAO) in 6-month-old 5XFAD mice and cholate and succinate in 9-month-old 5XFAD mice. These findings highlight the potential of fecal metabolomics as a non-invasive exploratory approach for understanding AD disease mechanisms and progression. Furthermore, to the best of our knowledge, this pilot study is the first to utilize NMR spectroscopy to investigate age-stratified cross-sectional changes in fecal metabolites in 5xFAD mice, thereby advancing our understanding of disease progression and potentially informing future therapeutic strategies. [GRAPHICS]
dc.description.issue1
dc.description.pages91
dc.description.sponsorshipOpen access funding provided by the Scientific and Technological Research Council of Turkiye (TUB & Idot;TAK).
dc.description.volume41
dc.identifier.doi10.1007/s11011-026-01848-2
dc.identifier.issn0885-7490
dc.identifier.issn1573-7365
dc.identifier.urihttps://doi.org/10.1007/s11011-026-01848-2
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/11440
dc.identifier.wosWOS:001748732100002
dc.language.isoen
dc.publisherSPRINGER/PLENUM PUBLISHERS
dc.relation.fundingAcibadem Mehmet Ali Aydinlar University
dc.relation.hasversion10.1007/s11011-026-01848-2
dc.relation.ispartofMETABOLIC BRAIN DISEASE
dc.subjectFecal metabolites
dc.subjectAlzheimer's disease
dc.subjectNuclear magnetic resonance spectroscopy
dc.subject5XFAD mice
dc.subjectCHAIN FATTY-ACIDS
dc.subjectMOUSE MODEL
dc.subjectTAURINE
dc.subjectPLASMA
dc.subjectEndocrinology & Metabolism
dc.subjectNeurosciences
dc.subjectNeurosciences & Neurology
dc.titleA perspective for alzheimer disease from gut microbiota-associated NMR-based fecal metabolomics: a study with 5XFAD mice
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.issue1
oaire.citation.volume41
person.identifier.ridMBV-5153-2025
person.identifier.ridNJR-0872-2025
person.identifier.ridPCT-4837-2025
person.identifier.ridC-3948-2013
person.identifier.ridNFT-3476-2025
person.identifier.ridV-7083-2018

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