Acetate reduces microglia inflammatory signaling in vitro
Open accessAbstract
Acetate supplementation increases brain acetyl‐CoA and histone acetylation and reduces lipopolysaccharide ( LPS )‐induced neuroglial activation and interleukin ( IL )‐1β expression in vivo . To determine how acetate imparts these properties, we tested the hypothesis that acetate metabolism reduces inflammatory signaling in microglia. To test this, we measured the effect acetate treatment had on cytokine expression, mitogen‐activated protein kinase ( MAPK ) signaling, histone H3 at lysine 9 acetylation, and alterations of nuclear factor‐kappa B ( NF‐κB ) in primary and BV‐2 cultured microglia. We found that treatment induced H3K9 hyperacetylation and reversed LPS‐induced H3K9 hypoacetylation similar to that found in vivo . LPS also increased IL‐1β, IL‐6, and tumor necrosis factor‐alpha ( TNF ‐α) mRNA and protein, whereas treatment returned the protein to control levels and only partially attenuated IL‐6 mRNA . In contrast, treatment increased mRNA levels of transforming growth factor‐β1 ( TGF ‐β1) and both IL‐4 mRNA and protein. LPS increased p38 MAPK and JNK phosphorylation at 4 and 2–4 h, respectively, whereas treatment reduced p38 MAPK and JNK phosphorylation only at 2 h. In addition, treatment reversed the LPS‐induced elevation of NF‐κB p65 protein and phosphorylation at serine 468 and induced acetylation at lysine 310. These data suggest that acetate metabolism reduces inflammatory signaling and alters histone and non‐histone protein acetylation.
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Acetate treatment of microglia primary culture reduces inflammatory signaling through reduced IL-1β, IL-6, and TNF-α expression and p38 MAPK, JNK, and NF-κB phosphorylation.
“acetate treatment of microglia primary culture has been shown to reduce inflammatory signaling through reduced IL-1β, IL-6, and TNF-α expression and p38 MAPK, JNK, and NF-κB phosphorylation (111).”
From The Role of Short-Chain Fatty Acids From Gut Microbiota in Gut-Brain Communication (2020) · cites this paper as [111]
The Results section (page unavailable) reports that acetate returned LPS-induced IL-1β, IL-6, and TNF-α protein increases to control levels in primary microglia. The phosphorylation findings were measured in BV-2 microglia, not primary cultures: p38 and JNK phosphorylation fell only at 2 hours, and NF-κB p65 phosphorylation fell at serine 468. The sentence conflates those cell types and omits the time- and site-specific limits. (LLM, conf=0.90)
Experimental — accuracy not yet measuredAcetate can be converted to acetyl-CoA, which leads to increased histone acetylation.
“acetate can be converted to acetyl-CoA, which leads to increased histone acetylation”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Soliman et al., 2012
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The language of covalent histone modifications
Strahl, B. D., & Allis, C. D. (2000) · Nature · doi:10.1038/47412 · Cited by 8,679 · see citing works
Mitogen-Activated Protein (MAP) Kinase Pathways: Regulation and Physiological Functions*
Pearson, G. W., Robinson, F. L., Gibson, T. B., Xu, B.-E., Karandikar, M. S., Berman, K. S., & Cobb, M. H. (2001) · Endocrine Reviews · doi:10.1210/edrv.22.2.0428 · Cited by 4,044 · see citing works
Microglia: Active sensor and versatile effector cells in the normal and pathologic brain
Hanisch, U.-K., & Kettenmann, H. (2007) · Nature Neuroscience · doi:10.1038/nn1997 · Cited by 3,676 · see citing works
Microglial physiology: unique stimuli, specialized responses
Ransohoff, R. M., & Perry, V. H. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132528 · Cited by 1,858 · see citing works
Acetylation and deacetylation of non-histone proteins
Glozak, M. A., Sengupta, N., Zhang, X., & Seto, E. (2005) · Gene · doi:10.1016/j.gene.2005.09.010 · Cited by 1,584 · see citing works
Duration of Nuclear NF-κB Action Regulated by Reversible Acetylation
Chen, L., Fischle, W., Verdin, E. M., & Greene, W. C. (2001) · Science · doi:10.1126/science.1062374 · Cited by 1,231 · see citing works
p38 MAP kinases: key signalling molecules as therapeutic targets for inflammatory diseases
Kumar, S., Boehm, J. C., & Lee, J. C. (2003) · Nature Reviews Drug Discovery · doi:10.1038/nrd1177 · Cited by 1,199 · see citing works
Streit, W. J., Walter, S. A., & Pennell, N. A. (1999) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00069-0 · Cited by 1,096 · see citing works
Mitogen-Activated Protein (MAP) Kinase Pathways: Regulation and Physiological Functions
Pearson, G. (2001) · Endocrine Reviews · doi:10.1210/er.22.2.153 · Cited by 1,060 · see citing works
Immortalization of murine microglial cells by a v-raf / v-myc carrying retrovirus
Blasi, E., Barluzzi, R., Bocchini, V., Mazzolla, R., & Bistoni, F. (1990) · Journal of Neuroimmunology · doi:10.1016/0165-5728(90)90073-v · Cited by 1,053 · see citing works
Cytokines and the nervous system II: actions and mechanisms of action
Rothwell, N. J., & Hopkins, S. J. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93890-a · Cited by 922 · see citing works
Acetylation of RelA at discrete sites regulates distinct nuclear functions of NF‐κB
Chen, L., Mu, Y., & Greene, W. C. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf660 · Cited by 827 · see citing works
Cytokines and the nervous system I: expression and recognition
Hopkins, S. J., & Rothwell, N. J. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)80029-2 · Cited by 793 · see citing works
MAPKAP kinase 2 is essential for LPS-induced TNF-α biosynthesis
Kotlyarov, A., Neininger, A., Schubert, C., Eckert, R., Birchmeier, C., Volk, H.-D., & Gaestel, M. (1999) · Nature Cell Biology · doi:10.1038/10061 · Cited by 763 · see citing works
SIRT1 Protects against Microglia-dependent Amyloid-β Toxicity through Inhibiting NF-κB Signaling
Chen, J., Zhou, Y., Mueller-Steiner, S., Chen, L.-F., Kwon, H., Yi, S., Mucke, L., & Gan, L. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m509329200 · Cited by 740 · see citing works
Regulation of NF-κB by Cyclin-Dependent Kinases Associated with the p300 Coactivator
Perkins, N. D., Felzien, L. K., Betts, J. C., Leung, K., Beach, D., & Nabel, G. J. (1997) · Science · doi:10.1126/science.275.5299.523 · Cited by 722 · see citing works
Regulation and Destabilization of HIF-1α by ARD1-Mediated Acetylation
Jeong, J.-W., Bae, M.-K., Ahn, M.-Y., Kim, S.-H., Sohn, T.-K., Bae, M.-H., Yoo, M.-A., Song, E. J., Lee, K.-J., & Kim, K.-W. (2002) · Cell · doi:10.1016/s0092-8674(02)01085-1 · Cited by 716 · see citing works
Histone methylation versus histone acetylation: new insights into epigenetic regulation
Rice, J. C., & Allis, C. D. (2001) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(00)00208-8 · Cited by 701 · see citing works
Beyaert, R., Cuenda, A., Berghe, W. V., Plaisance, S., Lee, J. C., Haegeman, G., Cohen, P., & Fiers, W. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00542.x · Cited by 650 · see citing works
Translational control by CPEB: a means to the end
Méndez, R., & Richter, J. D. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35080081 · Cited by 609 · see citing works
Lehnardt, S. (2009) · Glia · doi:10.1002/glia.20928 · Cited by 596 · see citing works
Li, Y., Liu, L., Barger, S. W., & Griffin, W. S. T. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01605.2003 · Cited by 563 · see citing works
Post-activation Turn-off of NF-κB-dependent Transcription Is Regulated by Acetylation of p65
Kiernan, R. E., Brès, V., Ng, R. W. M., Coudart, M.-P., Messaoudi, S. E., Sardet, C., Jin, D., Emiliani, S., & Benkirane, M. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m209572200 · Cited by 536 · see citing works
Hypusine-containing protein eIF5A promotes translation elongation
Saini, P., Eyler, D. E., Green, R., & Dever, T. E. (2009) · Nature · doi:10.1038/nature08034 · Cited by 425 · see citing works
Govindarajan, N., Agis-Balboa, R. C., Walter, J., Sananbenesi, F., & Fischer, A. (2011) · Journal of Alzheimer's Disease · doi:10.3233/jad-2011-110080 · Cited by 405 · see citing works
An immortalized cell line expresses properties of activated microglial cells
Bocchini, V., Mazzolla, R., Barluzzi, R., Blasi, E., Sick, P., & Kettenmann, H. (1992) · Journal of Neuroscience Research · doi:10.1002/jnr.490310405 · Cited by 364 · see citing works
Posttranslational modifications of NF-κB: Another layer of regulation for NF-κB signaling pathway
Huang, B., Yang, X., Lamb, A., & Chen, L. F. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2010.03.017 · Cited by 345 · see citing works
Inflammation and brain injury: Acute cerebral ischaemia, peripheral and central inflammation
Dénes, Á., Thornton, P., Rothwell, N. J., & Allan, S. M. (2009) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2009.09.010 · Cited by 307 · see citing works
Regulation of DNA binding by Rel/NF-κB transcription factors: structural views
Chen, F. E., & Ghosh, G. (1999) · Oncogene · doi:10.1038/sj.onc.1203224 · Cited by 301 · see citing works
Acetyl-CoA Synthetase 2, a Mitochondrial Matrix Enzyme Involved in the Oxidation of Acetate
Fujino, T., Kondo, J., Ishikawa, M., Morikawa, K., & Yamamoto, T. T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m008782200 · Cited by 298 · see citing works
Neuroinflammation is a key player in Parkinson’s disease and a prime target for therapy
Li, Q., Flood, P. M., & Hong, J. (2010) · Journal of Neural Transmission · doi:10.1007/s00702-010-0428-1 · Cited by 287 · see citing works
Osmotic regulation of cytokine synthesis in vitro.
Shapiro, L., & Dinarello, C. A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.26.12230 · Cited by 280 · see citing works
Ambivalent Aspects of Interleukin-6 in Cerebral Ischemia: Inflammatory versus Neurotrophic Aspects
Suzuki, S., Tanaka, K., & Suzuki, N. (2008) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2008.141 · Cited by 241 · see citing works
Ledeboer, A., Brev�, J. J. P., Poole, S., Tilders, F. J. H., & van Dam, A. (2000) · Glia · doi:10.1002/(sici)1098-1136(200004)30:2 · Cited by 225 · see citing works
Regulation of protein turnover by acetyltransferases and deacetylases
Sadoul, K., Boyault, C., Pabion, M., & Khochbin, S. (2007) · Biochimie · doi:10.1016/j.biochi.2007.06.009 · Cited by 223 · see citing works
Sawada, M., Suzumura, A., Hosoya, H., Marunouchi, T., & Nagatsu, T. (1999) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1999.721466.x · Cited by 223 · see citing works
HDAC inhibitors as anti‐inflammatory agents
Adcock, I. M. (2007) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707166 · Cited by 217 · see citing works
Cytokines and innate inflammation in the pathogenesis of human traumatic brain injury.
Helmy, A., Simoni, M. D., Guilfoyle, M., Carpenter, K., & Hutchinson, P. (2011) · Progress in neurobiology · doi:10.1016/j.pneurobio.2011.09.003 · Cited by 208 · see citing works
Theis, M., Si, K., & Kandel, E. R. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1133424100 · Cited by 194 · see citing works
Acetylation of mitogen-activated protein kinase phosphatase-1 inhibits Toll-like receptor signaling
Cao, W., Bao, C., Padalko, E. Y., & Lowenstein, C. J. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20071728 · Cited by 190 · see citing works
Lloyd, E., Somera-Molina, K., Eldik, L. J. V., Watterson, D. M., & Wainwright, M. S. (2008) · Journal of Neuroinflammation · doi:10.1186/1742-2094-5-28 · Cited by 180 · see citing works
Langley, B. C., Gensert, J. M., Beal, M. F., & Ratan, R. R. (2005) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1568007053005091 · Cited by 169 · see citing works
Chronic High-Fat Diet Drives Postnatal Epigenetic Regulation of μ-Opioid Receptor in the Brain
Vucetic, Z., Kimmel, J. N., & Reyes, T. M. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.4 · Cited by 165 · see citing works
Soliman, M. L., & Rosenberger, T. A. (2011) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-011-0751-3 · Cited by 158 · see citing works
Self-citationAtkins, C. M., Nozaki, N., Shigeri, Y., & Soderling, T. R. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0854-04.2004 · Cited by 156 · see citing works
Zhang, B., West, E., Van, K. C., Gurkoff, G. G., Zhou, J., Zhang, X.-M., Kozikowski, A., & Lyeth, B. G. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.085 · Cited by 138 · see citing works
eIF5A has a function in the elongation step of translation in yeast
Gregio, A. P. B., Cano, V. S. P., Avaca, J. S., Valentini, S. R., & Zanelli, C. F. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.01.148 · Cited by 127 · see citing works
Anti-Inflammatory Cytokines: Expression and Action in the Brain
Vitković, L., Maeda, S., & STERNBERG, E. M. (2001) · NeuroImmunoModulation · doi:10.1159/000059387 · Cited by 117 · see citing works
Assessing the contribution of inflammation in models of Alzheimer's disease
Johnston, H. R., Boutin, H., & Allan, S. M. (2011) · Biochemical Society Transactions · doi:10.1042/bst0390886 · Cited by 112 · see citing works
eIF5A binds to translational machinery components and affects translation in yeast
Zanelli, C. F., Maragno, A. L. C., Gregio, A. P. B., Komili, S., Pandolfi, J. R. C., Mestriner, C. A., Lustri, W. R., & Valentini, S. R. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.07.195 · Cited by 112 · see citing works
Transforming Growth Factor-β: A Neuroprotective Factor in Cerebral Ischemia
Dhandapani, K. M., & Brann, D. W. (2003) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:39:1:13 · Cited by 111 · see citing works
Schumann, R., Pfeil, D., Lamping, N., Kirschning, C. J., Scherzinger, G., Schlag, P., Karawajew, L., & Herrmann, F. (1996) · Blood · doi:10.1182/blood.v87.7.2805.bloodjournal8772805 · Cited by 109 · see citing works
Expression of mutant alpha-synuclein modulates microglial phenotype in vitro
Rojanathammanee, L., Murphy, E. J., & Combs, C. K. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-44 · Cited by 106 · see citing works
Self-citationSoliman, M. L., Smith, M. D., Houdek, H. M., & Rosenberger, T. A. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-51 · Cited by 104 · see citing works
Self-citationAmyloid-β oligomers stimulate microglia through a tyrosine kinase dependent mechanism
Manocha, G. D., Floden, A. M., & Combs, C. K. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.10.027 · Cited by 104 · see citing works
Self-citationMerson, T. D., Binder, M. D., & Kilpatrick, T. J. (2010) · NeuroMolecular Medicine · doi:10.1007/s12017-010-8112-z · Cited by 101 · see citing works
Ishfaq, M., Maeta, K., Maeda, S., Natsume, T., Ito, A., & Yoshida, M. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.06.042 · Cited by 82 · see citing works
Woo, M.-S., Jang, P., Park, J.-S., Kim, W.-K., Joh, T., & Kim, H.-S. (2003) · Brain Research. Molecular Brain Research · doi:10.1016/s0169-328x(03)00095-0 · Cited by 78 · see citing works
Selective Modulation of BV-2 Microglial Activation by Prostaglandin E2
Petrova, T. V., Akama, K. T., & Eldik, L. J. V. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.40.28823 · Cited by 77 · see citing works
Acetate supplementation attenuates lipopolysaccharide‐induced neuroinflammation
Reisenauer, C. J., Bhatt, D. P., Mitteness, D. J., Slanczka, E. R., Gienger, H. M., Watt, J. A., & Rosenberger, T. A. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07198.x · Cited by 73 · see citing works
Self-citationMetabolic Acetate Therapy for the Treatment of Traumatic Brain Injury
Arun, P., Ariyannur, P. S., Moffett, J. R., Xing, G., Hamilton, K. R., Grunberg, N. E., Ives, J. A., & Namboodiri, A. M. A. (2009) · Journal of Neurotrauma · doi:10.1089/neu.2009.0994 · Cited by 73 · see citing works
RNA-Binding Proteins: A Lesson in Repression
Wells, D. G. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1795-06.2006 · Cited by 73 · see citing works
Furlan, R., Bergami, A., Lang, R., Brambilla, E., Franciotta, D. M., Martinelli, V., Comı, G., Panina‐Bordignon, P., & Martino, G. (2000) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(00)00377-5 · Cited by 72 · see citing works
Metabolic acetate therapy improves phenotype in the tremor rat model of Canavan disease
Arun, P., Madhavarao, C. N., Moffett, J. R., Hamilton, K. R., Grunberg, N. E., Ariyannur, P. S., Gahl, W. A., Anikster, Y., Mog, S. R., Hallows, W. C., et al. (2010) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-010-9100-z · Cited by 71 · see citing works
Annunziato, A. T., Eason, M. B., & Perry, C. A. (1995) · Biochemistry · doi:10.1021/bi00009a023 · Cited by 70 · see citing works
Hu, W., Ranaivo, H. R., Roy, S. M., Behanna, H. A., Wing, L. K., Munoz, L., Guo, L., Eldik, L. J. V., & Watterson, D. M. (2006) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2006.10.028 · Cited by 66 · see citing works
Regulation of E2F-1 after DNA Damage by p300-Mediated Acetylation and Ubiquitination
Galbiati, L., Mendoza-Maldonado, R., Gutiérrez, M. I., & Giacca, M. (2005) · Cell Cycle · doi:10.4161/cc.4.7.1784 · Cited by 65 · see citing works
Mathew, R., Arun, P., Madhavarao, C. N., Moffett, J. R., & Namboodiri, M. A. A. (2005) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.105.087536 · Cited by 64 · see citing works
Nuclear‐cytoplasmic localization of acetyl coenzyme a synthetase‐1 in the rat brain
Ariyannur, P. S., Moffett, J. R., Madhavarao, C. N., Arun, P., Vishnu, N., Jacobowitz, D. M., Hallows, W. C., Denu, J. M., & Namboodiri, A. M. A. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22373 · Cited by 63 · see citing works
Seo, D. R., Kim, K. Y., & Lee, Y. B. (2004) · Neuroreport · doi:10.1097/00001756-200405190-00015 · Cited by 58 · see citing works
da Silva, P. F., Garcia, V. A., Dornelles, A. D. S., da Silva, V. K., Maurmann, N., Portal, B. C. D., Ferreira, R. D. P., Piazza, F. C., Roesler, R., & Schröder, N. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.10.038 · Cited by 56 · see citing works
Kohn, D. T., Tsai, K.-C., Cansino, V. V., Neve, R. L., & Perrone‐Bizzozero, N. I. (1996) · Molecular Brain Research · doi:10.1016/0169-328x(95)00239-o · Cited by 45 · see citing works
Shin, J. H., Li, R. W., Gao, Y., Baldwin, R. L., & Li, C. (2012) · Functional & Integrative Genomics · doi:10.1007/s10142-012-0263-6 · Cited by 38 · see citing works
Lee, S. B., Park, J. H., Folk, J. E., Deck, J. A., Pegg, A. E., Sokabe, M., Fraser, C. S., & Park, M. H. (2010) · Biochemical Journal · doi:10.1042/bj20101322 · Cited by 34 · see citing works
Kraatz, J. J., Clair, L., Bellingham, J. M., Wahlstrom, K., Rodriguez, J. L., & West, M. A. (1998) · doi:10.1097/00005373-199810000-00008 · Cited by 14 · see citing works
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Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286 · see citing works
The Role of Short-Chain Fatty Acids From Gut Microbiota in Gut-Brain Communication
Silva, Y. P., Bernardi, A., & Frozza, R. L. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00025 · Cited by 3,043 · see citing works
“Likewise, acetate treatment of microglia primary culture has been shown to reduce inflammatory signaling through reduced IL-1β, IL-6, and TNF-α expression and p38 MAPK, JNK, and NF-κB phosphorylation (111).”
BackgroundNey, L.-M., Wipplinger, M., Grossmann, M., Engert, N., Wegner, V. D., & Mosig, A. S. (2023) · Open Biology · doi:10.1098/rsob.230014 · Cited by 337 · see citing works
Feeding gut microbes to nourish the brain: unravelling the diet–microbiota–gut–brain axis
Schneider, E., O'Riordan, K. J., Clarke, G., & Cryan, J. (2024) · Nature Metabolism · doi:10.1038/s42255-024-01108-6 · Cited by 258 · see citing works
Aquaporin 4: a player in cerebral edema and neuroinflammation
Fukuda, A. M., & Badaut, J. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-279 · Cited by 265 · see citing works
Gut Microbiota and Their Metabolites in Stroke: A Double-Edged Sword
Peh, A., O’Donnell, J. A., Broughton, B. R. S., & Marques, F. Z. (2022) · Stroke · doi:10.1161/strokeaha.121.036800 · Cited by 259 · see citing works
Bhat, M. I., & Kapila, R. (2017) · Nutrition Reviews · doi:10.1093/nutrit/nux001 · Cited by 227 · see citing works
Inhibition of inflammatory microglia by dietary fiber and short-chain fatty acids
Caetano-Silva, M. E., Rund, L., Hutchinson, N. T., Woods, J. A., Steelman, A. J., & Johnson, R. W. (2023) · Scientific Reports · doi:10.1038/s41598-022-27086-x · Cited by 225 · see citing works
Chidambaram, S. B., Essa, M. M., Rathipriya, A. G., Bishir, M., Ray, B., Mahalakshmi, A. M., Tousif, A. H., Sakharkar, M. K., Kashyap, R. S., Friedland, R. P., et al. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107988 · Cited by 204 · see citing works
Moffett, J. R., Arun, P., Ariyannur, P. S., & Namboodiri, A. M. A. (2013) · Frontiers in Neuroenergetics · doi:10.3389/fnene.2013.00011 · Cited by 183 · see citing works
Short-chain fatty acids-producing probiotics: A novel source of psychobiotics
Cheng, Y., Liu, J., & Ling, Z. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1920884 · Cited by 155 · see citing works
Epigenetics Control Microglia Plasticity
Cheray, M., & Joseph, B. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00243 · Cited by 151 · see citing works
Lee, J., Venna, V. R., Durgan, D. J., Shi, H., Hudobenko, J., Putluri, N., Petrosino, J. F., McCullough, L. D., & Bryan, R. M. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1814107 · Cited by 151 · see citing works
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The gut microbiome: a key player in the complexity of amyotrophic lateral sclerosis (ALS)
Boddy, S. L., Giovannelli, I., Sassani, M., Cooper-Knock, J., Snyder, M. P., Segal, E., Elinav, E., Barker, L. A., Shaw, P. J., & McDermott, C. J. (2021) · BMC Medicine · doi:10.1186/s12916-020-01885-3 · Cited by 127 · see citing works
Cao, Q., Shen, M., Li, R., Liu, Y., Zeng, Z., Zhou, J., Niu, D., Zhang, Q., Wang, R., Yao, J., et al. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03454-y · Cited by 129 · see citing works
Szutowicz, A., Bielarczyk, H., Jankowska-Kulawy, A., Pawełczyk, T., & Ronowska, A. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1060-x · Cited by 116 · see citing works
Multiple roles of short-chain fatty acids in Alzheimer disease
Chen, H., Meng, L., & Shen, L. (2021) · Nutrition · doi:10.1016/j.nut.2021.111499 · Cited by 107 · see citing works
Unlocking gut-liver-brain axis communication metabolites: energy metabolism, immunity and barriers
Sun, X., Shukla, M., Wang, W., & Li, S. (2024) · npj Biofilms and Microbiomes · doi:10.1038/s41522-024-00610-9 · Cited by 98 · see citing works
Li, Y., Liu, A., Chen, K., Li, L., Zhang, X., Zou, F., Zhang, X., & Meng, X. (2024) · Environment International · doi:10.1016/j.envint.2024.108479 · Cited by 91 · see citing works
Soliman, M. L., Combs, C. K., & Rosenberger, T. A. (2013) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-012-9426-4 · Cited by 84 · see citing works
Self-citationAcorus calamus : a bio-reserve of medicinal values
Khwairakpam, A. D., Damayenti, Y. D., Deka, A., Monisha, J., Roy, N. K., Padmavathi, G., & Kunnumakkara, A. B. (2018) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp-2016-0132 · Cited by 78 · see citing works
Jiang, L., Wang, J., Liu, Z., Jiang, A., Li, S., Wu, D., Zhang, Y., Zhu, X., Zhou, E., Wei, Z., et al. (2020) · Frontiers in Veterinary Science · doi:10.3389/fvets.2020.579674 · Cited by 77 · see citing works
The Gut Microbiome as a Regulator of the Neuroimmune Landscape
Yu, L. W., Agirman, G., & Hsiao, E. Y. (2022) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101320-014237 · Cited by 75 · see citing works
Kien, C. L., Bunn, J. Y., Tompkins, C. L., Dumas, J. A., Crain, K. I., Ebenstein, D. B., Koves, T. R., & Muoio, D. M. (2013) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.112.051730 · Cited by 73 · see citing works
Inhibition of Neuroinflammation in LPS-Activated Microglia by Cryptolepine
Olajide, O. A., Bhatia, H. S., de Oliveira, A. C. P., Wright, C. W., & Fiebich, B. L. (2013) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2013/459723 · Cited by 72 · see citing works
Lo, J. Y., Kamarudin, M. N. A., Hamdi, O. A. A., Awang, K., & Kadir, H. A. (2015) · Food & Function · doi:10.1039/c5fo00607d · Cited by 70 · see citing works
Xu, M., Huang, H., Mo, X., Zhu, Y., Chen, X., Li, X., Peng, X., Xu, Z., Chen, L., Rong, S., et al. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000660 · Cited by 66 · see citing works
Gut Microbiota in Ischemic Stroke: Role of Gut Bacteria-Derived Metabolites
Zhang, W., Dong, X. Y., & Huang, R. (2022) · Translational Stroke Research · doi:10.1007/s12975-022-01096-3 · Cited by 66 · see citing works
Exploring the microbiota-gut-brain axis: impact on brain structure and function
Yassin, L. K., Nakhal, M. M., Alderei, A., Almehairbi, A., Mydeen, A. B., Akour, A. A., & Hamad, M. I. K. (2025) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2025.1504065 · Cited by 60 · see citing works
Fatty acids role in multiple sclerosis as “metabokines”
Yu, H., Bai, S., Hao, Y., & Guan, Y. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02502-1 · Cited by 58 · see citing works
Lim, H.-S., Kim, Y. J., Kim, B., & Jeong, S. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20143574 · Cited by 56 · see citing works
Lipid metabolism in homeostasis and disease
Li, Z., Deng, W., Yang, L., Tang, C., Yue, J.-M., Monteiro, O., Baptista‐Hon, D. T., & Li, T. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02357-x · Cited by 51 · see citing works
Short Chain Fatty Acid Acetate Protects against Ethanol-Induced Acute Gastric Mucosal Lesion in Mice
Liu, J., Wang, J., Shi, Y., SU, W. W., Chen, J., Zhang, Z., Wang, G., & Wang, F. (2017) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b17-00240 · Cited by 51 · see citing works
Chevalier, A. C., & Rosenberger, T. A. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14032 · Cited by 50 · see citing works
Self-citationThe complex relationship between gut microbiota and Alzheimer’s disease: A systematic review
Zhou, X.-P., Sun, L.-B., Liu, W., Zhu, W.-M., Li, L.-C., Song, X., Xing, J.-P., & Gao, S. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102637 · Cited by 50 · 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
Jackson, P. P. J., Wijeyesekera, A., Williams, C. M., Theis, S., Harsselaar, J. V., & Rastall, R. A. (2023) · American Journal of Clinical Nutrition · doi:10.1016/j.ajcnut.2023.08.016 · Cited by 48 · see citing works
Lee, B., Lee, S. M., Song, J. W., & Choi, J. W. (2024) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2024.009 · Cited by 48 · 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
Lim, H.-W., Kumar, H., Kim, B.-W., More, S. V., Kim, I.-W., Park, J.-I., Park, S., Kim, S., & Choi, D. (2014) · Food and Chemical Toxicology · doi:10.1016/j.fct.2014.07.018 · Cited by 45 · see citing works
APOE genetics influence murine gut microbiome
Zajac, D. J., Green, S. J., Johnson, L. A., & Estus, S. (2022) · Scientific Reports · doi:10.1038/s41598-022-05763-1 · Cited by 41 · see citing works
Brissette, C. A., Houdek, H. M., Floden, A. M., & Rosenberger, T. A. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-249 · Cited by 40 · see citing works
Self-citationPathophysiology and recent therapeutic insights of sickle cell disease
Shah, F., & Dwivedi, M. (2020) · Annals of Hematology · doi:10.1007/s00277-020-03977-9 · Cited by 39 · see citing works
Gao, H., Song, R., Li, Y., Zhang, W., Wan, Z., Wang, Y., Zhang, H., & Han, S. (2020) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c05677 · Cited by 38 · see citing works
Kim, B.-W., Koppula, S., Park, S., Kim, Y.-S., Park, P., Lim, J.-H., Kim, I., & Choi, D. (2014) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2014.11.004 · Cited by 35 · see citing works
Game of microbes: the battle within – gut microbiota and multiple sclerosis
Turner, T.-A. J., Lehman, P., Ghimire, S., Shahi, S. K., & Mangalam, A. K. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2387794 · Cited by 33 · see citing works
Dietary Fiber as a Counterbalance to Age-Related Microglial Cell Dysfunction
Vailati-Riboni, M., Rund, L. A., Caetano‐Silva, M. E., Hutchinson, N. T., Wang, S. S., Soto‐Díaz, K., Woods, J. A., Steelman, A. J., & Johnson, R. W. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.835824 · Cited by 32 · see citing works
Ramaiah, M. J., Kurappalli, R. K., Ramalingam, P. S., & Moparthi, N. R. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.120024 · Cited by 32 · see citing works
Liu, Y., Ju, Y., Cui, L., Liu, T., Hou, Y., Wu, Q., Ojo, O., Du, X., & Wang, X. (2021) · Nutrients · doi:10.3390/nu13114159 · Cited by 31 · see citing works
Sanguigno, L., Casamassa, A., Funel, N., Minale, M., Riccio, R., Riccio, S., Boscia, F., Brancaccio, P., Pollina, L. E., Anzilotti, S., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0197493 · Cited by 31 · see citing works
Microglia Sing the Prelude of Neuroinflammation-Associated Depression
Li, Q., Xie, Y., Lin, J., Li, M., Gu, Z., Xin, T., Zhang, Y., Lu, Q., Guo, Y., Xing, Y., et al. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04575-w · Cited by 30 · see citing works
Soliman, M. L., Ohm, J. E., & Rosenberger, T. A. (2013) · Lipids · doi:10.1007/s11745-013-3799-x · Cited by 30 · see citing works
Self-citationBorrelia burgdorferi hijacks cellular metabolism of immune cells: Consequences for host defense
Kerstholt, M., Netea, M. G., & Joosten, L. A. B. (2020) · Ticks and Tick-borne Diseases · doi:10.1016/j.ttbdis.2020.101386 · Cited by 29 · see citing works
Parasite infections, neuroinflammation, and potential contributions of gut microbiota
Alloo, J., Leleu, I., Grangette, C., & Pied, S. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1024998 · Cited by 28 · see citing works
Smith, M. D., Bhatt, D. P., Geiger, J. D., & Rosenberger, T. A. (2014) · Journal of Neuroinflammation · doi:10.1186/1742-2094-11-99 · Cited by 28 · see citing works
Self-citationThe Bidirectional Signal Communication of Microbiota‐Gut‐Brain Axis in Hypertension
Wang, X., Chen, Z., Geng, B., & Cai, J. (2021) · International Journal of Hypertension · doi:10.1155/2021/8174789 · Cited by 26 · see citing works
Wolugbom, J. A., Areloegbe, S. E. J., & Olaniyi, K. S. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03074-0 · Cited by 25 · see citing works
Bendriss, G., MacDonald, R. S., & McVeigh, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241511978 · Cited by 25 · see citing works
Bhatt, D. P., Houdek, H. M., Watt, J. A., & Rosenberger, T. A. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.01.004 · Cited by 24 · see citing works
Self-citationGut Microbiota as a Hidden Player in the Pathogenesis of Alzheimer’s Disease
Choi, H., Lee, D., & Mook‐Jung, I. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-215235 · Cited by 23 · see citing works
Kimura-Todani, T., Hata, T., Miyata, N., Takakura, S., Yoshihara, K., Zhang, X., Asano, Y., Altaisaikhan, A., Tsukahara, T., & Sudo, N. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.113004 · Cited by 22 · see citing works
Epigenetic Effects of Gut Metabolites: Exploring the Path of Dietary Prevention of Type 1 Diabetes
Theyab, A. A., Almutairi, T., Al-Suwaidi, A. M., Bendriss, G., McVeigh, C., & Châari, A. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.563605 · Cited by 22 · see citing works
The dual effect of acetate on microglial TNF-α production
de Fragas, M. G., de Oliveira, D. M., Hiyane, M. I., Braga, T. T., & Câmara, N. O. S. (2022) · Clinics · doi:10.1016/j.clinsp.2022.100062 · Cited by 21 · see citing works
Exogenous Short Chain Fatty Acid Effects in APP/PS1 Mice
Zajac, D. J., Shaw, B. C., Braun, D. J., Green, S. J., Morganti, J. M., & Estus, S. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.873549 · Cited by 21 · see citing works
Baby, N., Li, Y., Ling, E., Lu, J., & Dheen, S. T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0089326 · Cited by 21 · see citing works
Dong, B., Hou, Z., Zheng, Z., Xing, J., Zhao, N., Liu, Z., & Liu, S. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.138007 · Cited by 20 · see citing works
Viswanatha, G. L., Venkataranganna, M. V., Prasad, N. B. L., & Shylaja, H. (2018) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2018.09.018 · Cited by 20 · see citing works
Duong, M. T., Chen, Y. J., Doot, R. K., Young, A. J., Lee, H. S., Cai, J., Pilania, A., Wolk, D. A., & Nasrallah, I. M. (2021) · Nuclear Medicine Communications · doi:10.1097/mnm.0000000000001460 · Cited by 20 · see citing works
Churchward, M. A., Michaud, E. R., Mullish, B. H., Blanco, J. M., Perez, I. G., Marchesi, J. R., Xu, H., Kao, D. H., & Todd, K. G. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e16908 · Cited by 19 · see citing works
Viswanatha, G. L., Venkataranganna, M. V., & Prasad, N. B. L. (2019) · Europe PMC (PubMed Central) · doi:10.22038/ijbms.2018.30660.7389 · Cited by 18 · see citing works
Role of short chain fatty acids on astrocytes and microglia in Alzheimer's disease brain
Wtpsk, S., Burton, M., Fernando, W. M. K. T., Jayasena, V., Brennan, C. S., & Fernando, W. M. A. D. B. (2024) · International Journal of Food Science & Technology · doi:10.1111/ijfs.17380 · Cited by 17 · see citing works
Neuroprotective effects of Fructus Chebulae extracts on experimental models of cerebral ischemia
Gaire, B. P., & Kim, H. (2014) · 中医杂志:英文版 · doi:10.1016/s0254-6272(14)60057-1 · Cited by 17 · see citing works
Olajide, O. A., Velagapudi, R., Okorji, U. P., Sarker, S. D., & Fiebich, B. L. (2014) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2014.01.027 · Cited by 17 · see citing works
Funel, N., Dini, V., Janowska, A., Loggini, B., Minale, M., Grieco, F., Riccio, S., & Romanelli, M. (2020) · Mediators of Inflammation · doi:10.1155/2020/2851949 · Cited by 17 · see citing works
An altered gut microbiome in pre-eclampsia: cause or consequence
Deady, C., McCarthy, F. P., Barron, A., McCarthy, C., O’Keeffe, G. W., & O’Mahony, S. M. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1352267 · Cited by 15 · see citing works
Moriyama, M., Nishimura, Y., Kurebayashi, R., Minamihata, T., Kawabe, K., Takano, K., & Nakamura, Y. (2020) · Current Molecular Pharmacology · doi:10.2174/1874467213666200420101048 · Cited by 13 · 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 Human Microbiome—A Physiologic Perspective
Yang, X. J., Louwies, T., Mars, R. A. T., & Kashyap, P. (2024) · Comprehensive physiology · doi:10.1002/cphy.c230013 · Cited by 12 · see citing works
Felice, F., Falco, P. D., Milani, M., Castelli, S., Ragnini‐Wilson, A., Lazzarino, G., D’Ambrosi, N., Ciccarone, F., & Ciriolo, M. R. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01947-6 · Cited by 11 · see citing works
Intermittent hypoxia-induced cardiorespiratory long-term facilitation: A new role for microglia
Kim, S. J., Kim, S. J., Kakall, Z. M., Farnham, M. M. J., & Pilowsky, P. M. (2016) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2016.03.012 · Cited by 11 · see citing works
Jing, Y., Su, Z., Zhang, S., Han, Q., Wang, Z., Hu, B., Zhang, D., Sun, S., & Wu, L. (2023) · Plant Foods for Human Nutrition · doi:10.1007/s11130-023-01070-w · Cited by 11 · see citing works
Agranyoni, O., Sur, D., Amidror, S., Shidlovsky, N., Bagaev, A., Yissachar, N., Pinhasov, A., & Navon‐Venezia, S. (2024) · BMC Medicine · doi:10.1186/s12916-024-03323-0 · Cited by 11 · see citing works
The Antineuroinflammatory Effect of Simvastatin on Lipopolysaccharide Activated Microglial Cells
Zheng, X., Liao, Y. H., Wang, J., Hu, S., Rudramurthy, G. R., Swamy, M. K., Rohit, K. C., & Wang, Y. (2018) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2018/9691085 · Cited by 11 · see citing works
Ding, L., Wang, J., Qiu, S., Ren, Z., Li, Y., & An, P. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04176-7 · Cited by 10 · see citing works
Acetate Treatment Increases Fatty Acid Content in LPS‐Stimulated BV2 Microglia
Bhatt, D. P., & Rosenberger, T. A. (2014) · Lipids · doi:10.1007/s11745-014-3911-x · Cited by 10 · see citing works
Self-citationRay, P., Chakraborty, S., Ghosh, A., & Aich, P. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.08.430372 · Cited by 10 · see citing works
Souders, C. L., Zubcevic, J. A., & Martyniuk, C. J. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-021-01044-z · Cited by 9 · see citing works
Effect of melatonin on gut microbiome and metabolomics in diabetic cognitive impairment
Gao, M., Li, J., Han, X., Zhang, B., Chen, J., Lang, J., & Zhang, Q. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1489834 · Cited by 8 · see citing works
Zang, Z., Yang, F., Qu, L., Ge, M., Tong, L., Xue, L., Sun, X., & Hai, Y. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1640389 · Cited by 8 · see citing works
de Oliveira, L. I. G., Clementino, J. R., Salgaço, M. K., de Oliveira, S. P. A., Lima, M. D. S., Mesa, V., de Souza, E. L., Vinderola, C. G., Magnani, M., & Sivieri, K. (2023) · Food & Function · doi:10.1039/d3fo01156a · Cited by 8 · see citing works
Insights into host-microbe interaction: What can we do for the swine industry?
Fan, L., Liu, B., Han, Z., & Ren, W. (2020) · Animal nutrition · doi:10.1016/j.aninu.2020.10.003 · Cited by 8 · see citing works
Livshits, G., & Kalinkovich, A. (2021) · Pain Medicine · doi:10.1093/pm/pnab060 · Cited by 8 · see citing works
Gut microbiome dysregulation in noninfectious uveitis
Liu, M., Geng, J., Liu, T., & Liu, X. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1614304 · Cited by 7 · see citing works
Zhang, Y., Silang, Q., Wang, T., Wang, N., Gesang, L., Tang, L., & Liu, L. (2025) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s537129 · Cited by 7 · see citing works
Böswald, L. F., Wenderlein, J., Bachmann, M., Zeyner, A., Neuhaus, K., Schäfer, F., Imhof, A., Lahiri, S., Grützke, J., & Popper, B. (2025) · Scientific Reports · doi:10.1038/s41598-025-20986-8 · Cited by 7 · see citing works
Chauhan, V., Chauhan, N. K., Dutta, S., Pathak, D., & Nongthomba, U. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1153422 · Cited by 7 · see citing works
Exploring the Mechanisms of Gastroesophageal Reflux Disease Based on the Brain-Gut Axis Theory
Du, S., Zhang, L., Chen, Y., Zhang, Q., Chen, B., & Chen, S. (2025) · International Journal of General Medicine · doi:10.2147/ijgm.s558504 · Cited by 6 · see citing works
Mukhopadhyay, S., Ray, P., & Aich, P. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.121212 · Cited by 6 · see citing works
- Authors
- Soliman, M. L., Puig, K. L., Combs, C. K., & Rosenberger, T. A.
- Affiliations
- University of North Dakota (US)
- Corresponding author
- Rosenberger, Thad A.
- Venue
- Journal of Neurochemistry
- Publisher
- Wiley
- Published
- 2012-09-28
- Volume
- 123
- Issue
- 4
- Pages
- 555-567
- ISSN
- 0022-3042 (ISSN-L)
- 1471-4159
- PMC
- PMC3472042
- OpenAlex
- W2090091665
- Cited by
- 131
- References
- 75
- Citations by year
- 2026: 12 · 2025: 12 · 2024: 21 · 2023: 12 · 2022: 15 · 2021: 14 · 2020: 12 · 2019: 3 · 2018: 5 · 2017: 3 · 2016: 1 · 2015: 2 · 2014: 7 · 2013: 7 · 2012: 3
- FWCI
- 3.06
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Journal of Neurochemistry (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Center for Research Resources
- component of the National Institutes of Health
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- acetate, microglia, neuroinflammation, histone H3K9 acetylation, NF-κB, MAPK signaling, p38 MAPK, JNK, lipopolysaccharide, IL-1β, acetyl-CoA, histone acetylation, non-histone protein acetylation, acetate metabolism, cytokine expression, TGF-β1
- MeSH terms
- Acetates, Acetylation, Analysis of Variance, Animals, Brain, Cells, Cultured, Dose-Response Relationship, Drug, Histones, L-Lactate Dehydrogenase, Lipopolysaccharides, Lysine, Mice, Inbred C57BL, Phosphorylation, RNA, Messenger, Time Factors, Signal Transduction, Cytokines, Microglia, Mitogen-Activated Protein Kinases, Mice
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