Hydrogen sulfide improves colonic barrier integrity in DSS-induced inflammation in Caco-2 cells and mice

Intestinal permeability – a new target for disease prevention and therapy

Bischoff, S. C., Barbara, G., Buurman, W., Ockhuizen, T., Schulzke, J.-D., Serino, M., Tilg, H., Watson, A., & Wells, J. M. (2014) · BMC Gastroenterology · doi:10.1186/s12876-014-0189-7 · Cited by 1,755 · see citing works

Hydrogen sulfide protects neurons from oxidative stress

Kimura, Y., & Kimura, H. (2004) · The FASEB Journal · doi:10.1096/fj.04-1815fje · Cited by 874 · see citing works

Intestinal Permeability Regulation by Tight Junction: Implication on Inflammatory Bowel Diseases

Lee, S. H. (2015) · Intestinal Research · doi:10.5217/ir.2015.13.1.11 · Cited by 810 · see citing works

Intestinal barrier in inflammatory bowel disease

Antoni, L. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i5.1165 · Cited by 416 · see citing works

The Slow-Releasing Hydrogen Sulfide Donor, GYY4137, Exhibits Novel Anti-Cancer Effects In Vitro and In Vivo

Lee, Z., Zhou, J., Chen, C.-S., Zhao, Y., Tan, C., Li, L., Moore, P. K., & Deng, L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021077 · Cited by 382 · see citing works

l ‐Cysteine metabolism and its nutritional implications

Yin, J., Ren, W., Yang, G., Duan, J., Huang, X., Fang, R., Li, C.-Y., Li, Y., Yin, Y., Hou, Y., et al. (2015) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500031 · Cited by 355 · see citing works

Role of the intestinal barrier in inflammatory bowel disease

Laukoetter, M. G., Nava, P., & Nusrat, A. (2008) · World Journal of Gastroenterology · doi:10.3748/wjg.14.401 · Cited by 301 · see citing works

Inflammation and nerve fiber interaction in endometriotic pain

McKinnon, B. D., Bertschi, D., Bersinger, N. A., & Mueller, M. D. (2014) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2014.10.003 · Cited by 214 · see citing works

The hydrogen sulfide donor, GYY 4137, exhibits anti‐atherosclerotic activity in high fat fed apolipoprotein E −/− mice

Liu, Z., Han, Y., Li, L., Lu, H., Meng, G., Li, X., Atan, M. S. B. M., Peh, M. T., Xie, L., Zhou, S., et al. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12246 · Cited by 181 · see citing works

The IL-1 Pathway in Type 2 Diabetes and Cardiovascular Complications

Herder, C., Dalmas, É., Böni‐Schnetzler, M., & Donath, M. Y. (2015) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2015.08.001 · Cited by 169 · see citing works

MicroRNA-21 Knockout Improve the Survival Rate in DSS Induced Fatal Colitis through Protecting against Inflammation and Tissue Injury

Shi, C., Liang, Y., Yang, J., Xia, Y., Chen, H., Han, H., Yang, Y. P., Wu, W., Gao, R., & Qin, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0066814 · Cited by 163 · see citing works

Hydrogen Sulfide Protects the Retina from Light-induced Degeneration by the Modulation of Ca2+ Influx

Mikami, Y., Shibuya, N., Kimura, Y., Nagahara, N., Yamada, M., & Kimura, H. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.298208 · Cited by 141 · see citing works

Role of interleukins in obesity: implications for metabolic disease

Febbraio, M. A. (2014) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2014.02.004 · Cited by 130 · see citing works

TLR-independent anti-inflammatory function of intestinal epithelial TRAF6 signalling prevents DSS-induced colitis in mice

Vlantis, K., Polykratis, A., Welz, P.-S., Loo, G., Pasparakis, M., & Wullaert, A. (2015) · Gut · doi:10.1136/gutjnl-2014-308323 · Cited by 126 · see citing works

Hydrogen peroxide-induced oxidative stress activates NF-κB and Nrf2/Keap1 signals and triggers autophagy in piglets

Yin, J., Duan, J., Cui, Z., Ren, W., Li, Y., & Yin, Y. (2015) · RSC Advances · doi:10.1039/c4ra13557a · Cited by 125 · see citing works

Impaired hydrogen sulfide synthesis and IL-10 signaling underlie hyperhomocysteinemia-associated exacerbation of colitis

Flannigan, K. L., Agbor, T. A., Blackler, R. W., Kim, J., Khan, W. I., Verdu, E. F., Ferraz, J. G., & Wallace, J. L. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1413390111 · Cited by 97 · see citing works

Endogenous hydrogen sulfide is an anti-inflammatory molecule in dextran sodium sulfate-induced colitis in mice

Hirata, I., Naito, Y., Takagi, T., Mizushima, K., Suzuki, T., Omatsu, T., Handa, O., Ichikawa, H., Ueda, H., & Yoshikawa, T. (2011) · Digestive Diseases and Sciences · doi:10.1007/s10620-010-1461-5 · Cited by 72 · see citing works

Protective effect of hydrogen sulfide on TNF-α and IFN-γ-induced injury of intestinal epithelial barrier function in Caco-2 monolayers

Chen, S.-W., Zhu, J., Zuo, S., Zhang, J., Chen, Z., Chen, G., Wang, X., Pan, Y., Liu, Y., & Wang, P. (2015) · Inflammation Research · doi:10.1007/s00011-015-0862-5 · Cited by 69 · see citing works

Hydrogen sulfide attenuates cytokine production through the modulation of chromatin remodeling

Rios, E. C. S., Szczęsny, B., Soriano, F. G., Oláh, G., & Szabó, C. (2015) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2015.2176 · Cited by 65 · see citing works

Hydrogen Sulfide Inhalation Decreases Early Blood—Brain Barrier Permeability and Brain Edema Induced by Cardiac Arrest and Resuscitation

Geng, Y., Li, E., Mu, Q., Zhang, Y., Wei, X., Li, H., Cheng, L., & Zhang, B. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.223 · Cited by 59 · see citing works

Exogenous H2S protects H9c2 cardiac cells against high glucose-induced injury and inflammation by inhibiting the activation of the NF-κB and IL-1β pathways

Xu, W., Chen, J., LIN, J., LIU, D., Mo, L., Pan, W., Feng, J., Wu, W., & Zheng, D. (2014) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2014.2007 · Cited by 59 · see citing works

Type 1 Diabetes and Dysfunctional Intestinal Homeostasis

D’Addio, F., & Fiorina, P. (2016) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2016.04.005 · Cited by 47 · see citing works

Ghrelin ameliorates intestinal barrier dysfunction in experimental colitis by inhibiting the activation of nuclear factor-kappa B

Cheng, J., Zhang, L., Dai, W., Mao, Y., Li, S., Wang, J., Li, H., Guo, C., & Fan, X. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.01.083 · Cited by 37 · see citing works

Chloride Channel ClC-2 is a Key Factor in the Development of DSS-induced Murine Colitis

Nighot, P. K., Young, K. M., Nighot, M., Rawat, M., Sung, E. J., Maharshak, N., Plevy, S. E., Ma, T., & Blikslager, A. T. (2013) · Inflammatory Bowel Diseases · doi:10.1097/mib.0b013e3182a82ae9 · Cited by 33 · see citing works

Fermented milk derives bioactive peptides with antihypertensive effects

Shori, A. B., & Baba, A. S. (2015) · Integrative Food Nutrition and Metabolism · doi:10.15761/ifnm.1000126 · Cited by 21 · see citing works

Antibacterial effects of supernatant of lactic acid bacteria isolated from different Dough's in Gorgan city in north of Iran

Rashti, Z., & Koohsari, H. (2015) · Integrative Food Nutrition and Metabolism · doi:10.15761/ifnm.1000129 · Cited by 11 · see citing works

UNC 5B receptor deletion exacerbates DSS ‐induced colitis in mice by increasing epithelial cell apoptosis

Ranganathan, P. V., Jayakumar, C., Li, D. Y., & Ramesh, G. (2014) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12280 · Cited by 10 · see citing works

Gut Microbiota Cool-Down Burning Fat! The Immune Hypothesis

Burcelin, R., & Pomié, C. (2015) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2015.12.002 · Cited by 9 · see citing works

Status of food intake and elemental nutrition in patients with Crohn’s disease

Yamaguchi, M., & Emory University School of Medicine (2015) · Integrative Food Nutrition and Metabolism · doi:10.15761/ifnm.1000118 · Cited by 9 · see citing works

Iron sequestration is not the main mechanism in the inhibition of Staphylococcus aureus growth by cranberry phytochemicals

Howell, K. S., Yan, F., Tokich, A., & Ng, K. (2015) · Integrative Food Nutrition and Metabolism · doi:10.15761/ifnm.1000127 · Cited by 7 · see citing works

Effect of Broccoli Intake on Antioxidants in the Liver and Kidneys Tissues of Hyperglycemic Rats

El-Hendy, H. A. R., & El-Hendy, H. H. A. R. (2013) · Alexandria Science Exchange Journal · doi:10.21608/asejaiqjsae.2013.159251 · Cited by 6 · see citing works

Effect of body composition intake with nano-lactic acid in rats

centigrade, W. R. W. I. H. I. C. A. T. O. 2. ±. 1. D., feeding, A. 4.-6. H. A. B. 2. W. B. O. P., water, 2. R. W. D. 4. G. E. 5. R. A. W. F. S. C. P. F. D. A., control (group: C) as high-carb meal (344 kcal/100g), style, J., high-carb meal with high levels lactobacillus (group: CL), high-fat same calorifacient feed (597 kcal/100g) and water (group: F), high-fat meal with high levels lactobacillus (group: FL), law, A. F. C. T. O. A. D. I. W. D. T. L. 5. B. P. 1. B. O. R. S. T. T. A. E. W. C. O. I. A. W. T. J., which allows experiments on laboratory animals in Nippon Sport Science University accordance to the principle of laboratory animal care. During the experimental period of two weeks body weight was measured every one week. After two weeks of experimental feed, et al. (2015) · Integrative Food Nutrition and Metabolism · doi:10.15761/ifnm.1000120 · Cited by 2 · see citing works

International Union of Basic and Clinical Pharmacology. CII: Pharmacological Modulation of H2S Levels: H2S Donors and H2S Biosynthesis Inhibitors

Szabó, C., & Papapetropoulos, A. (2017) · Pharmacological Reviews · doi:10.1124/pr.117.014050 · Cited by 423 · see citing works

Desulfovibrio in the Gut: The Enemy within?

Singh, S., Carroll‐Portillo, A., & Lin, H. C. (2023) · Microorganisms · doi:10.3390/microorganisms11071772 · Cited by 268 · see citing works

Enterosalivary nitrate metabolism and the microbiome: Intersection of microbial metabolism, nitric oxide and diet in cardiac and pulmonary vascular health

Koch, C. D., Gladwin, M. T., Freeman, B. A., Lundberg, J. O., Weitzberg, E., & Morris, A. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.12.015 · Cited by 186 · see citing works

Production of hydrogen sulfide by the intestinal microbiota and epithelial cells and consequences for the colonic and rectal mucosa

Blachier, F., Andriamihaja, M., Larraufie, P., Ahn, E., Lan, A., & Kim, E. (2020) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00261.2020 · Cited by 175 · see citing works

Near-Infrared Fluorescent Probe with Large Stokes Shift for Imaging of Hydrogen Sulfide in Tumor-Bearing Mice

Yan, L., Gu, Q.-S., Jiang, W., Tan, M., Tan, Z.-K., Mao, G.-J., Fen, X., & Li, C. (2022) · Analytical Chemistry · doi:10.1021/acs.analchem.1c04169 · Cited by 153 · see citing works

The circulating microbiome signature and inferred functional metagenomics in alcoholic hepatitis

Puri, P., Liangpunsakul, S., Christensen, J. E., Shah, V. H., Kamath, P. S., Gores, G. J., Walker, S., Comerford, M., Katz, B. P., Borst, A. J., et al. (2017) · Hepatology · doi:10.1002/hep.29623 · Cited by 128 · see citing works

MPST deficiency promotes intestinal epithelial cell apoptosis and aggravates inflammatory bowel disease via AKT

Zhang, J., Li, C., Zhang, X., Tang, C., Chen, Y., Zhang, Y., Yu, M., Lü, C., Li, M., Li, S., et al. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102469 · Cited by 110 · see citing works

Activation of Resolution Pathways to Prevent and Fight Chronic Inflammation: Lessons From Asthma and Inflammatory Bowel Disease

Barnig, C., Bezema, T., Calder, P. C., Charloux, A., Frossard, N., Garssen, J., Haworth, O., Dilevskaya, K., Levi‐Schaffer, F., Lonsdorfer‐Wolf, E., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01699 · Cited by 99 · see citing works

Protective Actions of H 2 S in Acute Myocardial Infarction and Heart Failure

Donnarumma, E., Trivedi, R. K., & Lefer, D. J. (2017) · Comprehensive physiology · doi:10.1002/cphy.c160023 · Cited by 96 · see citing works

Development of Spleen Targeting H2S Donor Loaded Liposome for the Effective Systemic Immunomodulation and Treatment of Inflammatory Bowel Disease

Oh, C., Lee, W., Park, J., Choi, J., Lee, S., Li, S., Jung, H. N., Lee, J.-S., Hwang, J.-E., Park, J., et al. (2023) · ACS Nano · doi:10.1021/acsnano.2c08898 · Cited by 72 · see citing works

Role of Hydrogen Sulfide in Inflammatory Bowel Disease

Stummer, N., Feichtinger, R. G., Weghuber, D., Kofler, B., & Schneider, A.-M. (2023) · Antioxidants · doi:10.3390/antiox12081570 · Cited by 71 · see citing works

Rhein protects against barrier disruption and inhibits inflammation in intestinal epithelial cells

Zhuang, S., Zhong, J., Zhou, Q., Zhong, Y., Liu, P., & Liu, Z. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.03.030 · Cited by 69 · see citing works

Hydrogen sulfide protects against DSS-induced colitis by inhibiting NLRP3 inflammasome

Qin, M., Long, F., Wu, W., Yang, D., Huang, M., Xiao, C., Chen, X., Liu, X., & Zhu, Y. Z. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.04.025 · Cited by 66 · see citing works

Gasotransmitters and the immune system: Mode of action and novel therapeutic targets

Fagone, P., Mazzon, E., Bramanti, P., Bendtzen, K., & Nicoletti, F. (2018) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2018.07.026 · Cited by 63 · see citing works

Role of hydrogen sulfide in health and disease

Jin, Y., Yuan, H., Liu, Y., Zhu, Y., Wang, Y., Liang, X., Gao, W., Ren, Z., Ji, X., & Wu, D. (2024) · MedComm · doi:10.1002/mco2.661 · Cited by 54 · see citing works

Contribution of sulfate-reducing bacteria to homeostasis disruption during intestinal inflammation

Figliuolo, V. R., Coutinho‐Silva, R., & Coutinho, C. M. L. M. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.11.009 · Cited by 51 · see citing works

Update on the Pathogenesis of the Hirschsprung-Associated Enterocolitis

Li, S., Zhang, Y., Li, K., Liu, Y., Chi, S., Wang, Y., & Tang, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054602 · Cited by 48 · see citing works

Recent Development of the Molecular and Cellular Mechanisms of Hydrogen Sulfide Gasotransmitter

Liu, J., Mesfin, F. M., Hunter, C., Olson, K. R., Shelley, W. C., Brokaw, J. P., Manohar, K., & Markel, T. A. (2022) · Antioxidants · doi:10.3390/antiox11091788 · Cited by 43 · see citing works

Neutrophil elastase inhibitor (MPH-966) improves intestinal mucosal damage and gut microbiota in a mouse model of 5-fluorouracil–induced intestinal mucositis

Chen, K.-J., Chen, Y., Ueng, S., Hwang, T., Kuo, L.-M., & Hsieh, P. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.111152 · Cited by 42 · see citing works

Effects of gut microbiota on atherosclerosis through hydrogen sulfide

Gui, D.-D., Luo, W., Yan, B., Ren, Z., Tang, Z., Liu, L.-S., Zhang, J., & Jiang, Z.-S. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.173916 · Cited by 40 · see citing works

Role of Gut Microbial Metabolites in Cardiovascular Diseases—Current Insights and the Road Ahead

Datta, S., Pasham, S., Sandeep, I. S., Boini, K. M., & Koka, S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251810208 · Cited by 42 · see citing works

Hydrogen Sulfide Plays an Important Role by Influencing NLRP3 inflammasome

Wang, H., Shi, X., Qiu, M., Lv, S., Zheng, H., Niu, B., & Liu, H. (2020) · International Journal of Biological Sciences · doi:10.7150/ijbs.47595 · Cited by 40 · see citing works

Organic fluorescent probe for concurrent imaging and apoptosis induction in cancer cells in vivo and in vitro by utilizing endogenous hydrogen sulfide

Xu, Z., Yan, Z., Qiao, R., Cao, S., Fang, Y., Bo, X., Zhu, H., Ying, C., Sun, Y. X., & Zheng, J. (2022) · Chemical Engineering Journal · doi:10.1016/j.cej.2022.141000 · Cited by 34 · see citing works

The causal relationship between gut microbiota and leukemia: a two-sample Mendelian randomization study

Chen, G., Kuang, Z., Li, F., & Li, J. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1293333 · Cited by 30 · see citing works

Engineered bacteria titrate hydrogen sulfide and induce concentration-dependent effects on the host in a gut microphysiological system

Hayes, J. A., Lunger, A. W., Sharma, A. S., Fernez, M. T., Carrier, R. L., Koppes, A. N., Koppes, R. A., & Woolston, B. M. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113481 · Cited by 27 · see citing works

Gut sensory neurons as regulators of neuro-immune-microbial interactions: from molecular mechanisms to precision therapy for IBD/IBS

Sun, N., Cao, L.-S., Xia, W.-Y., Wang, J., & Wu, Q. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03500-9 · Cited by 24 · see citing works

Immunobiotic Lactobacillus jensenii TL2937 Alleviates Dextran Sodium Sulfate-Induced Colitis by Differentially Modulating the Transcriptomic Response of Intestinal Epithelial Cells

Sato, N., García-Castillo, V., Yuzawa, M., Islam, M. A., Albarracín, L., Tomokiyo, M., Ikeda‐Ohtsubo, W., García, A., Takahashi, H., Villena, J., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.02174 · Cited by 23 · see citing works

Reduction of hydrogen sulfide synthesis enzymes cystathionine-β-synthase and cystathionine-γ-lyase in the colon of patients with Hirschsprungs disease

Tomuschat, C., O’Donnell, A. M., Coyle, D., & Puri, P. (2017) · Journal of Pediatric Surgery · doi:10.1016/j.jpedsurg.2017.06.011 · Cited by 22 · see citing works

Protective role of casuarinin from Melastoma malabathricum against a mouse model of 5-fluorouracil–induced intestinal mucositis: Impact on inflammation and gut microbiota dysbiosis

Chen, K.-J., Huang, Y., Kuo, L.-M., Chen, Y., Hung, C., & Hsieh, P. (2022) · Phytomedicine · doi:10.1016/j.phymed.2022.154092 · Cited by 22 · see citing works

Protective properties of grape-seed proanthocyanidins in human ex vivo acute colonic dysfunction induced by dextran sodium sulfate

González-Quilen, C., Grau‐Bové, C., Jorba, R., Caro, A., Pinent, M., Ardèvol, A., Beltrán‐Debón, R., Terra, X., & Blay, M. (2020) · European Journal of Nutrition · doi:10.1007/s00394-020-02222-3 · Cited by 22 · see citing works

TLR2 and TLR4 interact with sulfide system in the modulation of mouse colonic motility

Grasa, L., Abecia, L., Peña‐Cearra, A., Robles, S., Layunta, E., Latorre, E., Mesonero, J. E., & Forcén, R. (2019) · Neurogastroenterology & Motility · doi:10.1111/nmo.13648 · Cited by 13 · see citing works

Exogenous H 2 S Protects Colon Cells in Ulcerative Colitis by Inhibiting NLRP3 and Activating Autophagy

Liu, Y., Liao, R., Qiang, Z., Yang, W., Cao, J., & Zeng, H. (2021) · DNA and Cell Biology · doi:10.1089/dna.2020.6380 · Cited by 13 · see citing works

The Role of H2S in the Gastrointestinal Tract and Microbiota

Xiao, A., Liu, C., & Li, J. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-981-16-0991-6_4 · Cited by 13 · see citing works

Plantamajoside alleviates DSS-induced ulcerative colitis by modulating gut microbiota, upregulating CBS, and inhibiting NF-κB

Jia, Y., Liu, X., Gao, X., Yin, S., Wu, K., Meng, X., Ren, H. J., Liu, J., Liu, Z., Li, H., et al. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.156827 · Cited by 11 · see citing works

Searching for Novel Sources of Hydrogen Sulfide Donors: Chemical Profiling of Polycarpa aurata Extract and Evaluation of the Anti-Inflammatory Effects

Casertano, M., Esposito, E., Bello, I., Indolfi, C., Putra, M. Y., Mannelli, L. D. C., Ghelardini, C., Menna, M., Sorrentino, R., Cirino, G., et al. (2023) · Marine Drugs · doi:10.3390/md21120641 · Cited by 10 · see citing works

Protective Actions of H 2 S in Acute Myocardial Infarction and Heart Failure

Donnarumma, E., Trivedi, R. K., & Lefer, D. J. (2017) · Comprehensive physiology · doi:10.1002/j.2040-4603.2017.tb00754.x · Cited by 10 · see citing works

Role of Pyroptosis in inflammatory bowel disease.

Xiao, Z., Xie, J.-L., Zhao, X., Chen, X.-J., Lu, Y.-H. C. S., Xu, Y., Wu, M., An, L., & Li, Q. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114619 · Cited by 11 · see citing works

Identification and Characterization of Two Novel Members of the Family Eubacteriaceae, Anaerofustis butyriciformans sp. nov. and Pseudoramibacter faecis sp. nov., Isolated from Human Feces

Wang, X.-M., Huang, H., Sun, X., Wei, R.-Q., Chen, H. Y., Liu, C., & Liu, S. (2025) · Microorganisms · doi:10.3390/microorganisms13040916 · Cited by 10 · see citing works

Bidirectional Mendelian randomization links gut microbiota to primary biliary cholangitis

Zhou, Z., Li, W., Wu, Y., Wang, T., Zhang, J., You, L., Li, H., Zheng, C., Gao, Y., & Sun, X. (2024) · Scientific Reports · doi:10.1038/s41598-024-79227-z · Cited by 8 · see citing works

The Physicochemical, Sensory, and Functional Properties of Yogurt Containing Millet and Milk

Wang, H., Zhang, Y., Han, Y., Hou, J., Zuo, Y., Li, Y., & Wu, H. (2025) · Foods · doi:10.3390/foods14203491 · Cited by 8 · see citing works

Intestinal Fibrogenesis in Inflammatory Bowel Diseases: Exploring the Potential Role of Gut Microbiota Metabolites as Modulators

Cicchinelli, S., Gemma, S., Pignataro, G., Piccioni, A., Ojetti, V., Gasbarrini, A., Franceschi, F., & Candelli, M. (2024) · Pharmaceuticals · doi:10.3390/ph17040490 · Cited by 8 · see citing works

A novel colorimetric NIR fluorescent probe for turn-on detection and imaging of hydrogen sulfide

Lu, G., Duan, L., Hu, Q., Meng, S., Cai, P., Chen, Y., Wang, X., & Dong, T. (2023) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2023.115309 · Cited by 8 · see citing works

pH-responsive Oral liposomal delivery of hydrogen sulfide donor GYY4137 enables colon-targeted therapy for inflammatory bowel disease

Oh, C., Hwang, J.-E., Yim, H., Park, H., Kim, S.-Y., Lee, J. K., & Im, H. (2025) · Journal of Nanobiotechnology · doi:10.1186/s12951-025-03753-9 · Cited by 7 · see citing works

Mice Deficient in Epithelial or Myeloid Cell Iκκβ Have Distinct Colonic Microbiomes and Increased Resistance to Citrobacter rodentium Infection

Mackos, A. R., Allen, J. M., Kim, E., Ladaika, C., Gharaibeh, R. Z., Moore, C. C., Parry, N. M., Boyaka, P. N., & Bailey, M. T. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02062 · Cited by 6 · see citing works

GYY4137, as a slow-releasing H2S donor, ameliorates sodium deoxycholate–induced chronic intestinal barrier injury and gut microbiota dysbiosis

Pan, S., Yan, H., Zhu, J., Ma, Y., Wang, P., Liu, Y., & Chen, Z. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1476407 · Cited by 6 · see citing works

Identification of SLC15A4/PHT1 Gene Products Upregulation Marking the Intestinal Epithelial Monolayer of Ulcerative Colitis Patients

Mazzei, A., Serino, G., Romano, A., Piccinno, E., Scalavino, V., Valentini, A. M., Armentano, R., Schiavone, R., Giannelli, G., Verri, T., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113170 · Cited by 6 · see citing works

Update of gut gas metabolism in ulcerative colitis

Zhang, X., Zhang, X., & Yang, Y. (2024) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2024.2383635 · Cited by 6 · see citing works

A Promising Biomimetic Hydrogen Sulfide System for Advancing Inflammatory Disease Treatment

Qiao, C., Wang, L., Zhang, R., Shi, Y., Huang, C., Ji, Y., Yang, Z., Feng, Y., Chen, Z., Liu, J., et al. (2025) · Advanced Materials · doi:10.1002/adma.202510602 · Cited by 5 · see citing works

CSE/H2S ameliorates colitis in mice via protection of enteric glial cells and inhibition of the RhoA/ROCK pathway

Wang, S., Ding, Y., & Jiang, W. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.966881 · Cited by 5 · see citing works

The effect of microbial metabolites from colonic protein fermentation on bacteria‐induced cytokine production in dendritic cells

Xie, Z., Eriksen, D. B., Johnsen, P. R., Nielsen, D. S., & Frøkiær, H. (2025) · BioFactors · doi:10.1002/biof.70007 · Cited by 4 · see citing works

Gas entrapping materials for damage control

Alves, P. K. N., Sutton, I. C., Byrne, J. D., & Otterbein, L. E. (2026) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2026.115813 · Cited by 3 · see citing works

Differential Roles of Cystathionine Gamma-Lyase and Mercaptopyruvate Sulfurtransferase in Hapten-Induced Colitis and Contact Dermatitis in Mice

Akahoshi, N., Hasegawa, R., Yamamoto, S., Takemoto, R., Yoshizawa, T., Kamichatani, W., & Ishii, I. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032659 · Cited by 3 · see citing works

Insights into the Gut Microbiome of the South American Leaf-Toed Gecko (Phylodactylus gerropygus) Inhabiting the Core of the Atacama Desert

Rivera, D. S., Beltrán, V., Gutiérrez-Cortés, I., Vargas, C., & Alfaro, F. D. (2024) · Microorganisms · doi:10.3390/microorganisms12061194 · Cited by 3 · see citing works

Flagellin in blood and Bifidobacterium pseudocatenulatum in gut are associated with live birth upon IVF-frozen embryo transfer

Chin, K. T.-C., Yiu, J. H. C., Cheung, K. W., Yuen, L. C., Wong, W. Y.-L., Cai, J., Cheung, S. W. M., Li, R., & Woo, C. W. (2025) · iScience · doi:10.1016/j.isci.2025.111933 · Cited by 2 · see citing works

Cystathionine Gamma-Lyase Regulates TNF-α-Mediated Injury Response in Human Colonic Epithelial Cells and Colonoids

Almenas, F. A., Törő, G., Szaniszlo, P., Maskey, M., Thanki, K. K., Koltun, W. A., Yochum, G. S., Pinchuk, I. V., Chao, C., Hellmich, M. R., et al. (2024) · Antioxidants · doi:10.3390/antiox13091067 · Cited by 2 · see citing works

Rhamnogalacturonan rich fractions isolated from Saururus chinensis alleviate ulcerative colitis via regulation of MAPK/NF-κB pathway and tight junction

Kim, T. E., Son, S., Rho, Y., & Shin, K. (2026) · Nutrition Research and Practice · doi:10.4162/nrp.2026.20.2.182 · Cited by 1 · see citing works

Microbially derived glutathione from Eubacterium rectale alleviates oxidative stress and promotes intestinal epithelial recovery

Richie, T. G., Wiechman, H., Vogt, B., Ingold, C., Heeren, L., Kamke, A., Pogranichniy, S., Monk, K., Summers, T., Ran, Q., et al. (2026) · Microbiome · doi:10.1186/s40168-026-02457-y · Cited by 5 · see citing works

DXFD-1 alleviates DSS-induced ulcerative colitis by targeting NF-κB and Nrf2 signaling

Li, S., Fu, X., Cheng, C., Zhao, Y., Wu, T., & Xu, G. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115934

A cascade-activated nanotheranostic platform for MRI-guided hydrogen sulfide therapy and microenvironment remodeling in inflammatory bowel disease

Hou, W., Wang, S., Tan, M., & Ran, H. (2026) · Biomaterials Advances · doi:10.1016/j.bioadv.2026.214941

Plant-Derived Extracellular Vesicle-Like Nanoparticles and Decoction Nanoparticles Exhibit Distinct Therapeutic Effects in Alcoholic Liver Disease via Gut Homeostasis and Macrophage Regulation.

Yuan, Y., Zhang, Z.-Y., Li, X., Liu, X.-Y., Ma, Z.-X., Lv, M.-C., Yu, Z.-P., & Li, Y. (2026) · Small · doi:10.1002/smll.74979

Arctic Fox-Derived Lactiplantibacillus plantarum J3 Alleviates Colitis in Mice in Association with Strengthening of the Intestinal Barrier and Reshaping of the Intestinal Flora

Sun, Y., Lv, J., Meng, X., Sun, Y., Fu, H., Xu, W., & Du, Z. (2026) · Life · doi:10.3390/life16081355

Endogenous hydrogen sulfide is an anti-inflammatory molecule in dextran sodium sulfate-induced colitis in mice

Hirata, I., Naito, Y., Takagi, T., Mizushima, K., Suzuki, T., Omatsu, T., Handa, O., Ichikawa, H., Ueda, H., & Yoshikawa, T. (2011) · Digestive Diseases and Sciences · doi:10.1007/s10620-010-1461-5 · Cited by 72 · see citing works

GYY4137 Attenuates Sodium Deoxycholate-Induced Intestinal Barrier Injury Both In Vitro and In Vivo

Chen, Z., Tang, J., Wang, P., Zhu, J., & Liu, Y. (2019) · BioMed Research International · doi:10.1155/2019/5752323 · Cited by 11 · see citing works

ADT-OH improves intestinal barrier function and remodels the gut microbiota in DSS-induced colitis

Bi, Z., Chen, J., Chang, X., Li, D., Yao, Y., Cai, F., Xu, H., Cheng, J. G., Hua, Z., & Zhuang, H. (2023) · Frontiers of Medicine · doi:10.1007/s11684-023-0990-1 · Cited by 17 · see citing works

P45 Endogenous hydrogen sulfide suppresses intestinal inflammation through the regulation of macrophage polarization

Higashimura, Y., Naito, Y., Takagi, T., Hirata, I., Mizushima, K., & Yoshikawa, T. (2014) · Nitric Oxide · doi:10.1016/j.niox.2014.03.095 · Cited by 2 · see citing works

Protective effect of hydrogen sulfide on TNF-α and IFN-γ-induced injury of intestinal epithelial barrier function in Caco-2 monolayers

Chen, S.-W., Zhu, J., Zuo, S., Zhang, J., Chen, Z., Chen, G., Wang, X., Pan, Y., Liu, Y., & Wang, P. (2015) · Inflammation Research · doi:10.1007/s00011-015-0862-5 · Cited by 69 · see citing works