The DOI matches its Crossref record; 102 of the 103 references it cites were found in a registry or an index.
Effects of bile acids on neurological function and disease
Open accessAbstract
Bile acids are synthesized from cholesterol and are known to be involved with the emulsification and digestion of dietary lipids and fat-soluble vitamins. Outside of this role, bile acids can act as cell signaling effectors through binding and activating receptors on both the cell membrane and nucleus. Numerous reports have investigated these signaling pathways in conditions where the liver is damaged. More recently, effort has been made to investigate the role of bile acids in diseases outside of those associated with liver damage. This review summarizes recent findings on the influences that bile acids can exert in normal neurological function and their contribution to diseases of the nervous system, with the intent of highlighting the role of these metabolites as potential players in neurological disorders.-McMillin, M., DeMorrow, S. Effects of bile acids on neurological function and disease.
Overview
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
Verification
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?
In the citing paper
“BAs modulate HPA axis activity by inhibiting CRH release through FXR activation, expressed in the hypothalamus (309).”
From Signalling cognition: The gut microbiota and hypothalamic-pituitary-adrenal axis (2023) · cites this paper as [309]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The amyloid hypothesis of Alzheimer's disease at 25 years
Selkoe, D. J., & Hardy, J. (2016) · EMBO Molecular Medicine · doi:10.15252/emmm.201606210 · Cited by 6,164
The Enzymes, Regulation, and Genetics of Bile Acid Synthesis
Russell, D. W. (2003) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.72.121801.161712 · Cited by 2,069
Endogenous Bile Acids Are Ligands for the Nuclear Receptor FXR/BAR
Wang, H., Chen, J., Hollister, K., Sowers, L. C., & Forman, B. M. (1999) · Molecular Cell · doi:10.1016/s1097-2765(00)80348-2 · Cited by 1,636
A G Protein-coupled Receptor Responsive to Bile Acids
Kawamata, Y., Fujii, R., Hosoya, M., Harada, M., Yoshida, H., Miwa, M., Fukusumi, S., Habata, Y., Itoh, T., Shintani, Y., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m209706200 · Cited by 1,628
Lehmann, J., McKee, D. D., Watson, M. A., Willson, T. M., Moore, J. T., & Kliewer, S. A. (1998) · Journal of Clinical Investigation · doi:10.1172/jci3703 · Cited by 1,577
The nuclear receptor PXR is a lithocholic acid sensor that protects against liver toxicity
Staudinger, J. L., Goodwin, B. J., Jones, S. A., Hawkins‐Brown, D., MacKenzie, K. I., Latour, A. M., Liu, Y., Klaassen, C. D., Brown, K. K., Reinhard, J. F., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051551698 · Cited by 1,378
Anatomical profiling of nuclear receptor expression reveals a hierarchical transcriptional network
Bookout, A. L., Jeong, Y., Downes, M., Yu, R. T., Evans, R. M., & Mangelsdorf, D. J. (2006) · Cell · doi:10.1016/j.cell.2006.06.049 · Cited by 1,015
Identification of membrane-type receptor for bile acids (M-BAR)
Maruyama, T., Miyamoto, Y., Nakamura, T., Tamai, Y., Okada, H., Sugiyama, E., Nakamura, T., Itadani, H., & Tanaka, K. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)02550-0 · Cited by 993
The Continuing Importance of Bile Acids in Liver and Intestinal Disease
Hofmann, A. F. (1999) · Archives of Internal Medicine · doi:10.1001/archinte.159.22.2647 · Cited by 972
