The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
The Microbiome and Butyrate Regulate Energy Metabolism and Autophagy in the Mammalian Colon
Open accessAbstract
The microbiome is being characterized by large-scale sequencing efforts, yet it is not known whether it regulates host metabolism in a general versus tissue-specific manner or which bacterial metabolites are important. Here, we demonstrate that microbiota have a strong effect on energy homeostasis in the colon compared to other tissues. This tissue specificity is due to colonocytes utilizing bacterially produced butyrate as their primary energy source. Colonocytes from germfree mice are in an energy-deprived state and exhibit decreased expression of enzymes that catalyze key steps in intermediary metabolism including the TCA cycle. Consequently, there is a marked decrease in NADH/NAD(+), oxidative phosphorylation, and ATP levels, which results in AMPK activation, p27(kip1) phosphorylation, and autophagy. When butyrate is added to germfree colonocytes, it rescues their deficit in mitochondrial respiration and prevents them from undergoing autophagy. The mechanism is due to butyrate acting as an energy source rather than as an HDAC inhibitor.
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
“The pathophysiological consequences of this condition are predictable (epithelial cell death and dysregulated inflammation), but the clinical consequences are unknown.”
From The microbiome and critical illness (2016) · cites this paper as [75]
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
An obesity-associated gut microbiome with increased capacity for energy harvest
Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444
Smyth, G. K. (2004) · Statistical Applications in Genetics and Molecular Biology · doi:10.2202/1544-6115.1027 · Cited by 11,829
A human gut microbial gene catalogue established by metagenomic sequencing
MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624
Self-citationDiversity of the Human Intestinal Microbial Flora
Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913 · cited 2×
“INTRODUCTION Diverse microbial communities reside at various sites within the human body (Camp et al., 2009; Eckburg et al., 2005; Savage, 1977).”
A core gut microbiome in obese and lean twins
Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823 · cited 3×
“These microbiota and their genomes, referred to collectively as the microbiome, are being characterized by metagenomic sequencing as part of the Human Microbiome Project (Gill et al., 2006; Hildebrandt et al., 2009; Kurokawa et al., 2007; Qin et al.; Turnbaugh et al., 2009; Turnbaugh et al., 2007).”
The gut microbiota as an environmental factor that regulates fat storage
Bäckhed, F., Ding, H., Wang, T., Hooper, L. V., Koh, G. Y., Nagy, A., Semenkovich, C. F., & Gordon, J. I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407076101 · Cited by 6,245 · cited 8×
“These studies support the idea that microbes increase host metabolic efficiency (Backhed et al., 2004; Turnbaugh et al., 2008; Turnbaugh and Gordon, 2009; Turnbaugh et al., 2009; Turnbaugh et al., 2006).”
InfluentialTurnbaugh, P. J., Ley, R. E., Hamady, M., Fraser-Liggett, C. M., Knight, R., & Gordon, J. I. (2007) · Nature · doi:10.1038/nature06244 · Cited by 6,091 · cited 1×
“These microbiota and their genomes, referred to collectively as the microbiome, are being characterized by metagenomic sequencing as part of the Human Microbiome Project (Gill et al., 2006; Hildebrandt et al., 2009; Kurokawa et al., 2007; Qin et al.; Turnbaugh et al., 2009; Turnbaugh et al., 2007).”
Metagenomic Analysis of the Human Distal Gut Microbiome
Gill, S. R., Pop, M., DeBoy, R. T., Eckburg, P. B., Turnbaugh, P. J., Samuel, B. S., Gordon, J. I., Relman, D. A., Fraser-Liggett, C. M., & Nelson, K. E. (2006) · Science · doi:10.1126/science.1124234 · Cited by 4,699 · cited 2×
“These microbiota and their genomes, referred to collectively as the microbiome, are being characterized by metagenomic sequencing as part of the Human Microbiome Project (Gill et al., 2006; Hildebrandt et al., 2009; Kurokawa et al., 2007; Qin et al.; Turnbaugh et al., 2009; Turnbaugh et al., 2007).”
Regulation mechanisms and signaling pathways of autophagy
He, C., & Klionsky, D. J. (2009) · Annual Review of Genetics · doi:10.1146/annurev-genet-102808-114910 · Cited by 3,609 · cited 1×
“In response to nutrient deprivation, AMPK activation induces autophagy, which is a catabolic process where the cell degrades its own cellular components in an attempt to maintain energy homeostasis (He and Klionsky, 2009; Yang and Klionsky, 2009).”
Turnbaugh, P. J., Bäckhed, F., Fulton, L., & Gordon, J. I. (2008) · Cell Host & Microbe · doi:10.1016/j.chom.2008.02.015 · Cited by 2,915 · cited 1×
“These studies support the idea that microbes increase host metabolic efficiency (Backhed et al., 2004; Turnbaugh et al., 2008; Turnbaugh and Gordon, 2009; Turnbaugh et al., 2009; Turnbaugh et al., 2006).”
Flagged first, then by citations
Cited by
Sorted by citations
Items 801–900 of 1,000
Ilie, O., Ciobica, A. S., Riga, S., Dhunna, N., McKenna, J., Mavroudis, I. A., Doroftei, B., Ciobanu, A. M., & Riga, D. (2020) · Medicina · doi:10.3390/medicina56110626 · Cited by 34
Wang, J., Yang, M., Wu, Q., Chen, J., Deng, S.-F., Chen, L., Wei, D., & Liang, F. (2021) · Chinese Medicine · doi:10.1186/s13020-020-00417-8 · Cited by 34
How autophagy, a potential therapeutic target, regulates intestinal inflammation
Chen, S.-L., Li, C., Li, W., Liu, Q., Hu, S., Zhao, M., Hu, D.-S., Hao, Y., Zeng, J., & Zhang, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1087677 · Cited by 36
Cheng, J., Ye, K., Fu, C., Zhou, Y., Chen, Y., Ma, G., Chen, S., Tu, J., & Xiao, H. (2024) · Food Research International · doi:10.1016/j.foodres.2024.115231 · Cited by 31
The Role of Gut Microbiota in the Onset and Progression of Obesity and Associated Comorbidities
Enache, R. M., Profir, M., Roşu, O. A., Creţoiu, S. M., & Gașpar, B. S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212321 · Cited by 34
Han, A., Bennett, N. E., MacDonald, A., Johnstone, M. E., Whelan, J. N., & Donohoe, D. R. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25287 · Cited by 31
Living Therapeutics: The Next Frontier of Precision Medicine
Kelly, V. W., Liang, B. K., & Sirk, S. J. (2020) · ACS Synthetic Biology · doi:10.1021/acssynbio.0c00444 · Cited by 30
“(30) den Besten, G., et al. (2013) The role of short-chain fatty acids in”
BackgroundHow Changes in the Nutritional Landscape Shape Gut Immunometabolism
Tan, J., Ni, D., Ribeiro, R. V., Pinget, G. V., & Macia, L. (2021) · Nutrients · doi:10.3390/nu13030823 · Cited by 29
“This process inhibits autophagia that is significantly increased in germ-free mice devoid of luminal butyrate [194].”
BackgroundSolé-Jiménez, P., Naya-Català, F., Piazzon, M. C., Estensoro, I., Calduch-Giner, J. À., Sitjà‐Bobadilla, A., Mullem, D. V., & Pérez‐Sánchez, J. (2021) · Frontiers in Marine Science · doi:10.3389/fmars.2021.705041 · Cited by 31
Khan, S., & Chousalkar, K. K. (2021) · Animal Microbiome · doi:10.1186/s42523-021-00112-5 · Cited by 31
A Special Network Comprised of Macrophages, Epithelial Cells, and Gut Microbiota for Gut Homeostasis
Chen, W., Liu, D., Ren, C., Su, L., Wong, C. K., & Yang, R. (2022) · Cells · doi:10.3390/cells11020307 · Cited by 31
“Luminal butyrate can serve as a source of energy for gut epithelial cells in metabolic processes, and act to inhibit HDAC activity in intestinal epithelial stem cells [87,88].”
BackgroundMa, S., Tong, Q., Zhao, Z., Cong, L., Yu, J., Fu, J., Han, P., Pan, L., Gu, R., Peng, R., et al. (2019) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-019-01793-3 · Cited by 31
Luan, M., Niu, M., Yang, P., Han, D., Zhang, Y., Li, W., He, Q., Zhao, Y., Mao, B., Chen, J., et al. (2023) · BMC Microbiology · doi:10.1186/s12866-023-03020-7 · Cited by 32
Jia, J., Zheng, W., Tang, S., Song, S., & Ai, C. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.127337 · Cited by 30
Cold exposure, gut microbiota and health implications: A narrative review
Zhou, E., Zhang, L., He, L., Xiao, Y., Zhang, K., & Luo, B. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.170060 · Cited by 33
Wang, Y., Dou, W., Qian, X., Chen, H., Zhang, Y., Yang, L., Wu, Y., & Xu, X. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123528 · Cited by 33
Integrative systems biology approaches for analyzing microbiome dysbiosis and species interactions
Rehman, S. S. U., Nasar, M. I., Mesquita, C. S., Khodor, S. A., Notebaart, R. A., Ott, S., Mundra, S., Arasardanam, R. P., Muhammad, K., & Alam, M. T. (2025) · Briefings in Bioinformatics · doi:10.1093/bib/bbaf323 · Cited by 35
Hong, M. Y., Turner, N. D., Murphy, M. E., Carroll, R. J., Chapkin, R. S., & Lupton, J. R. (2015) · Cancer Prevention Research · doi:10.1158/1940-6207.capr-15-0147 · Cited by 30
“Among the short chain fatty acids, butyrate is used as a major energy source by colonocytes (10, 11).”
