Sodium butyrate attenuates high-fat diet-induced steatohepatitis in mice by improving gut microbiota and gastrointestinal barrier

Introducing mothur: Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities

Schloss, P. D., Westcott, S. L., Ryabin, T., Hall, J. R., Hartmann, M., Hollister, E. B., Lesniewski, R. A., Oakley, B. B., Parks, D. H., Robinson, C. J., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01541-09 · Cited by 20,966 · see citing works

Global epidemiology of nonalcoholic fatty liver disease-Meta-analytic assessment of prevalence, incidence, and outcomes

Younossi, Z. M., Koenig, A. B., Abdelatif, D., Fazel, Y., Henry, L., & Wymer, M. (2016) · Hepatology · doi:10.1002/hep.28431 · Cited by 10,781 · see citing works

A metagenome-wide association study of gut microbiota in type 2 diabetes

Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762 · see citing works

Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa

De Filippo, C., Cavalieri, D., Di Paola, M., Ramazzotti, M., Poullet, J. B., Massart, S., Collini, S., Pieraccini, G., & Lionetti, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005963107 · Cited by 5,579 · see citing works

The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism

den Besten, G., van Eunen, K., Groen, A. K., Venema, K., Reijngoud, D.-J., & Bakker, B. M. (2013) · Journal of Lipid Research · doi:10.1194/jlr.r036012 · Cited by 5,048 · see citing works

Richness of human gut microbiome correlates with metabolic markers

Le Chatelier, E., Nielsen, T., Qin, J., Prifti, E., Hildebrand, F., Falony, G., Almeida, M., Arumugam, M., Batto, J.-M., Kennedy, S., et al. (2013) · Nature · doi:10.1038/nature12506 · Cited by 4,662 · see citing works

Functional interactions between the gut microbiota and host metabolism

Tremaroli, V., & Bäckhed, F. (2012) · Nature · doi:10.1038/nature11552 · Cited by 4,387 · see citing works

Interactions Between the Microbiota and the Immune System

Hooper, L. V., Littman, D. R., & Macpherson, A. J. (2012) · Science · doi:10.1126/science.1223490 · Cited by 4,173 · see citing works

The gut microbiota--masters of host development and physiology

Sommer, F., & Bäckhed, F. (2013) · Nature Reviews Microbiology · doi:10.1038/nrmicro2974 · Cited by 3,681 · see citing works

Human Genetics Shape the Gut Microbiome

Goodrich, J. K., Waters, J. L., Poole, A. C., Sutter, J. L., Koren, O., Blekhman, R., Beaumont, M., Van Treuren, W., Knight, R., Bell, J. T., et al. (2014) · Cell · doi:10.1016/j.cell.2014.09.053 · Cited by 3,164 · see citing works

Gut metagenome in European women with normal, impaired and diabetic glucose control

Karlsson, F. H., Tremaroli, V., Nookaew, I., Bergström, G., Behre, C. J., Fagerberg, B., Nielsen, J., & Bäckhed, F. (2013) · Nature · doi:10.1038/nature12198 · Cited by 3,115 · see citing works

The gut flora as a forgotten organ

O'Hara, A. M., & Shanahan, F. (2006) · The EMBO Reports · doi:10.1038/sj.embor.7400731 · Cited by 2,791 · see citing works

Microbiota and SCFA in lean and overweight healthy subjects

Schwiertz, A., Taras, D., Schäfer, K., Beijer, S., Bos, N. A., Donus, C., & Hardt, P. D. (2010) · Obesity · doi:10.1038/oby.2009.167 · Cited by 2,457 · see citing works

Nonalcoholic Fatty Liver Disease

Rinella, M. E. (2015) · JAMA · doi:10.1001/jama.2015.5370 · Cited by 2,289 · see citing works

Butyrate improves insulin sensitivity and increases energy expenditure in mice

Gao, Z., Yin, J., Zhang, J., Ward, R. E., Martin, R. J., Lefevre, M., Cefalu, W. T., & Ye, J. (2009) · Diabetes · doi:10.2337/db08-1637 · Cited by 2,204 · see citing works

Bifidobacteria and Butyrate-Producing Colon Bacteria: Importance and Strategies for Their Stimulation in the Human Gut

Rivière, A., Selak, M., Lantin, D., Leroy, F., & Vuyst, L. D. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00979 · Cited by 1,746 · see citing works

The severity of nonalcoholic fatty liver disease is associated with gut dysbiosis and shift in the metabolic function of the gut microbiota

Boursier, J., Mueller, O., Barret, M., Machado, M., Fizanne, L., Araujo‐Perez, F., Guy, C. D., Seed, P. C., Rawls, J. F., David, L. A., et al. (2016) · Hepatology · doi:10.1002/hep.28356 · Cited by 1,483 · see citing works

Effects of targeted delivery of propionate to the human colon on appetite regulation, body weight maintenance and adiposity in overweight adults

Chambers, E. S., Viardot, A., Psichas, A., Morrison, D. J., Murphy, K. G., Zac-Varghese, S. E. K., MacDougall, K., Preston, T., Tedford, C., Finlayson, G. S., et al. (2015) · Gut · doi:10.1136/gutjnl-2014-307913 · Cited by 1,424 · see citing works

Short-chain fatty acids induce both effector and regulatory T cells by suppression of histone deacetylases and regulation of the mTOR–S6K pathway

Park, J., Kim, M., Kang, S. G., Jannasch, A. H., Cooper, B., Patterson, J., & Kim, C. H. (2015) · Mucosal Immunology · doi:10.1038/mi.2014.44 · Cited by 1,307 · see citing works

The global burden of liver disease: The major impact of China

Wang, F., Fan, J., Zhang, Z., Gao, B., & Wang, H. (2014) · Hepatology · doi:10.1002/hep.27406 · Cited by 1,258 · see citing works

Gut Microbiota and Metabolic Endotoxemia in Young Obese Mexican Subjects

Radilla-Vázquez, R. B., Parra‐Rojas, I., Martínez-Hernández, N. E., Márquez‐Sandoval, F., Illades‐Aguiar, B., & Castro-Alarcón, N. (2016) · Obesity Facts · doi:10.1159/000442479 · Cited by 1,200 · see citing works

Minireview: Gut microbiota: The neglected endocrine organ

Clarke, G., Stilling, R. M., Kennedy, P. J., Stanton, C., Cryan, J. F., & Dinan, T. G. (2014) · Molecular Endocrinology · doi:10.1210/me.2014-1108 · Cited by 1,192 · see citing works

Comparison of the Levels of Bacterial Diversity in Freshwater, Intertidal Wetland, and Marine Sediments by Using Millions of Illumina Tags

Wang, Y., Sheng, H.-F., He, Y., Wu, J.-Y., Jiang, Y., Tam, N. F. Y., & Zhou, H. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.01821-12 · Cited by 894 · see citing works

Modulation of gut microbiota during probiotic-mediated attenuation of metabolic syndrome in high fat diet-fed mice

Wang, J., Tang, H., Zhang, C., Zhao, Y., Derrien, M., Rocher, E., Vlieg, J. E. V. H., Strissel, K. J., Zhao, L., Obin, M. S., et al. (2014) · The ISME Journal · doi:10.1038/ismej.2014.99 · Cited by 833 · see citing works

From the gut to the peripheral tissues: the multiple effects of butyrate

Guilloteau, P., Martin, L., Eeckhaut, V., Ducatelle, R., Zabielski, R., & Immerseel, F. V. (2010) · Nutrition Research Reviews · doi:10.1017/s0954422410000247 · Cited by 813 · see citing works

Gut microbiota-derived short-chain Fatty acids, T cells, and inflammation

Kim, C. H., Park, J., & Kim, M. (2014) · Immune Network · doi:10.4110/in.2014.14.6.277 · Cited by 704 · see citing works

Fecal Microbiome and Volatile Organic Compound Metabolome in Obese Humans With Nonalcoholic Fatty Liver Disease

Raman, M., Ahmed, I., Gillevet, P. M., Probert, C. S., Ratcliffe, N. M., Smith, S., Greenwood, R., Sikaroodi, M., Lam, V., Crotty, P., et al. (2013) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2013.02.015 · Cited by 672 · see citing works

Insights into the role of the microbiome in obesity and type 2 diabetes

Hartstra, A. V., Bouter, K. E. C., Bäckhed, F., & Nieuwdorp, M. (2015) · Diabetes Care · doi:10.2337/dc14-0769 · Cited by 641 · see citing works

Lactobacillus rhamnosus GG-supplemented formula expands butyrate-producing bacterial strains in food allergic infants

Canani, R. B., Sangwan, N., Stefka, A. T., Nocerino, R., Paparo, L., Aitoro, R., Calignano, A., Khan, A. A., Gilbert, J. A., & Nagler‐Anderson, C. (2015) · The ISME Journal · doi:10.1038/ismej.2015.151 · Cited by 525 · see citing works

A microbiota signature associated with experimental food allergy promotes allergic sensitization and anaphylaxis

Rivas, M. N., Burton, O. T., Wise, P. M., Zhang, Y., Hobson, S. A., Lloret, M. G., Chehoud, C., Kuczynski, J., DeSantis, T. Z., Warrington, J. A., et al. (2012) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.10.026 · Cited by 488 · see citing works

A phylo-functional core of gut microbiota in healthy young Chinese cohorts across lifestyles, geography and ethnicities

Zhang, J., Guo, Z., Xue, Z., Sun, Z., Zhang, M., Wang, L., Wang, G., Wang, F., Xu, J., Cao, H., et al. (2015) · The ISME Journal · doi:10.1038/ismej.2015.11 · Cited by 459 · see citing works

Microbial butyrate and its role for barrier function in the gastrointestinal tract

Plöger, S., Stumpff, F., Penner, G. B., Schulzke, J., Gäbel, G., Märtens, H., Shen, Z., Günzel, D., & Aschenbach, J. R. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06553.x · Cited by 445 · see citing works

Role of the Microbiome in Energy Regulation and Metabolism

Nieuwdorp, M., Gilijamse, P. W., Pai, N., & Kaplan, L. M. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.02.008 · Cited by 421 · see citing works

Illumina Sequencing of 16S rRNA Tag Revealed Spatial Variations of Bacterial Communities in a Mangrove Wetland

Jiang, X.-T., Peng, X., Deng, G.-H., Sheng, H., Wang, Y., Zhou, H.-W., & Tam, N. (2013) · Microbial Ecology · doi:10.1007/s00248-013-0238-8 · Cited by 366 · see citing works

Butyrate

Leonel, A. J., & Alvarez-Leite, J. I. (2012) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e32835665fa · Cited by 362 · see citing works

Molecular mechanisms of NF-κB activation induced by bacterial lipopolysaccharide through Toll-like receptors:

Zhang, G.-L., & Ghosh, S. (2000) · Journal of Endotoxin Research · doi:10.1179/096805100101532414 · Cited by 307 · see citing works

SCFAs Induce Mouse Neutrophil Chemotaxis through the GPR43 Receptor

Vinolo, M. A. R., Ferguson, G. J., Kulkarni, S., Damoulakis, G., Anderson, K. E., Bohlooly‐Y, M., Stephens, L., Hawkins, P. T., & Curi, R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021205 · Cited by 292 · see citing works

Importance of changes in adipose tissue insulin resistance to histological response during thiazolidinedione treatment of patients with nonalcoholic steatohepatitis

Gastaldelli, A., Harrison, S. A., Belfort-Aguilar, R., Hardies, L. J., Balas, B., Schenker, S., & Cusi, K. (2009) · Hepatology · doi:10.1002/hep.23116 · Cited by 285 · see citing works

Anti-inflammatory effects of short chain fatty acids in IFN-γ-stimulated RAW 264.7 murine macrophage cells: Involvement of NF-κB and ERK signaling pathways

Park, J.-S., Lee, E.-J., Lee, J.-C., Kim, W.-K., & Kim, H.-S. (2007) · International Immunopharmacology · doi:10.1016/j.intimp.2006.08.015 · Cited by 278 · see citing works

Guidelines for the diagnosis and management of nonalcoholic fatty liver disease: Update 2010

Fan, J., Jia, J. D., Li, Y. M., Wang, B. Y., Lu, L., Shi, J., & Chan, L.-Y. (2010) · Journal of Digestive Diseases · doi:10.1111/j.1751-2980.2010.00476.x · Cited by 277 · see citing works

Butyrate affects differentiation, maturation and function of human monocyte-derived dendritic cells and macrophages