Transcriptional integration of metabolism by the nuclear sterol-activated receptors LXR and FXR
Calkin, A. C., & Tontonoz, P. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3312 · Cited by 779
Research works printed but not linked: 2
- Roberts J., 2015, Cereb. Blood Flow Metab
- Naqvi S. H., 1969, J. LipidRes
Cited by
Sorted by citations
Functions of Gut Microbiota Metabolites, Current Status and Future Perspectives
Liu, J., Tan, Y., Cheng, H., Zhang, D., Feng, W., & Peng, C. (2022) · Aging and disease · doi:10.14336/ad.2022.0104 · Cited by 529
Bile Acids as Metabolic Regulators and Nutrient Sensors
Chiang, J. Y. L., & Ferrell, J. M. (2019) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-082018-124344 · Cited by 456
Signalling cognition: The gut microbiota and hypothalamic-pituitary-adrenal axis
Rusch, J. A., Layden, B. T., & Dugas, L. R. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1130689 · Cited by 415
Gut microbial molecules in behavioural and neurodegenerative conditions
Needham, B. D., Kaddurah-Daouk, R., & Mazmanian, S. K. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-00381-0 · Cited by 379
Bile acid signaling pathways from the enterohepatic circulation to the central nervous system
Mertens, K. L., Kalsbeek, A., Soeters, M. R., & Eggink, H. M. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00617 · Cited by 287
Kusaczuk, M. (2019) · Cells · doi:10.3390/cells8121471 · Cited by 250
Bhargava, P., Smith, M. D., Mische, L., Harrington, E., Fitzgerald, K. C., Martin, K. A., Kim, S., Reyes, A. A., Cardona, J. G., Volsko, C. M., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci129401 · Cited by 243
Ji, Y. S., Yin, Y., Li, Z., & Zhang, W. (2019) · Nutrients · doi:10.3390/nu11081712 · Cited by 235
Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer’s Disease
Baloni, P., Funk, C. C., Yan, J., Yurkovich, J. T., Kueider-Paisley, A., Nho, K., Heinken, A., Jia, W., Mahmoudiandehkordi, S., Louie, G., et al. (2020) · Cell Reports Medicine · doi:10.1016/j.xcrm.2020.100138 · Cited by 211
Turk, B. R., Theda, C., Fatemi, A. S., & Moser, A. B. (2020) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.10003 · Cited by 212
Microbial-derived metabolites as a risk factor of age-related cognitive decline and dementia
Connell, E., Le Gall, G., Pontifex, M. G., Sami, S., Cryan, J. F., Clarke, G., Müller, M., & Vauzour, D. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-022-00548-6 · Cited by 208
Sasso, J. M., Ammar, R. M., Tenchov, R., Lemmel, S. A., Kelber, O., Grieswelle, M., & Zhou, Q. A. (2023) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.3c00127 · Cited by 229
Central anorexigenic actions of bile acids are mediated by TGR5
Perino, A., Velázquez‐Villegas, L. A., Bresciani, N., Sun, Y., Huang, Q. D., Fénelon, V. S., Castellanos-Jankiewicz, A., Zizzari, P., Bruschetta, G., Jin, S., et al. (2021) · Nature Metabolism · doi:10.1038/s42255-021-00398-4 · Cited by 159
Gut Microbiota Dysbiosis Is Associated with Elevated Bile Acids in Parkinson’s Disease
Li, P., Killinger, B. A., Ensink, E., Beddows, I., Yilmaz, A., Lubben, N., Lamp, J., Schilthuis, M., Vega, I. E., Woltjer, R., et al. (2021) · Metabolites · doi:10.3390/metabo11010029 · Cited by 146
Jia, B., Park, D., Hahn, Y., & Jeon, C. O. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1748261 · Cited by 139
The bile acid TUDCA and neurodegenerative disorders: An overview
Zangerolamo, L., Vettorazzi, J. F., Rosa, L. R. D. O., Carneiro, E. M., & Barbosa, H. C. L. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119252 · Cited by 128
Huang, F., Pariante, C. M., & Borsini, A. (2022) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2021.09.021 · Cited by 117
Wei, L., Singh, R., Ro, S., & Ghoshal, U. C. (2021) · JGH Open · doi:10.1002/jgh3.12528 · Cited by 134
Bile acids as key modulators of the brain-Gut-Microbiota axis in alzheimer’s disease
Mulak, A. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210608 · Cited by 114
Probiotics ameliorate intestinal pathophysiology in a mouse model of Alzheimer’s disease
Kaur, H., Nagamoto‐Combs, K., Golovko, S. A., Golovko, M. Y., Klug, M. G., & Combs, C. K. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.04.009 · Cited by 115
Zhang, H., Wang, L., Wang, X., Deng, L., He, B., Xia, Y., & Li, J. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176724 · Cited by 112
Pathogenesis of Hepatic Encephalopathy in Chronic Liver Disease
Ochoa‐Sanchez, R., & Rose, C. F. (2018) · Journal of Clinical and Experimental Hepatology · doi:10.1016/j.jceh.2018.08.001 · Cited by 89
O’Donovan, S. M., Crowley, E. K., Brown, J. R. ‐., O’Sullivan, O., O’Leary, O. F., Timmons, S., Nolan, Y. M., Clarke, D. J., Hyland, N. P., Joyce, S. A., et al. (2020) · Neurogastroenterology & Motility · doi:10.1111/nmo.13726 · Cited by 86
Wang, H., Tan, Y.-Z., Mu, R.-H., Tang, S., Liu, X., Xing, S.-Y., Long, Y., Yuan, D.-H., & Hong, H. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.11.018 · Cited by 81
Carotenoids Diet: Digestion, Gut Microbiota Modulation, and Inflammatory Diseases
Rocha, H. R., Coelho, M. C., Gomes, A., & Pintado, M. (2023) · Nutrients · doi:10.3390/nu15102265 · Cited by 90
Hou, Y., Luan, J., Huang, T., Deng, T., Li, X., Xiao, Z., Zhan, J., Luo, D., Hou, Y., Xu, L., et al. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02248-2 · Cited by 81
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 82
Mondo, E., Barone, M., Soverini, M., D’Amico, F., Cocchi, M., Petrulli, C. A., Mattioli, M., Marliani, G., Candela, M., & Accorsi, P. A. (2020) · Heliyon · doi:10.1016/j.heliyon.2020.e03311 · Cited by 82
Unraveling the Role of the Human Gut Microbiome in Health and Diseases
Khalil, M., Ciaula, A. D., Mahdi, L., Jaber, N., Palo, D. M. D., Graziani, A., Baffy, G., & Portincasa, P. (2024) · Microorganisms · doi:10.3390/microorganisms12112333 · Cited by 100
Daruich, A., Picard, É., Boatright, J. H., & Béhar‐Cohen, F. (2019) · PubMed Central · Cited by 73
Estrada, J. A., & Contreras, I. (2019) · Nutrients · doi:10.3390/nu11051076 · Cited by 65
Choroid Plexus Blood-CSF Barrier: Major Player in Brain Disease Modeling and Neuromedicine
Johanson, C. E. (2018) · Journal of Neurology and Neuromedicine · doi:10.29245/2572.942x/2018/4.1194 · Cited by 65
Wei, L., Singh, R., & Ghoshal, U. C. (2022) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm22008 · Cited by 71
Gut-Brain Axis a Key Player to Control Gut Dysbiosis in Neurological Diseases
Pan, I., Issac, P. K., Rahman, M. M., Guru, A., & Arockiaraj, J. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03691-3 · Cited by 62
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 63
The gut microbiota-bile acid axis: a crucial regulator of immune function and metabolic health
Tyagi, A., & Kumar, V. (2025) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-025-04395-7 · Cited by 68
The contribution of age-related changes in the gut-brain axis to neurological disorders
Khan, R., Gesù, C. M. D., Lee, J., & McCullough, L. D. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2302801 · Cited by 62
Charach, G., Karniel, E., Novikov, I., Galin, L., Vons, S., Grosskopf, I., & Charach, L. (2019) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2019.12.010 · Cited by 56
The pathophysiological function of non-gastrointestinal farnesoid X receptor
Yan, N., Yan, T., Xia, Y., Hao, H., Wang, G., & Gonzalez, F. J. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107867 · Cited by 56
Rodríguez-Morató, J., & Matthan, N. R. (2020) · Current Atherosclerosis Reports · doi:10.1007/s11883-020-00863-7 · Cited by 54
Che, H., Gao, Y., Xu, Y., Xu, H., Eils, R., & Tian, M. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02329-1 · Cited by 57
Implications of glial metabolic dysregulation in the pathophysiology of neurodegenerative diseases
Afridi, R., Rahman, M. H., & Suk, K. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105874 · Cited by 53
Fitz, N. F., Nam, K. N., Koldamova, R. P., & Lefterov, I. M. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14668 · Cited by 52
Bordeleau, M., Comin, C. H., de Cossío, L. F., Lacabanne, C., Freitas-Andrade, M., Ibáñez, F. G., Raman-Nair, J., Wakem, M., Chakravarty, M., Costa, L. D. F., et al. (2022) · Communications Biology · doi:10.1038/s42003-021-02947-9 · Cited by 53
Gut Biofactory—Neurocompetent Metabolites within the Gastrointestinal Tract. A Scoping Review
Skonieczna‐Żydecka, K., Jakubczyk, K., Maciejewska, D., Janda, K., Kaźmierczak-Siedlecka, K., Kaczmarczyk, M., Łoniewski, I., & Marlicz, W. M. (2020) · Nutrients · doi:10.3390/nu12113369 · Cited by 52
Anwar, S., Shamsi, A., Kar, R. K., Queen, A., Islam, A., Ahmad, F., & Hassan, M. I. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.06.078 · Cited by 49
Coconut oil as a therapeutic treatment for alzheimer's disease: a review
Sandupama, P., Munasinghe, D., & Jayasinghe, M. A. (2022) · Journal of Future Foods · doi:10.1016/j.jfutfo.2022.03.016 · Cited by 47
Chen, Q., Wu, C., Xu, J., Ye, C., Chen, X., Tian, H., Zong, N., Zhang, S., Li, L., Gao, Y., et al. (2024) · Cell Host & Microbe · doi:10.1016/j.chom.2024.01.013 · Cited by 49
Redox‐Dependent Effects in the Physiopathological Role of Bile Acids
Orozco-Aguilar, J., Simón, F., & Cabello‐Verrugio, C. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/4847941 · Cited by 45
Petakh, P., Duve, K. V., Oksenych, V., Behzadi, P., & Kamyshnyi, O. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1394953 · Cited by 50
Huang, R., Gao, Y., Chen, J., Duan, Q., He, P., Zhang, J., Huang, H., Zhang, Q., Ma, G., Zhang, Y., et al. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.02.028 · Cited by 41
The Role of Bile Acids in the Human Body and in the Development of Diseases
Shulpekova, Y. O., Жаркова, М. С., Tkachenko, P. E., Тихонов, И. Н., Stepanov, A. A., Sinitsyna, A. A., Izotov, A., Butkova, T. V., Shulpekova, N. V., Лапина, Н. В., et al. (2022) · Molecules · doi:10.3390/molecules27113401 · Cited by 46
Wu, M., Cheng, Y., Zhang, R., Han, W., Jiang, H., Bi, C., Zhang, Z., Ye, M., Lin, X., & Liu, Z. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117228 · Cited by 40
McMillin, M., Grant, S. M., Frampton, G. A., Petrescu, A. D., Kain, J., Williams, E., Haines, R., Canady, L., & DeMorrow, S. (2018) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2018.02.008 · Cited by 39
Self-citationPeripheral neuronal activation shapes the microbiome and alters gut physiology
Griffiths, J. A., Yoo, B. B., Thuy-Boun, P. S., Cantu, V., Weldon, K. C., Challis, C., Sweredoski, M. J., Chan, K. Y., Thron, T., Sharon, G., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113953 · Cited by 37
Hypothalamus-Pituitary-Adrenal Dysfunction in Cholestatic Liver Disease
Petrescu, A. D., Kain, J., Liere, V., Heavener, T. E., & DeMorrow, S. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00660 · Cited by 38
Self-citationLiver Bile Acid Changes in Mouse Models of Alzheimer’s Disease
Kaur, H., Seeger, D. R., Golovko, S. A., Golovko, M. Y., & Combs, C. K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147451 · Cited by 36
Role of Microglia in Regulating Cholesterol and Tau Pathology in Alzheimer’s Disease
Nanjundaiah, S., Chidambaram, H., Chandrashekar, M., & Chinnathambi, S. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00883-6 · Cited by 36
Metabolic Diffusion in Neuropathologies: The Relevance of Brain-Liver Axis
Vegas‐Suárez, S., Simón, J., Martínez‐Chantar, M. L., & Moratalla, R. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.864263 · Cited by 35
Stanimirov, B., Đanić, M., Pavlović, N., Zaklan, D., Lazarević, S., Mikov, M., & Stankov, K. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262412167 · Cited by 39
Linking Nonalcoholic Fatty Liver Disease and Brain Disease: Focusing on Bile Acid Signaling
Ren, Z., Li, C.-X., Ma, C., Chen, D., Chen, J., Xu, W., Chen, C.-A., Cheng, F., & Wang, X. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113045 · Cited by 32
Paraiso, I. L., Tran, T. Q., Magaña, A. A., Kundu, P., Choi, J., Maier, C. S., Bobe, G., Raber, J., Kioussi, C., & Stevens, J. F. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.643857 · Cited by 31
Liver’s influence on the brain through the action of bile acids
Yeo, X. Y., Tan, L. Y., Chae, W. R., Lee, D., Lee, Y., Wüestefeld, T., & Jung, S. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1123967 · Cited by 35
Effects of dietary restriction on gut microbiota and CNS autoimmunity
Cantoni, C., Dorsett, Y., Fontana, L., Zhou, Y., & Piccio, L. M. (2020) · Clinical Immunology · doi:10.1016/j.clim.2020.108575 · Cited by 32
Fecal Microbiota Transplantation in Gastrointestinal and Extraintestinal Disorders
Ianiro, G., Segal, J. P., Mullish, B. H., Quraishi, M. N., Porcari, S., Fabiani, G., Gasbarrini, A., & Cammarota, G. (2020) · Future Microbiology · doi:10.2217/fmb-2020-0061 · Cited by 31
A critical review of bile acids and their receptors in hepatic encephalopathy
Williams, E., Chu, C. S., & DeMorrow, S. (2021) · Analytical Biochemistry · doi:10.1016/j.ab.2021.114436 · Cited by 34
Self-citationPharmacological and Metabolic Significance of Bile Acids in Retinal Diseases
Win, A. S., Delgado, A. M., Jadeja, R. N., Martin, P. M., Bartoli, M., & Thounaojam, M. C. (2021) · Biomolecules · doi:10.3390/biom11020292 · Cited by 30
Gut-microbiota-directed strategies to treat epilepsy: clinical and experimental evidence
Granados, D. M. M., Villasana‐Salazar, B., Lozano‐García, L., Cavalheiro, É. A., & Striano, P. (2021) · Seizure · doi:10.1016/j.seizure.2021.03.009 · Cited by 32
Fu, X., Xiao, Y., Golden, J. M., Niu, S., & Gayer, C. P. (2019) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm-2019-0354 · Cited by 29
Bile acid signalling and its role in anxiety disorders
Chen, S., Shao, Q., Chen, J., Lv, X., Ji, J., Liu, Y., & Song, Y. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1268865 · Cited by 34
Fiaschini, N., Mancuso, M., Tanori, M., Colantoni, E., Vitali, R., Diretto, G., Lorenzo-Rebenaque, L., Stronati, L., & Negroni, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232214254 · Cited by 31
Huang, F. (2021) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2021.100348 · Cited by 28
Genetically personalised organ-specific metabolic models in health and disease
Foguet, C., Xu, Y., Ritchie, S. C., Lambert, S. A., Persyn, E., Nath, A. P., Davenport, E. E., Roberts, D. J., Paul, D. S., Angelantonio, E. D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35017-7 · Cited by 26
Metabolomic signature of the Dravet syndrome: A genetic mouse model study
Miljanovic, N., van Dijk, R. M., Buchecker, V., & Potschka, H. (2021) · Epilepsia · doi:10.1111/epi.16976 · Cited by 28
Collaborative Metabolism: Gut Microbes Play a Key Role in Canine and Feline Bile Acid Metabolism
Rowe, J. C., & Winston, J. A. (2024) · Veterinary Sciences · doi:10.3390/vetsci11020094 · Cited by 26
Ao, Z., Li, Z., Wang, X., Zhao, C., Gan, Y., Wu, X. F., Zeng, F., Shi, J., Gu, T., Hong, L., et al. (2019) · Molecular Reproduction and Development · doi:10.1002/mrd.23102 · Cited by 23
The role of the gut microbiome in disorders of gut–brain interaction
Gawey, B. J., Mars, R. A. T., & Kashyap, P. (2024) · FEBS Journal · doi:10.1111/febs.17200 · Cited by 30
Research Progress on the Mechanism of Bile Acids and Their Receptors in Depression
Zhao, X., Zheng, I., Huang, W., Tang, D., Zhao, M., Hou, R., Huang, Y., Shi, Y., Zhu, W., & Wang, S. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26094023 · Cited by 25
Kiriyama, Y., & Nochi, H. (2023) · Genes · doi:10.3390/genes14040825 · Cited by 22
Darmanto, A. G., Yen, T., Jan, J., Linh, T. T. D., Taliyan, R., Yang, C. H., & Sheu, J. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107564 · Cited by 23
Microbiome influences on neuro-immune interactions in neurodegenerative disease
Menees, K. B., Otero, B. A., & Tansey, M. G. (2022) · International review of neurobiology · doi:10.1016/bs.irn.2022.07.006 · Cited by 24
Hadavi, D., Borzova, M., Siegel, T. P., & Honing, M. (2022) · Analytica Chimica Acta · doi:10.1016/j.aca.2022.339617 · Cited by 20
Emerging Anti-Diabetic Drugs for Beta-Cell Protection in Type 1 Diabetes
Ajmal, N., Bogart, M. C., Khan, P., Max-Harry, I. M., & Nunemaker, C. S. (2023) · Cells · doi:10.3390/cells12111472 · Cited by 20
Xing, C., Zhang, X., Wang, D., Chen, H., Gao, X., Sun, C., Guo, W., Roshan, S., Li, Y., Hang, Z., et al. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.08.047 · Cited by 20
Wang, X., Wang, F., Zhang, Y., Xiong, H., Zhang, Y., Zhuang, P., & Zhang, Y. (2018) · Toxicology Letters · doi:10.1016/j.toxlet.2018.01.006 · Cited by 20
Vishweswaraiah, S., Akyol, S., Yılmaz, A., Ugur, Z., Gordevičius, J., Oh, K. J., Brundin, P., Radhakrishna, U., Labrie, V., & Graham, S. F. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.804261 · Cited by 18
Bile acid modulation by gut microbiota: a bridge to understanding cognitive health
Sabahat, S. E., Saqib, M., Talib, M., Shaikh, T. G., Khan, T., & Kailash, S. J. (2024) · Annals of Medicine and Surgery · doi:10.1097/ms9.0000000000002433 · Cited by 22
Late-Stage Glioma Is Associated with Deleterious Alteration of Gut Bacterial Metabolites in Mice
Herbreteau, A., Aubert, P., Croyal, M., Naveilhan, P., Billon‐Crossouard, S., Neunlist, M., Delneste, Y., Couez, D., & Aymeric, L. (2022) · Metabolites · doi:10.3390/metabo12040290 · Cited by 19
Bile acids as novel enhancers of CNS targeting antitumor drugs: a comprehensive review
Gvoic, M., Vukmirović, S., Al‐Salami, H., Mooranian, A., Mikov, M., & Stankov, K. (2021) · Pharmaceutical Development and Technology · doi:10.1080/10837450.2021.1916032 · Cited by 17
Sancho‐Alonso, M., Arenas, Y. M., Izquierdo‐Altarejos, P., Martinez‐García, M., Llansola, M., & Felipo, V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242417251 · Cited by 19
Duarte‐Silva, S., Silva, J. D. D., Monteiro‐Fernandes, D., Costa, M. D., Neves‐Carvalho, A., Raposo, M., Soares‐Cunha, C., Correia, J. S., Nogueira-Goncalves, G., Fernandes, H. S., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci162246 · Cited by 19
Bálentová, S., Hnilicová, P., Kalenská, D., Baranovičová, E., Muríň, P., Bittšanský, M., Hajtmanová, E., Lehotský, J., & Adamkov, M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.12.022 · Cited by 17
Untargeted Metabolomics of Slc13a5 Deficiency Reveal Critical Liver–Brain Axis for Lipid Homeostasis
Milosavljevic, S., Glinton, K. E., Li, X., Medeiros, C., Gillespie, P. J., Seavitt, J. R., Graham, B. H., & Elsea, S. H. (2022) · Metabolites · doi:10.3390/metabo12040351 · Cited by 17
Lahariya, R., Anand, G., Kumari, B., & Priyadarshi, K. (2026) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2026.578870 · Cited by 20
Kundu, P., Holden, S. J., Paraiso, I. L., Sudhakar, R., McQuesten, C., Choi, J., Miranda, C. L., Maier, C. S., Bobe, G., Stevens, J. F., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.954980 · Cited by 17
Hepatic interoception in health and disease
Berthoud, H., Münzberg, H., Morrison, C. D., & Neuhuber, W. (2024) · Autonomic Neuroscience · doi:10.1016/j.autneu.2024.103174 · Cited by 17
Turk, B. R., Theda, C., Fatemi, A. S., & Moser, A. B. (2019) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2019.11.002 · Cited by 17
TUDCA receptors and their role on pancreatic beta cells
Rosa, L. R. D. O., Vettorazzi, J. F., Zangerolamo, L., Carneiro, E. M., & Barbosa, H. C. L. (2021) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2021.09.003 · Cited by 17
Research progress on intranasal treatment for Parkinson's disease
Wen, P., & Ren, C. (2024) · Neuroprotection/Neuroprotection (Chichester, England. Print) · doi:10.1002/nep3.42 · Cited by 18
Bile Acids in Pancreatic Carcinogenesis
Sharma, B., Twelker, K., Nguyen, C., Ellis, S., Bhatia, N. D., Kuschner, Z. D., Agriantonis, A., Agriantonis, G., Arnold, M., Dave, J., et al. (2024) · Metabolites · doi:10.3390/metabo14070348 · Cited by 15
Metadata
- Authors
- McMillin, M., & DeMorrow, S.
- Affiliations
- Texas A&M Health Science Center (US)
- Corresponding author
- DeMorrow, Sharon
- Venue
- The FASEB Journal
- Publisher
- Wiley
- Published
- 2016-07-28
- Volume
- 30
- Issue
- 11
- Pages
- 3658-3668
- ISSN
- 0892-6638 (ISSN-L)
- 1530-6860
- PMC
- PMC5067249
- OpenAlex
- W2491463486
- Cited by
- 192
- References
- 103
- Citations by year
- 2026: 24 · 2025: 20 · 2024: 27 · 2023: 18 · 2022: 29 · 2021: 28 · 2020: 19 · 2019: 15 · 2018: 8 · 2017: 3 · 2016: 1
- FWCI
- 0.90
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The FASEB Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Health Services Research and Development
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases (R01 DK082435)
- Biomedical Laboratory Research and Development, VA Office of Research and Development (BX002638-01)
- Topics
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Cholesterol and Lipid Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Aldose Reductase and Taurine
- Keywords
- bile acids, neurological function, neurological disorders, bile acid receptors, signal transduction, neuroprotection, liver injury, cholesterol metabolism, lipid emulsification
- MeSH terms
- Animals, Bile Acids and Salts, Cholesterol, Homeostasis, Humans, Liver, Signal Transduction, Receptors, Cytoplasmic and Nuclear
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