Cited by 268Gut microbiota and healthGastrointestinal motility and disordersProbiotics and Fermented Foods

The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index.

The Effect of Diet and Exercise on Intestinal Integrity and Microbial Diversity in Mice

Open access

Campbell, Sara C., Wisniewski, Paul J., Noji, Michael, McGuinness, Lora R., Häggblom, Max M., Lightfoot, Stanley A., Joseph, Laurie B., Kerkhof, Lee J.·2016·PLOS ONE

DOI 10.1371/journal.pone.0150502PMC PMC4783017

Open this paper in CoChat — free account Open PDF

Abstract

BACKGROUND: The gut microbiota is now known to play an important role contributing to inflammatory-based chronic diseases. This study examined intestinal integrity/inflammation and the gut microbial communities in sedentary and exercising mice presented with a normal or high-fat diet. METHODS: Thirty-six, 6-week old C57BL/6NTac male mice were fed a normal or high-fat diet for 12-weeks and randomly assigned to exercise or sedentary groups. After 12 weeks animals were sacrificed and duodenum/ileum tissues were fixed for immunohistochemistry for occludin, E-cadherin, and cyclooxygenase-2 (COX-2). The bacterial communities were assayed in fecal samples using terminal restriction fragment length polymorphism (TRFLP) analysis and pyrosequencing of 16S rRNA gene amplicons. RESULTS: Lean sedentary (LS) mice presented normal histologic villi while obese sedentary (OS) mice had similar villi height with more than twice the width of the LS animals. Both lean (LX) and obese exercise (OX) mice duodenum and ileum were histologically normal. COX-2 expression was the greatest in the OS group, followed by LS, LX and OX. The TRFLP and pyrosequencing indicated that members of the Clostridiales order were predominant in all diet groups. Specific phylotypes were observed with exercise, including Faecalibacterium prausnitzi, Clostridium spp., and Allobaculum spp. CONCLUSION: These data suggest that exercise has a strong influence on gut integrity and host microbiome which points to the necessity for more mechanistic studies of the interactions between specific bacteria in the gut and its host.

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

Crossref · 10.1371/journal.pone.0150502

Cites

60 of 60 references verified0 citation errors · 0 not checkable

Statistics

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

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
Human gut microbes associated with obesity
Ley, R. E., Turnbaugh, P. J., Klein, S., & Gordon, J. I. (2006) · Nature · doi:10.1038/4441022a · Cited by 8,785
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
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
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
Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients
Sokol, H., Pigneur, B., Watterlot, L., Lakhdari, O., Bermúdez-Humarán, L. G., Gratadoux, J.-J., Blugeon, S., Bridonneau, C., Furet, J.-P., Corthier, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804812105 · Cited by 4,413
Inflammatory Mechanisms in Obesity
Gregor, M. F., & Hotamisligil, G. S. (2011) · Annual Review of Immunology · doi:10.1146/annurev-immunol-031210-101322 · Cited by 3,754
Mechanisms underlying the resistance to diet-induced obesity in germ-free mice
Bäckhed, F., Manchester, J. K., Semenkovich, C. F., & Gordon, J. I. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605374104 · Cited by 2,615
The gut microbiota and host health: a new clinical frontier
Marchesi, J. R., Adams, D. H., Fava, F., Hermes, G. D. A., Hirschfield, G. M., Hold, G., Quraishi, M. N., Kinross, J., Smidt, H., Tuohy, K. M., et al. (2016) · Gut · doi:10.1136/gutjnl-2015-309990 · Cited by 2,302 · cited 1×
“Microbiome dysbiosis has proven to be a major contributor to chronic gut inflammatory diseases, like Irritable Bowel Syndrome (IBS) and ulcerative colitis [1].”
Background
Metabolic Syndrome and Altered Gut Microbiota in Mice Lacking Toll-Like Receptor 5
Vijay-Kumar, M., Aitken, J. D., Carvalho, F. A., Cullender, T. C., Mwangi, S., Srinivasan, S., Sitaraman, S. V., Knight, R., Ley, R. E., & Gewirtz, A. T. (2010) · Science · doi:10.1126/science.1179721 · Cited by 2,068

Flagged first, then by citations

Show all 60 references

Research works printed but not linked: 1

WH Martin, 1993, Effect of endurance training on plasma FFA turnover and oxidation during exercise, Am. J. Physiol, 265, E708

