Cited by 378Gut microbiota and healthGastrointestinal motility and disordersRegulation of Appetite and Obesity

The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.

Gut microbiota, enteroendocrine functions and metabolism

Cani, Patrice D, Everard, Amandine, Duparc, Thibaut·2013·Current Opinion in Pharmacology

DOI 10.1016/j.coph.2013.09.008

Open this paper in CoChat — free account

Abstract

The gut microbiota affects host metabolism through a number of physiological processes. Emerging evidence suggests that gut microbes interact with the host through several pathways involving enteroendocrine cells (e.g. L cells). The activation of specific G protein coupled receptors expressed on L cells (e.g. GPR41, GPR43, GPR119 and TGR5) triggers the secretion of glucagon-like peptides (GLP-1 and GLP-2) and PYY. These gut peptides are known to control energy homeostasis, glucose metabolism, gut barrier function and metabolic inflammation. Here, we explore how crosstalk between the ligands produced by the gut microbiota (short chain fatty acids, or SCFAs), or produced by the host but influenced by gut microbes (endocannabinoids and bile acids), impact host physiology.

Integrity signals

Registry

Crossref · 10.1016/j.coph.2013.09.008

Cites

61 of 61 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

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
Metabolic Endotoxemia Initiates Obesity and Insulin Resistance
Cani, P. D., Amar, J., Iglesias, M. A., Poggi, M., Knauf, C., Bastelica, D., Neyrinck, A. M., Fava, F., Tuohy, K. M., Chabo, C., et al. (2007) · Diabetes · doi:10.2337/db06-1491 · Cited by 6,638
Self-citation
Obesity alters gut microbial ecology
Ley, R. E., Bäckhed, F., Turnbaugh, P., Lozupone, C. A., Knight, R. D., & Gordon, J. I. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504978102 · Cited by 6,176
The gut microbiota shapes intestinal immune responses during health and disease
Round, J. L., & Mazmanian, S. K. (2009) · Nature Reviews Immunology · doi:10.1038/nri2515 · Cited by 5,029
Changes in gut microbiota control metabolic endotoxemia-induced inflammation in high-fat diet-induced obesity and diabetes in mice
Cani, P. D., Bibiloni, R., Knauf, C., Waget, A., Neyrinck, A. M., Delzenne, N. M., & Burcelin, R. (2008) · Diabetes · doi:10.2337/db07-1403 · Cited by 4,819
Self-citation
Cross-talk between Akkermansia muciniphila and intestinal epithelium controls diet-induced obesity
Everard, A., Belzer, C., Geurts, L., Ouwerkerk, J. P., Druart, C., Bindels, L. B., Guiot, Y., Derrien, M., Muccioli, G. G., Delzenne, N. M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219451110 · Cited by 4,511
Self-citation
Functional interactions between the gut microbiota and host metabolism
Tremaroli, V., & Bäckhed, F. (2012) · Nature · doi:10.1038/nature11552 · Cited by 4,387
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
Human nutrition, the gut microbiome and the immune system
Kau, A. L., Ahern, P. P., Griffin, N. W., Goodman, A. L., & Gordon, J. I. (2011) · Nature · doi:10.1038/nature10213 · Cited by 2,588
Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability
Cani, P. D., Possemiers, S., Van de Wiele, T., Guiot, Y., Everard, A., Rottier, O., Geurts, L., Naslain, D., Neyrinck, A., Lambert, D. M., et al. (2009) · Gut · doi:10.1136/gut.2008.165886 · Cited by 2,518
Self-citation

