The DOI matches its Crossref record; 88 of the 88 references it cites were found in a registry or an index.
Neuromodulatory effects and targets of the SCFAs and gasotransmitters produced by the human symbiotic microbiota
Open accessAbstract
The symbiotic gut microbiota plays an important role in the development and homeostasis of the host organism. Its physiological, biochemical, behavioral, and communicative effects are mediated by multiple low molecular weight compounds. Recent data on small molecules produced by gut microbiota in mammalian organisms demonstrate the paramount importance of these biologically active molecules in terms of biology and medicine. Many of these molecules are pleiotropic mediators exerting effects on various tissues and organs. This review is focused on the functional roles of gaseous molecules that perform neuromediator and/or endocrine functions. The molecular mechanisms that underlie the effects of microbial fermentation-derived gaseous metabolites are not well understood. It is possible that these metabolites produce their effects via immunological, biochemical, and neuroendocrine mechanisms that involve endogenous and microbial modulators and transmitters; of considerable importance are also changes in epigenetic transcriptional factors, protein post-translational modification, lipid and mitochondrial metabolism, redox signaling, and ion channel/gap junction/transporter regulation. Recent findings have revealed that interactivity among such modulators/transmitters is a prerequisite for the ongoing dialog between microbial cells and host cells, including neurons. Using simple reliable methods for the detection and measurement of short-chain fatty acids (SCFAs) and small gaseous molecules in eukaryotic tissues and prokaryotic cells, selective inhibitors of enzymes that participate in their synthesis, as well as safe chemical and microbial donors of pleiotropic mediators and modulators of host intestinal microbial ecology, should enable us to apply these chemicals as novel therapeutics and medical research tools.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“It was described that SCFAs may modulate the levels of neurotransmitters and neurotrophic factors.”
From The Role of Short-Chain Fatty Acids From Gut Microbiota in Gut-Brain Communication (2020) · cites this paper as [115]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Propionate and butyrate exert an influence on the intracellular potassium level, which implies the involvement of SCFAs in the operation of cell signaling systems (115).”
From The Role of Short-Chain Fatty Acids From Gut Microbiota in Gut-Brain Communication (2020) · cites this paper as [115]
In the citing paper
“Propionate and butyrate can influence the cell signaling system via modification of the intracellular potassium levels (104), and they regulate the expression levels of tryptophan 5-hydroxylase 1, involved in the synthesis of serotonin, and tyrosine hydroxylase, which is involved in the biosynthesis of dopamine, adrenaline, and noradrenaline (105).”
From The gut-brain axis: how microbiota and host inflammasome influence brain physiology and pathology (2020) · cites this paper as [104]
In the citing paper
“First of all, the microbiota composition of MS patients is different from the one of healthy individuals (104).”
From The gut-brain axis: how microbiota and host inflammasome influence brain physiology and pathology (2020) · cites this paper as [104]
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
Hill (2014) · doi:10.1038/nrgastro.2014.66 · Cited by 9,592
Physiological Implications of Hydrogen Sulfide: A Whiff Exploration That Blossomed
Wang, R. (2012) · Physiological Reviews · doi:10.1152/physrev.00017.2011 · Cited by 1,962
Regulation of inflammation by short chain fatty acids
Vinolo, M. A. R., Rodrigues, H. G., Nachbar, R. T., & Curi, R. (2011) · Nutrients · doi:10.3390/nu3100858 · Cited by 1,724
Psychobiotics: A novel class of psychotropic
Dinan, T. G., Stanton, C., & Cryan, J. F. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.001 · Cited by 1,287
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
Hemarajata, P., & Versalovic, J. (2013) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756283x12459294 · Cited by 1,083
The role of microbiome in central nervous system disorders
Wang, Y., & Kasper, L. H. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.12.015 · Cited by 803