Sorted by citations

Items 201–268 of 268

Exploring gut microbiota and spinal cord injury: pathogenesis, treatment strategies and prospects
Chen, Q., Zhong, M., & Ye, L. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1693883 · Cited by 3
Multifactorial Mechanisms and Therapeutic Role of the Gut Microbiota in Sarcopenic Obesity: Role of Lifestyle and Gut Microbiota–Derived Metabolites
Tao, Y., Wang, Z., Wang, Q., & Zhong, S. (2025) · Nutrition Reviews · doi:10.1093/nutrit/nuaf274 · Cited by 4
The Gut Microbiota: An Essential Component in Understanding Pediatric Obesity: A Narrative Review
Lupu, V. V., Nedelcu, A. H., Balas, R. B., Anton, C., Tarnita, I., Azoicai, A. N., Forna, L., Munteanu, D., Anton, S. C., Shawais, S. K., et al. (2026) · Nutrients · doi:10.3390/nu18060952 · Cited by 3
Ketogenic diet as a therapeutic strategy for neurodegenerative diseases: from mechanisms to translational challenges
Salgueiro, A. M., Ferreira‐Marques, M., Ribeiro, R. F. N., Lopes, S. M., Pereira, D., Costa, D. G., Santana, M. M., de Almeida, L. P., & Cavadas, C. (2026) · Translational Neurodegeneration · doi:10.1186/s40035-026-00557-1 · Cited by 4
Relationship between Gut-Microbiota and Sport Activity
Mokarrami, A., Capacci, A., Trio, B., Merra, G., & Canosci, D. D. M. (2024) · Central European Journal of Sport Sciences and Medicine · doi:10.18276/cej.2024.1-03 · Cited by 4
Enviromimetics: From exercise mimetics to cognitomimetics in the quest for enhanced brain health and cognition
Hannan, A. J. (2025) · The Journal of Physiology · doi:10.1113/jp287484 · Cited by 3
Surfeit folic acid, protein, and exercise modify oncogenic inflammatory biomarkers and fecal microbiota
Tuska, R., Helm, S. M., Graf, C. F., James, C., Kong, G., Stiemsma, L. T., Green, D. B., & Helm, S. E. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1060212 · Cited by 4
From symbiosis to dysbiosis in gut-consequence includes metabolic syndrome
Mohan, N., & Sunder, A. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-95715-1.00005-4 · Cited by 3
Effect of oligosaccharides and aerobic training on hyperglycemia, growth and intestinal microbial diversity of diabetic rats
Choneva, M., Hristozov, M. V., Dimov, I., Boyanov, K., Dimitrov, I. V., Murdjeva, M., Hrischev, P., Vasilev, V., Georgieva, K. N., & Bivolarska, A. V. (2023) · Turkish Journal of Biochemistry · doi:10.1515/tjb-2023-0070 · Cited by 3
Parental cardiorespiratory fitness influences early life energetics and metabolic health
Sadler, D. G., Treas, L. D., Ross, T., Sikes, J. D., Britton, S. L., Koch, L. G., Piccolo, B. D., Børsheim, E., & Porter, C. C. (2023) · Physiological Genomics · doi:10.1152/physiolgenomics.00045.2023 · Cited by 3
МІКРОБІОМ ТА ОЖИРІННЯ
Мельник, Т., & Pivtorak, K. V. (2024) · ГРААЛЬ НАУКИ · doi:10.36074/grail-of-science.12.04.2024.065 · Cited by 3
The Nerves to Conduct a Multiple Sclerosis Crime Investigation
Chopra, S., Myers, Z., Sekhon, H., & Dufour, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052498 · Cited by 2
The Effect of 6 Weeks Aerobic Training and Aqueous Extract of Caraway Seed (Carum Carvi) on the Expression of CTRP12 Gene, Body Weight Changes and Subcutaneous Adipose Tissue in Obese Male Rats: An Experimental Study
Taherzadeh, S., Mogharnasi, M., Rasoulian, B., Kaeidi, A., & Khosravi, A. (2020) · مجله علمی دانشگاه علوم پزشکی رفسنجان · doi:10.29252/jrums.19.1.39 · Cited by 3
Are conventional antidepressants enough? The gut microbiome and nanocarrier-based delivery systems as future prospects for depression treatment
Gastaldo-Jordán, I., Villalba-Pita, C., Martínez-Raga, J., Sanz, Y., & Medina-Rodriguez, E. M. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106421 · Cited by 2
Late-in-life treadmill training mitigates gut microbiome imbalances and cardiovascular disease risk in mice
Cho, J. M., Park, S.-K., Babu, A. K. S., Mookherjee, S., Hansen, M., Petersen, C., Zhong, Y., Jalili, T., Robeson, M. S., Wankhade, U. D., et al. (2026) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00354.2025 · Cited by 2
Link between physical activity, nutrition, and antimicrobial pharmacokinetics and therapeutic efficacy: Implications for resistance management
Clemente‐Suárez, V. J., Beltrán-Velasco, A. I., Ramos‐Campo, D. J., Rubio-Zarapuz, A., Tornero-Aguilera, J. F., Martín-Rodríguez, A., Sepulveda, R. A. Y., & López-Gil, J. F. (2026) · SAGE Open Medicine · doi:10.1177/20503121261462838 · Cited by 3
The role of microbiota-gut-brain axis in neurodegenerative diseases: biochemical and therapeutic aspects
Ernesto, J. T., Damásio, C. M., Gontijo, V. S., Gasparotto, J., & Viegas, C. (2023) · Exploration of Neuroprotective Therapy · doi:10.37349/ent.2023.00038 · Cited by 2
Interaction between high-intensity interval training and high-protein diet on gut microbiota composition and body weight in obese male rats
Aliabadi, M., Saghebjoo, M., Yakhchali, B., & Shariati, V. (2023) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2023-0071 · Cited by 3
Correlation between gut microbiota and musculoskeletal diseases
Alessandro de, S. I. R. E., Marotta, N., Zito, R., Invernizzi, M., & Ammendolia, A. (2024) · International Journal of Bone Fragility · doi:10.57582/ijbf.240402.054 · Cited by 3
Contourner la résistance à l’immunothérapie des cancers : interventions centrées sur le microbiome intestinal
Fidelle, M., Derosa, L., Routy, B., & Zitvogel, L. (2021) · Bulletin de l Académie Nationale de Médecine · doi:10.1016/j.banm.2021.01.022 · Cited by 2
Microbiota intestinale ed esercizio fisico: nuova possibile area di intervento?
Cella, V., Migliaccio, S., & Paoli, A. (2020) · L Endocrinologo · doi:10.1007/s40619-020-00777-1 · Cited by 2
Although host-related factors are important for the formation of gut microbiota, environmental factors cannot be ignoredPreprint
Jung, Y., Kerfahi, D., Pham, H. Q., Son, H., Ibal, J. C., Park, M., Park, Y.-J., Park, C. E., Choi, S.-D., Jo, Y., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.03.933317 · Cited by 2
Role of the Gut Flora in Human Nutrition and Gut Health
Alvarado‐Martinez, Z., Filho, S., Mihalik, M., Rha, R., & Snyder, M. (2020) · Springer eBooks · doi:10.1007/978-3-030-47384-6_5 · Cited by 2
Mechanisms of Musculoskeletal Frailty in People Living with HIV
Nelson, A. K., Fiskum, G. M., Renn, C. L., Zhu, S., Kottilil, S., & Klinedinst, N. J. (2021) · The Journal of Frailty & Aging · doi:10.14283/jfa.2021.44 · Cited by 1
Exercise and the Brain–Gut Axis
Godinho, D. B., Fighera, M. R., & Royes, L. F. F. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99971-7.00019-9 · Cited by 1
Microbial Partners In Disease: Understanding The Role Of Gut Microbiota In Diabetes
NUNES, T. C. C., Santos, F. C., LIRIO, L. R., COSSARI, J. F., RODRIGUES, Y. B., BERALDO, A., SILVA, A. P. F., SILVA, S. S., CADAMURO, M. P. D. R., Duran, A., et al. (2024) · International Journal of Health Science · doi:10.22533/at.ed.1594272419033 · Cited by 2
Getting to the Heart of the Matter: Exploring the Intersection of Cardiovascular Disease, Sex and Race and How Exercise, and Gut Microbiota Influence these Relationships
Guers, J. J., Heffernan, K. S., & Campbell, S. C. (2025) · Reviews in Cardiovascular Medicine · doi:10.31083/rcm26430 · Cited by 1
Self-citation
Future Perspectives in the Management of Obesity
Garcha, S. C., & Kalra, S. (2025) · Springer eBooks · doi:10.1007/978-981-96-1651-0_6 · Cited by 1
Gut microbiota and intervention of probiotics in spaceflight
Pradeep, N., Green, S. J., & Chaudhary, A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-32904-3.00024-8 · Cited by 1
Moderate physical activity during late pregnancy enhances gut microbial network stability in pregnant women
Tye, K. D., Ran, X., & Liu, X. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1731350 · Cited by 2
Interweaving microglial senescence and gut microbiome dynamics in Alzheimer's disease – Mechanisms and therapeutic frontiers
Waghmare, A., Rahangdale, S. R., Khare, K., Taksande, B. G., Umekar, M. J., & Mangrulkar, S. V. (2026) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2026.104075 · Cited by 1
Disruption of the gut microbiota in regulator of G protein signaling 14 knockout (RGS14 KO) mice alters the metabolome and reduces enhanced exercise capacity
Longoria, C. R., DeSio, D. D., Oydanich, M. K., Su, X., Chiles, E. N., Kerkhof, L. J., Ibironke, O. A., Häggblom, M. M., Wages, N. P., Guers, J. J., et al. (2026) · European Journal of Applied Physiology · doi:10.1007/s00421-026-06191-z · Cited by 1
Self-citation
High-intensity exercise training alters gut microbiota to mitigate the development of experimental autoimmune encephalomyelitis
Hamdi, L., Agranyoni, O., Goldberg, Y., Zarka, N., Fainstein, N., Theotokis, P., Salamotas, I., Grigoriadis, N., Katz, A., Ben‐Hur, T., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-48522-2 · Cited by 1
Sarcopenia
Barry, D. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-43044-9.00217-x · Cited by 1
Exercise and Gut Microbiome: Trends and Advances in Research Methods
Baek, K., Ahn, K., Ahn, Y. J., Xiang, Y.-Y., & Kim, J. (2022) · Exercise Science · doi:10.15857/ksep.2022.00479 · Cited by 2
МІКРОБІОТА ЛЮДЕЙ ТА ТВАРИН: ВПЛИВ ФІЗИЧНОЇ АКТИВНОСТІ ТА ДІЄТИ
Куйбіда, В., Lopatynska, V. V., & Коханець, П. (2022) · Scientia et societus · doi:10.31470/2786-6327/2022/2/108-117 · Cited by 2
Gut Microbiome and Diet: Promising Approach for Treatment of Cognitive Impairment
Soni, A., Gupta, P., & Verma, A. (2022) · Nutritional neurosciences · doi:10.1007/978-981-19-4530-4_12 · Cited by 1
Energy Balance: Through the Looking Glass
Brilla, L. R. (2016) · Journal of Sports Medicine & Doping Studies · doi:10.4172/2161-0673.1000e149
Exercise and Dietary Factors Affecting the Microbiota: Current Knowledge and Future Perspectives
Marroquín, F. E. M. (2017) · Journal of Nutritional Health & Food Engineering · doi:10.15406/jnhfe.2017.06.00199
Efeitos do treinamento aeróbio sobre a morfologia e função barreira da mucosa intestinal em ratos wistar
da Costa, A. V. (2017) · doi:10.11606/d.39.2017.tde-01062017-151656
Exercise and Sport Sciences Reviews: 2019 Paper of the Year
Campbell, S. C. (2020) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000228
Self-citation
EFFECT OF PHYSICAL EXERCISE ON COLORECTAL CANCER: SYSTEMATIC REVIEW
Neves, M. B., Gonçalves, A. D. F., Alves, G. R., Takita, L. C., Fagundes, L. S., Rocha, A. K. D. S., da Silva, U. N., Toniello, J. F., & Ramalho, R. T. (2021) · International Journal for Innovation Education and Research · doi:10.31686/ijier.vol9.iss2.2930
Research in Exercise Science and Gut Microbiota: A Two-way Relationship
Petriz, B. A., de Almeida, J. A., Ribeiro, F. M., & Franco, O. L. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00066-8
Gene-Environment-Gut Interactions in Huntington's Disease Mice Are Associated with Environmental Modulation of the Gut MicrobiomePreprint
Gubert, C., Love, C. J., Kodikara, S., Liew, J. J. M., Renoir, T., Cao, K. L., & Hannan, A. J. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3904352
Peer Review #1 of "Diets with and without edible cricket support a similar level of diversity in the gut microbiome of dogs (v0.1)"
(2019) · PeerJ · doi:10.7287/peerj.7661v0.1/reviews/1
References
(2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811351-6.00026-7
Involvement of Body Temperature Increase and Sympathetic Nerve Activation in Exercise-Induced Microbiota Changes in MicePreprint
Sasaki, H., Miyakawa, H., Watanabe, A., Tamura, K., Shiga, K., Lyu, Y., Ichikawa, N., Fu, Y., Hayashi, K., Imamura, M., et al. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3920240
Peer Review #2 of "Diets with and without edible cricket support a similar level of diversity in the gut microbiome of dogs (v0.1)"
(2019) · PeerJ · doi:10.7287/peerj.7661v0.1/reviews/2
Applications of Microbial Fermentation to Food Products, Chemicals and Pharmaceuticals
(2021) · Wiley eBooks · doi:10.1002/9781119042792.part2
Nutritional and lifestyle procedures to reduce symptoms associated with dysbiosis in women
Ferreira, C. D. S., de Brito, L. T. T., Albuquerque, G. M., Vieira, J. N., & Torres, R. D. A. (2024) · REVISTA INTERDISCIPLINAR E DO MEIO AMBIENTE (RIMA) · doi:10.52664/rima.v6.n1.2024.e247
Investigating the role of gut microbiome in the association between ambient air pollution and type-2 diabetes mellitus: a causal inference approach using review of evidence to date
Mandal, S., Kuriakose, S., & Shridhar, K. (2024) · Frontiers in Environmental Health · doi:10.3389/fenvh.2024.1339674
Comparing the Impact of Continuous Endurance and High-intensity Interval Training on Cecal Butyrate and Propionate Levels in Diabetic Rats Induced by High-fat Diet
Solouki, S., Gorgani‐Firuzjaee, S., Jafary, H., & Delfan, M. (2024) · Annals of Military and Health Sciences Research · doi:10.5812/amh-147901
References
(2024) · Elsevier eBooks · doi:10.1016/b978-0-443-23565-8.09996-8
Lifestyle Factors Affecting Biological Processes and Health
Anisman, H., Hayley, S. P., & Kusnecov, A. W. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-23565-8.00009-0
Practical applications for diet and lifestyle to improve microbial and epigenetic health
Habibian, J. S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18979-1.00015-0
Evaluation of the intestinal microbiota and correlation with functioning in patients suffering from knee osteoarthritis: a cross-sectional study
Zito, R., Marotta, N., Bartalotta, I., Sgro, M., Massimino, M., Averta, C., Mannino, G. C., Andreozzi, F., Ammendolia, A., & Alessandro de, S. I. R. E. (2024) · International Journal of Bone Fragility · doi:10.57582/ijbf.240401.038
16S rRNA NGS sequencing of fecal bacterial microbiota in some obese and healthy horses of Ukrainian origin
Боровков, С. Б., Kolchyk, O. V., Тарасов, О. А., & Bezymennyi, M. (2025) · Agricultural science and practice · doi:10.15407/agrisp11.03.072
The Role of the Microbiome in Surgical Diseases and Their Management
Thomas, R. M. (2025) · Success in academic surgery · doi:10.1007/978-3-031-83034-1_18
Ameliorative Effects of Aerobic Exercise Combined With Lycium barbarum Polysaccharide‐Mediated Gut Microbiota Remodeling on Glycolipid Abnormalities in Type 2 Diabetic Rats
Wang, J., Feng, S., Cao, X., & Li, X. (2026) · Food Science & Nutrition · doi:10.1002/fsn3.71503
Gut bacteriome alterations during high altitude exposure: a comprehensive analysis of different species
Yin, X., Zeng, J., Li, Z., Chen, S., Xie, C., Li, X., Zhang, L., Pan, Y., & An, J. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1762563 · Cited by 1
Exercise, eating, and estrogen: What in the gut is going on?
Campbell, S. C., Cheng, A., & Snyder, K. M. (2026) · Sports Medicine and Health Science · doi:10.1016/j.smhs.2026.02.004
Self-citation
Étude des effets des acides gras oméga-3 et de nouvelles bactéries probiotiques pour contrer les désordres associés à l'obésité au niveau métabolique et intestinal
Barz, M. L. (2017) · theses.fr (ABES) · doi:10.70675/d1f0a7a2z6eadz445dzb191za197a6f08824
Effets de différentes modalités d’entrainement et/ou d’une complémentation à base d’extraits végétaux sur la composition corporelle et l’équilibre glycémique
Dupuit, M. (2021) · theses.fr (ABES) · doi:10.70675/01833b89z2397z4126z961dz74652e7b2a54
Acute high-intensity exercise alters gut microbiota composition and energy metabolism in different strains of mice
Gao, R., Wang, J., Song, J., Zhang, W., & Quan, L. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1790697
Gut Microbiota and Skeletal Muscle Interaction: The Role of Short-Chain Fatty Acids, G-Protein Receptor Signaling and Metabolic Adaptation
Kalkan, H. (2026) · Physiology · doi:10.5772/intechopen.1015465 · Cited by 1
Fecal microbiota transplantation in obesity: a comprehensive overview from basic research to clinical application
Ji, Y., Zhao, L., Wang, L., Wang, A., Zhang, C., Xie, Y., & Luo, X. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1840517 · Cited by 1
Prescribing Exercise as a Lifestyle Intervention
Karatzaferi, C., Osório, T. G., Conde, J., Arosa, L., Roditi, E.-E., & Sakkas, G. K. (2026) · Advances in predictive, preventive and personalised medicine · doi:10.1007/978-3-032-32838-0_11
Interactions between physical activity, diet, and gut microbiota in gastrointestinal health: celiac disease as a model in children and athletes
Montano, A., Paolini, A., Felli, C., Bruno, S. P., Baldassarre, A., Sandal, S., & Masotti, A. (2026) · Frontiers in Sports and Active Living · doi:10.3389/fspor.2026.1940762

Authors: Campbell, S. C., Wisniewski, P. J., Noji, M., McGuinness, L. R., Häggblom, M. M., Lightfoot, S. A., Joseph, L. B., & Kerkhof, L. J.
Affiliations: Rutgers, The State University of New Jersey (US)
Corresponding author: Campbell, Sara C.
ORCID: Campbell, Sara C.
Noji, Michael
Häggblom, Max M.
Joseph, Laurie B.
Kerkhof, Lee J.
Venue: PLOS ONE
Publisher: Public Library of Science (PLoS)
Published: 2016-03-08
Volume: 11
Issue: 3
Pages: e0150502
ISSN: 1932-6203 (ISSN-L)
DOI: 10.1371/journal.pone.0150502
PMC: PMC4783017
OpenAlex: W2295140408
Cited by: 268
References: 60
Citations by year: 2026: 18 · 2025: 18 · 2024: 33 · 2023: 24 · 2022: 33 · 2021: 34 · 2020: 33 · 2019: 25 · 2018: 16 · 2017: 26 · 2016: 8
FWCI: 12.99
Type: journal article
Language: en
Open access: gold
doi.org
Licence: cc-by
creativecommons.org/licenses/by/4.0/ (vor)
Locations: PLoS ONE (publishedVersion, cc-by)
Europe PMC (PubMed Central) (publishedVersion, cc-by)
PubMed Central (publishedVersion, cc-by)
PubMed (publishedVersion)
Rutgers University Community Repository (Rutgers University) (submittedVersion)
DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Figshare (submittedVersion, cc-by)
Funders: National Institutes of Health
National Institute of Arthritis and Musculoskeletal and Skin Diseases (U54AR055073)
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: gut microbiota, high-fat diet, physical activity, intestinal integrity, intestinal inflammation, cyclooxygenase-2, occludin, E-cadherin, villus morphology, Clostridiales, Faecalibacterium prausnitzii, Clostridium, Allobaculum, obesity, sedentary behavior, host-microbe interactions
MeSH terms: Animals, Animal Feed, Bacteria, Body Weight, Feces, Intestines, Male, Phylogeny, Physical Conditioning, Animal, RNA, Ribosomal, 16S, Biomarkers, Cadherins, Biodiversity, Mice, Metagenome, Occludin, 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

The Effect of Diet and Exercise on Intestinal Integrity and Microbial Diversity in Mice

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks