Intestinal Flora and Disease Mutually Shape the Regional Immune System in the Intestinal Tract

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

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

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

Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns

Dominguez-Bello, M. G., Costello, E. K., Contreras, M., Magris, M., Hidalgo, G., Fierer, N., & Knight, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002601107 · Cited by 4,774

The gut microbiota--masters of host development and physiology

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

Gut microbiota, metabolites and host immunity

Rooks, M. G., & Garrett, W. S. (2016) · Nature reviews. Immunology · doi:10.1038/nri.2016.42 · Cited by 3,409

Intestinal epithelial cells: regulators of barrier function and immune homeostasis

Peterson, L. W., & Artis, D. (2014) · Nature reviews. Immunology · doi:10.1038/nri3608 · Cited by 3,367

The Treatment-Naive Microbiome in New-Onset Crohn’s Disease

Gevers, D., Kugathasan, S., Denson, L. A., Vázquez-Baeza, Y., Van Treuren, W., Ren, B., Schwager, E., Knights, D., Song, S. J., Yassour, M., et al. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.02.005 · Cited by 3,220

Metabolomics — the link between genotypes and phenotypes

Fiehn, O. (2002) · Springer eBooks · doi:10.1007/978-94-010-0448-0_11 · Cited by 3,168

Gut Microbiota Metabolism of Dietary Fiber Influences Allergic Airway Disease and Hematopoiesis

Trompette, A., Gollwitzer, E. S., Yadava, K., Sichelstiel, A. K., Sprenger, N., Ngom-Bru, C., Blanchard, C., Junt, T., Nicod, L. P., Harris, N. L., et al. (2014) · Nature Medicine · doi:10.1038/nm.3444 · Cited by 2,862

Succession of microbial consortia in the developing infant gut microbiome

Koenig, J. E., Spor, A., Scalfone, N., Fricker, A. D., Stombaugh, J., Knight, R., Angenent, L. T., & Ley, R. E. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000081107 · Cited by 2,540

Probiotics Mechanism of Action on Immune Cells and Beneficial Effects on Human Health

Mazziotta, C., Tognon, M., Martini, F., Torreggiani, E., & Rotondo, J. C. (2023) · Cells · doi:10.3390/cells12010184 · Cited by 889

Microbiota‐derived extracellular vesicles in interkingdom communication in the gut

Díaz‐Garrido, N., Badı́a, J., & Baldomà, L. (2021) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12161 · Cited by 418

Weaning stress and intestinal health of piglets: A review

Tang, X., Xiong, K., Fang, R., & Li, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1042778 · Cited by 444

Integration strategy of network pharmacology in Traditional Chinese Medicine: a narrative review.

Wu, J., Fangqing, Z., Zhuangzhuang, L. I., Weiyi, J., & Yue, S. (2022) · PubMed Central · doi:10.19852/j.cnki.jtcm.20220408.003 · Cited by 213

Microrobots for Targeted Delivery and Therapy in Digestive System

Wang, Y., Shen, J., Handschuh‐Wang, S., Qiu, M., Du, S., & Wang, B. (2022) · ACS Nano · doi:10.1021/acsnano.2c04716 · Cited by 141

Mucin O-glycans facilitate symbiosynthesis to maintain gut immune homeostasis

Yamada, T., Hino, S., Iijima, H., Genda, T., Aoki, R., Nagata, R., Han, K., Hirota, M., Kinashi, Y., Oguchi, H., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.09.008 · Cited by 130

Metabolic crosstalk in the tumor microenvironment regulates antitumor immunosuppression and immunotherapy resisitance

Wei, F., Wang, D., Wei, J., Tang, N., Tang, L. M., Xiong, F., Guo, C. J., Zhou, M., Li, X., Li, G., et al. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03581-0 · Cited by 128

Bioactive compounds in coffee and their role in lowering the risk of major public health consequences: A review

Urugo, M. M., Tola, Y. B., Ogah, O., & Endale, F. (2023) · Food Science & Nutrition · doi:10.1002/fsn3.3848 · Cited by 114

Exploring immune-related pathogenesis in lung injury: Providing new insights Into ALI/ARDS

Zheng, J., Li, Y., Kong, X., & Guo, J. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116773 · Cited by 103

Microalgae—Sustainable Source for Alternative Proteins and Functional Ingredients Promoting Gut and Liver Health

Eilam, Y., Khattib, H., Pintel, N., & Avni, D. (2023) · Global Challenges · doi:10.1002/gch2.202200177 · Cited by 101

Dietary nutrition, intestinal microbiota dysbiosis and post-weaning diarrhea in piglets

Han, X., Hu, X., Jin, W., & Liu, G. (2024) · Animal nutrition · doi:10.1016/j.aninu.2023.12.010 · Cited by 112

Biogenesis and Biological Functions of Extracellular Vesicles in Cellular and Organismal Communication With Microbes

Fang, Y., Wang, Z., Liu, X., & Tyler, B. M. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.817844 · Cited by 100

Recent advances in the design and fabrication of probiotic delivery systems to target intestinal inflammation

Jiang, Z., Li, M., McClements, D. J., Liu, X., & Liu, F. (2021) · Food Hydrocolloids · doi:10.1016/j.foodhyd.2021.107438 · Cited by 100

Ginsenoside Rb1 ameliorates heart failure through DUSP-1-TMBIM-6-mediated mitochondrial quality control and gut flora interactions

Pu, X., Zhang, Q., Liu, J., Wang, Y., Guan, X., Wu, Q., Liu, Z., Liu, Z., & Chang, X. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155880 · Cited by 87

The Implication of the Gut Microbiome in Heart Failure

Lupu, V. V., Răileanu, A. A., Mihai, C. M., Morariu, I. D., Lupu, A., Stârcea, I. M., Frăsinariu, O. E., Mocanu, A., Dragan, F., & Fotea, S. (2023) · Cells · doi:10.3390/cells12081158 · Cited by 88

Short‐chain fatty acids mediate gut microbiota–brain communication and protect the blood–brain barrier integrity

Chenghan, M., Li, W., Zhao, B., He, Y., Li, Q., Zhang, T., Xiaojie, L., Zhang, K., Yingqian, Z., & Zhong, Z. (2025) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.15299 · Cited by 91

The Role of Autophagy in Inflammatory Bowel Disease

Shao, B., Yao, Y., Zhai, J., Zhu, J.-H., Li, J., & Wu, K. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.621132 · Cited by 82

A new paradigm for a new simple chemical: butyrate & immune regulation

Dang, G., Wu, W., Zhang, H., & Everaert, N. (2021) · Food & Function · doi:10.1039/d1fo02116h · Cited by 66

Study on the toxic-mechanism of triclosan chronic exposure to zebrafish (Danio rerio) based on gut-brain axis

Wang, Y., Song, J., Wang, X., Qian, Q., & Wang, H. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2022.156936 · Cited by 56

Cryptotanshinone alleviates radiation‐induced lung fibrosis via modulation of gut microbiota and bile acid metabolism

Li, Z., Shen, Y., Xin, J., Xu, X., Ding, Q., Chen, W., Wang, J., Lv, Y., Wei, X., Wei, Y., et al. (2023) · Phytotherapy Research · doi:10.1002/ptr.7926 · Cited by 55

The Regulatory effect of chlorogenic acid on gut-brain function and its mechanism: A systematic review

Zeng, L., Xiang, R., Fu, C.-Y., Qu, Z., & Liu, C. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.112831 · Cited by 54

The mechanism of intestinal flora dysregulation mediated by intestinal bacterial biofilm to induce constipation

Fu, R., Li, Z., Zhou, R., Li, C., Shao, S., & Li, J. (2021) · Bioengineered · doi:10.1080/21655979.2021.1973356 · Cited by 53

Curcumin regulates the homeostasis of Th17/Treg and improves the composition of gut microbiota in type 2 diabetic mice with colitis

Xiao, Q., Zhong, Y., Kang, Z.-P., Huang, J., Fang, W., Wei, S., Long, J., Li, S., Zhao, H., & Liu, D. (2022) · Phytotherapy Research · doi:10.1002/ptr.7404 · Cited by 51

The gut microbiome, immune modulation, and cognitive decline: insights on the gut-brain axis

Zhang, R., Ding, N., Feng, X., & Liao, W. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1529958 · Cited by 58

Effects of the potential probiotic Bacillus subtilis D1-2 on growth, digestion, immunity and intestinal flora in juvenile sea cucumber, Apostichopus japonicus

Wang, M. E., Lv, C., Chen, Y., Bi, X., Yang, D., & Zhao, J. (2022) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2022.03.043 · Cited by 44

Yanghe decoction inhibits inflammation-induced lung metastasis of colorectal cancer

Zhang, L., Liu, S., Ding, K., Zeng, B., Li, B., Zhou, J., Li, J., Wang, J., Su, X., & Sun, R. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.119257 · Cited by 44

Molecular Hydrogen Therapy: Mechanisms, Delivery Methods, Preventive, and Therapeutic Application

Jin, J., Yue, L., Du, M., Geng, F., Gao, X., Zhou, Y., Lu, Q., & Pan, X. (2025) · MedComm · doi:10.1002/mco2.70194 · Cited by 46

In vitro fermentation of seaweed polysaccharides and tea polyphenol blends by human intestinal flora and their effects on intestinal inflammation

Shen, S., Yang, W., Li, L., Zhu, Y., Yang, Y., Ni, H., Jiang, Z., & Zheng, M. (2023) · Food & Function · doi:10.1039/d2fo03390a · Cited by 43

Microbiota-Gut-Brain Axis Dysregulation in Alzheimer's Disease: Multi-Pathway Effects and Therapeutic Potential

Qu, L., Li, Y., Liu, F., Fang, Y., He, J., Ma, J., Xu, T., Wang, L., Lei, P., Dong, H., et al. (2023) · Aging and Disease · doi:10.14336/ad.2023.0823-2 · Cited by 46

Mechanism of Iron Ion Homeostasis in Intestinal Immunity and Gut Microbiota Remodeling

Bao, H., Wang, Y., Xiong, H., Xia, Y., Cui, Z., & Liu, L. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25020727 · Cited by 48

Lactobacillus plantarum attenuates glucocorticoid-induced osteoporosis by altering the composition of rat gut microbiota and serum metabolic profile

Li, S., Han, X., Liu, N., Chang, J., Liu, G., & Hu, S. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1285442 · Cited by 43

The gut-retina axis: a new perspective in the prevention and treatment of diabetic retinopathy

Zhang, H., & Mo, Y. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1205846 · Cited by 42

Integrating Omics Technologies for a Comprehensive Understanding of the Microbiome and Its Impact on Cattle Production

Kaur, H., Kaur, G., Gupta, T., Mittal, D., & Ali, S. A. (2023) · Biology · doi:10.3390/biology12091200 · Cited by 47

Role of metabolites derived from gut microbiota in inflammatory bowel disease

Zheng, L., Wen, X., & Duan, S.-L. (2022) · World Journal of Clinical Cases · doi:10.12998/wjcc.v10.i9.2660 · Cited by 43

Bifidobacterium bifidum Ameliorates DSS-Induced Colitis in Mice by Regulating Microbial Metabolome and Targeting Gut Microbiota

Han, M., Liang, J., Hou, M., Liu, Y., Li, H., & Gao, Z. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.4c00365 · Cited by 41

Selenium Deficiency Leads to Inflammation, Autophagy, Endoplasmic Reticulum Stress, Apoptosis and Contraction Abnormalities via Affecting Intestinal Flora in Intestinal Smooth Muscle of Mice

Wang, F., Sun, N., Zeng, H., Gao, Y., Zhang, N., & Zhang, W. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.947655 · Cited by 42

Gut microbiota mediated inflammation, neuroendocrine and neurotrophic functions involved in the antidepressant-like effects of diosgenin in chronic restraint stress

Cui, J.-J., Huang, Z.-Y., Xie, Y.-H., Wu, J.-B., Xu, G., Li, C., Zhang, M., & Yi, L. (2022) · Journal of Affective Disorders · doi:10.1016/j.jad.2022.10.045 · Cited by 40

Rosmarinic acid alleviates intestinal inflammatory damage and inhibits endoplasmic reticulum stress and smooth muscle contraction abnormalities in intestinal tissues by regulating gut microbiota

Li, K., Wu, J., Xu, S., Li, X., Zhang, Y., & Gao, X. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.01914-23 · Cited by 40

Modulation of the gut–brain axis via the gut microbiota: a new era in treatment of amyotrophic lateral sclerosis

Hong, D., Zhang, C., Wu, W., Lu, X., & Zhang, L. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1133546 · Cited by 38