Flagged first, then by citations

Show all 61 references

Sorted by citations

Items 201–300 of 376

Fecal microbiome alterations in pediatric patients with short bowel syndrome receiving a rotating cycle of gastrointestinal prophylactic antibiotics
Phyo, L. Y., Singkhamanan, K., Laochareonsuk, W., Surachat, K., Phutong, N., Boonsanit, K., Chiengkriwate, P., & Sangkhathat, S. (2021) · Pediatric Surgery International · doi:10.1007/s00383-021-04948-5 · Cited by 20
Chronic Perigestational Exposure to Chlorpyrifos Induces Perturbations in Gut Bacteria and Glucose and Lipid Markers in Female Rats and Their Offspring
Djekkoun, N., Dépeint, F., Guibourdenche, M., Sabbouri, H. E. K. E., Corona, A., Rhazi, L., Gay‐Queheillard, J., Rouabah, L., Hamdad, F., Bach, V., et al. (2022) · Toxics · doi:10.3390/toxics10030138 · Cited by 20
Plasma Levels of Endocannabinoids and Their Analogues Are Related to Specific Fecal Bacterial Genera in Young Adults: Role in Gut Barrier Integrity
Ortiz-Alvarez, L., Xu, H., Di, X., Köhler, I., Osuna‐Prieto, F. J., Acosta, F. M., Vilchez‐Vargas, R., Link, A., Plaza‐Díaz, J., van der Stelt, M., et al. (2022) · Nutrients · doi:10.3390/nu14102143 · Cited by 22
Butyrate Produced by Gut Microbiota Regulates Atherosclerosis: A Narrative Review of the Latest Findings
Dicks, L. M. T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26146744 · Cited by 22
Impact of Enteric Nervous Cells on Irritable Bowel Syndrome: Potential Treatment Options
Pastras, P., Aggeletopoulou, I., & Triantos, C. K. (2024) · Microorganisms · doi:10.3390/microorganisms12102036 · Cited by 18
Bacterial metabolite S-equol modulates glucagon-like peptide-1 secretion from enteroendocrine L cell line GLUTag cells via actin polymerization
Harada, K., Sada, S., Sakaguchi, H., Takizawa, M., Ishida, R., & Tsuboi, T. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.05.100 · Cited by 18
The Role of Nutri(epi)genomics in Achieving the Body’s Full Potential in Physical Activity
Petracci, I., Gabbianelli, R., & Bordoni, L. (2020) · Antioxidants · doi:10.3390/antiox9060498 · Cited by 19
Probiotics for glycemic control in patients with type 2 diabetes mellitus: protocol for a systematic review
Rittiphairoj, T., Pongpirul, K., Mueller, N. T., & Li, T. (2019) · Systematic Reviews · doi:10.1186/s13643-019-1145-y · Cited by 17
The role of gut microbiota in the treatment of irritable bowel syndrome
Leylabadlo, H. E., Heravi, F. S., Soltani, E., Abbasi, A., Kafil, H. S., Parsaei, M., Sanaie, S., Ahmadian, Z., & Ghotaslou, R. (2021) · Reviews in Medical Microbiology · doi:10.1097/mrm.0000000000000284 · Cited by 16
Dietary Inulin Regulated Gut Microbiota and Improved Neonatal Health in a Pregnant Sow Model
Li, H., Ma, L., Zhang, L., Liu, N., Li, Z., Zhang, F., Liu, X., & Ma, X. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.716723 · Cited by 16
Alterations in Fecal Microbiota Linked to Environment and Sex in Red Deer (Cervus elaphus)
Sun, Y., Yu, Y., Guo, J., Zhong, L., & Zhang, M. (2023) · Animals · doi:10.3390/ani13050929 · Cited by 16
Effects of the Gut Microbiota and Barrier Function on Melatonin Efficacy in Alleviating Liver Injury
Zhang, H., Liu, X., Elsabagh, M., Zhang, Y., Ma, Y., Jin, Y., Wang, M., Wang, H., & Jiang, H. (2022) · Antioxidants · doi:10.3390/antiox11091727 · Cited by 15
Mental Disorders Linked to Crosstalk between The Gut Microbiome and The Brain
Choi, T.-Y., Choi, Y. P., & Koo, J. W. (2020) · Experimental Neurobiology · doi:10.5607/en20047 · Cited by 18
Simulated spatial radiation impacts learning and memory ability with alterations of neuromorphology and gut microbiota in mice
Song, C., Gao, X., Song, W., Zeng, D., Shan, S., Yin, Y., Li, Y., Baranenko, D., & Lu, W. (2020) · RSC Advances · doi:10.1039/d0ra01017k · Cited by 14
Gut Microorganisms and Neurological Disease Perspectives
Faruqui, N. A., Prium, D. H., Mowna, S. A., Ullah, M. A., Araf, Y., Sarkar, B., Zohora, U. S., & Rahman, M. S. (2021) · Future Neurology · doi:10.2217/fnl-2020-0026 · Cited by 15
An overview of basic pathophysiological interactions between gut bacteria and their host
Simonson, M., Simonson, T., & Nobécourt, E. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1565609 · Cited by 14
Exploring the intestinal ecosystem: from gut microbiota to associations with subtypes of inflammatory bowel disease
Li, F., Yu, C., Zhao, Q., Wang, Z., Wang, Z., Chang, Y., Xu, Z., Han, X., Li, H., Liu, Y., et al. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1304858 · Cited by 15
Gut Microbiota and Metabolism
Ryan, P. M., & Delzenne, N. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802304-4.00018-9 · Cited by 12
Roles of intestinal microbiota in response to cancer immunotherapy
Cong, J., & Zhang, X. (2018) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-018-3374-8 · Cited by 13
Comparison of Structural and Functional Characterizations of Arabinoxylans from Different Wheat Processing Varieties
Sun, N., Wang, L., Tong, L., Zhou, X., Liu, L., Sun, Y., & Zhou, S. (2019) · Plant Foods for Human Nutrition · doi:10.1007/s11130-019-00734-w · Cited by 13
Polysaccharides from Trametes versicolor as a Potential Prebiotic to Improve the Gut Microbiota in High-Fat Diet Mice
Bai, M., Huang, Z., Zheng, X., Hou, M., & Zhang, S. (2024) · Microorganisms · doi:10.3390/microorganisms12081654 · Cited by 13
Dipeptidyl Peptidase-4 and Adolescent Idiopathic Scoliosis: Expression in Osteoblasts
Normand, É., Franco, A., Moreau, A., & Marcil, V. (2017) · Scientific Reports · doi:10.1038/s41598-017-03310-x · Cited by 12
A Mechanistic Model of Gut–Brain Axis Perturbation and High-Fat Diet Pathways to Gut Microbiome Homeostatic Disruption, Systemic Inflammation, and Type 2 Diabetes
Lew, K. N., Starkweather, A. R., Cong, X. S., & Judge, M. P. (2019) · Biological Research For Nursing · doi:10.1177/1099800419849109 · Cited by 12
Gut microbiota on human health and disease
Duttaroy, A. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822405-2.00006-2 · Cited by 11
Preliminary Evaluation of Potential Properties of Three Probiotics and Their Combination with Prebiotics on GLP-1 Secretion and Type 2 Diabetes Alleviation
Xiao, R., Wang, R., Shusen, L., Kang, X., Ren, Y., Sun, E., Wang, C., He, J., & Zhan, J. (2022) · Journal of Food Quality · doi:10.1155/2022/8586843 · Cited by 12
Xanthan gum oligosaccharides ameliorate glucose metabolism and related gut microbiota dysbiosis in type 2 diabetic mice
Xu, J., Sun, W., Li, H., Gao, Z., Hu, G.-A., Wu, J., Zhang, H., Li, Z., Gao, M., Zhu, L., et al. (2022) · Food Bioscience · doi:10.1016/j.fbio.2022.102002 · Cited by 12
Absorption and Transport Mechanism of Red Meat-Derived N-glycolylneuraminic Acid and Its Damage to Intestinal Barrier Function through the NF-κB Signaling Pathway
He, E., Quan, W., Luo, J., Liu, C., Zheng, W., & Shen, Q. W. (2023) · Toxins · doi:10.3390/toxins15020132 · Cited by 12
INTESTINAL MICROBIOTA MUTUALISM AND GASTROINTESTINAL DISEASES
Tomasello, G., Sinagra, E., Zeenny, M., Jurjus, A. R., Giammanco, M., Majo, D. D., Traina, G., Damiani, P., Zein, R. J., & Leone, A. (2026) · EuroMediterranean Biomedical Journal · doi:10.3269/1970-5492.2015.10.1 · Cited by 13
Lipid malabsorption from altered hormonal signaling changes early gut microbial responses
Terry, N. A., Ngaba, L. V., Wilkins, B. J., Pi, D., Gheewala, N., & Kaestner, K. H. (2018) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00135.2018 · Cited by 12
Akkermansia muciniphila bacteria: a new perspective on the management of obesity: an updated review
Payahoo, L., Khajebishak, Y., & Ostadrahimi, A. (2018) · Reviews in Medical Microbiology · doi:10.1097/mrm.0000000000000161 · Cited by 12
Microbiotes et maladies métaboliques
Burcelin, R., Nicolas, S., & Blasco‐Baqué, V. (2016) · médecine/sciences · doi:10.1051/medsci/20163211010 · Cited by 11
Bile-processed Rhizoma Coptidis alleviates type 2 diabetes mellitus through modulating the gut microbiota and short-chain fatty acid metabolism
Zhu, Y., Tian, Q., Huang, Q., & Wang, J. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114645 · Cited by 11
Clostridioides difficile toxin A-mediated Caco-2 cell barrier damage was attenuated by insect-derived fractions and corresponded to increased gene transcription of cell junctional and proliferation proteins
Dong, L., Tomassen, M. M. M., Ariëns, R. M. C., Oosterink, E., Wichers, H. J., Veldkamp, T., Mes, J. J., & Govers, C. (2021) · Food & Function · doi:10.1039/d1fo00673h · Cited by 11
New perspectives on microbiome-dependent gut-brain pathways for the treatment of depression with gastrointestinal symptoms: from bench to bedside
Liu, M., Fan, G., Meng, L., Yang, K., & Liu, H. (2024) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2300343 · Cited by 10
Comparison of the prebiotic properties of native chicory and synthetic inulins using swine fecal cultures
Nakayama, Y., Kawasaki, N., Tamiya, T., Anzai, S., Toyohara, K., Nishiyama, A., & Kitazono, E. (2020) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2020.1749553 · Cited by 10
Whole genome metagenomic analysis of the gut microbiome of differently fed infants identifies differences in microbial composition and functional genes, including an absent CRISPR/Cas9 gene in the formula-fed cohort
Guglielmo, M. D. D., Franke, K., Cox, C. L., & Crowgey, E. L. (2019) · Human Microbiome Journal · doi:10.1016/j.humic.2019.100057 · Cited by 10
Food obesogens as emerging metabolic disruptors; A toxicological insight
Ravichandran, G., Kumar, D., Arunachalam, A., & Thilagar, S. (2021) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2021.106042 · Cited by 13
Medicine‐Food Plant Polysaccharides Modulate Diabetes and Diabetic Complications Through Maintaining Gut Function: A Review
Long, Y., Yu, W., Yang, P., Xu, M., Ling, J., Wu, Y., Liu, X., Ouyang, L., Xiong, Y., Liu, J., et al. (2025) · Food Frontiers · doi:10.1002/fft2.70122 · Cited by 10
The Cognitive Improvement and Alleviation of Brain Hypermetabolism Caused by FFAR3 Ablation in Tg2576 Mice Is Persistent under Diet-Induced Obesity
Solas, M., Zamarbide, M., Ardanaz, C. G., Ramírez, M. J., & Pérez‐Mediavilla, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113591 · Cited by 9
Behavioral activation for smoking cessation and the prevention of smoking cessation-related weight gain: A randomized trial
Audrain-McGovern, J. E., Wileyto, E. P., Ashare, R. L., Albelda, B., Manikandan, D., & Perkins, K. A. (2023) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2023.109792 · Cited by 10
The association of antibiotic exposure with new-onset inflammatory bowel disease: A systematic review and meta-analysis
Dar, S. H., Maniya, M. T., Merza, N., Musheer, A., Zahid, M., Ahmed, F., Shurjeel, Q., Qazi, S., Ahmed, A. B., Shah, H., et al. (2023) · Clinics and Research in Hepatology and Gastroenterology · doi:10.1016/j.clinre.2023.102129 · Cited by 9
Weight and Glucose Reduction Observed with a Combination of Nutritional Agents in Rodent Models Does Not Translate to Humans in a Randomized Clinical Trial with Healthy Volunteers and Subjects with Type 2 Diabetes
Hodge, R. J., Paulik, M. A., Walker, A. C., Boucheron, J. A., McMullen, S. L., Gillmor, D., & Nunez, D. J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0153151 · Cited by 9
High and Mighty? Cannabinoids and the microbiome in pain
Rea, K., O’Mahony, S. M., & Cryan, J. F. (2021) · Neurobiology of Pain · doi:10.1016/j.ynpai.2021.100061 · Cited by 9
İnsan Mikrobiyomu: Beslenme ve Sağlık Üzerindeki Etkileri
Cetinbas, S., Kemeriz, F., Göker, G., Biçer, İ., & Velioğlu, Y. S. (2017) · Akademik Gıda · doi:10.24323/akademik-gida.370267 · Cited by 9
Bacillus licheniformis Alleviates Clostridium perfringens-Induced Intestinal Injury in Mice Model by Modulating Inflammation, Apoptosis, and Cecal Microbial–Metabolic Responses
Zhong, Y., Zhang, M., Xu, H., Yu, X., Hu, Y., Xu, Y., Xiao, X., & Yang, C. (2025) · Animals · doi:10.3390/ani15101409 · Cited by 8
The Interplay of Cross‐Organ Immune Regulation in Inflammation and Cancer
Dou, J., Jiang, J., Xue, Y., Jiang, X., Jiang, Y., Xiao, P., & Xu, J. (2025) · MedComm · doi:10.1002/mco2.70249 · Cited by 9
Enteric glial cells contribute to chronic stress-induced alterations in the intestinal microbiota and barrier in rats
Lu, T., Huang, C., Weng, R., Wang, Z., Sun, H., & Ma, X. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e24899 · Cited by 9
Nav1.8-expressing neurons control daily oscillations of food intake, body weight and gut microbiota in mice
Bullich‐Vilarrubias, C., Romaní‐Pérez, M., López‐Almela, I., Rubio, T., García, C. J., Tomás-Barberán, F. A., & Sanz, Y. (2024) · Communications Biology · doi:10.1038/s42003-024-05905-3 · Cited by 8
Effect of glucose oxidase and pentosanase on the prebiotic potentials of wheat arabinoxylans in an in vitro fermentation system
Sun, N., Wang, L., Liu, L., Tong, L., Tran, C. D., Awais, M., Zhou, X., & Zhou, S. (2019) · RSC Advances · doi:10.1039/c9ra02474c · Cited by 8
The role of the stem cell epigenome in normal aging and rejuvenative therapy
Jayarajan, J., & Milsom, M. D. (2020) · Human Molecular Genetics · doi:10.1093/hmg/ddaa167 · Cited by 8
Effects of Intestinal Flora on Irritable Bowel Syndrome and Therapeutic Significance of Polysaccharides
Ye, Y., Liu, Y., Cheng, K., Wu, Z., Zhang, P., & Zhang, X. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.810453 · Cited by 8
A discriminant analysis of plasma metabolomics for the assessment of metabolic responsiveness to red raspberry consumption
Barbe, V., de Toro‐Martín, J., San-Cristóbal, R., Garneau, V., Pilon, G., Couture, P., Roy, D., Couillard, C., Marette, A., & Vohl, M. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1104685 · Cited by 8
Regular low‐calorie sweetener consumption is associated with increased secretion of glucose‐dependent insulinotropic polypeptide
Chia, C. W., Shardell, M. D., Gravenstein, K. S., Carlson, O. D., Simonsick, E. M., Ferrucci, L., & Egan, J. M. (2018) · Diabetes Obesity and Metabolism · doi:10.1111/dom.13328 · Cited by 8
A bélflóra patofiziológai jelentősége és szerepe mint terápiás célpont májbetegségekben
Hagymási, K., Bacsárdi, A., Egresi, A., Berta, E., Tulassay, Z., & Lengyel, G. (2018) · Orvosi Hetilap · doi:10.1556/650.2018.31178 · Cited by 8
CLINICAL EFFICIENCY OF VAGINAL TRAINING DEVICE IN TREATMENT OF PELVIC ORGAN PROLAPSE IN ELDERLY WOMEN
KOROTKEVITCH, O. S., Эйзенах, И. А., Мозес, В. Г., & Захаров, И. С. (2018) · Fundamental and Clinical Medicine · doi:10.23946/2500-0764-2018-3-4-32-38 · Cited by 8
Childhood Obesity and Diabetes: Role of Probiotics and Prebiotics
Vyas, N., Nair, S., Rao, M., & Miraj, S. S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-812840-4.00029-3 · Cited by 8
Importance of Gut Microbiota Dysbiosis and Circadian Disruption–Associated Biomarkers in Emergence of Alzheimer’s Disease
Kaur, S., Kumari, D., & Dandekar, M. P. (2025) · Molecular Neurobiology · doi:10.1007/s12035-024-04685-5 · Cited by 7
Exploring the human small intestinal luminal microbiome via a newly developed ingestible sampling device
Tronel, A., Roger‐Margueritat, M., Plazy, C., Biennier, S., Craspay, A., Mohanty, I., Cools-Portier, S., Laiola, M., Roeselers, G., Mathieu, N., et al. (2025) · ISME Communications · doi:10.1093/ismeco/ycaf224 · Cited by 11
Navigating through 65 years of insights: lessons learned on functional abdominal pain in children
Rajindrajith, S., Boey, C., Devanarayana, N., Niriella, M., Thapar, N., & Benninga, M. (2024) · European Journal of Pediatrics · doi:10.1007/s00431-024-05667-4 · Cited by 8
Immunomodulatory effects of probiotics
Plotnikova, E. Y., & Zakharova, Y. V. (2020) · Meditsinskiy sovet = Medical Council · doi:10.21518/2079-701x-2020-15-135-144 · Cited by 7
A role of human microbiota in the development of neurodegenerative diseases
Epishina, I. V., & Budanova, E. V. (2022) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro202212210157 · Cited by 8
Lean and obese microbiota: differences in in vitro fermentation of food-by-products
de Souza, C. B., Saad, S. M. I., & Venema, K. (2021) · Beneficial Microbes · doi:10.3920/bm2020.0151 · Cited by 7
Experimental and Emerging Free Fatty Acid Receptor Agonists for the Treatment of Type 2 Diabetes
Patti, A. M., Giglio, R. V., Παπάνας, Ν., Şerban, D., Stoian, A. P., Pafili, K., Al‐Rasadi, K., Rajagopalan, K., Rizvi, A. A., Ciaccio, M., et al. (2022) · Medicina · doi:10.3390/medicina58010109 · Cited by 7
An Overview of the Roles of the Gut Microbiome in Obesity and Diabetes
Barlow, G. M., Lin, E. A., & Mathur, R. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812019-4.00006-4 · Cited by 7
GRK2 levels in myeloid cells modulate adipose-liver crosstalk in high fat diet-induced obesity
Vila‐Bedmar, R., Cruces‐Sande, M., Arcones, A. C., Willemen, H. L. D. M., Prieto, P., Moreno‐Indias, I., Díaz‐Rodríguez, D., Francisco, S., Jaén, R. I., Gutiérrez‐Repiso, C., et al. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03442-5 · Cited by 7
Billroth II anastomosis maintains SMI and BMI better than Roux-en-Y anastomosis following totally laparoscopic distal gastrectomy: a propensity score-matched study
Jiang, L., Zhang, J., & Zhu, X. (2022) · Langenbeck s Archives of Surgery · doi:10.1007/s00423-022-02459-y · Cited by 6
A Gluten Free Diet in the Management of Epilepsy in People with Coeliac Disease or Gluten Sensitivity
Gilbey, Z., & Bold, J. (2020) · Gastrointestinal Disorders · doi:10.3390/gidisord2030026 · Cited by 7
INTERAKSI ANTARA MIKROBIOTA USUS DAN SISTEM KEKEBALAN TUBUH MANUSIA
Hasibuan, F. E., & Kolondam, B. J. (2017) · JURNAL ILMIAH SAINS · doi:10.35799/jis.17.1.2017.15221 · Cited by 6
Probiyotik ve Prebiyotiklerin Bağırsak-Beyin Aksına Etkisi
Özer, M., Özyurt, G., & Harsa, Ş. (2019) · Akademik Gıda · doi:10.24323/akademik-gida.613637 · Cited by 7
Intestinal Immune Homeostasis and Inflammatory Bowel Disease: A Perspective on Intracellular Response Mechanisms
Ranjan, K. (2020) · Gastrointestinal Disorders · doi:10.3390/gidisord2030024 · Cited by 6
Effects of mannan oligosaccharide, Bacillus clausii, and their synbiotic supplementation on growth performance, humoral immunity, intestinal morphology, and ghrelin gene expression in broiler chickens
Al-Khalaifah, H., Mushtaq, M., Khan, A., Chand, N., Shah, S. S. A., Shah, M., Sultan, A., Khan, R., Naz, S., Abudabos, A., et al. (2025) · Poultry Science · doi:10.1016/j.psj.2025.105862 · Cited by 5
Association between inflammation, lipopolysaccharide binding protein, and gut microbiota composition in a New Hampshire Bhutanese refugee population with a high burden of type 2 diabetes
Moser, B., Moore, D., Khadka, B., Lyons, C., Foxall, T., Andam, C. P., Parker, C. J., Ochin, C., Garelnabi, M., Sevigny, J. L., et al. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1059163 · Cited by 5
HAND HYGIENE IN PATIENT CARE
Kampf, G. (2018) · Fundamental and Clinical Medicine · doi:10.23946/2500-0764-2018-3-4-60-72 · Cited by 5
Maternal Magnolol Supplementation during Pregnancy and Lactation Promotes Antioxidant Capacity, Improves Gut Health, and Alters Gut Microbiota and Metabolites of Weanling Piglets
Fan, Q., Du, E., Chen, F., Tao, W., Zhao, N., Huang, S., Guo, W., Huang, J., & Wei, J. (2023) · Metabolites · doi:10.3390/metabo13070797 · Cited by 8
FOURTH UNIVERSAL DEFINITION OF MYOCARDIAL INFARCTION. FOCUS ON THE TYPE 2 MYOCARDIAL INFARCTION
Барбараш, О. Л., & Кашталап, В. В. (2018) · Fundamental and Clinical Medicine · doi:10.23946/2500-0764-2018-3-4-73-82 · Cited by 5
The gut-brain axis: interactions between microbiota and nervous systems
Akpınar, O. (2018) · Journal of Cellular Neuroscience and Oxidative Stress · doi:10.37212/jcnos.610103 · Cited by 5
Microbial Impact on Host Metabolism: Opportunities for Novel Treatments of Nutritional Disorders?
Plovier, H., & Cani, P. D. (2018) · ASM Press eBooks · doi:10.1128/9781555819705.ch5 · Cited by 5
Self-citation
How the gut affects bone metabolism
Lafage‐Proust, M. (2017) · Joint Bone Spine · doi:10.1016/j.jbspin.2016.12.015 · Cited by 5
Probiotics and prebiotics, including fibers and medicinal foods
Jana, T., Acker, B. W., & Cash, B. D. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813037-7.00042-x · Cited by 4
Effects of Dietary Supplementation of Stimbiotics to Sows on Lactation Performance, Immune Function, and Anti-Inflammatory and Antioxidant Capacities during Late Gestation and Lactation
Li, J., Chen, W., Sun, W., Cordero, G., Hasan, S., Bontempo, V., Xiao, J.-F., Li, Y., Pi, Y., Li, X., et al. (2024) · Veterinary Sciences · doi:10.3390/vetsci11020053 · Cited by 4
Consumption patterns of nonnutritive sweeteners among university students at a Caribbean institution
Webb, M. C., Chong, D., & Bawa, S. (2020) · Journal of American College Health · doi:10.1080/07448481.2019.1706531 · Cited by 5
Bacillus subtilis JATP-3 Improves Nitrogen Metabolism by Regulating Intestinal Flora and AKG in Weaned Piglets
He, F., Jin, X., Sun, K., Zhao, L., Yang, W., Zhang, X., Dong, X., Zhao, Y., Li, P., Bao, N., et al. (2023) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-023-10196-x · Cited by 4
Enteroendocrine and adipokine associations with type 2 diabetes: Phenotypic risk scoring approaches
Cox, A. J., Zhang, P., Bowden, D. W., Devereaux, B., Davoren, P. M., Cripps, A. W., & West, N. P. (2017) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.14057 · Cited by 4
Adsorptive granulomonocytapheresis alters the gut bacterial microbiota in patients with active ulcerative colitis
Chen, X., Lou, L., Tang, H., Tan, X., Bi, J., Wu, H., Li, N., Wang, Y.-D., & Mao, J. (2021) · Journal of Clinical Apheresis · doi:10.1002/jca.21887 · Cited by 5
Metabolism of gut microbiota and its role in state of diabetes mellitus
Demidova, T. Y., Kochina, A. S., & Korotkova, T. N. (2023) · Meditsinskiy sovet = Medical Council · doi:10.21518/2079-701x-2022-16-23-192-198 · Cited by 3
Impact of the Gut Microbiome on Behavior and Emotions
Rivera‐Íñiguez, I., Román, S., Ojeda‐Granados, C., & Arturo, P. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-815249-2.00040-3 · Cited by 3
Psychobiotics
Mörkl, S., Butler, M., Cichini, F., Cryan, J. F., & Dinan, T. G. (2020) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190931544.013.7 · Cited by 3
Evaluation of Diet and Symptom Severity in Disorder of Gut–Brain Interaction
Faruga‐Lewicka, W., Bielaszka, A., Staśkiewicz‐Bartecka, W., Opiołka, S., Kiciak, A., & Kardas, M. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13144132 · Cited by 3
Microbiota and Lipotoxicity
Engin, D. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-63657-8_12 · Cited by 3
Astrocyte Pathophysiology in Liver Disease
Pérez‐Monter, C., & Torre-Delgadillo, A. (2018) · InTech eBooks · doi:10.5772/intechopen.72506 · Cited by 3
En Önemli Miras Anne Mikrobiyotası
Öz, H. G., & Yangın, H. B. (2020) · Hacettepe Üniversitesi Hemşirelik Fakültesi Dergisi · doi:10.31125/hunhemsire.834219 · Cited by 3
The role of probiotics on the roadmap to a healthy microbiota: a symposium report
Lockyer, S., Aguirre, M., Durrant, L., Pot, B., & Suzuki, K. (2020) · Gut Microbiome · doi:10.1017/gmb.2020.2 · Cited by 3
Plasma Levels of Endocannabinoids and Their Analogues Are Related to Specific Fecal Bacterial Genera in Young Adults: Role on Gut Barrier IntegrityPreprint
Ortiz-Alvarez, L., Xu, H., Di, X., Köhler, I., Osuna‐Prieto, F. J., Acosta, F. M., Vilchez‐Vargas, R., Link, A., Plaza‐Díaz, J., van der Stelt, M., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4000450 · Cited by 3
Plasma and Urinary TMAO and Methylamine Responses to Meat and Egg Ingestion: Links to Gut Microbiota Composition in Subjects With and Without Metabolic Syndrome
Hefni, M. E., Esberg, A., Hellström, P., Johansson, I., & Witthöft, C. M. (2025) · Nutrients · doi:10.3390/nu17233719 · Cited by 2
The roles of gut microbiota and their metabolites in uric acid–related metabolic diseases: mechanisms and therapeutic targets
Li, H., Zhou, H., Li, M., Wu, J., & Pan, L. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1781413 · Cited by 2
RETRACTED: Gut-Colonizing Bacteria Promote C. elegans Innate Immunity by Producing Nitric Oxide
Xiao, Y., Liu, F., Zhang, Z., Tang, J., Zou, C., & Zhang, K. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.01.032 · Cited by 2
Retracted
Microbiota and Lipotoxicity
Engin, D. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-48382-5_10 · Cited by 2
Potential Role of Microbiota in the Prevention and Therapeutic Management of Infectious Diseases
Shahid, A., Nasir, K., Aslam, S., Kamran, M., Sarfraz, M. H., Saleem, H. G. M., & Khurshid, M. (2022) · Pakistan Journal of Biochemistry and Biotechnology · doi:10.52700/pjbb.v3i1.75 · Cited by 3
Abordaje nutricional en el tratamiento de la depresión, revisión bibliográfica.
Quishpe, E. T. V., Lara, V. E. G., & Morales, K. P. H. (2023) · Ciencia Latina Revista Científica Multidisciplinar · doi:10.37811/cl_rcm.v7i3.6599 · Cited by 2
Health-Related Composition and Bioactivity of an Agave Sap/Prickly Pear Juice Beverage
Duque-Buitrago, L. F., Solórzano-Lugo, I. E., González-Vázquez, M., Jiménez‐Martínez, C., Hernández-Aguirre, M. A., Osorio‐Díaz, P., Calderón‐Domínguez, G., Loera‐Castañeda, V., & Mora‐Escobedo, R. (2024) · Molecules · doi:10.3390/molecules29122742 · Cited by 3

Authors: Cani, P. D., Everard, A., & Duparc, T.
Affiliations: Walloon Excellence in Lifesciences and Biotechnology (BE)
Corresponding author: Cani, Patrice D
ORCID: Cani, Patrice D
Everard, Amandine
Duparc, Thibaut
Venue: Current Opinion in Pharmacology
Publisher: Elsevier BV
Published: 2013-12
Volume: 13
Issue: 6
Pages: 935-940
ISSN: 1471-4892 (ISSN-L)
DOI: 10.1016/j.coph.2013.09.008
OpenAlex: W2044719746
Cited by: 378
References: 61
Citations by year: 2026: 16 · 2025: 17 · 2024: 21 · 2023: 26 · 2022: 31 · 2021: 37 · 2020: 45 · 2019: 34 · 2018: 48 · 2017: 36 · 2016: 29 · 2015: 21 · 2014: 16 · 2013: 1
FWCI: 2.10
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Current Opinion in Pharmacology (publishedVersion)
PubMed (publishedVersion)
Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)) (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 › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
Keywords: gut microbiota, enteroendocrine cells, L cells, G protein-coupled receptors, GPR41, GPR43, GPR119, TGR5, glucagon-like peptide-1, glucagon-like peptide-2, peptide YY, short-chain fatty acids, endocannabinoids, bile acids, energy homeostasis, glucose metabolism, intestinal barrier, metabolic inflammation
MeSH terms: Animals, Gastrointestinal Hormones, Humans, Enteroendocrine Cells, Gastrointestinal Tract, Microbiota

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

Gut microbiota, enteroendocrine functions and metabolism

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks