The gut microbiome modulates the transformation of microglial subtypes

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Gut microbiome remodeling induces depressive-like behaviors through a pathway mediated by the host’s metabolism

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Single-Cell Map of Diverse Immune Phenotypes in the Breast Tumor Microenvironment

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Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice

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Microglia development and function

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The Gut Microbiota Mediates the Anti-Seizure Effects of the Ketogenic Diet

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Spatial Transcriptomics and In Situ Sequencing to Study Alzheimer’s Disease

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Single-cell genomics identifies cell type–specific molecular changes in autism

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Signaling inflammation across the gut-brain axis

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Microbiome Influences Prenatal and Adult Microglia in a Sex-Specific Manner

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Single cell RNA sequencing of human microglia uncovers a subset associated with Alzheimer’s disease

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The gut microbiome from patients with schizophrenia modulates the glutamate-glutamine-GABA cycle and schizophrenia-relevant behaviors in mice

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Potential roles of gut microbiome and metabolites in modulating ALS in mice

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Neuroinflammatory astrocyte subtypes in the mouse brain

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Peripheral lipopolysaccharide (LPS) challenge promotes microglial hyperactivity in aged mice that is associated with exaggerated induction of both pro-inflammatory IL-1β and anti-inflammatory IL-10 cytokines

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Adult hippocampal neurogenesis is involved in anxiety-related behaviors

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Anti-human TREM2 induces microglia proliferation and reduces pathology in an Alzheimer’s disease model

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Single-cell analysis reveals T cell infiltration in old neurogenic niches

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Mild cognitive impairment has similar alterations as Alzheimer's disease in gut microbiota

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Microbiota modulate sympathetic neurons via a gut–brain circuit

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Using single nuclei for RNA-seq to capture the transcriptome of postmortem neurons

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The microbiota regulate neuronal function and fear extinction learning

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Landscapes of bacterial and metabolic signatures and their interaction in major depressive disorders

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Microbiota regulate social behaviour via stress response neurons in the brain

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Spatial memory dissociations in mice lacking GluR1

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Prefrontal Cortex Development in Health and Disease: Lessons from Rodents and Humans

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Single-cell analyses of Crohn’s disease tissues reveal intestinal intraepithelial T cells heterogeneity and altered subset distributions

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Associations between gut microbiota and Alzheimer’s disease, major depressive disorder, and schizophrenia

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Single-nucleus transcriptome analysis reveals cell-type-specific molecular signatures across reward circuitry in the human brain

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A Single-Cell Transcriptional Atlas of the Developing Murine Cerebellum

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Uncoupling the dopamine D1-D2 receptor complex exerts antidepressant-like effects

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Gut Microbial Signatures Can Discriminate Unipolar from Bipolar Depression

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Interleukin-10 Prevents Pathological Microglia Hyperactivation following Peripheral Endotoxin Challenge

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Peripheral apoE4 enhances Alzheimer’s pathology and impairs cognition by compromising cerebrovascular function

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Systematic Analysis of Gut Microbiome Reveals the Role of Bacterial Folate and Homocysteine Metabolism in Parkinson’s Disease

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Obesity impairs short-term and working memory through gut microbial metabolism of aromatic amino acids

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Identification of Faecalibacterium prausnitzii strains for gut microbiome-based intervention in Alzheimer’s-type dementia

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AD-linked R47H- <i>TREM2</i> mutation induces disease-enhancing microglial states via AKT hyperactivation

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Single-Cell RNA Sequencing: Unraveling the Brain One Cell at a Time

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How gut microbes could drive brain disorders

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Pyramidal neuron subtype diversity governs microglia states in the neocortex

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Primate gastrulation and early organogenesis at single-cell resolution

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Isoform cell-type specificity in the mouse primary motor cortex

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Chronic stress alters the dendritic morphology of callosal neurons and the acute glutamate stress response in the rat medial prefrontal cortex

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Exploratory and locomotor activity, learning and memory functions in somatostatin receptor subtype 4 gene-deficient mice in relation to aging and sex

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Microbiota–gut–brain axis and its therapeutic applications in neurodegenerative diseases

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The communication mechanism of the gut-brain axis and its effect on central nervous system diseases: A systematic review

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Gut microbiome-targeted therapies for Alzheimer’s disease

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Emerging role of the host microbiome in neuropsychiatric disorders: overview and future directions