Diarrhea with deficiency kidney-yang syndrome caused by adenine combined with Folium senna was associated with gut mucosal microbiota

Zhu, J., Li, X., Deng, N., Peng, X., & Tan, Z. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1007609 · Cited by 38

Traditional Chinese medicine for the treatment of Alzheimer's disease: A focus on the microbiota–gut–brain axis

Ma, L., Jiang, X., Huang, Q.-Y., Chen, W., Zhang, H., Pei, H., Cao, Y., Wang, H., & Li, H. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115244 · Cited by 39

Fecal microbiota transplantation for the management of autoimmune diseases: Potential mechanisms and challenges

Liu, X., Liu, M., Zhao, M., Li, P., Gao, C., Fan, X., Cai, G., Lu, Q., & Chen, X. (2023) · Journal of Autoimmunity · doi:10.1016/j.jaut.2023.103109 · Cited by 41

Vanillin Has Potent Antibacterial, Antioxidant, and Anti-Inflammatory Activities In Vitro and in Mouse Colitis Induced by Multidrug-Resistant Escherichia coli

Wang, J., An, W., Wang, Z., Zhao, Y., Han, B., Tao, H., Wang, J., & Wang, X. (2024) · Antioxidants · doi:10.3390/antiox13121544 · Cited by 41

Lactic acid bacteria in Asian fermented foods and their beneficial roles in human health

Doo, H., Kwak, J., Keum, G. B., Ryu, S., Choi, Y., Kang, J., Kim, H., Chae, Y., Kim, S., Kim, H. B., et al. (2024) · Food Science and Biotechnology · doi:10.1007/s10068-024-01634-9 · Cited by 44

Microbiota–gut–brain axis: Natural antidepressants molecular mechanism

Lu, Y., Yu, X., Wang, Z., Kong, L., Jiang, Z., Shang, R., Zhong, X., Lv, S., Zhang, G., Gao, H., et al. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.156012 · Cited by 39

Fecal microbiota transplantation for diseases: Therapeutic potential, methodology, risk management in clinical practice

Qu, Z., Tian, P., Yang, B. K., Zhao, J., Wang, G., & Chen, W. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120719 · Cited by 37

Inflammatory Response: A Crucial Way for Gut Microbes to Regulate Cardiovascular Diseases

Wang, W., Zhu, L., Leng, Y.-Q., Wang, Y.-W., Shi, T., Wang, W., & Sun, J. (2023) · Nutrients · doi:10.3390/nu15030607 · Cited by 35

Effects of intestinal flora on polycystic ovary syndrome

Liu, J., Liu, Y., & Li, X. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1151723 · Cited by 35

The Mechanism of Zinc Oxide in Alleviating Diarrhea in Piglets after Weaning: A Review from the Perspective of Intestinal Barrier Function

Tang, X., Xiong, K., Zeng, Y., & Fang, R. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251810040 · Cited by 39

Gut microbiota and their metabolites in the immune response of rheumatoid arthritis: Therapeutic potential and future directions

Cai, X. T., Ren, F., & Yao, Y. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114034 · Cited by 34

Multifaceted Impacts of Periodontal Pathogens in Disorders of the Intestinal Barrier

Liu, Y., Huang, W., Wang, J., Ma, J., Zhang, M., Lü, X., Liu, J., & Kou, Y. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.693479 · Cited by 34

Recent advance in the biological activity of chlorogenic acid and its application in food industry

Li, Z., Niu, L., Chen, Y., Qiu, X., Du, T., Zhu, M., Wang, M., Mo, H., & Xiao, S. (2023) · International Journal of Food Science & Technology · doi:10.1111/ijfs.16617 · Cited by 31

Effect of different delivery modes on intestinal microbiota and immune function of neonates

Lai, C., Huang, L., Wang, Y., Huang, C., Luo, Y., Qin, X., & Zeng, J. (2024) · Scientific Reports · doi:10.1038/s41598-024-68599-x · Cited by 30

Comparative Analysis of Metabolic Dysfunctions Associated with Pristine and Aged Polyethylene Microplastic Exposure via the Liver-Gut Axis in Mice

Cui, H., Jiang, X., Cao, J., Yang, W., Yang, B., & Li, M. (2025) · ACS Nano · doi:10.1021/acsnano.5c00945 · Cited by 33