H 2 S: A Universal Defense Against Antibiotics in Bacteria
Shatalin, K. Y., Shatalina, E., Mironov, A. S., & Nudler, E. (2011) · Science · doi:10.1126/science.1209855 · Cited by 769
Dietary Inorganic Nitrate Improves Mitochondrial Efficiency in Humans
Larsen, F. J., Schiffer, T. A., Borniquel, S., Sahlin, K., Ekblom, B., Lundberg, J. O., & Weitzberg, E. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.01.004 · Cited by 689
The Gut Microbiome and the Brain
Galland, L. (2014) · Journal of Medicinal Food · doi:10.1089/jmf.2014.7000 · Cited by 648
Behavioural abnormalities in male mice lacking neuronal nitric oxide synthase
Nelson, R. J., Demas, G. E., Huang, P. L., Fishman, M. C., Dawson, V. L., Dawson, T. M., & Snyder, S. H. (1995) · Nature · doi:10.1038/378383a0 · Cited by 595
Regulation of the stress response by the gut microbiota: implications for psychoneuroendocrinology
Dinan, T. G., & Cryan, J. F. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.03.007 · Cited by 577
A novel pathway for the production of hydrogen sulfide from D-cysteine in mammalian cells
Shibuya, N., Koike, S., Tanaka, M., Ishigami‐Yuasa, M., Kimura, Y., Ogasawara, Y., Fukui, K., Nagahara, N., & Kimura, H. (2013) · Nature Communications · doi:10.1038/ncomms2371 · Cited by 558
Endogenous hydrogen sulfide production is essential for dietary restriction benefits
Hine, C., Harputlugil, E., Zhang, Y., Ruckenstuhl, C., Lee, B. C., Brace, L., Longchamp, A., Treviño-Villarreal, J. H., Mejia, P., Ozaki, C. K., et al. (2015) · Cell · doi:10.1016/j.cell.2014.11.048 · Cited by 558
Lyte, M. (2011) · BioEssays · doi:10.1002/bies.201100024 · Cited by 549
Microbial pathways in colonic sulfur metabolism and links with health and disease
Carbonero, F., Benefiel, A. C., Alizadeh-Ghamsari, A. H., & Gaskins, H. R. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00448 · Cited by 544
Hydrogen sulfide as a gasotransmitter
Gadalla, M. M., & Snyder, S. H. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06580.x · Cited by 493
A Source of Hydrogen Sulfide and a Mechanism of Its Release in the Brain
Ishigami, M., Hiraki-Kamon, K., Umemura, K., Ogasawara, Y., Ishii, K., & Kimura, H. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2008.2132 · Cited by 478
Emergence of Hydrogen Sulfide as an Endogenous Gaseous Signaling Molecule in Cardiovascular Disease
Polhemus, D. J., & Lefer, D. J. (2014) · Circulation Research · doi:10.1161/circresaha.114.300505 · Cited by 442
MacFabe, D. F. (2012) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v23i0.19260 · Cited by 438
Distribution, diversity and ecology of aerobic CO-oxidizing bacteria
King, G. M., & Weber, C. F. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1595 · Cited by 436
Endogenous Nitric Oxide Protects Bacteria Against a Wide Spectrum of Antibiotics
Gusarov, I., Shatalin, K., Starodubtseva, M., & Nudler, E. (2009) · Science · doi:10.1126/science.1175439 · Cited by 417
Wang, L., Christophersen, C. T., Sorich, M. J., Gerber, J. P., Angley, M. T., & Conlon, M. A. (2012) · Digestive Diseases and Sciences · doi:10.1007/s10620-012-2167-7 · Cited by 412
Ingested nitrate and nitrite and stomach cancer risk: An updated review
Bryan, N. S., Alexander, D. D., Coughlin, J. R., Milkowski, A. L., & Boffetta, P. (2012) · Food and Chemical Toxicology · doi:10.1016/j.fct.2012.07.062 · Cited by 335
Hydrogen Sulfide: From Brain to Gut
Kimura, H. (2009) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2919 · Cited by 315
NO-mediated cytoprotection: Instant adaptation to oxidative stress in bacteria
Gusarov, I., & Nudler, E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504307102 · Cited by 282
Liu, W.-H., Chuang, H.-L., Huang, Y.-T., Wu, C.-C., Chou, G.-T., Wang, S., & Tsai, Y.-C. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.10.046 · Cited by 269
Methanogens, Methane and Gastrointestinal Motility
Triantafyllou, K., Chang, C., & Pimentel, M. (2014) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm.2014.20.1.31 · Cited by 254
Methane and the Gastrointestinal Tract
Sahakian, A. B., Jee, S.-R., & Pimentel, M. (2009) · Digestive Diseases and Sciences · doi:10.1007/s10620-009-1012-0 · Cited by 222
Hydrogen Sulfide Signaling in the Gastrointestinal Tract
Linden, D. R. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5312 · Cited by 222
Bacterial Nitric Oxide Extends the Lifespan of C. elegans