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Multi-omics data reveals aberrant gut microbiota-host glycerophospholipid metabolism in association with neuroinflammation in APP/PS1 mice

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Microbiota–gut–brain axis in health and neurological disease: Interactions between gut microbiota and the nervous system

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The potential role of mitochondria in the microbiota-gut-brain axis: Implications for brain health

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Exploring the microbiota-gut-brain axis: impact on brain structure and function

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The contribution of age-related changes in the gut-brain axis to neurological disorders

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Microglia and gut microbiota: A double-edged sword in Alzheimer's disease

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Microglia: a promising therapeutic target in spinal cord injury

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Bridging gap in the treatment of Alzheimer’s disease via postbiotics: Current practices and future prospects

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Gut microbes in central nervous system development and related disorders

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The Hallmarks of Ageing in Microglia

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The central role of microglia in major depressive disorder and its potential as a therapeutic target

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The potential of the gut microbiome for identifying Alzheimer’s disease diagnostic biomarkers and future therapies

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Alcohol Use Disorder and the Gut–Brain Axis: A Narrative Review of the Role of Gut Microbiota and Implications for Treatment

Shukla, S., & Hsu, C. L. (2025) · Microorganisms · doi:10.3390/microorganisms13010067 · Cited by 31 · see citing works

Therapeutic targeting the cGAS−STING pathway associated with protein and gene: An emerging and promising novel strategy for aging-related neurodegenerative disease

Zhou, Q., Luo, J., Chai, X., Yang, J., Zhong, S., Zhang, Z., Chang, X., & Wang, H. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114679 · Cited by 28 · see citing works

Exploring the Role of Microglial Cells in the Gut–Brain Axis Communication: A Systematic Review

Ortiz‐Samur, N. S., Vijaya, A. K., Burokas, A., & Mela, V. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70154 · Cited by 29 · see citing works

Linking depression and neuroinflammation: Crosstalk between glial cells

Yang, X., Wang, H., Wang, Z.-Z., & Chen, N. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177408 · Cited by 26 · see citing works

Pathways linking microbiota-gut-brain axis with neuroinflammatory mechanisms in Alzheimer’s pathophysiology

Hochuli, N., Kadyan, S., Park, G., Patoine, C., & Nagpal, R. (2023) · Microbiome Research Reports · doi:10.20517/mrr.2023.39 · Cited by 24 · see citing works

Microglial Mechanisms and Therapeutic Potential in Brain Injury Post-Intracerebral Hemorrhage

Gong, Y., Li, H., Cui, H., & Gong, Y. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s498809 · Cited by 21 · see citing works

Huangqin decoction attenuates spared nerve injury (SNI)-induced neuropathic pain by modulating microglial M1/M2 polarization partially mediated by intestinal nicotinamide metabolism

Gao, L., Zhang, A., Fu, L., Li, Q.-W., Qin, X., & Zhao, J. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155594 · Cited by 18 · see citing works

Advances in the study of the effects of gut microflora on microglia in Alzheimer’s disease

Wu, J.-J., & Wei, Z. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1295916 · Cited by 16 · see citing works

The Hidden Dangers of Sedentary Living: Insights into Molecular, Cellular, and Systemic Mechanisms

Diniz, D. G., Bento‐Torres, J., da Costa, V. O., Carvalho, J. P. R., Tomás, A. M., de Oliveira, T. C. G., Soares, F. C., de Macedo, L. D. E. D., Jardim, N. Y. V., Bento-Torres, N. V. O., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251910757 · Cited by 17 · see citing works

The emerging role of the gut microbiome in depression: implications for precision medicine

Liu, L., Wang, H., Guo, S., Liu, S., Du, Y., Wang, L. Y., He, D., Mo, X., Zhang, H., Cheng, Q., et al. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03191-x · Cited by 16 · see citing works

Spinal Cord Injury Management Based on Microglia-Targeting Therapies

Schreiner, T. G., Schreiner, O. D., & Ciobanu, R. C. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13102773 · Cited by 13 · see citing works

The microbiome’s influence on obesity: mechanisms and therapeutic potential

Tadese, D. A., Mwangi, J., Luo, L., Zhang, H., Huang, X., Michira, B. B., Zhou, S., Kamau, P. M., Lu, Q., & Lai, R. (2024) · Science China Life Sciences · doi:10.1007/s11427-024-2759-3 · Cited by 18 · see citing works

Multi Layered Omics Approaches Reveal Glia Specific Alterations in Alzheimer's Disease: A Systematic Review and Future Prospects

İş, Ö., Min, Y., Wang, X., Oatman, S. R., Daniel, A. A., & Ertekin‐Taner, N. (2024) · Glia · doi:10.1002/glia.24652 · Cited by 13 · see citing works

Evolving insights on the role of microglia in neuroinflammation, plasticity, and regeneration of the injured spinal cord

Swarts, E. A., & Brennan, F. H. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1621789 · Cited by 12 · see citing works

The aging gut–glia–immune axis in alzheimer’s disease: microbiome-derived mediators of neuroinflammation and therapeutic innovation

Mir, P. A., Kumar, N. G., Bhutia, G. T., Chaudhary, P., Kaur, G., & Gupta, S. K. (2026) · GeroScience · doi:10.1007/s11357-025-02062-1 · Cited by 13 · see citing works

Gut–brain axis in health and brain disease

Olasunkanmi, O. I., Zheng, L., & Zheng, P. (2026) · Chinese Medical Journal · doi:10.1097/cm9.0000000000003920 · Cited by 12 · see citing works

Host–gut microbiota interactions in health and disease: mechanisms and intervention strategies

Han, Y., Wang, Z., Xie, J., Yang, G., Su, M., Wang, S., Yang, M., Yu, H., Li, M., Wang, L., et al. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1785607 · Cited by 12 · see citing works

Early-life obesogenic environment integrates immunometabolic and epigenetic signatures governing neuroinflammation

Ontiveros‐Ángel, P., Vega-Torres, J. D., Simon, T. B., Williams, V., Inostroza‐Nieves, Y., Alvarado-Crespo, N., Gonzalez, Y. V., Pompolius, M., Katzka, W. R., Lou, J., et al. (2024) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2024.100879 · Cited by 12 · see citing works

Unveiling the hidden culprit: How the brain-gut axis fuels neuroinflammation in ischemic stroke

Ma, B. D. Y., Chan, T. Y. H., & Lo, B. (2024) · Surgical Neurology International · doi:10.25259/sni_703_2024 · Cited by 12 · see citing works

The interconnection between obesity and executive function in adolescence: The role of the gut microbiome

Lane, J. M., Wright, R. O., & Eggers, S. I. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105337 · Cited by 13 · see citing works

Bibliometric Analysis of Alzheimer's Disease and Depression

Li, S., Zhang, Q., Liu, J., Zhang, N., Li, X., Liu, Y., Qiu, H., Li, J., & Cao, H. (2024) · Current Neuropharmacology · doi:10.2174/1570159x22666240730154834 · Cited by 11 · see citing works

Peptide discovery across the spectrum of neuroinflammation; microglia and astrocyte phenotypical targeting, mediation, and mechanistic understanding

Benita, B. A., & Koss, K. M. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1443985 · Cited by 11 · see citing works

Treatment of preterm brain injury via gut‐microbiota–metabolite–brain axis

Li, L., Liu, T., & Shi, Y. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14556 · Cited by 10 · see citing works

Repurposing Ketamine in the Therapy of Depression and Depression-Related Disorders: Recent Advances and Future Potential

Deng, Q., Parker, E., Wu, C., Zhu, L., Liu, T. C., Duan, R., & Yang, L. (2024) · Aging and Disease · doi:10.14336/ad.2024.0239 · Cited by 10 · see citing works

Biospecimens in the HEALthy Brain and Child Development (HBCD) Study: Rationale and protocol

Sullivan, E. L., Bogdan, R., Bakhireva, L. N., Levitt, P. R., Jones, J., Sheldon, M., Croff, J. M., Thomason, M. E., Lo, J. O.-T., MacIntyre, L., et al. (2024) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2024.101451 · Cited by 10 · see citing works

The Metabolomic Mind: Microbial Metabolite Programming of Microglia

Verosky, B. G., Bailey, M. T., & Gur, T. (2025) · NeuroImmunoModulation · doi:10.1159/000545484 · Cited by 9 · see citing works

Parallel Pathways, Divergent Outcomes: Adipose Tissue–Neural Crosstalk in Depression and Obesity

Prodaniuc, A., Amălinei, C., Căruntu, I.-D., Riscanu, L., & Grigoraş, A. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14238307 · Cited by 9 · see citing works

Akkermansia muciniphila vesicles attenuate smoking-induced cognitive decline via ILA-mediated AhR-dependent microglial reprogramming

Zhu, B., Huang, J., Zhang, H., Lin, H., Chen, T., Min, L., Yang, Y., Liu, Y., & Guo, S. (2026) · Journal of Nanobiotechnology · doi:10.1186/s12951-026-04044-7 · Cited by 9 · see citing works

Probiotics derived sodium benzoate improves social behavior of offspring exposed in the maternal immune activation through regulation of histone lysine benzoylation in astrocytes

Li, T., Chen, J., Mi, K., Lei, J., Ning, Z., Lu, L., Su, Z., Zhu, Q., Lin, M., Wang, Y., et al. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03164-0 · Cited by 9 · see citing works

Identification of Potential Biomarkers for Major Depressive Disorder: Based on Integrated Bioinformatics and Clinical Validation

Zhong, X., Chen, Y., Chen, W., Liu, Y., Gui, S., Pu, J., Wang, D., He, Y., Chen, X., Chen, X., et al. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04217-1 · Cited by 8 · see citing works

Gut microbiota is necessary for pair-housing to protect against post-stroke depression in mice

Jiang, S.-T., Sun, Y.-H., Ya, L., Wang, M., Wang, X., & Dong, Y. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114834 · Cited by 8 · see citing works

Microglia and Microbiome-Gut-Brain Axis

Filho, A. M. C., Gomes, N. S., Lós, D. B., Leite, I. B., Tremblay, M., & Macêdo, D. S. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-55529-9_17 · Cited by 8 · see citing works

Importance of Gut Microbiota Dysbiosis and Circadian Disruption–Associated Biomarkers in Emergence of Alzheimer’s Disease

Kaur, S., Kumari, D., & Dandekar, M. P. (2025) · Molecular Neurobiology · doi:10.1007/s12035-024-04685-5 · Cited by 7 · see citing works

Alzheimer's disease and gut-brain axis: Drosophila melanogaster as a model

Alves, S. D. M., Lisboa‐Filho, P. N., Vieira, C. L. Z., & Piacenti‐Silva, M. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1543826 · Cited by 7 · see citing works

Systematic review and meta-analysis of microbiota-gut-astrocyte axis perturbation in neurodegeneration, brain injury, and mood disorders

Radford‐Smith, D. E., Oke, K., Costa, C. F. F. A., & Anthony, D. C. (2025) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2025.101013 · Cited by 8 · see citing works

Navigating the Complex Terrain of Dysregulated Microglial Function in Depressive Disorders: Insights, Challenges and Future Directions

Zhang, Y., & Tang, C. (2024) · Aging and Disease · doi:10.14336/ad.2024.0326 · Cited by 7 · see citing works

Perturbations in the microbiota-gut-brain axis shaped by social status loss

Yang, R., Wang, X., Yang, J., Zhou, X., Wu, Y., Li, Y., Huang, Y., Zhang, J., Liu, P., Yuan, M., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-07850-1 · Cited by 7 · see citing works

Association between self-reported multimorbidity and longitudinal brain Aβ deposition in Alzheimer’s disease

Bu, X., Zhu, W., Wang, Q.-H., Liu, Z., Bao, Y.-Y., Bai, Y., Li, J.-H., Liu, Z.-H., Zhao, J.-L., Xiang, Y., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60748-8 · Cited by 7 · see citing works

Rehmannia glutinosa DC.-Lilium lancifolium Thunb. in the treatment of depression: a comprehensive review and perspectives

Wang, Z. Q., Wang, X., Mou, X., Wang, C., Sun, Y., & Wang, J. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1471307 · Cited by 6 · see citing works

Microbiota-induced inflammation mediates the impacts of a Western diet on hippocampal-dependent memory

Crain, E., Minaya, D. M., & Serre, C. B. D. L. (2025) · Nutrition Research · doi:10.1016/j.nutres.2025.04.002 · Cited by 6 · see citing works

Symposium: What Does the Microbiome Tell Us about Prevention and Treatment of AD/ADRD?

Capocchi, J., Figueroa-Romero, C., Dunham, S. J. B., Faraci, G., Rothman, J. A., Whiteson, K., Seo, D.-O., Holtzman, D., Grabrucker, S., Nolan, Y., et al. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1295-24.2024 · Cited by 5 · see citing works

Modified neuroimmune processes and emotional behaviour in weaned and late adolescent male and female mice born via caesarean section

Miceli, M. D., Rossitto, M., Martinat, M., Marchaland, F., Kharbouche, S., GRALAND, M., Younes, F., Séré, A., Aubert, A., Khabbaz, L. R., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-80770-y · Cited by 4 · see citing works

Gut microbiome and glial cell dialog: Role of TCM in the treatment of depression

Zhang, X., Chen, X., Ruan, S., Wang, H., Xu, Y., Fu, H., Lin, S., Efferth, T., Tian, Y., Li, C., et al. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.157196 · Cited by 4 · see citing works

Applications and potential mechanisms of transcranial magnetic stimulation in autism spectrum disorders

Liao, X., Li, H., Han, K., Long, J., Liu, Y., Tang, Z., Chen, J., Liu, H., & Zhang, H. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-026-07754-6 · Cited by 4 · see citing works

Muribaculum intestinale alleviates depressive-like behaviors by inhibiting Th17 cell differentiation and M1 microglia polarization

He, J., Wang, M.-N., Chen, H.-J., Zuo, G., Li, J.-L., Yin, W., Pan, X.-G., Cheng, Y., Xia, C., Xu, J., et al. (2026) · Microbiome · doi:10.1186/s40168-026-02354-4 · Cited by 6 · see citing works

Early Gut Microbiota and Neurodevelopmental Trajectories: Implications for Pediatric Neuropsychiatric Vulnerability—A Narrative Review

Lupu, V. V., Nedelcu, A. H., Miron, I. C., Anton, S. C., Săsăran, M. O., Frăsinariu, O. E., Jechel, E., Bozomitu, L. I., Chisnoiu, T., Anton, C., et al. (2026) · Nutrients · doi:10.3390/nu18101541 · Cited by 4 · see citing works

Microbiome and metabolites impact enteric and central nervous systems in ALS

Walton, E. I., & Sun, J. (2026) · Gut Microbes · doi:10.1080/19490976.2026.2692737 · Cited by 4 · see citing works

Multi-site investigation of gut microbiota in CDKL5 deficiency disorder mouse models: Targeting dysbiosis to improve neurological outcomes

Damiani, F., Giuliano, M. G., Cornuti, S., Putignano, E., Tognozzi, A., Suckow, V., Kalscheuer, V. M., Pizzorusso, T., & Tognini, P. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115546 · Cited by 4 · see citing works

The mechanism of disease progression by aging and age-related gut dysbiosis in multiple sclerosis

Yadav, S. K., Chen, C., Dhib-Jalbut, S. S., & Ito, K. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.106956 · Cited by 4 · see citing works

Intestinal epithelial Dicer1 regulates gut microbiome and Alzheimer’s pathology in App-knock-in mice

Hao, W., Luo, Q., Szabo, I. M., Gasparoni, G., Tierling, S., Quan, W., Chang, H., Wu, G., Schulze-Hentrich, J. M., & Liu, Y. (2025) · Alzheimer s Research & Therapy · doi:10.1186/s13195-025-01849-w · Cited by 4 · see citing works

Mechanisms of aerobic exercise effects on the gut microbiota and its metabolites in anxiety disorders

Zheng, Y., Qu, Y., Yao, M., Li, K., Dong, Y., Xing, X., Yang, T., Guo, H., & Huang, P. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1721497 · Cited by 3 · see citing works

Neuroinflammation in Alzheimer’s Disease: The Role of Obesity, Gut Microbiota, and Therapeutic Potential of Omega-3 Fatty Acids and Neural Stem Cells

Morovati, A., Moussa, Y., Kalupahana, N. S., Zu, Y., Jun, H., Fokar, M., & Moustaïd‐Moussa, N. (2026) · Journal of Nutrition · doi:10.1016/j.tjnut.2026.101407 · Cited by 3 · see citing works

The Causal Relationship Between Gut Microbiomes, Inflammatory Mediators, and Traumatic Brain Injury in Europeans: Evidence from Genetic Correlation and Functional Mapping Annotation Analyses

Song, B., Qiu, Y., Wang, Z., Tao, Y., Wang, M., Duan, A., Xie, M., Yin, Z., Chen, Z., Ma, C., et al. (2025) · Biomedicines · doi:10.3390/biomedicines13030753 · Cited by 3 · see citing works

Integrated analysis of transcriptional changes in major depressive disorder: Insights from blood and anterior cingulate cortex

Zhong, X., Chen, X., Liu, Y., Gui, S., Pu, J., Wang, D., Wei, T., Chen, Y., Chen, X., Chen, W., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e28960 · Cited by 3 · see citing works

Microglial Regulation of Neural Networks in Neuropsychiatric Disorders

Cao, Z.-L., Zhu, L., Wang, H., & Zhu, L. (2025) · The Neuroscientist · doi:10.1177/10738584251316558 · Cited by 2 · see citing works

Restoration of gamma-aminobutyric acid homeostasis: A novel approach to alleviating central nervous system injury–associated immunodepression syndrome

Yang, P., Tian, D., Li, Z., & Yao, Z. (2025) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-25-00147 · Cited by 2 · see citing works

Protective effects of Parabacteroides distasonis against high-fat diet-induced brain injury in mice

Xie, J., Sun, Y., Li, Q., Nie, X., Zhang, W., Dong, L., Chen, X., & Nie, S. (2025) · npj Science of Food · doi:10.1038/s41538-025-00591-9 · Cited by 2 · see citing works

IL-15 receptor alpha deficiency triggers depressive-like behaviors via enhanced microglial synapse pruning

Tang, Y., Huang, Y., Pan, J., Li, C., Yang, J., Tan, X., 胡康安, Wen, L., Xie, P., Liu, Y., et al. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03593-5 · Cited by 2 · see citing works

Long-term rapamycin treatment suppresses IL-17-producing gamma delta T cells and blunts neuroinflammation in aging

Torrent, C., Gagliardi, C., Fülle, N., Antignano, I., Bernis, M. E., Stork, M., Bano, D., Capasso, M., & Keane, L. (2026) · PLoS ONE · doi:10.1371/journal.pone.0343183 · Cited by 2 · see citing works

Visualising the Knowledge Structure of Microglia in Alzheimer’s Disease: A CiteSpace Analysis

Wang, Q., Zhang, X. C., Wang, D., Jiang, X., Zhou, Y., Zhang, T., Yang, X., Liu, L.-Z., & Li, Q. (2025) · Journal of Multidisciplinary Healthcare · doi:10.2147/jmdh.s521350 · Cited by 1 · see citing works

Advances in the Study of Intestinal Microbiota and Neuropathic Pain

Jiang, Y., Xu, H., Zhang, W., Jin, S., Piao, H., Yu, J., Yao, H., Shi, J., Liu, Q., Li, N., et al. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl43051 · Cited by 1 · see citing works

Gut microbiota shape diurnal rhythms of amino acid metabolism in the mouse prefrontal cortex

Tofani, G. S. S., & Cryan, J. F. (2026) · Molecular Metabolism · doi:10.1016/j.molmet.2026.102319 · Cited by 1 · see citing works

Nutraceuticals and the Microbiota–Gut–Brain Axis: A Pathway for Preventing Cognitive Decline

Castillo-Moral, Á., Toda-Ferran, C., Bulló, M., Teichenné, J., & Escoté, X. (2026) · Nutrition Reviews · doi:10.1093/nutrit/nuag017 · Cited by 1 · see citing works

Microbiota-Driven microglia reprogramming reverses depressive-like behaviors through Peripheral-to-Central immune crosstalk

Wu, J., Zhou, X., Luo, T., Wang, X., Zuo, H., Yang, R., Tian, R., Wu, Y., Wu, Y. F., Jiang, W., et al. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03545-z · Cited by 1 · see citing works

The oral-gut-brain axis: how periodontitis influence depression

Li, Z., Xie, C., & Pan, C. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1778744 · Cited by 1 · see citing works

Nutrition as a systems regulator of brain aging trajectories

Müller, L., Benedetto, S. D., & Müller, V. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1825800 · Cited by 1 · see citing works

Targeting the Gut–Brain Axis: Protective Effects of NMN in Alleviating D-Galactose-Induced Cognitive Deficits

Zang, Z., Chen, F., Tang, Q., Luo, W., Lin, Y., Li, J., & Yu, Y. (2026) · Metabolites · doi:10.3390/metabo16050314 · Cited by 1 · see citing works

Butyrate-producing gut bacteria restrain PBAT microplastic-triggered brain microglial lipotoxicity via a microbiota–butyrate–mTORC1–ISR relay along the gut–brain axis

Wang, M.-Z., Du, Z., Xu, W.-Q., Xie, Y.-H., Wang, L. S., He, X.-X., Wang, Y., Zheng, H.-Y., Yao, Y.-L., Ya-bin, S., et al. (2026) · Journal of Neuroinflammation · doi:10.1186/s12974-026-03869-1 · Cited by 1 · see citing works

Peripheral to central: Exploring the neural, endocrine, and immune pathways of the gut-brain axis in postoperative neurocognitive dysfunction

Cao, R., Shi, Z., Ou, W., & Liu, Z. (2026) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2026.111975 · Cited by 1 · see citing works

РОЛЬ И ОСОБЕННОСТИ МИКРОБИОТЫ КИШЕЧНИКА ПРИ БОЛЕЗНИ АЛЬЦГЕЙМЕРА

Турсуметова, Д. Р., Хан, Ю., Ткачёва, Л. В., & Раевский, К. П. (2024) · Успехи геронтологии · doi:10.34922/ae.2024.37.4.016 · Cited by 1 · see citing works

Sedentary Life Is an Invisible Trap: Molecular, Cellular, and Systemic Reasons to Leave It BehindPreprint

Diniz, D. G., Bento‐Torres, J., da Costa, V. O., Carvalho, J. P. R., Tomás, A. M., de Oliveira, T. C. G., Soares, F. C., de Macedo, L. D. E. D., Jardim, N. Y. V., Bento-Torres, N. V. O., et al. (2024) · Preprints.org · doi:10.20944/preprints202408.1277.v1 · Cited by 1 · see citing works

Gut miRNA regulates gut microbiome and Alzheimer’s pathology in App -knock-in micePreprint

Hao, W., Luo, Q., Szabo, I. M., Gasparoni, G., Tierling, S., Quan, W., Chang, H., Wu, G., Schulze-Hentrich, J. M., & Liu, Y. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.05.658056 · Cited by 1 · see citing works

Multi-Site Investigation of Gut Microbiota in CDKL5 Deficiency Disorder Mouse Models: Targeting Dysbiosis to Improve Neurological OutcomesPreprint

Damiani, F., Giuliano, M. G., Cornuti, S., Putignano, E., Tognozzi, A., Suckow, V., Kalscheuer, V. M., & Tognini, P. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.19.581742

Mapping gene expression across the microbiome-gut-brain axis of germ- and specific pathogen-free micePreprint

Dritsa, C., Hoffmann, S., Hulme, H., Lynch, C. P., Taylor, V., Burchmore, R., Cole, J., Goodwin, R. J. A., & Wall, D. M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.15.648950

Onkolojik Acillerde Görüntüleme

Öztürk, M. Ö., & Reşorlu, M. (2025) · Türk Radyoloji Seminerleri · doi:10.4274/trs.2025.24185

The role of gut dysbiosis in the pathogenesis of neurodegenerative diseases

Roudenský, P. (2025) · Neurologie pro praxi · doi:10.36290/neu.2025.036

NMN alleviates cognitive impairment in Alzheimer's disease by regulating the gut microbiota through the Nrf2/HO-1 pathwayPreprint

Zang, Z., Chen, F., Gao, L., Tang, Q., Luo, W., Lin, Y., & Yu, Y. (2025) · Research Square · doi:10.21203/rs.3.rs-7928145/v1

The Influence of Gut Microbiota on the Development of Schizophrenia. Ways of Pharmacologic Correction (Systematic Scoping Review)

Abdullina, L. K., Алексеевна, М. А., Sorokina, Y. A., & Strueva, E. P. (2025) · Health Food & Biotechnology · doi:10.36107/hfb.2025.i2.s254

Xuefu Zhuyu Capsule alleviates depression in post-stroke depression model rats via modulation of the gut microbiota–gut–brain axis

Jin, B., Wang, Y., Zhang, Z., Fan, X., Zhang, Y., & Zhuang, P. (2026) · Drug Discoveries & Therapeutics · doi:10.5582/ddt.2025.01120

Outcomes of the lifestyle on microglial aging and neurodegenerative diseases along the aging trajectory: diet and the gut-brain axis

Nicolas, S., & Nolan, Y. M. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-27340-7.00003-6

Involvement of microglial aging in neurodegenerative diseases: a focus on amyotrophic lateral sclerosis

Catalano, M., & Limatola, C. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-27340-7.00004-8

Electroacupuncture alleviates comorbid obesity and depression via the gut-brain axis: orchestrating SCFA-producing bacteria and hippocampal synaptic plasticity

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GPR68, a proton-sensing GPCR, as a therapeutic target in depression: structural, signalling, and mechanistic perspectives

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