Altered Gut Microbiota in HIV Infection: Future Perspective of Fecal Microbiota Transplantation Therapy

Kang, Y., & Cai, Y. (2018) · AIDS Research and Human Retroviruses · doi:10.1089/aid.2017.0268 · Cited by 30

Role of Akkermansia muciniphila in insulin resistance

Zeng, Z., Chen, M., Liu, Y., Zhou, Y., Liu, H., Wang, S., & Ji, Y. (2024) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.16747 · Cited by 30

Buyang Huanwu Decoction stabilizes atherosclerotic vulnerable plaques by regulating intestinal flora, TLR4-NF-κB-NLRP3 inflammatory pathway and mitophagy

Chang, S.-Y., Li, Y., Zhu, H.-Y., He, Z., You, Y., & Liu, Y.-H. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.156751 · Cited by 32

Evolving interplay between natural products and gut microbiota

Zhang, N., Jiang, Z., Li, S., Yang, X. S., & Liu, E. (2023) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2023.175557 · Cited by 32

A Comparative Study on the Effects of Different Sources of Carboxymethyl Poria Polysaccharides on the Repair of DSS-Induced Colitis in Mice

Tan, Z., Zhang, Q., Zhao, R., Huang, T., Tian, Y., & Lin, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24109034 · Cited by 29

Relationship between trimethylamine N-oxide and the risk of hypertension in patients with cardiovascular disease: A meta-analysis and dose-response relationship analysis

Han, J., Guo, L., Chen, X.-H., Xie, Q., Song, X.-Y., & Ma, Y.-L. (2024) · Medicine · doi:10.1097/md.0000000000036784 · Cited by 28

Spirulina polysaccharide-based prebiotic foods preparations-a promising approach for modulating gut microbiota and improving health

Guan, F., Fu, G., Ma, Y., Zhou, L., Li, G., Sun, C., & Zhang, T. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106158 · Cited by 29

Gut bacterial and fungal dysbiosis in tuberculosis patients

Han, M., Wang, X., Zhang, J., Su, L., Ishaq, H. M., Duan, L., Cui, J., Zhao, H., & Yang, F. (2024) · BMC Microbiology · doi:10.1186/s12866-024-03275-8 · Cited by 28

Analysis of Intestinal Microflora and Metabolites From Mice With DSS-Induced IBD Treated With Schistosoma Soluble Egg Antigen

Zhu, T., Xue, Q., Liu, Y., Xu, Y., Xiong, C., Jin, L., Yang, H., Zhang, Q., & Huang, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.777218 · Cited by 28

The efficacy and neural mechanism of acupuncture therapy in the treatment of visceral hypersensitivity in irritable bowel syndrome

Yang, Y., Wang, J., Zhang, C., Guo, Y. M., Zhao, M., Zhang, M., Li, Z., Gao, F., Luo, Y., Wang, Y., et al. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1251470 · Cited by 30

Intestinal Mucosal Immune Barrier: A Powerful Firewall Against Severe Acute Pancreatitis-Associated Acute Lung Injury via the Gut-Lung Axis

Li, F., Wang, Z., Cao, Y., Pei, B., Luo, X., Liu, J., Ge, P., Luo, Y., Ma, S., & Chen, H. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s448819 · Cited by 30

How do probiotics alleviate constipation? A narrative review of mechanisms

Huang, Y.-P., Shi, J.-Y., Luo, X.-T., Luo, S.-C., Cheung, P. C. K., Corke, H., Yang, Q.-Q., & Zhang, B. (2024) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2024.2336531 · Cited by 28

Effects of oral supplementation of probiotics on body weight and visceral fat in obese patients: a meta-analysis and systematic review

Guo, M., Li, J., Zhang, L., Chen, C., Wei, Y., & Shen, Z. (2025) · Scientific Reports · doi:10.1038/s41598-025-90820-8 · Cited by 33

Caspase‐8 in endothelial cells maintains gut homeostasis and prevents small bowel inflammation in mice

Tisch, N., Mogler, C., Stojanovic, A., Luck, R., Korhonen, E. A., Ellerkmann, A., Adler, H., Singhal, M., Schermann, G., Erkert, L., et al. (2022) · EMBO Molecular Medicine · doi:10.15252/emmm.202114121 · Cited by 26

The interaction between tea polyphenols and host intestinal microorganisms: an effective way to prevent psychiatric disorders

Sun, Q., Cheng, L., Zhang, X., Wu, Z., & Weng, P. (2021) · Food & Function · doi:10.1039/d0fo02791j · Cited by 26

Simo decoction curing spleen deficiency constipation was associated with brain-bacteria-gut axis by intestinal mucosal microbiota

Yi, X., Zhou, K., Deng, N., Cai, Y., Peng, X., & Tan, Z. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1090302 · Cited by 25

Gymnema sylvestre extract ameliorated streptozotocin‐induced hyperglycemia in T2DM rats via gut microbiota

Chen, G., Xu, Y., Zhang, H., Muema, F. W., & Guo, M. (2023) · Food Frontiers · doi:10.1002/fft2.238 · Cited by 26

Phyllanthus emblica polysaccharide (PEP) attenuates cyclophosphamide-induced immunosuppression through microbiota-dependent or –independent regulation of immune responses

Xu, D.-H., Xie, H., Li, Y.-L., Wang, L., Qing-Lu, Yu-Sun, Zhao, J.-L., & Zeng, H. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106065 · Cited by 24

Protective Effect of Prim-O-Glucosylcimifugin on Ulcerative Colitis and Its Mechanism

Yin, Y., Liu, K., & Li, G. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.882924 · Cited by 24

Huangqi Guizhi Wuwu decoction alleviates oxaliplatin-induced peripheral neuropathy via the gut-peripheral nerve axis

Zhang, Z., Ye, J., Liu, X., Zhao, W., Zhao, B., Gao, X., Lan, H., Wu, Y., Yang, Y., & Cao, P. (2023) · Chinese Medicine · doi:10.1186/s13020-023-00826-5 · Cited by 24

Alginate oligosaccharide extends the service lifespan by improving the sperm metabolome and gut microbiota in an aging Duroc boars model

Zhou, Y., Wei, Z., Tan, J., Sun, H., Jiang, H., Gao, Y., Zhang, H., & Schroyen, M. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1308484 · Cited by 24

PFOA/PFOS Facilitated Intestinal Fatty Acid Absorption by Activating the PPARα Pathway: Insights from Organoids Model

Zhang, W., Tian, Y., Chen, B., Xu, S., & Wu, L. (2023) · Environment & Health · doi:10.1021/envhealth.3c00129 · Cited by 24

Gut microbiota dysbiosis and intestinal barrier impairment in diarrhea caused by cold drink and high-fat diet

Tian, Y., Fu, M., Su, J., Yan, M., Yu, J., Wang, C., Niu, Z., Du, Y., Hu, X., Zheng, J., et al. (2024) · Toxicology · doi:10.1016/j.tox.2024.153728 · Cited by 23

New approach methodologies to enhance human health risk assessment of immunotoxic properties of chemicals — a PARC (Partnership for the Assessment of Risk from Chemicals) project

Snapkow, I., Smith, N. M., Arnesdotter, E., Beekmann, K., Blanc, É., Braeuning, A., Corsini, E., Dolenc, M. S., Duivenvoorde, L. P. M., Eriksen, G. S., et al. (2024) · Frontiers in Toxicology · doi:10.3389/ftox.2024.1339104 · Cited by 23

Mechanisms of action and applications of Polygonatum sibiricum polysaccharide at the intestinal mucosa barrier: a review

Ren, Y., Sun, Y., Liao, Y., Wang, S., Liu, Q., Duan, C.-Y., Sun, L., Li, X., & Yuan, J. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1421607 · Cited by 24

Portulaca oleracea Polysaccharides Modulate Intestinal Microflora in Aged Rats in vitro

Fu, Q., Zhou, S., Yu, M., Lu, Y., He, G., Huang, X. B., & Huang, Y. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.841397 · Cited by 23

The diarrheal mechanism of mice with a high-fat diet in a fatigued state is associated with intestinal mucosa microbiota

Liu, J., Qiao, B., Deng, N., Wu, Y., Li, D., & Tan, Z. (2023) · 3 Biotech · doi:10.1007/s13205-023-03491-5 · Cited by 23

Comparison of the effects of chlorogenic acid isomers and their compounds on alleviating oxidative stress injury in broilers

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