Gusarov, I., Gautier, L., Смоленцева, О. А., Shamovsky, I., Eremina, S. Y., Mironov, A. S., & Nudler, E. (2013) · Cell · doi:10.1016/j.cell.2012.12.043 · Cited by 204
The oral microbiome and nitric oxide homoeostasis
Hezel, M., & Weitzberg, E. (2015) · Oral Diseases · doi:10.1111/odi.12157 · Cited by 201
Biology of nitrogen oxides in the gastrointestinal tract
Lundberg, J. O., & Weitzberg, E. (2013) · Gut · doi:10.1136/gutjnl-2011-301649 · Cited by 200
Farrugia, G., & Szurszewski, J. H. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.04.041 · Cited by 192
Differential immunostimulatory effects of Gram-positive bacteria due to their lipoteichoic acids
Ryu, Y. H., Baik, J. E., Yang, J. S., Kang, S., Im, J., Yun, C., Kim, D. W., Lee, K., Chung, D. K., Ju, H. R., et al. (2008) · International Immunopharmacology · doi:10.1016/j.intimp.2008.10.014 · Cited by 189
Hydrogen sulfide in signaling pathways
Olas, B. (2014) · Clinica Chimica Acta · doi:10.1016/j.cca.2014.10.037 · Cited by 171
Mechanisms of nitrite bioactivation
Kim-Shapiro, D. B., & Gladwin, M. T. (2014) · Nitric Oxide · doi:10.1016/j.niox.2013.11.002 · Cited by 157
A Gastroenterologist's Guide to Probiotics
Ciorba, M. A. (2012) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2012.03.024 · Cited by 156
An overview of the biological significance of endogenous gases: new roles for old molecules
Li, L., & Moore, P. K. (2007) · Biochemical Society Transactions · doi:10.1042/bst0351138 · Cited by 151
Frye, R. E., Rose, S., Slattery, J. M., & MacFabe, D. F. (2015) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v26.27458 · Cited by 145
Pathogenesis of Hepatic Encephalopathy and Brain Edema in Acute Liver Failure
Butterworth, R. F. (2014) · Journal of Clinical and Experimental Hepatology · doi:10.1016/j.jceh.2014.02.004 · Cited by 145
Stilling, R. M., Bordenstein, S. R., Dinan, T. G., & Cryan, J. F. (2014) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2014.00147 · Cited by 139
Gaseotransmitters: New Frontiers for Translational Science
Szabó, C. (2010) · Science Translational Medicine · doi:10.1126/scitranslmed.3000721 · Cited by 139
Richardson, A. J., McKain, N., & Wallace, R. J. (2013) · BMC Microbiology · doi:10.1186/1471-2180-13-6 · Cited by 134
Cystathionine β-synthase is enriched in the brains of Down’s patients
Ichinohe, A., Kanaumi, T., Takashima, S., Enokido, Y., Nagai, Y., & Kimura, H. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.10.118 · Cited by 128
The Diversity of Microbial Responses to Nitric Oxide and Agents of Nitrosative Stress
Bowman, L. A. H., McLean, S., Poole, R. K., & Fukuto, J. M. (2011) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/b978-0-12-387661-4.00006-9 · Cited by 118
The Role of Glutamine Synthetase and Glutamate Dehydrogenase in Cerebral Ammonia Homeostasis
Cooper, A. J. L. (2012) · Neurochemical Research · doi:10.1007/s11064-012-0803-4 · Cited by 114
Carbon monoxide and mitochondria—modulation of cell metabolism, redox response and cell death
Almeida, A. S., Figueiredo-Pereira, C., & Vieira, H. L. A. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00033 · Cited by 113
Cerebral effects of ammonia in liver disease: current hypotheses
Ott, P., & Vilstrup, H. (2014) · Metabolic Brain Disease · doi:10.1007/s11011-014-9494-7 · Cited by 106
The microbial organ in the gut as a driver of homeostasis and disease
Lyte, M. (2009) · Medical Hypotheses · doi:10.1016/j.mehy.2009.10.025 · Cited by 105
Characterization of the rat oral microbiome and the effects of dietary nitrate
Hyde, E. R., Luk, B., Cron, S., Kusic, L., McCue, T., Bauch, T., Kaplan, H., Tribble, G., Petrosino, J. F., & Bryan, N. S. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.09.017 · Cited by 103
The social network of carbon monoxide in medicine
Wegiel, B., Hanto, D. W., & Otterbein, L. E. (2012) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2012.10.001 · Cited by 99
Osmotic and oxidative/nitrosative stress in ammonia toxicity and hepatic encephalopathy
Görg, B., Schliess, F., & Häussinger, D. (2013) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2013.03.010 · Cited by 97
Low Doses of Carbon Monoxide Protect Against Experimental Focal Brain Ischemia
Zeynalov, E., & Doré, S. (2009) · Neurotoxicity Research · doi:10.1007/s12640-009-9014-4 · Cited by 90
Hypothesis: Bacteria Control Host Appetites
Norris, V., Molina, F., & Gewirtz, A. T. (2012) · Journal of Bacteriology · doi:10.1128/jb.01384-12 · Cited by 87
Muñoz, M. F., Puebla, M., & Figueroa, X. F. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00059 · Cited by 82
Biological warfare: Microorganisms as drivers of host–parasite interactions
Dheilly, N. M., Poulin, R., & Frédéric Thomas, A. (2015) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2015.05.027 · Cited by 80
Probiotic (symbiotic) bacterial languages
Ba, S. (2011) · Anaerobe · doi:10.1016/j.anaerobe.2011.05.009 · Cited by 80
Approaches to studying and manipulating the enteric microbiome to improve autism symptoms
Frye, R. E., Slattery, J. M., MacFabe, D. F., Allen‐Vercoe, E., Parker, W., Rodakis, J., Adams, J. B., Krajmalnik‐Brown, R., Bolte, E. R., Kahler, S. G., et al. (2015) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v26.26878 · Cited by 78
Oleskin, A. V., El-Registan, G. I., & Ba, S. (2016) · Microbiology · doi:10.1134/s0026261716010082 · Cited by 74
Self-citationTRP channels: sensors and transducers of gasotransmitter signals
Takahashi, N., Kozai, D., & Mori, Y. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00324 · Cited by 72
Diverse mechanisms underlying the regulation of ion channels by carbon monoxide
Peers, C., Boyle, J. P., Scragg, J. L., Dallas, M. L., Al‐Owais, M. M., Hettiarachichi, N. T., Elíes, J., Johnson, E., Gamper, N. L., & Steele, D. S. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12760 · Cited by 69
Inorganic nitrite supplementation for healthy arterial aging
Sindler, A. L., DeVan, A. E., Fleenor, B. S., & Seals, D. R. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01100.2013 · Cited by 68
Bueno, M., Wang, J., Mora, A. L., & Gladwin, M. T. (2013) · Antioxidants & Redox Signaling · doi:10.1089/ars.2012.4833 · Cited by 68
Microbiome to Brain: Unravelling the Multidirectional Axes of Communication
Aidy, S. E., Stilling, R. M., Dinan, T. G., & Cryan, J. F. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-20215-0_15 · Cited by 65
Therapeutic applications of the gaseous mediators carbon monoxide and hydrogen sulfide
Bannenberg, G. L., & Vieira, H. L. A. (2009) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543770902858824 · Cited by 62
Epigenomic programing: a future way to health?
Ba, S., & Midtvedt, T. (2014) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v25.24145 · Cited by 60
Metabolic Turnover of Hydrogen Sulfide
Kimura, H. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00101 · Cited by 55
Oleskin, A. V., Zhilenkova, O. G., Ba, S., Amerhanova, A. M., Кудрин, В. С., & Михайлович, К. П. (2014) · Journal of Pharmacy and Nutrition Sciences · doi:10.6000/1927-5951.2014.04.03.5 · Cited by 51
Self-citationInfluence of a probiotic lactobacillus strain on the intestinal ecosystem in a stress model mouse
Palomar, M. M., Galdeano, C. M., & Perdigón, G. (2013) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.08.015 · Cited by 46
A biochemical rationale for the interaction between gastrointestinal yeast and autism
Burrus, C. J. (2012) · Medical Hypotheses · doi:10.1016/j.mehy.2012.08.029 · Cited by 44
Deciphering nitric oxide stress in bacteria with quantitative modeling
Robinson, J. L., Adolfsen, K. J., & Brynildsen, M. P. (2014) · Current Opinion in Microbiology · doi:10.1016/j.mib.2014.05.018 · Cited by 43
Lyte, M. (2013) · PharmaNutrition · doi:10.1016/j.phanu.2012.11.002 · Cited by 40
Smith, H. K., Mann, B. E., Motterlini, R., & Poole, R. K. (2011) · IUBMB Life · doi:10.1002/iub.476 · Cited by 39
Gasotransmitters, poisons, and antimicrobials: it's a gas, gas, gas!
Tinajero‐Trejo, M., Jesse, H. E., & Poole, R. K. (2013) · F1000Prime Reports · doi:10.12703/p5-28 · Cited by 34
Histidine ligand variants of a flavo-diiron protein: effects on structure and activities
Fang, H., Caranto, J. D., Mendoza, R., Taylor, A. B., Hart, P. J., & Kurtz, D. M. J. (2012) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-012-0938-4 · Cited by 33
The gasotransmitter hydrogen sulphide decreases Na+transport across pulmonary epithelial cells
Althaus, M., Urness, K., Clauss, W., Baines, D. L., & Fronius, M. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.01909.x · Cited by 31
Concentrations and Correlations of Faecal Short-chain Fatty Acids and Faecal Water Content in Man
Siigur, U., Norin, K. E., Allgood, G. S., Schlagheck, T. G., & Midtvedt, T. (1994) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v7i6.8310 · Cited by 27
Gasotransmitters: Novel Regulators of Epithelial Na+ Transport?
Althaus, M. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00083 · Cited by 26
Unexpected NO-dependent DNA binding by the CooA homolog from Carboxydothermus hydrogenoformans
Clark, R. W., Lanz, N. D., Lee, A. J., Kerby, R. L., Roberts, G. P., & Burstyn, J. N. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505919103 · Cited by 26
Carbon Monoxide Protects Against Ischemia-reperfusion Injuryin Vitrovia Antioxidant Properties
Berne, J.-P., Lauzier, B., Rochette, L., & Vergely, C. (2012) · Cellular Physiology and Biochemistry · doi:10.1159/000338501 · Cited by 24
Nitrosothiols in Bacterial Pathogens and Pathogenesis
Laver, J. R., McLean, S., Bowman, L. A. H., Harrison, L. J., Read, R. C., & Poole, R. K. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.4767 · Cited by 22
Hydrogen sulfide: role in ion channel and transporter modulation in the eye
Njie‐Mbye, Y. F., Opere, C. A., Chitnis, M. K., & Ohia, S. E. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00295 · Cited by 18
Hettiarachchi, N. T., Boyle, J. P., Bauer, C. C., Dallas, M. L., Pearson, H. A., Hara, S., Gamper, N. L., & Peers, C. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4398 · Cited by 17
Vaginal microbiota in healthy women and patients with bacterial vaginosis and nonspecific vaginitis
Aleshkin, V. A., Александровна, В. Е., & Ba, S. (2006) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v18i2.7694 · Cited by 17
Gasotransmitters: novel regulators of ion channels and transporters
Althaus, M., & Clauss, W. G. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00027 · Cited by 14
Modulation of ion transport across rat distal colon by cysteine
Pouokam, E. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00043 · Cited by 11
Zı́dek, Z., Kmonı́čková, E., Kostecká, P., & Tlaskalová‐Hogenová, H. (2010) · Folia Microbiologica · doi:10.1007/s12223-010-0027-4 · Cited by 11
Flagged first, then by citations
Research works printed but not linked: 2
- Oleskin, 2013, Biopolitical approach to rehabilitation: potential role of microbial neurochemistry, Regen Med J, N1, 60
- El Aidy, 2016, Microbial endocrinology: interkingdom signaling in infectious disease and health. Advances in experimental medicine and biology 874, 301
Cited by
Sorted by citations
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
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
“Propionate and butyrate exert an influence on the intracellular potassium level, which implies the involvement of SCFAs in the operation of cell signaling systems (115).”
BackgroundNeurotransmitter modulation by the gut microbiota
Strandwitz, P. (2018) · Brain Research · doi:10.1016/j.brainres.2018.03.015 · Cited by 1,527
The gut-brain axis: how microbiota and host inflammasome influence brain physiology and pathology
Rutsch, A., Kantsjö, J. B., & Ronchi, F. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.604179 · Cited by 821
Short chain fatty acids: Microbial metabolites for gut-brain axis signalling
O’Riordan, K. J., Collins, M., Moloney, G. M., Knox, E. G., Aburto, M. R., Fülling, C., Morley, S. J., Clarke, G. A., Schellekens, H., & Cryan, J. F. (2022) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2022.111572 · Cited by 788
Metadata
- Authors
- Oleskin, A. V., & Shenderov, B. A.
- Affiliations
- Lomonosov Moscow State University (RU)
- Venue
- Microbial Ecology in Health & Disease
- Publisher
- Co-Action Publishing
- Published
- 2016-07-05
- Volume
- 27
- Issue
- 0
- Pages
- 30971-30971
- ISSN
- 0891-060X (ISSN-L)
- 1651-2235
- PMC
- PMC4937721
- OpenAlex
- W2472180307
- Cited by
- 145
- References
- 88
- Citations by year
- 2026: 3 · 2025: 16 · 2024: 14 · 2023: 15 · 2022: 28 · 2021: 25 · 2020: 12 · 2019: 10 · 2018: 12 · 2017: 8 · 2016: 2
- FWCI
- 5.55
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc
- Locations
- Microbial Ecology in Health and Disease (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Keywords
- short-chain fatty acids, gasotransmitters, gut microbiota, neuromodulation, neuroendocrine signaling, microbial metabolites, host-microbe interactions, microbial fermentation, redox signaling, ion channel modulation, epigenetic regulation, post-translational modification, gut-brain axis, therapeutic target
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