MILLARD, A. L., MERTES, P. M., ITTELET, D., VILLARD, F., JEANNESSON, P., & BERNARD, J. (2002) · Clinical and Experimental Immunology · doi:10.1046/j.0009-9104.2002.01977.x · Cited by 220 · see citing works

Guidelines for the diagnosis and management of alcoholic liver disease: Update 2010

Li, Y. M., Fan, J., Wang, B. Y., Lu, L., Shi, J., Niu, J. Q., & Wei, S. H. E. N. (2010) · Journal of Digestive Diseases · doi:10.1111/j.1751-2980.2010.00477.x · Cited by 219 · see citing works

Effects of Sodium Butyrate and Its Synthetic Amide Derivative on Liver Inflammation and Glucose Tolerance in an Animal Model of Steatosis Induced by High Fat Diet

Raso, G. M., Simeoli, R., Russo, R., Iacono, A., Santoro, A. N., Paciello, O., Ferrante, M. C., Canani, R. B., Calignano, A., & Meli, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068626 · Cited by 196 · see citing works

Sodium butyrate maintains growth performance by regulating the immune response in broiler chickens

Zhang, W. H., Jiang, Y., Zhu, Q., Gao, F., Dai, S., Chen, J., & Zhou, G. (2011) · British Poultry Science · doi:10.1080/00071668.2011.578121 · Cited by 188 · see citing works

Sodium butyrate epigenetically modulates high‐fat diet‐induced skeletal muscle mitochondrial adaptation, obesity and insulin resistance through nucleosome positioning

Henagan, T. M., Stefañska, B., Fang, Z., Navard, A. M., Ye, J., Lenard, N. R., & Devarshi, P. P. (2015) · British Journal of Pharmacology · doi:10.1111/bph.13058 · Cited by 172 · see citing works

Histone Deacetylase Inhibitors Up-Regulate the Expression of Tight Junction Proteins

Bordin, M., D'Atri, F., Guillemot, L., & Citi, S. (2004) · Molecular Cancer Research · doi:10.1158/1541-7786.692.2.12 · Cited by 168 · see citing works

Obesity: An overview of possible role(s) of gut hormones, lipid sensing and gut microbiota

Mishra, A. K., Dubey, V., & Ghosh, A. R. (2016) · Metabolism · doi:10.1016/j.metabol.2015.10.008 · Cited by 161 · see citing works

Supplementation of sodium butyrate protects mice from the development of non-alcoholic steatohepatitis (NASH)

Jin, C. J., Sellmann, C., Engstler, A. J., Ziegenhardt, D., & Bergheim, I. (2015) · British Journal Of Nutrition · doi:10.1017/s0007114515003621 · Cited by 130 · see citing works

Mechanism of Butyrate Stimulation of Triglyceride Storage and Adipokine Expression during Adipogenic Differentiation of Porcine Stromovascular Cells

Yan, H., & Ajuwon, K. M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0145940 · Cited by 90 · see citing works

Establishing a causal link between gut microbes, body weight gain and glucose metabolism in humans – towards treatment with probiotics

Stenman, L. K., Burcelin, R., & Lahtinen, S. J. (2015) · Beneficial Microbes · doi:10.3920/bm2015.0069 · Cited by 78 · see citing works

Gut microbiota and non-alcoholic fatty liver disease

Gkolfakis, P., Dimitriadis, G., & Τriantafyllou, Κ. (2015) · Hepatobiliary & pancreatic diseases international · doi:10.1016/s1499-3872(15)60026-1 · Cited by 78 · see citing works

Lactobacillus acidophilus counteracts enteropathogenic E. coli-induced inhibition of butyrate uptake in intestinal epithelial cells

Kumar, A., Alrefai, W. A., Borthakur, A., & Dudeja, P. K. (2015) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00186.2015 · Cited by 72 · see citing works

Butyrate enhances antibacterial effects while suppressing other features of alternative activation in IL-4-induced macrophages

Fernando, M., Saxena, A., Reyes, J. L., & McKay, D. M. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00440.2015 · Cited by 67 · see citing works

The Role of Probiotics on the Microbiota

Nova, E., de Heredia, F. P., Gómez‐Martínez, S., & Marcos, A. (2016) · Nutrition in Clinical Practice · doi:10.1177/0884533615620350 · Cited by 65 · see citing works

Gut microbiota and non-alcoholic fatty liver disease

Paraskevas, Gkolfakis, George, Dimitriadis, Κωνσταντίνος, & Triantafyllou (2015) · Acta Scientiarum Naturalium Universitatis Sunyatseni · Cited by 47 · see citing works

Effects of Sodium Butyrate on the Intestinal Morphology and DNA-Binding Activity of Intestinal Nuclear Factor-κB in Weanling Pigs

Lu, J., Wen, Z., & Zou, X. (2012) · Journal of Animal and Veterinary Advances · doi:10.3923/javaa.2012.814.821 · Cited by 30 · see citing works

Short chain fatty acids in human gut and metabolic health

Blaak, E. E., Canfora, E. E., Theis, S., Frost, G., Groen, A. K., Mithieux, G., Nauta, A., Scott, K., Stahl, B., van Harsselaar, J., et al. (2020) · Beneficial Microbes · doi:10.3920/bm2020.0057 · Cited by 1,103 · see citing works

Short-chain fatty acids in diseases

Zhang, D., Jian, Y., Zhang, Y., Li, Y., Gu, L.-T., Sun, H.-H., Liu, M., Zhou, H., Wang, Y., & Xu, Z. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01219-9 · Cited by 763 · see citing works

Role of gut microbiota-generated short-chain fatty acids in metabolic and cardiovascular health

Chambers, E. S., Preston, T., Frost, G., & Morrison, D. J. (2018) · Current Nutrition Reports · doi:10.1007/s13668-018-0248-8 · Cited by 691 · see citing works

The role of the microbiome in NAFLD and NASH

Kolodziejczyk, A. A., Zheng, D., Shibolet, O., & Elinav, E. (2019) · EMBO Molecular Medicine · doi:10.15252/emmm.201809302 · Cited by 523 · see citing works

Effects and Mechanisms of Probiotics, Prebiotics, Synbiotics, and Postbiotics on Metabolic Diseases Targeting Gut Microbiota: A Narrative Review

Li, H., Zhou, D.-D., Gan, R., Huang, S., Zhao, C., Shang, A., Xu, X., & Li, H. (2021) · Nutrients · doi:10.3390/nu13093211 · Cited by 514 · see citing works

Contribution of the Intestinal Microbiome and Gut Barrier to Hepatic Disorders

Chopyk, D. M., & Grakoui, A. (2020) · Gastroenterology · doi:10.1053/j.gastro.2020.04.077 · Cited by 495 · see citing works

Role of the gut microbiota in type 2 diabetes and related diseases

Yang, G., Wei, J., Liu, P., Zhang, Q., Tian, Y., Hou, G., Meng, L., Xin, Y., & Jiang, X. (2021) · Metabolism · doi:10.1016/j.metabol.2021.154712 · Cited by 418 · see citing works

The Role of Short Chain Fatty Acids in Inflammation and Body Health

Du, Y., He, C., An, Y., Huang, Y., Zhang, H., Fu, W., Wang, M., Shan, Z., Xie, J., Yang, Y., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25137379 · Cited by 411 · see citing works

Short-Chain Fatty Acids and Human Health: From Metabolic Pathways to Current Therapeutic Implications

Facchin, S., Bertin, L., Bonazzi, E., Lorenzon, G., Barba, C. D., Barberio, B., Zingone, F., Maniero, D., Scarpa, M., Ruffolo, C., et al. (2024) · Life · doi:10.3390/life14050559 · Cited by 422 · see citing works

Targeted therapeutics and novel signaling pathways in non-alcohol-associated fatty liver/steatohepatitis (NAFL/NASH)

Xu, X., Poulsen, K. L., Wu, L., Liu, S., Miyata, T., Song, Q., Wei, Q., Zhao, C., Lin, C., & Yang, J. B. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01119-3 · Cited by 370 · see citing works

Gut Microbiota Metabolites in NAFLD Pathogenesis and Therapeutic Implications

Chen, J., & Vitetta, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155214 · Cited by 357 · see citing works

Indole-3-propionic acid inhibits gut dysbiosis and endotoxin leakage to attenuate steatohepatitis in rats

Zhao, Z., Xin, F., Xue, Y., Hu, Z., Han, Y., Ma, F., Zhou, D., Liu, X., Cui, A., Liu, Z., et al. (2019) · Experimental & Molecular Medicine · doi:10.1038/s12276-019-0304-5 · Cited by 353 · see citing works

Lean NAFLD: A Distinct Entity Shaped by Differential Metabolic Adaptation

Chen, F., Esmaili, S., Rogers, G. B., Bugianesi, E., Petta, S., Marchesini, G., Bayoumi, A., Metwally, M., Azardaryany, M. K., Coulter, S., et al. (2019) · Hepatology · doi:10.1002/hep.30908 · Cited by 330 · see citing works

Biological Function of Short-Chain Fatty Acids and Its Regulation on Intestinal Health of Poultry

Liu, L., Li, Q., Yang, Y., & Guo, A. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.736739 · Cited by 318 · see citing works

Dietary fructose-induced gut dysbiosis promotes mouse hippocampal neuroinflammation: a benefit of short-chain fatty acids

Li, J.-M., Yu, R., Zhang, L.-P., Wen, S.-Y., Wang, S.-J., Zhang, X.-Y., Xu, Q., & Kong, L.-D. (2019) · Microbiome · doi:10.1186/s40168-019-0713-7 · Cited by 300 · see citing works

Gut Microbiota Mediates the Protective Effects of Dietary Capsaicin against Chronic Low-Grade Inflammation and Associated Obesity Induced by High-Fat Diet

Kang, C., Wang, B., Kaliannan, K., Wang, X., Lang, H., Hui, S., Huang, L., Zhang, Y., Zhou, M., Chen, M., et al. (2017) · mBio · doi:10.1128/mbio.00470-17 · Cited by 273 · see citing works

The Protective Role of Butyrate against Obesity and Obesity-Related Diseases

Coppola, S., Avagliano, C., Calignano, A., & Canani, R. B. (2021) · Molecules · doi:10.3390/molecules26030682 · Cited by 267 · see citing works

Lactobacillus and intestinal diseases: Mechanisms of action and clinical applications

Huang, R., Wu, F. L., Zhou, Q., Wei, W., Juan, Y., Xiao, B., & Luo, Z. (2022) · Microbiological Research · doi:10.1016/j.micres.2022.127019 · Cited by 258 · see citing works

Role of gut microbiota on intestinal barrier function in acute pancreatitis

Li, X.-Y., He, C., Zhu, Y., & Lü, N. (2020) · World Journal of Gastroenterology · doi:10.3748/wjg.v26.i18.2187 · Cited by 251 · see citing works

Gut Microbiota-Derived Components and Metabolites in the Progression of Non-Alcoholic Fatty Liver Disease (NAFLD)

Ji, Y. S., Yin, Y., Li, Z., & Zhang, W. (2019) · Nutrients · doi:10.3390/nu11081712 · Cited by 230 · see citing works

Sodium butyrate reduces high-fat diet-induced non-alcoholic steatohepatitis through upregulation of hepatic GLP-1R expression

Zhou, D., Chen, Y., Zhao, Z., Yang, R., Xin, F., Liu, X., Pan, Q., Zhou, H., & Fan, J. (2018) · Experimental & Molecular Medicine · doi:10.1038/s12276-018-0183-1 · Cited by 218 · see citing works

Prebiotic Inulin and Sodium Butyrate Attenuate Obesity-Induced Intestinal Barrier Dysfunction by Induction of Antimicrobial Peptides

Beisner, J., Rosa, L. F., Kaden-Volynets, V., Stolzer, I., Günther, C., & Bischoff, S. C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.678360 · Cited by 215 · see citing works

Butyrate Protects Mice Against Methionine–Choline-Deficient Diet-Induced Non-alcoholic Steatohepatitis by Improving Gut Barrier Function, Attenuating Inflammation and Reducing Endotoxin Levels

Ye, J., Lv, L., Wu, W., Li, Y., Shi, D., Fang, D., Guo, F., Jiang, H., Ren, Y., Ye, W., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01967 · Cited by 211 · see citing works

Gut Microbiota and Nonalcoholic Fatty Liver Disease: Insights on Mechanisms and Therapy

Ma, J., Zhou, Q., & Li, H. (2017) · Nutrients · doi:10.3390/nu9101124 · Cited by 197 · see citing works

Fructose: A Dietary Sugar in Crosstalk with Microbiota Contributing to the Development and Progression of Non-Alcoholic Liver Disease

Lambertz, J., Weiskirchen, S., Landert, S., & Weiskirchen, R. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01159 · Cited by 184 · see citing works

Metformin attenuated sepsis-related liver injury by modulating gut microbiota

Liang, H., Song, H., Zhang, X., Song, G., Wang, Y., Ding, X., Duan, X., Li, L., Sun, T., & Kan, Q. (2022) · Emerging Microbes & Infections · doi:10.1080/22221751.2022.2045876 · Cited by 175 · see citing works

Comparison of Fecal Collection Methods for Microbiome and Metabolomics Studies

Wang, Z., Zolnik, C. P., Qiu, Y., Usyk, M., Wang, T., Strickler, H. D., Isasi, C. R., Kaplan, R. C., Kurland, I. J., Qi, Q., et al. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00301 · Cited by 166 · see citing works

Infectious Threats, the Intestinal Barrier, and Its Trojan Horse: Dysbiosis

Iacob, S. A., & Iacob, D. G. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01676 · Cited by 152 · see citing works

Butyrate to combat obesity and obesity‐associated metabolic disorders: Current status and future implications for therapeutic use

van Deuren, T., Blaak, E. E., & Canfora, E. E. (2022) · Obesity Reviews · doi:10.1111/obr.13498 · Cited by 162 · see citing works

Indole-3-carbinol prevents colitis and associated microbial dysbiosis in an IL-22–dependent manner

Busbee, P. B., Menzel, L. P., Alrafas, H. R., Dopkins, N., Becker, W., Miranda, K., Tang, C., Chatterjee, S., Singh, U. P., Nagarkatti, M., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.127551 · Cited by 153 · see citing works

Possible Benefits of Faecalibacterium prausnitzii for Obesity-Associated Gut Disorders

Maioli, T. U., Nogués, E. B., Torres, L., Barbosa, S. C., Martins, V. D., Langella, P., Azevedo, V., & Chatel, J. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.740636 · Cited by 151 · see citing works

Short-Chain Fatty Acids—A Product of the Microbiome and Its Participation in Two-Way Communication on the Microbiome-Host Mammal Line

Lange, O., Proczko-Stepaniak, M., & Mika, A. (2023) · Current Obesity Reports · doi:10.1007/s13679-023-00503-6 · Cited by 155 · see citing works

Modulation of the Gut Microbiota in Rats by Hugan Qingzhi Tablets during the Treatment of High‐Fat‐Diet‐Induced Nonalcoholic Fatty Liver Disease

Tang, W., Yao, X., Xia, F., Yang, M., Chen, Z., Zhou, B., & Liu, Q. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/7261619 · Cited by 148 · see citing works

Microbiota-derived butyrate regulates intestinal inflammation: Focus on inflammatory bowel disease

Couto, M. R., Gonçalves, P., Magro, F., & Martel, F. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.104947 · Cited by 148 · see citing works

Resveratrol attenuates high-fat diet-induced non-alcoholic steatohepatitis by maintaining gut barrier integrity and inhibiting gut inflammation through regulation of the endocannabinoid system

Chen, M., Hou, P., Zhou, M., Ren, Q., Wang, X., Huang, L., Hui, S., Yi, L., & Mi, M. (2019) · Clinical Nutrition · doi:10.1016/j.clnu.2019.05.020 · Cited by 148 · see citing works

Activation of a Specific Gut Bacteroides-Folate-Liver Axis Benefits for the Alleviation of Nonalcoholic Hepatic Steatosis

Qiao, S., Li, B., Wang, K., Sun, S., Liao, M., Liu, C., Zhou, N., Ma, K., Zhang, Y., Chen, Y., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108005 · Cited by 147 · see citing works

Dietary sodium butyrate improves intestinal development and function by modulating the microbial community in broilers

Wu, W., Xiao, Z., An, W., Dong, Y., & Zhang, B. (2018) · PLoS ONE · doi:10.1371/journal.pone.0197762 · Cited by 146 · see citing works

The Role of Gut–Liver Axis in Gut Microbiome Dysbiosis Associated NAFLD and NAFLD-HCC

Song, Q., & Zhang, X. (2022) · Biomedicines · doi:10.3390/biomedicines10030524 · Cited by 147 · see citing works

The polysaccharides from the fruits of Lycium barbarum L. confer anti-diabetic effect by regulating gut microbiota and intestinal barrier

Zhou, W., Yang, T., Xu, W., Huang, Y., Ran, L., Yan, Y., Mi, J., Lu, L., Sun, Y., Zeng, X., et al. (2022) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2022.119626 · Cited by 148 · see citing works

The Role of Probiotics in Nonalcoholic Fatty Liver Disease: A New Insight into Therapeutic Strategies

Meroni, M., Longo, M., & Dongiovanni, P. (2019) · Nutrients · doi:10.3390/nu11112642 · Cited by 146 · see citing works

Butyrate as a bioactive human milk protective component against food allergy

Paparo, L., Nocerino, R., Ciaglia, E., Scala, C. D., Caro, C. D., Russo, R., Trinchese, G., Aitoro, R., Amoroso, A., Bruno, C., et al. (2020) · Allergy · doi:10.1111/all.14625 · Cited by 140 · see citing works

Mitotherapy for Fatty Liver by Intravenous Administration of Exogenous Mitochondria in Male Mice

Fu, A., Shi, X., Zhang, H., & Fu, B. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00241 · Cited by 139 · see citing works

Intestinal dysbiosis in nonalcoholic fatty liver disease (NAFLD): focusing on the gut–liver axis

Han, H. L., Jiang, Y., Wang, M., Melaku, M., Liu, L., Zhao, Y. M., Everaert, N., Yi, B., & Zhang, H. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1966738 · Cited by 130 · see citing works

Colon Carcinogenesis: The Interplay Between Diet and Gut Microbiota

Loke, Y. L., Chew, M. T., Ngeow, Y. F., Lim, W. W.-D., & Peh, S. C. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.603086 · Cited by 129 · see citing works

Butyrate ameliorated ferroptosis in ulcerative colitis through modulating Nrf2/GPX4 signal pathway and improving intestinal barrier

Chen, H., Qian, Y., Jiang, C., Tang, L., Yu, J., Zhang, L., Dai, Y., & Jiang, G. Z. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166984 · Cited by 127 · see citing works

Understanding the Effects of Gut Microbiota Dysbiosis on Nonalcoholic Fatty Liver Disease and the Possible Probiotics Role: Recent Updates

Khan, A., Ding, Z., Ishaq, M. H., Bacha, A. S., KHAN, I. A., Hanif, A., Li, W., & Guo, X. (2021) · International Journal of Biological Sciences · doi:10.7150/ijbs.56214 · Cited by 126 · see citing works

Correlations between α-Linolenic Acid-Improved Multitissue Homeostasis and Gut Microbiota in Mice Fed a High-Fat Diet

Gao, X., Chang, S., Liu, S., Peng, L., Xie, J., Dong, W., Tian, Y., & Sheng, J. (2020) · mSystems · doi:10.1128/msystems.00391-20 · Cited by 120 · see citing works

Sodium Butyrate Supplementation Inhibits Hepatic Steatosis by Stimulating Liver Kinase B1 and Insulin-Induced Gene

Zhao, Z., Wang, Z., Zhou, D., Han, Y., Ma, F., Hu, Z., Xin, F., Liu, X., Ren, T., Zhang, F., et al. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.05.006 · Cited by 112 · see citing works

A bridge for short-chain fatty acids to affect inflammatory bowel disease, type 1 diabetes, and non-alcoholic fatty liver disease positively: by changing gut barrier

Liu, W., Luo, X., Tang, J., Mo, Q., Zhong, H., Zhang, H., & Feng, F. (2020) · European Journal of Nutrition · doi:10.1007/s00394-020-02431-w · Cited by 111 · see citing works

Sodium Butyrate Ameliorates High-Fat-Diet-Induced Non-alcoholic Fatty Liver Disease through Peroxisome Proliferator-Activated Receptor α-Mediated Activation of β Oxidation and Suppression of Inflammation

Sun, B., Jia, Y., Hong, J., Sun, Q., Gao, S., Hu, Y., Zhao, N., & Zhao, R. (2018) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.8b01189 · Cited by 106 · see citing works

Enhancing intestinal barrier efficiency: A novel metabolic diseases therapy

Zhang, Y., Xiao, Z., Yu, X., Novák, P., Gui, Q., & Yin, K. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1120168 · Cited by 110 · see citing works

Dietary butyrate suppresses inflammation through modulating gut microbiota in high-fat diet-fed mice

Zhai, S., Qin, S., Li, L., Zhu, L., Zou, Z., & Wang, L. (2019) · FEMS Microbiology Letters · doi:10.1093/femsle/fnz153 · Cited by 101 · see citing works

Age- and diet-specific effects of chronic exposure to chlorpyrifos on hormones, inflammation and gut microbiota in rats

Li, J., Fang, B., Pang, G., Zhang, M., & Ren, F. (2019) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2019.05.018 · Cited by 104 · see citing works

Whole food-based approaches to modulating gut microbiota and associated diseases

Han, Y., & Xiao, H. (2020) · Annual Review of Food Science and Technology · doi:10.1146/annurev-food-111519-014337 · Cited by 101 · see citing works

Lactobacillus plantarum ZY08 relieves chronic alcohol-induced hepatic steatosis and liver injury in mice via restoring intestinal flora homeostasis

Ding, Q., Cao, F., Lai, S., Zhuge, H., Chang, K., Valencak, T. G., Liu, J., Li, S., & Ren, D. (2022) · Food Research International · doi:10.1016/j.foodres.2022.111259 · Cited by 101 · see citing works

Sodium butyrate in both prevention and supportive treatment of colorectal cancer

Kaźmierczak-Siedlecka, K., Marano, L., Merola, E., Roviello, F., & Połom, K. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.1023806 · Cited by 106 · see citing works

Microbial Metabolites: Critical Regulators in NAFLD

Dai, X., Hou, H., Zhang, W., Liu, T., Li, Y., Wang, S., Wang, B., & Cao, H. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.567654 · Cited by 102 · see citing works

Capsaicin and Gut Microbiota in Health and Disease

Roşca, A. E., Ieșanu, M. I., Zahiu, C. D. M., Voiculescu, S. E., Paslaru, A. C., & Zăgrean, A. (2020) · Molecules · doi:10.3390/molecules25235681 · Cited by 102 · see citing works

Effects of a multispecies synbiotic on glucose metabolism, lipid marker, gut microbiome composition, gut permeability, and quality of life in diabesity: a randomized, double-blind, placebo-controlled pilot study

Horvath, A., Leber, B., Feldbacher, N., Tripolt, N. J., Rainer, F., Blesl, A., Trieb, M., Marsche, G., Sourij, H., & Stadlbauer, V. (2019) · European Journal of Nutrition · doi:10.1007/s00394-019-02135-w · Cited by 99 · see citing works

Microbial metabolites in non-alcoholic fatty liver disease

Zhou, D., & Fan, J. (2019) · World Journal of Gastroenterology · doi:10.3748/wjg.v25.i17.2019 · Cited by 94 · see citing works

Liraglutide modulates gut microbiome and attenuates nonalcoholic fatty liver in db/db mice

Liu, Q., Cai, B.-Y., Zhu, L., Xin, X., Wang, X., An, Z., Li, S., Hu, Y., & Feng, Q. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118457 · Cited by 92 · see citing works

Overview of the Importance of Biotics in Gut Barrier Integrity

Kocot, A. M., Jarocka‐Cyrta, E., & Drabińska, N. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052896 · Cited by 95 · see citing works

Recent advances and potentiality of postbiotics in the food industry: Composition, inactivation methods, current applications in metabolic syndrome, and future trends

Zhong, Y., Wang, T., Luo, R., Liu, J., Jin, R., & Peng, X. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2158174 · Cited by 96 · see citing works

The Therapeutic Effect of SCFA-Mediated Regulation of the Intestinal Environment on Obesity

You, H., Tan, Y., Yu, D., Qiu, S., Bai, Y., He, J., Cao, H., Che, Q., Guo, J., & Su, Z. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.886902 · Cited by 93 · see citing works

SIRT3 Deficiency Promotes High‐Fat Diet‐Induced Nonalcoholic Fatty Liver Disease in Correlation with Impaired Intestinal Permeability through Gut Microbial Dysbiosis

Chen, M., Hui, S., Lang, H., Zhou, M., Zhang, Y., Kang, C., Zeng, X., Zhang, Q., Yi, L., & Mi, M. (2018) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201800612 · Cited by 85 · see citing works

Maternal sucralose intake alters gut microbiota of offspring and exacerbates hepatic steatosis in adulthood

Dai, X., Guo, Z., Chen, D., Li, L., Song, X., Liu, T., Jin, G., Li, Y., Liu, Y., Ajiguli, A., et al. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1738187 · Cited by 87 · see citing works

Rosmarinic Acid Restores Colonic Mucus Secretion in Colitis Mice by Regulating Gut Microbiota-Derived Metabolites and the Activation of Inflammasomes

Wang, Q., Xu, K., Cai, X., Wang, C., Cao, Y., & Xiao, J. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c08444 · Cited by 87 · see citing works

Butyrate: A potential mediator of obesity and microbiome via different mechanisms of actions

Güler, M. S., Arslan, S., Ağagündüz, D., Cerqua, I., Pagano, E., Canani, R. B., & Capasso, R. (2024) · Food Research International · doi:10.1016/j.foodres.2024.115420 · Cited by 87 · see citing works

Intestinal environmental disorders associate with the tissue damages induced by perfluorooctane sulfonate exposure

Wang, G., Sun, S., Wu, X., Yang, S., Wu, Y., Zhao, J., Zhang, H., & Chen, W. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.110590 · Cited by 84 · see citing works

New insights in gut microbiota and mucosal immunity of the small intestine

Million, M., Tomas, J., Wagner, C., Lelouard, H., Raoult, D., & Gorvel, J. (2018) · Human Microbiome Journal · doi:10.1016/j.humic.2018.01.004 · Cited by 83 · see citing works

Molecular and Pathophysiological Links between Metabolic Disorders and Inflammatory Bowel Diseases

Hyun, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179139 · Cited by 84 · see citing works

Neuroprotective Effects of Sodium Butyrate by Restoring Gut Microbiota and Inhibiting TLR4 Signaling in Mice with MPTP-Induced Parkinson’s Disease

Guo, T.-T., Zhang, Z., Sun, Y., Zhu, R.-Y., Wang, F.-X., Ma, L.-J., Jiang, L., & Liu, H.-D. (2023) · Nutrients · doi:10.3390/nu15040930 · Cited by 82 · see citing works

A double‐edged sword: Role of butyrate in the oral cavity and the gut

Guan, X., Li, W., & Meng, H. (2020) · Molecular Oral Microbiology · doi:10.1111/omi.12322 · Cited by 79 · see citing works

Butyrate prevents valproate‐induced liver injury: In vitro and in vivo evidence

Pirozzi, C., Lama, A., Annunziata, C., Cavaliere, G., Caro, C. D., Citraro, R., Russo, E., Tallarico, M., Iannone, M., Ferrante, M. C., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201900927rr · Cited by 77 · see citing works

Advances in the Involvement of Gut Microbiota in Pathophysiology of NAFLD

Jiang, X., Zheng, J., Zhang, S., Wang, B., Wu, C., & Guo, X. (2020) · Frontiers in Medicine · doi:10.3389/fmed.2020.00361 · Cited by 79 · see citing works

Removal of the cecum affects intestinal fermentation, enteric bacterial community structure, and acute colitis in mice

Brown, K., Abbott, D., Uwiera, R., & Inglis, G. (2018) · Gut microbes · doi:10.1080/19490976.2017.1408763 · Cited by 66 · see citing works

Escherichia fergusonii Promotes Nonobese Nonalcoholic Fatty Liver Disease by Interfering With Host Hepatic Lipid Metabolism Through Its Own msRNA 23487

Xin, F., Zhao, Z., Liu, X., Pan, Q., Wang, Z., Zeng, L., Zhang, Q., Ye, L., Wang, M., Zhang, R.-N., et al. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.12.003 · Cited by 76 · see citing works

Butyrate and obesity: Current research status and future prospect

Peng, K., Dong, W., Luo, T., Tang, H., Zhu, W., Huang, Y., & Yang, X. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1098881 · Cited by 80 · see citing works

Non-estrogenic Xanthohumol Derivatives Mitigate Insulin Resistance and Cognitive Impairment in High-Fat Diet-induced Obese Mice

Miranda, C. L., Johnson, L. A., de Montgolfier, O., Elias, V. D., Ullrich, L. S., Hay, J. J., Paraiso, I. L., Choi, J., Reed, R. L., Revel, J. S., et al. (2018) · Scientific Reports · doi:10.1038/s41598-017-18992-6 · Cited by 74 · see citing works

Geniposide and Chlorogenic Acid Combination Ameliorates Non-alcoholic Steatohepatitis Involving the Protection on the Gut Barrier Function in Mouse Induced by High-Fat Diet

Peng, J., Leng, J., Tian, H., Yang, T., Fang, Y., Feng, Q., Zhao, Y., & Hu, Y. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01399 · Cited by 75 · see citing works

Dietary Fiber from Oat and Rye Brans Ameliorate Western Diet–Induced Body Weight Gain and Hepatic Inflammation by the Modulation of Short‐Chain Fatty Acids, Bile Acids, and Tryptophan Metabolism

Kundi, Z. M., Lee, J. C., Pihlajamäki, J., Chan, C. B., Leung, K. S., So, S. S. Y., Nordlund, E., Kolehmainen, M., & El-Nezami, H. S. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201900580 · Cited by 74 · see citing works

High-Fat Diet Alters the Intestinal Microbiota in Streptozotocin-Induced Type 2 Diabetic Mice

Liu, S., Qin, P., & Wang, J. (2019) · Microorganisms · doi:10.3390/microorganisms7060176 · Cited by 77 · see citing works

Fecal Transplantation from db/db Mice Treated with Sodium Butyrate Attenuates Ischemic Stroke Injury

Wang, H., Song, W., Wu, Q., Gao, X., Li, J., Tan, C., Zhou, H., Zhu, J., He, Y., & Yin, J. (2021) · Microbiology Spectrum · doi:10.1128/spectrum.00042-21 · Cited by 75 · see citing works

Gut Microbiota, Glucose, Lipid, and Water-Electrolyte Metabolism in Children With Nonalcoholic Fatty Liver Disease

Pan, X., Kaminga, A. C., Liu, A., Wen, S. W., Luo, M., & Luo, J. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.683743 · Cited by 68 · see citing works

The effect of increasing intestinal short‐chain fatty acid concentration on gut permeability and liver injury in the context of liver disease: A systematic review

Pohl, K., Moodley, P., & Dhanda, A. (2022) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.15899 · Cited by 70 · see citing works

Microbiota-derived short-chain fatty acids and modulation of host-derived peptides formation: Focused on host defense peptides

Liu, T., Sun, Z., Yang, Z., & Qiao, X. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114586 · Cited by 67 · see citing works

The Role of Fatty Acids in Non-Alcoholic Fatty Liver Disease Progression: An Update

Hliwa, A., Ramos‐Molina, B., Łaski, D., Mika, A., & Śledziński, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136900 · Cited by 66 · see citing works

Sodium butyrate supplementation in high-soybean meal diets for juvenile rice field eel (Monopterus albus): Effects on growth, immune response and intestinal health

Zhang, J., Zhong, L., Chi, S., Chu, W., Liu, Y., & Hu, Y. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.734952 · Cited by 66 · see citing works

Connecting the Dots Between Inflammatory Bowel Disease and Metabolic Syndrome: A Focus on Gut-Derived Metabolites

Verdugo‐Meza, A., Ye, J., Dadlani, H., Ghosh, S., & Gibson, D. L. (2020) · Nutrients · doi:10.3390/nu12051434 · Cited by 69 · see citing works

Role of Dietary Lipids in Modulating Inflammation through the Gut Microbiota

Wisniewski, P. J., Dowden, R. A., & Campbell, S. C. (2019) · Nutrients · doi:10.3390/nu11010117 · Cited by 65 · see citing works

Understanding Dietary Intervention-Mediated Epigenetic Modifications in Metabolic Diseases

Asif, S., Morrow, N. M., Mulvihill, E. E., & Kim, K.-H. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.590369 · Cited by 69 · see citing works

The Effects of Erchen Decoction on Gut Microbiota and Lipid Metabolism Disorders in Zucker Diabetic Fatty Rats

Zhao, T., Zhan, L., Zhou, W., Chen, W., Luo, J., Zhang, L., Weng, Z., Zhao, C., & Liu, S. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.647529 · Cited by 60 · see citing works

Butyrate protects against MRSA pneumonia via regulating gut-lung microbiota and alveolar macrophage M2 polarization

Zhao, Y., Sun, H., Chen, Y., Niu, Q., Dong, Y., Li, M., Yuan, Y., Yang, X., & Sun, Q. (2023) · mBio · doi:10.1128/mbio.01987-23 · Cited by 60 · see citing works

Self-assembling polymer-based short chain fatty acid prodrugs ameliorate non-alcoholic steatohepatitis and liver fibrosis

Shashni, B., Tajika, Y., Ikeda, Y., Nishikawa, Y., & Nagasaki, Y. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122047 · Cited by 59 · see citing works

Sodium Alginate Prevents Non-Alcoholic Fatty Liver Disease by Modulating the Gut–Liver Axis in High-Fat Diet-Fed Rats

Zhao, H., Gao, X., Liu, Z., Zhang, L., Fang, X., Sun, J., Zhang, Z., & Sun, Y. (2022) · Nutrients · doi:10.3390/nu14224846 · Cited by 58 · see citing works

Protective effect of sodium butyrate on intestinal barrier damage and uric acid reduction in hyperuricemia mice

Li, Y., Li, H., Wang, R., Yu, Y., Liu, X., & Tian, Z. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114568 · Cited by 58 · see citing works

The Role of Intestinal Flora in the Regulation of Bone Homeostasis

Li, C., Pi, G., & Li, F. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.579323 · Cited by 57 · see citing works

Structural Modification of Natural Product Ganomycin I Leading to Discovery of a α-Glucosidase and HMG-CoA Reductase Dual Inhibitor Improving Obesity and Metabolic Dysfunction in Vivo

Wang, K., Li, B., Zhou, N., Zhang, J., Liao, M., Zheng, Z., Wang, Y., Liu, C., Wang, J., Wang, L., et al. (2018) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.8b00107 · Cited by 57 · see citing works

Non-alcoholic fatty liver diseases: from role of gut microbiota to microbial-based therapies

Leylabadlo, H. E., Ghotaslou, R., Kafil, H. S., Feizabadi, M. M., Moaddab, S. Y., Farajnia, S., Sheykhsaran, E., Sanaie, S., Shanehbandi, D., & Baghi, H. B. (2019) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-019-03746-1 · Cited by 56 · see citing works

The Gut Microbial Endocrine Organ in Type 2 Diabetes

Massey, W. J., & Brown, J. M. (2020) · Endocrinology · doi:10.1210/endocr/bqaa235 · Cited by 61 · see citing works

Sodium butyrate ameliorates non‐alcoholic fatty liver disease by upregulating miR‐150 to suppress CXCR4 expression

Zhang, N., Qu, Y., & Qin, B. (2021) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.13497 · Cited by 21 · see citing works

Oral Supplementation of Sodium Butyrate Attenuates the Progression of Non-Alcoholic Steatohepatitis

Baumann, A., Jin, C. J., Brandt, A., Sellmann, C., Nier, A., Burkard, M., Venturelli, S., & Bergheim, I. (2020) · Nutrients · doi:10.3390/nu12040951 · Cited by 51 · see citing works

Efficacy of sodium butyrate in improving nonalcoholic fatty liver disease: A meta-analysis of preclinical studies

Xu, H., Wang, X., Song, S., & Zhang, L. (2025) · Medicine · doi:10.1097/md.0000000000042101 · Cited by 6 · see citing works

Sodium butyrate alleviates fructose-induced non-alcoholic fatty liver disease by remodeling gut microbiota to promote γ -amino butyric acid production

Chen, Q., Wu, L., Zhang, A., Wu, C., Cai, L., Xiao, Y., & Ni, Y. (2023) · Food Science and Human Wellness · doi:10.26599/fshw.2022.9250082 · Cited by 17 · see citing works

Amelioration of non-alcoholic fatty liver disease by sodium butyrate is linked to the modulation of intestinal tight junctions in db/db mice

Yang, T., Yang, H., Cai, H., Wang, H., Chen, S., Hu, Y., Jiang, Z., Yu, Q., Wang, Z., Qian, S., et al. (2020) · Food & Function · doi:10.1039/d0fo01954b · Cited by 63 · see citing works