BackgroundYang, X., Gao, X., Liu, J., & Ren, H. (2017) · World Journal of Gastroenterology · doi:10.3748/wjg.v23.i26.4744 · Cited by 30
Regulation of axial and head patterning during planarian regeneration by a commensal bacterium
Williams, K. B., Bischof, J., Lee, F. J., Miller, K. A., LaPalme, J. V., Wolfe, B. E., & Levin, M. G. (2020) · Mechanisms of Development · doi:10.1016/j.mod.2020.103614 · Cited by 27
Role of Low FODMAP Diet and Probiotics on Gut Microbiome in Irritable Bowel Syndrome (IBS)
Selvaraj, S. M., Wong, S. H., Ser, H., & Lee, L. (2020) · Progress In Microbes & Molecular Biology · doi:10.36877/pmmb.a0000069 · Cited by 31
Hul, M. V., Karnik, K., Canene‐Adams, K., de Souza, M., den Abbeele, P. V., Marzorati, M., Delzenne, N. M., Everard, A., & Cani, P. D. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00108.2020 · Cited by 33
“For example, Allobaculum is a known producer of butyrate, a SCFA that is rapidly taken up by enterocytes, where it serves as an energy source (23).”
BackgroundAmbrożkiewicz, F., Karczmarski, J., Kulecka, M., Paziewska, A., Niemira, M., Żeber‐Lubecka, N., Zagórowicz, E., Kretowski, A. J., & Ostrowski, J. (2020) · BMC Gastroenterology · doi:10.1186/s12876-020-01444-3 · Cited by 30
Role and mechanism of action of butyrate in atherosclerotic diseases: a review
Xiao, Y., Guo, Z., Li, Z., Ling, H., & Song, C. (2020) · Journal of Applied Microbiology · doi:10.1111/jam.14906 · Cited by 30
“Thus, butyrate can significantly alleviate mitochondrial respiratory defects and autophagy by serving as an energy substrate (Donohoe et al. 2011).”
BackgroundKang, M., Lee, S., Park, Y. M., Kim, B. S., Lee, M.-J., Kim, J., Jeong, S., Lee, S., Park, M. J., Rhee, E. S., et al. (2021) · Allergy Asthma and Immunology Research · doi:10.4168/aair.2021.13.3.404 · Cited by 33
Olivier, S., Pochard, C., Ilchmann-Diounou, H., Castillo, V., Divoux, J., Alcantara, J. A., Leclerc, J., Guilmeau, S., Huet, C., Charifi, W., et al. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101183 · Cited by 31
“Interestingly, disruption of the gut microbiota has been associated with activation of AMPK in germ-free mice as reported in skeletal muscle and liver as well as in colonocytes to influence energy balance homeostasis [39,40].”
BackgroundCho, K. M., Kim, Y. S., Lee, M., Lee, H. Y., & Bae, Y. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16482 · Cited by 29
Zhang, S., Xu, M., Sun, X., Liu, X., Choueiry, F., Xu, R., Shi, H., & Zhu, J. (2021) · Journal of Chromatography B · doi:10.1016/j.jchromb.2021.123027 · Cited by 30
Jansen, S. A., Nieuwenhuis, E. E. S., Hanash, A. M., & Lindemans, C. A. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00527-6 · Cited by 30
Distinct colon mucosa microbiomes associated with tubular adenomas and serrated polyps
Avelar‐Barragan, J., DeDecker, L. C., Lu, Z. N., Coppedge, B., Karnes, W. E., & Whiteson, K. (2022) · npj Biofilms and Microbiomes · doi:10.1038/s41522-022-00328-6 · Cited by 32
Sun, Y., Tang, Z., Hao, T., Qiu, Z., & Zhang, B. (2022) · Foods · doi:10.3390/foods11244016 · Cited by 30
“In addition, butyrate can regulate host immunological function and metabolism by exerting anti-inflammatory effects, hence maintaining intestinal homeostasis [46,47].”
BackgroundA Comprehensive Metabolomic Investigation in Urine of Mice Exposed to Strontium-90
Goudarzi, M., Weber, W., Mak, T. D., Chung, J., Doyle‐Eisele, M., Melo, D. R., Strawn, S. J., Brenner, D. J., Guilmette, R. A., & Fornace, A. J. (2015) · Radiation Research · doi:10.1667/rr14011.1 · Cited by 30
“shown that butanoate deficiency in colonocytes can lead to energy deprivation and ultimately autophagy (13).”
BackgroundGarcía, K. E., de Souza, T. C. R., Landín, G. M., Barreyro, A. A., Santos, M. G. B., & Soto, J. G. G. (2014) · Food and Nutrition Sciences · doi:10.4236/fns.2014.518191 · Cited by 30
“In turn, acetic acid can be transformed to butyric acid, which provides between 70% and 90% of the energy required by colonocytes metabolism [22], thus sparing about 30% of the energy requirement of piglets during the stressful period weaning represents [1] [22] [23].”
BackgroundCompound probiotics can improve intestinal health by affecting the gut microbiota of broilers
Liu, X., Ma, Z., Wang, Y., Li, L., Jia, H., & Zhang, L. (2023) · Journal of Animal Science · doi:10.1093/jas/skad388 · Cited by 29
Nutritional strategies to reduce intestinal cell apoptosis by alleviating oxidative stress
Li, B., Zhang, X., Zhang, Q., Zheng, T., Li, Q., Yang, S., Shao, J., Guan, W., & Zhang, S. (2024) · Nutrition Reviews · doi:10.1093/nutrit/nuae023 · Cited by 29
Govaert, M., Rotsaert, C., Vannieuwenhuyse, C., Duysburgh, C., Medlin, S., Marzorati, M., & Jarrett, H. (2024) · Nutrients · doi:10.3390/nu16162791 · Cited by 35
Triff, K., Kim, E., & Chapkin, R. S. (2015) · Current Pharmacology Reports · doi:10.1007/s40495-014-0005-7 · Cited by 30
Chen, Z., Wu, Y., Shrestha, R., Gao, Z., Zhao, Y., Miura, Y., Tamakoshi, A., Chiba, H., & Hui, S. (2018) · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · doi:10.1177/0004563218801393 · Cited by 29
“Taking butyrate as an example, evidence has shown the uptake of butyrate by the colonic epithelium, confirming that butyrate is preferentially utilized by colonocytes as the primary energy source.(7) After absorbed, butyrate is involved in various types of therapeutic effects, such as the improvement of type 2 diabete…”
The role of chronic kidney disease-associated dysbiosis in cardiovascular disease
Bryniarski, M. A., Hamarneh, F., & Yacoub, R. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219826526 · Cited by 31
Titan, S., Venturini, G., Padilha, K., Goulart, A. C., Lotufo, P. A., Benseñor, I. M., Krieger, J. E., Thadhani, R., Rhee, E. P., & Pereira, A. C. (2019) · PLoS ONE · doi:10.1371/journal.pone.0213764 · Cited by 29
Bhushan, B., Singh, B. P., Saini, K., Kumari, M., Tomar, S. K., & Mishra, V. (2019) · Environmental Chemistry Letters · doi:10.1007/s10311-019-00914-9 · Cited by 29
“Besides other fatty acids, butyrate is the most important fuel source for colonocytes (Donohoe et al. 2011) and will be explained much in the present review.”
BackgroundFuentes, S., den Hartog, G., Nanlohy, N. M., Wijnands, L. M., Ferreira, J. A., Nicolaie, M. A., Pennings, J. L. A., Jacobi, R. H. J., de Wit, J., van Beek, J., et al. (2021) · The Lancet Healthy Longevity · doi:10.1016/s2666-7568(20)30034-9 · Cited by 28
Antibiotic use and colorectal neoplasia: a systematic review and meta-analysis
Aneke-Nash, C. S., Yoon, G. H., Du, M., & Liang, P. S. (2021) · BMJ Open Gastroenterology · doi:10.1136/bmjgast-2021-000601 · Cited by 33
Rebelos, E., Iozzo, P., Guzzardi, M. A., Brunetto, M. R., & Bonino, F. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i30.4999 · Cited by 32
Lokesh, J., Ghislain, M., Reyrolle, M., Béchec, M. L., Pigot, T., Terrier, F., Roy, J., Panserat, S., & Ricaud, K. (2021) · Aquaculture · doi:10.1016/j.aquaculture.2022.738699 · Cited by 35
Chu, X., Hou, Y., Meng, Q., Croteau, D. L., Wei, Y. Q., De, S., Becker, K. G., & Bohr, V. A. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.993615 · Cited by 28
Wang, A., Li, Q., Sun, Z., Zhang, D., & Ma, X. (2023) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2023.109370 · Cited by 30
Targeting gut microbiota in aging-related cardiovascular dysfunction: focus on the mechanisms
Liu, S., He, Y., Zhang, Y., Zhang, Z., Huang, K., Deng, L., Liao, B., Zhong, Y., & Feng, J. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2290331 · Cited by 31
Le microbiote intestinal et la digestion des polysaccharides
Kaoutari, A. E., Armougom, F., Raoult, D., & Henrissat, B. (2014) · médecine/sciences · doi:10.1051/medsci/20143003013 · Cited by 39
“Ce produit constitue la première source d’énergie pour les cellules du côlon (colonocytes), et son manque provoque l’autophagie ou l’autolyse de ces dernières qui finissent par se dégrader [22].”
BackgroundBevilacqua, A., Costabile, A., Bergillos-Meca, T., Gonzalez, I., Landriscina, L., Ciuffreda, E., D’Agnello, P., Corbo, M. R., Sinigaglia, M., & Lamacchia, C. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162770 · Cited by 29
Tissue metabolism and host-microbial interactions in the intestinal mucosa
Chun, C. L., Zheng, L., & Colgan, S. P. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.09.027 · Cited by 31
Microbiota regulate the development and function of the immune cells
Yu, Q., Jia, A., Li, Y., Bi, Y., & Liu, G. (2018) · International Reviews of Immunology · doi:10.1080/08830185.2018.1429428 · Cited by 30
Muenzner, P., & Hauck, C. R. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.03.010 · Cited by 28
Ortega‐Hernández, A., Martínez‐Martínez, E., Gómez-Gordo, R., López‐Andrés, N., Fernández‐Celis, A., Gutiérrez-Miranda, B., Nieto, M. L., Alarcón, T., Alba, C., Gómez‐Garré, D., et al. (2020) · Antioxidants · doi:10.3390/antiox9070640 · Cited by 28
“By contrast, metabolites produced by GM modulate mitochondrial energy metabolism and activities [20,22,23].”
BackgroundUnderstanding connections and roles of gut microbiome in cardiovascular diseases
Rajendiran, E., Ramadass, B., & Ramprasath, V. R. (2020) · Canadian Journal of Microbiology · doi:10.1139/cjm-2020-0043 · Cited by 29
New perspective toward nutritional support for malnourished cancer patients: Role of lipids
Wang, Y., Zhang, T., Liu, R., Chang, M., Wei, W., Jin, Q., & Wang, X. (2021) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12706 · Cited by 30
Shimizu, Y., Nakamura, K., Kikuchi, M., Ukawa, S., Nakamura, K., Okada, E., Imae, A., Nakagawa, T., Yamamura, R., Tamakoshi, A., et al. (2021) · GeroScience · doi:10.1007/s11357-021-00398-y · Cited by 32
Gut microbiota-derived metabolites as key mucosal barrier modulators in obesity
Wei, Y., Zheng, K., & Wang, Y.-G. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i33.5555 · Cited by 29
Liu, H., Zhao, J., Zhang, W., & Nie, C. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1041885 · Cited by 39
“Butyrate is also the main energy source for colonocytes, with at least 95% of luminally derived butyrate being utilized and absorbed in the colon (Donohoe et al., 2011; den Besten et al., 2013).”
BackgroundLamas, B., Evariste, L., & Houdeau, É. (2023) · Environmental Pollution · doi:10.1016/j.envpol.2023.121795 · Cited by 31
A comprehensive review for gut microbes: technologies, interventions, metabolites and diseases
Qi, C., Wang, P., Fu, T., Lu, M., Cai, Y., Chen, X., & Cheng, L. (2020) · Briefings in Functional Genomics · doi:10.1093/bfgp/elaa029 · Cited by 28
Mafra, D., Borges, N. A., Lindholm, B., & Stenvinkel, P. (2019) · Mitochondrion · doi:10.1016/j.mito.2018.11.006 · Cited by 27
Nieva, C., Pryor, J., Williams, G. M., Hoedt, E. C., Burns, G. L., Eslick, G. D., Talley, N. J., Duncanson, K., & Keely, S. (2023) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjad204 · Cited by 29
“18 This underscores diet as a key modifiable factor that can directly influence the GI environment.”
BackgroundThe role of short-chain fatty acids in cancer prevention and cancer treatment
Kalyanaraman, B., Cheng, G., & Hardy, M. (2024) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2024.110172 · Cited by 29
“Thus, they are essential for the normal functioning of the colon cells (colonocytes) [17].”
Crouch, L. I., Rodrigues, C. S., Bakshani, C. R., Tavares-Gomes, L., Gaifem, J., & Pinho, S. S. (2024) · Seminars in Immunology · doi:10.1016/j.smim.2024.101891 · Cited by 29
Short-chain fatty acids: key antiviral mediators of gut microbiota
Xu, Z., Wang, T., Wang, Y., Li, Y., Sun, Y., & Qiu, H. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1614879 · Cited by 37
Summers, S., Quimby, J. M., Phillips, R. K., Stockman, J. A., Isaiah, A., Lidbury, J. A., Steiner, J. M., & Suchodolski, J. S. (2019) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.15634 · Cited by 28
Ke, W., Bonilla‐Rosso, G., Engel, P., Wang, P., Chen, F., & Hu, X. (2020) · Journal of Nutrition · doi:10.1093/jn/nxaa159 · Cited by 27
Montanari, C., Parolisi, S., Borghi, E., Putignani, L., Bassanini, G., Zuvadelli, J., Bonfanti, C., Tummolo, A., Dionisi‐Vici, C., Biasucci, G., et al. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.716520 · Cited by 28
Sibinelli‐Sousa, S., Silva, A. L. D. A., Hespanhol, J. T., & Bayer‐Santos, E. (2021) · FEBS Journal · doi:10.1111/febs.16211 · Cited by 28
Role of Maternal Microbiota and Nutrition in Early-Life Neurodevelopmental Disorders
Daliry, A., & Pereira, E. N. G. D. S. (2021) · Nutrients · doi:10.3390/nu13103533 · Cited by 31
“energy source, while propionate and acetate are utilized by the liver for lipogenesis and gluconeogenesis [137,138].”
BackgroundDietrich, A., Matchado, M. S., Zwiebel, M., Ölke, B., Lauber, M., Lagkouvardos, I., Baumbach, J., Haller, D., Brandl, B., Skurk, T., et al. (2022) · Microbial Genomics · doi:10.1099/mgen.0.000852 · Cited by 31
IFI16 Partners with KAP1 to Maintain Epstein-Barr Virus Latency
Xu, H., Li, X., Rousseau, B. A., Akinyemi, I. A., Frey, T. R., Zhou, K., Droske, L. E., Mitchell, J. A., McIntosh, M. T., & Bhaduri‐McIntosh, S. (2022) · Journal of Virology · doi:10.1128/jvi.01028-22 · Cited by 28
“That said also, the relevance of the short-chain fatty acid butyrate in this context cannot be dismissed because butyrate is produced by bacterial fermentation by gut microbes (45), resulting in ample exposure of infected B cells within the gut, the largest immune organ.”
BackgroundZhang, X., Shi, L. S., Li, Q., Song, C., Han, N., Yan, T., Zhang, L., Ren, D., Zhao, Y., & Yang, X. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c06162 · Cited by 29
Effects of Lysophosphatidylcholine on Intestinal Health of Turbot Fed High-Lipid Diets
Li, S., Luo, X., Liao, Z., Liang, M., Xu, H., Mai, K., & Zhang, Y. (2022) · Nutrients · doi:10.3390/nu14204398 · Cited by 27
“Butyrate, the preferred fuel of intestinal epithelial cells, can regulate the expression of cytokines or their receptors in the intestine, and enhance the intestinal barrier integrity [69].”
BackgroundEpigenetic Aberrations in Major Psychiatric Diseases Related to Diet and Gut Microbiome Alterations
Nohesara, S., Abdolmaleky, H. M., & Thiagalingam, S. (2023) · Genes · doi:10.3390/genes14071506 · Cited by 32
“Butyrate is another SCFA and a secondary metabolite of the gut microbiome which acts as an endogenous inhibitor of class I HDACs, a well-known class of epigenetic modulatory genes [174,175].”
Panasevich, M. R., Allen, J. M., Wallig, M. A., Woods, J. A., & Dilger, R. N. (2015) · Journal of Nutrition · doi:10.3945/jn.115.218578 · Cited by 28
Meijerink, M., Rösch, C., Taverne, N., Venema, K., Gruppen, H., Schols, H. A., & Wells, J. M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01972 · Cited by 27
Vai, A., Noberini, R., Ghirardi, C., de Paula, D. R., Carminati, M., Pallavi, R., Araújo, N. V. P., Varga‐Weisz, P., & Bonaldi, T. (2024) · Molecular & Cellular Proteomics · doi:10.1016/j.mcpro.2024.100799 · Cited by 26
“Therefore, antibiotic treatment should decrease the formation of acyl-CoAs and, consequently, the level of histone acylations, as reported in (52 – 54).”
Butyrate: a bridge between intestinal flora and rheumatoid arthritis
Cao, Y., Chen, J., Xiao, J., Hong, Y., Xu, K., & Zhu, Y. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1475529 · Cited by 26
“Additionally, the remaining butyrate (extremely low concentration) enters the circulation to be metabolized (14, 15).”
BackgroundMicrobiota-derived metabolites in inflammatory bowel disease
Guggeis, M. A., Harris, D. M. M., Welz, L., Rosenstiel, P. C., & Aden, K. (2025) · Seminars in Immunopathology · doi:10.1007/s00281-025-01046-9 · Cited by 31
“…microbiota influence host NAD + bioavailability: For example, in germ-free mice, a total reduction of NADH/NAD + redox ratio in colonocytes has been observed [85]; and microbiota fulfil a critical function in supplying the host with NAD + precursors, e.g. by converting NA into NAM [86, 87].”
Gut Microbiota Modulation in IBD: From the Old Paradigm to Revolutionary Tools
Murgiano, M., Bartocci, B., Puca, P., Vincenzo, F. D., GAUDIO, A. D., Papa, A., Cammarota, G., Gasbarrini, A., Scaldaferri, F., & Lopetuso, L. R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26073059 · Cited by 30
“In contrast, a fiber-rich plant-based diet promotes microbial diversity and increases the production of SCFAs, which help maintain intestinal health [27].”
Microbial metabolites and their influence on the tumor microenvironment
Duan, H., Xu, B., Luo, P., Chen, T., & Zou, J. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1675677 · Cited by 31
“…evidence has demonstrated their pleiotropic functions in maintaining human health: they act not only as a major energy substrate for speci fi c cell types (e.g., intestinal epithelial cells) (66), but also exhibit signi fi cant immunomodulatory properties with implications for tumor immunity (67).”
Mobile Technologies for the Discovery, Analysis, and Engineering of the Global Microbiome
Ballard, Z. S., Brown, C., & Özcan, A. (2018) · ACS Nano · doi:10.1021/acsnano.7b08660 · Cited by 26
Short-Chain Fatty Acid Production and Functional Aspects on Host Metabolism
Tungland, B. C. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814649-1.00002-8 · Cited by 29
Zhou, F., Liu, B.-D., Liu, X., Li, Y., Wang, L., Huang, J., Luo, G., & Wang, X. (2021) · Metabolites · doi:10.3390/metabo11050298 · Cited by 26
“Short-chain fatty acids are the most abundant metabolites produced by the fermentation of undigested dietary fiber by intestinal microorganisms and provide the main energy source for the host intestinal cells [3].”
Backgroundde León, A. V., Jahnes, B. C., Otero-Bravo, A., & Sabree, Z. L. (2021) · mSystems · doi:10.1128/msystems.00802-21 · Cited by 26
“Similarly, reduced mitochondrial respiration and ATP synthase activity were observed in colonocytes of GF mice, which was linked to energy stress (36).”
BackgroundJardou, M., Provost, Q., Brossier, C., Pinault, É., Sauvage, F., & Lawson, R. (2021) · BMC Pharmacology and Toxicology · doi:10.1186/s40360-021-00536-4 · Cited by 29
“Butyrate can also be a source of energy for the colonocytes and can improve epithelial barrier functions through up-regulation of tight junctions proteins such as Claudin-1 and ZO-1 [35, 36].”
BackgroundKang, R., Wang, W., Liu, Y., Huang, S., Xu, J., Zhao, L., Zhang, J., Ji, C., Wang, Z., Hu, Y., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.928865 · Cited by 26
“abundance of Lachnospiraceae and Clostridium, which could utilize dietary carbohydrate and fiber metabolism to produce butyric acid, regulating both energy metabolism and the immune response of intestinal epithelial cells (55, 56).”
BackgroundNatural Compounds Targeting the Autophagy Pathway in the Treatment of Colorectal Cancer
Du, Y.-X., Mamun, A. A., Lü, A., & Zhang, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087310 · Cited by 25
Sasaki, H., Hayashi, K., Imamura, M., Hirota, Y., Hosoki, H., Nitta, L., Furutani, A., & Shibata, S. (2023) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2023.109420 · Cited by 29
Tezacaftor/Ivacaftor therapy has negligible effects on the cystic fibrosis gut microbiome
Marsh, R., Santos, C. D., Hanson, L., Ng, C., Major, G., Smyth, A. R., Rivett, D. W., & Gast, C. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.01175-23 · Cited by 26
“This is unsurprising, given the relation ship of butyrate in particular with antiinflammatory properties and enhancement of epithelial integrity (37–39).”
BackgroundThe Interaction between Stress and Inflammatory Bowel Disease in Pediatric and Adult Patients
Belei, O., Basaca, D.-G., Olariu, L., Pantea, M., Bozgan, D., Nanu, A.-M., Sîrbu, I., Mărginean, O., & Enătescu, I. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13051361 · Cited by 30
“…cell proliferation [52], barrier function [53], and cellular metabolism, ff erent signals from the lumen of the intestine are also known to control behavior, sleep, and stress responses through enteric, spinal, and vagal nerve cells [39]. as thoroughly reviewed by Parada Venegas et al. [54,55].”
BackgroundZhdanov, A. V., Okkelman, I. A., Golubeva, A. V., Doerr, B., Hyland, N. P., Melgar, S., Shanahan, F., Cryan, J. F., & Papkovsky, D. B. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2323-x · Cited by 26
Recent advances in developing butyrogenic functional foods to promote gut health
Zhang, M., Li, R. W., Yang, H., Tan, Z., & Liu, F. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2142194 · Cited by 27
“Up to 95% of microbe-derived butyrate is utilized in the colon; as a preferred oxidative substrate for colonocytes, butyrate plays a vital role in regulating host energy metabolism and promoting intestinal epithelial cell regeneration (Donohoe et al. 2011).”
BackgroundShmuel-Galia, L., Humphries, F., Vierbuchen, T., Jiang, Z., Santos, N., Johnson, J. L., Shklyar, B., Joannas, L. D., Mustone, N., Sherman, S., et al. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.06.019 · Cited by 25
Zhao, J., Duan, L., Li, J., Yao, C., Wang, G., Mi, J., Yu, Y., Ding, L., Zhao, Y., Yan, G., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116807 · Cited by 26
Lu, H., Xu, P., Sun, G., Chen, B., Zheng, Y., Zhang, J., & Wang, G. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.176802 · Cited by 26
The intricate connection between diet, microbiota, and cancer: A jigsaw puzzle
Arkan, M. C. (2017) · Seminars in Immunology · doi:10.1016/j.smim.2017.08.009 · Cited by 25
Regulation of Intestinal Stem Cell Stemness by the Aryl Hydrocarbon Receptor and Its Ligands
Wisniewski, P. J., Nagarkatti, M., & Nagarkatti, P. S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.638725 · Cited by 27
“Interestingly, butyrate is a critical energy source for colonocytes (89) and exhibits therapeutic effects like that of other AhR agonists including induction of Treg cells, anti-inflammatory responses as well as the induction of IL-22 (90–93).”
Background
Metadata
- Authors
- Donohoe, D. R., Garge, N., Zhang, X., Sun, W., O'Connell, T. M., Bunger, M. K., & Bultman, S. J.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- RTI International (US)
- Corresponding author
- Bultman, Scott J.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2011-05
- Volume
- 13
- Issue
- 5
- Pages
- 517-526
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC3099420
- OpenAlex
- W2082578477
- Cited by
- 2,003
- References
- 47
- Citations by year
- 2026: 203 · 2025: 192 · 2024: 170 · 2023: 171 · 2022: 190 · 2021: 228 · 2020: 182 · 2019: 148 · 2018: 115 · 2017: 104 · 2016: 96 · 2015: 68 · 2014: 56 · 2013: 44 · 2012: 23
- FWCI
- 17.16
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 844 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
- UNC Libraries
- Funders
- National Institutes of Health (CA125237)
- Prevent Cancer Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Nutrition and Physiology
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- gut microbiota, butyrate, colonic epithelial cells, energy metabolism, autophagy, germ-free mice, TCA cycle, oxidative phosphorylation, AMPK, p27, mitochondrial respiration, bacterial metabolites, energy homeostasis
- MeSH terms
- Animals, Autophagy, Butyrates, Cells, Cultured, Colon, Energy Metabolism, Germ-Free Life, Glucose, Male, Mice, Inbred C57BL, Mitochondria, NAD, Magnetic Resonance Spectroscopy, Oxidative Phosphorylation, Phosphorylation, Blotting, Western, Signal Transduction, Biomarkers, Oligonucleotide Array Sequence Analysis, Gene Expression Profiling, Cyclin-Dependent Kinase Inhibitor p27, Mice, Metagenome, AMP-Activated Protein Kinases, Metabolomics
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