Loss of Gut Microbiota Alters Immune System Composition and Cripples Postinfarction Cardiac Repair

Heart Disease and Stroke Statistics—2017 Update: A Report From the American Heart Association

Benjamin, E. J., Blaha, M. J., Chiuve, S. E., Cushman, M., Das, S. R., Deo, R., de Ferranti, S. D., Floyd, J., Fornage, M., Gillespie, C., et al. (2017) · Circulation · doi:10.1161/cir.0000000000000485 · Cited by 12,591 · see citing works

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 · see citing works

Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences

Langille, M. G. I., Zaneveld, J., Caporaso, J. G., McDonald, D., Knights, D., Reyes, J. A., Clemente, J. C., Burkepile, D. E., Vega Thurber, R. L., Knight, R., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2676 · Cited by 9,116 · see citing works

Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease

Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., DuGar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y.-M., et al. (2011) · Nature · doi:10.1038/nature09922 · Cited by 5,597 · see citing works

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 · see citing works

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 · see citing works

Host microbiota constantly control maturation and function of microglia in the CNS

Erny, D., Hrabě de Angelis, A. L., Jaitin, D., Wieghofer, P., Staszewski, O., David, E., Keren-Shaul, H., Mahlakoiv, T., Jakobshagen, K., Buch, T., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4030 · Cited by 3,569 · see citing works

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 · see citing works

Transient Regenerative Potential of the Neonatal Mouse Heart

Porrello, E. R., Mahmoud, A. I., Simpson, E., Hill, J. A., Richardson, J. A., Olson, E. N., & Sadek, H. A. (2011) · Science · doi:10.1126/science.1200708 · Cited by 2,545 · see citing works

The healing myocardium sequentially mobilizes two monocyte subsets with divergent and complementary functions

Nahrendorf, M., Swirski, F. K., Aikawa, E., Stangenberg, L., Wurdinger, T., Figueiredo, J.-L., Libby, P., Weissleder, R., & Pittet, M. J. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070885 · Cited by 2,300 · see citing works

Diet–microbiota interactions as moderators of human metabolism

Sonnenburg, J. L., & Bäckhed, F. (2016) · Nature · doi:10.1038/nature18846 · Cited by 2,257 · see citing works

Nonresolving Inflammation

Nathan, C., & Ding, A. (2010) · Cell · doi:10.1016/j.cell.2010.02.029 · Cited by 2,183 · see citing works

The microbial metabolite butyrate regulates intestinal macrophage function via histone deacetylase inhibition.

Chang, P. V., Hao, L., Offermanns, S., & Medzhitov, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1322269111 · Cited by 2,175 · see citing works

The microbiome and innate immunity

Thaiss, C. A., Zmora, N., Levy, M., & Elinav, E. (2016) · Nature · doi:10.1038/nature18847 · Cited by 2,012 · see citing works

Intestinal homeostasis and its breakdown in inflammatory bowel disease

Maloy, K. J., & Powrie, F. M. (2011) · Nature · doi:10.1038/nature10208 · Cited by 1,876 · see citing works

The microbiota in adaptive immune homeostasis and disease

Honda, K., & Littman, D. R. (2016) · Nature · doi:10.1038/nature18848 · Cited by 1,846 · see citing works

Gut microbiota in cardiovascular health and disease

Tang, W. H. W., Kitai, T., & Hazen, S. L. (2017) · Circulation Research · doi:10.1161/circresaha.117.309715 · Cited by 1,670 · see citing works

Regulation of the Inflammatory Response in Cardiac Repair

Frangogiannis, N. G. (2012) · Circulation Research · doi:10.1161/circresaha.111.243162 · Cited by 1,196 · see citing works

ATP drives lamina propria TH17 cell differentiation

Atarashi, K., Nishimura, J., Shima, T., Umesaki, Y., Yamamoto, M., Onoue, M., Yagita, H., Ishii, N., Evans, R., Honda, K., et al. (2008) · Nature · doi:10.1038/nature07240 · Cited by 1,089 · see citing works

High-Fiber Diet and Acetate Supplementation Change the Gut Microbiota and Prevent the Development of Hypertension and Heart Failure in Hypertensive Mice

Marques, F. Z., Nelson, E., Chu, P.-Y., Horlock, D., Fiedler, A., Ziemann, M., Tan, J. K., Kuruppu, S., Rajapakse, N. W., El-Osta, A., et al. (2017) · Circulation · doi:10.1161/circulationaha.116.024545 · Cited by 1,065 · see citing works

The negative impact of antibiotic resistance

Friedman, N. D., Temkin, E., & Carmeli, Y. (2015) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2015.12.002 · Cited by 882 · see citing works

Diet, metabolites, and “western-lifestyle” inflammatory diseases

Thorburn, A. N., Macia, L., & Mackay, C. R. (2014) · Immunity · doi:10.1016/j.immuni.2014.05.014 · Cited by 879 · see citing works

Macrophages are required for neonatal heart regeneration

Aurora, A. B., Porrello, E. R., Tan, W. H., Mahmoud, A. I., Hill, J. A., Bassel‐Duby, R., Sadek, H. A., & Olson, E. N. (2014) · Journal of Clinical Investigation · doi:10.1172/jci72181 · Cited by 823 · see citing works

Gut Microbiota Promote Hematopoiesis to Control Bacterial Infection

Khosravi, A., Yáñez, A., Price, J. G., Chow, A. T., Mérad, M., Goodridge, H. S., & Mazmanian, S. K. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.02.006 · Cited by 651 · see citing works

Microbiota restoration: natural and supplemented recovery of human microbial communities

Reid, G., Younes, J. A., van der Mei, H. C., Gloor, G. B., Knight, R. D., & Busscher, H. J. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2473 · Cited by 585 · see citing works

Transplantation of fecal microbiota from patients with irritable bowel syndrome alters gut function and behavior in recipient mice

De Palma, G., Lynch, M. D. J., Lu, J., Dang, V. T., Deng, Y., Jury, J., Umeh, G., Miranda, P. M., Pigrau Pastor, M., Sidani, S., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf6397 · Cited by 505 · see citing works

Metagenomic analyses reveal antibiotic-induced temporal and spatial changes in intestinal microbiota with associated alterations in immune cell homeostasis

Hill, D. A., Hoffmann, C., Abt, M. C., Du, Y., Kobuley, D. E., Kirn, T. J., Bushman, F. D., & Artis, D. (2009) · Mucosal Immunology · doi:10.1038/mi.2009.132 · Cited by 425 · see citing works

Effect of Lactobacillus plantarum 299v on cardiovascular disease risk factors in smokers

Naruszewicz, M., Johansson, M.-L., Zapolska‐Downar, D., & Bukowska, H. (2002) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/76.6.1249 · Cited by 365 · see citing works

Physiological concentrations of short-chain fatty acids immediately suppress colonic epithelial permeability

Suzuki, T., Yoshida, S., & Hara, H. (2008) · British Journal Of Nutrition · doi:10.1017/s0007114508888733 · Cited by 356 · see citing works

Probiotic Administration Attenuates Myocardial Hypertrophy and Heart Failure After Myocardial Infarction in the Rat

Gan, X. T., Ettinger, G., Huang, C. X., Burton, J. P., Haist, J. V., Rajapurohitam, V., Sidaway, J. E., Martin, G., Gloor, G. B., Swann, J. R., et al. (2014) · Circulation: Heart Failure · doi:10.1161/circheartfailure.113.000978 · Cited by 329 · see citing works

Commensal Fungi Recapitulate the Protective Benefits of Intestinal Bacteria

Jiang, T. T., Shao, T., Ang, W. X. G., Kinder, J. M., Turner, L. H., Pham, G. H., Whitt, J., Alenghat, T., & Way, S. S. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.10.013 · Cited by 296 · see citing works

Probiotics in foods not containing milk or milk constituents, with special reference to Lactobacillus plantarum 299v

Molin, G. (2001) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/73.2.380s · Cited by 261 · see citing works

Short-Chain Fatty Acids Activate AMP-Activated Protein Kinase and Ameliorate Ethanol-Induced Intestinal Barrier Dysfunction in Caco-2 Cell Monolayers

Elamin, E. E., Masclee, A., Jan, D., Pieters, H., & Jonkers, D. M. A. E. (2013) · Journal of Nutrition · doi:10.3945/jn.113.179549 · Cited by 237 · see citing works

Mortality in Patients After a Recent Myocardial Infarction

Camm, A. J., Pratt, C. M., Schwartz, P. J., Al‐Khalidi, H. R., Spyt, M. J., Holroyde, M. J., Karam, R., Sonnenblick, E. H., & Brum, J. M. (2004) · Circulation · doi:10.1161/01.cir.0000117090.01718.2a · Cited by 226 · see citing works

Depletion of Cultivatable Gut Microbiota by Broad-Spectrum Antibiotic Pretreatment Worsens Outcome After Murine Stroke

Winek, K., Engel, O., Bäcker‐Koduah, P., Heimesaat, M. M., Fischer, A., Bereswill, S., Dames, C., Kershaw, O., Gruber, A. D., Curato, C., et al. (2016) · Stroke · doi:10.1161/strokeaha.115.011800 · Cited by 214 · see citing works

Use of the second-generation antipsychotic, risperidone, and secondary weight gain are associated with an altered gut microbiota in children

Bahr, S. M., Tyler, B. C., Wooldridge, N., Butcher, B. D., Burns, T. L., Teesch, L. M., Oltman, C. L., Azcarate-Peril, M. A., Kirby, J. R., & Calarge, C. A. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.135 · Cited by 197 · see citing works

Depressed Liver Regeneration After Partial Hepatectomy of Germ–Free, Athymic and Lipopolysaccharide–Resistant Mice

Cornell, R. P., Liljequist, B. L., & Bartizal, K. F. (1990) · Hepatology · doi:10.1002/hep.1840110603 · Cited by 178 · see citing works

Use of Antibiotics and Risk of Type 2 Diabetes: A Population-Based Case-Control Study

Mikkelsen, S. U., Knop, F. K., Frost, M., Hallas, J., & Pottegård, A. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2015-2696 · Cited by 173 · see citing works

Intestinal Microbial Metabolites Are Linked to Severity of Myocardial Infarction in Rats

Lam, V., Su, J., Hsu, A., Gross, G. J., Salzman, N. H., & Baker, J. E. (2016) · PLoS ONE · doi:10.1371/journal.pone.0160840 · Cited by 138 · see citing works

Immune Responses to Broad-Spectrum Antibiotic Treatment and Fecal Microbiota Transplantation in Mice

Ekmekçiu, I., von Klitzing, E., Fiebiger, U., Escher, U., Neumann, C., Bächer, P., Scheffold, A., Kühl, A. A., Bereswill, S., & Heimesaat, M. M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00397 · Cited by 135 · see citing works

Oral Antibiotic Treatment Induces Skin Microbiota Dysbiosis and Influences Wound Healing

Zhang, M., Jiang, Z., Li, D., Jiang, D., Wu, Y., Ren, H., Hua, P., & Lai, Y. (2014) · Microbial Ecology · doi:10.1007/s00248-014-0504-4 · Cited by 103 · see citing works

Prostaglandin E2 promotes post‐infarction cardiomyocyte replenishment by endogenous stem cells

Hsueh, Y., Wu, J. M. F., Yu, C., Wu, K. K., & Hsieh, P. C. H. (2014) · EMBO Molecular Medicine · doi:10.1002/emmm.201303687 · Cited by 68 · see citing works

Circulating Cells Contribute to Cardiomyocyte Regeneration After Injury

Wu, J. M. F., Hsueh, Y.-C., Ch’ang, H.-J., Luo, C.-Y., Wu, L., Nakauchi, H., & Hsieh, P. C. H. (2014) · Circulation Research · doi:10.1161/circresaha.116.304564 · Cited by 53 · see citing works

Gut microbiota in human metabolic health and disease

Fan, Y., & Pedersen, O. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-020-0433-9 · Cited by 4,724 · see citing works

Gut microbiota and cardiovascular disease.

Witkowski, M., Weeks, T. L., & Hazen, S. L. (2020) · Circulation Research · doi:10.1161/circresaha.120.316242 · Cited by 1,051 · see citing works

Intestinal Microbiota in Cardiovascular Health and Disease

Tang, W. H. W., Bäckhed, F., Landmesser, U., & Hazen, S. L. (2019) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2019.03.024 · Cited by 508 · see citing works

Health Benefits and Side Effects of Short-Chain Fatty Acids

Xiong, R.-G., Zhou, D.-D., Wu, S.-X., Huang, S., Saimaiti, A., Yang, Z., Shang, A., Zhao, C., Gan, R., & Li, H. (2022) · Foods · doi:10.3390/foods11182863 · Cited by 489 · see citing works

The gut microbiome in coronary artery disease and heart failure: Current knowledge and future directions

Trøseid, M., Andersen, G. Ø., Broch, K., & Hov, J. R. (2020) · EBioMedicine · doi:10.1016/j.ebiom.2020.102649 · Cited by 406 · see citing works

Propionate attenuates atherosclerosis by immune-dependent regulation of intestinal cholesterol metabolism

Haghikia, A., Zimmermann, F., Schumann, P., Jasina, A., Roessler, J., Schmidt, D., Heinze, P., Kaisler, J., Nageswaran, V., Aigner, A., et al. (2021) · European Heart Journal · doi:10.1093/eurheartj/ehab644 · Cited by 376 · see citing works

TMAO: how gut microbiota contributes to heart failure

Zhang, Y., Wang, Y., Ke, B., & Du, J. (2020) · Translational research · doi:10.1016/j.trsl.2020.08.007 · Cited by 306 · see citing works

Trimethylamine-N-Oxide Promotes Vascular Calcification Through Activation of NLRP3 (Nucleotide-Binding Domain, Leucine-Rich-Containing Family, Pyrin Domain-Containing-3) Inflammasome and NF-κB (Nuclear Factor κB) Signals

Zhang, X., Li, Y., Yang, P., Liu, X., Lu, L., Chen, Y., Zhong, X., Li, Z., Liu, H., Ou, C., et al. (2020) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.119.313414 · Cited by 291 · see citing works

The gut microbiome and hypertension

O’Donnell, J. A., Zheng, T., Méric, G., & Marques, F. Z. (2023) · Nature Reviews Nephrology · doi:10.1038/s41581-022-00654-0 · Cited by 294 · see citing works

Altered Gut Microbial Metabolites in Amnestic Mild Cognitive Impairment and Alzheimer’s Disease: Signals in Host–Microbe Interplay

Wu, L., Han, Y., Zheng, Z., Peng, G., Liu, P., Yue, S., Zhu, S., Chen, J., Lv, H., Shao, L., et al. (2021) · Nutrients · doi:10.3390/nu13010228 · Cited by 227 · see citing works

Short-chain fatty acid, acylation and cardiovascular diseases

Chen, X., Chen, X., & Tang, X. (2020) · Clinical Science · doi:10.1042/cs20200128 · Cited by 186 · see citing works

Targeting the gut microbiota-related metabolites for osteoporosis: The inextricable connection of gut-bone axis

Zhang, Y., Wu, Y. Q., Liu, X.-F., Chen, X., & Su, J. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102196 · Cited by 153 · see citing works

Androgen-induced gut dysbiosis disrupts glucolipid metabolism and endocrinal functions in polycystic ovary syndrome

Han, Q., Wang, J., Li, W., Chen, Z., & Du, Y. (2021) · Microbiome · doi:10.1186/s40168-021-01046-5 · Cited by 152 · see citing works

Gut dysbiosis induced by cardiac pressure overload enhances adverse cardiac remodeling in a T cell-dependent manner

Carrillo-Salinas, F. J., Anastasiou, M., Ngwenyama, N., Kaur, K., Tai, A., Smolgovsky, S. A., Jetton, D., Aronovitz, M. J., & Alcaide, P. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1823801 · Cited by 144 · see citing works

Beneficial effect of the short-chain fatty acid propionate on vascular calcification through intestinal microbiota remodelling

Yan, J., Pan, Y., Shao, W., Wang, C., Wang, R., He, Y., Zhang, M., Wang, Y., Li, T., Wang, Z., et al. (2022) · Microbiome · doi:10.1186/s40168-022-01390-0 · Cited by 148 · see citing works

Implication of Gut Microbiota in Cardiovascular Diseases

Zhou, W., Cheng, Y., Zhu, P., Nasser, M. I., Zhang, X., & Zhao, M. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/5394096 · Cited by 138 · see citing works

Short-Chain Fatty Acids Outpace Ketone Oxidation in the Failing Heart

Carley, A. N., Maurya, S. K., Fasano, M. J., Wang, Y., Selzman, C. H., Drakos, S. G., & Lewandowski, E. D. (2021) · Circulation · doi:10.1161/circulationaha.120.052671 · Cited by 135 · see citing works

Microbial Peer Pressure

Muralitharan, R. R., Jama, H. A., Xie, L., Peh, A., Snelson, M., & Marques, F. Z. (2020) · Hypertension · doi:10.1161/hypertensionaha.120.14473 · Cited by 131 · see citing works

Role of the intestinal microbiome and its therapeutic intervention in cardiovascular disorder

Luqman, A., Hassan, A., Ullah, M., Naseem, S., Ullah, M., Zhang, L., Din, A. U., Ullah, K., Ahmad, W., & Wang, G. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1321395 · Cited by 138 · see citing works

Gut microbiota-derived short-chain fatty acids and hypertension: Mechanism and treatment

Yang, F., Chen, H., Gao, Y., An, N., Li, X., Pan, X., Yang, X., Tian, L., Sun, J., Xiong, X., et al. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110503 · Cited by 131 · see citing works

Heart–gut microbiota communication determines the severity of cardiac injury after myocardial ischaemia/reperfusion

Zhao, J., Qi, Z., Cheng, W., Dai, Q., Wei, Z., Guo, M., Chen, F., Qiao, S., Hu, J., Wang, J., et al. (2023) · Cardiovascular Research · doi:10.1093/cvr/cvad023 · Cited by 126 · see citing works

Fecal g. Streptococcus and g. Eubacterium_coprostanoligenes_group combined with sphingosine to modulate the serum dyslipidemia in high-fat diet mice

Wei, W., Jiang, W., Tian, Z., Wu, H., Ning, H., Yan, G., Zhang, Z., Li, Z., Dong, F., Sun, Y., et al. (2021) · Clinical Nutrition · doi:10.1016/j.clnu.2021.01.031 · Cited by 125 · see citing works

Role and Effective Therapeutic Target of Gut Microbiota in Heart Failure

Jia, Q., Li, H., Zhou, H., Zhang, X., Zhang, A., Xie, Y., Li, Y., Lv, S., & Zhang, J. (2019) · Cardiovascular Therapeutics · doi:10.1155/2019/5164298 · Cited by 118 · see citing works

Gut microbiome mediates the protective effects of exercise after myocardial infarction

Zhou, Q., Deng, J., Pan, X., Meng, D., Zhu, Y., Bai, Y., Shi, C., Duan, Y., Wang, T., Li, X., et al. (2022) · Microbiome · doi:10.1186/s40168-022-01271-6 · Cited by 106 · see citing works

Polyamine metabolism links gut microbiota and testicular dysfunction

Zhao, Q., Huang, J., Cheng, Y., Dai, M., Zhu, W., Yang, X., Gonzalez, F. J., & Li, F. (2021) · Microbiome · doi:10.1186/s40168-021-01157-z · Cited by 106 · see citing works

Microbiota-derived short-chain fatty acids: Implications for cardiovascular and metabolic disease

Lu, Y., Zhang, Y., Zhao, X., Shang, C., Xiang, M., Li, L., & Cui, X. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.900381 · Cited by 109 · see citing works

Gut microbiome - A potential mediator of pathogenesis in heart failure and its comorbidities: State-of-the-art review

Mamic, P., Chaikijurajai, T., & Tang, W. H. W. (2020) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2020.12.001 · Cited by 99 · see citing works

Gut-Heart Axis: The Role of Gut Microbiota and Metabolites in Heart Failure

Snelson, M., Muralitharan, R. R., Liu, C., Markó, L., Forslund, S. K., Marques, F. Z., & Tang, W. H. W. (2025) · Circulation Research · doi:10.1161/circresaha.125.325516 · Cited by 106 · see citing works

Gut microbiota and microbiota-derived metabolites in cardiovascular diseases

Chen, X., Zhang, H., Ren, S., Ding, Y.-N., Remex, N. S., Bhuiyan, M. S., Qu, J.-H., & Tang, X. (2023) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002206 · Cited by 98 · see citing works

Importance of gut microbiota metabolites in the development of cardiovascular diseases (CVD)

Hemmati, M., Kashanipoor, S., Mazaheri, P., Alibabaei, F., Babaeizad, A., Asli, S., Mohammadi, S., Gorgin, A. H., Ghods, K., Yousefi, B., et al. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121947 · Cited by 102 · see citing works

Oral bacteria relative abundance in faeces increases due to gut microbiota depletion and is linked with patient outcomes

Liao, C., Rolling, T., Djuković, A., Fei, T., Mishra, V., Liu, H., Lindberg, C., Dai, L., Zhai, B., Peled, J. U., et al. (2024) · Nature Microbiology · doi:10.1038/s41564-024-01680-3 · Cited by 94 · see citing works

Akkermansia muciniphila-derived acetate activates the hepatic AMPK/SIRT1/PGC-1α axis to alleviate ferroptosis in metabolic-associated fatty liver disease

Zhuge, A., Li, S., Han, S., Yuan, Y., Shen, J., Wu, W., Wang, K., Xia, J., Wang, Q., Gu, Y., et al. (2024) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2024.10.010 · Cited by 94 · see citing works

Symbiotic Firmicutes establish mutualism with the host via innate tolerance and resistance to control systemic immunity

Jordan, C. K. I., Brown, R. L., Larkinson, M. L. Y., Sequeira, R. P., Edwards, A. M., & Clarke, T. B. (2023) · Cell Host & Microbe · doi:10.1016/j.chom.2023.07.008 · Cited by 88 · see citing works

Cross-omics analysis revealed gut microbiome-related metabolic pathways underlying atherosclerosis development after antibiotics treatment

Kappel, B. A., Angelis, L. D., Heiser, M., Ballanti, M., Stoehr, R., Goettsch, C., Mavilio, M., Artati, A., Paoluzi, O. A., Adamski, J., et al. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.100976 · Cited by 89 · see citing works

Therapeutic and Improving Function of Lactobacilli in the Prevention and Treatment of Cardiovascular-Related Diseases: A Novel Perspective From Gut Microbiota

Zhao, X., Zhong, X., Liu, X., Wang, X., & Gao, X. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.693412 · Cited by 91 · see citing works

Gut-Derived Metabolite Indole-3-Propionic Acid Modulates Mitochondrial Function in Cardiomyocytes and Alters Cardiac Function

Gesper, M., Nonnast, A., Kumowski, N., Stoehr, R., Schuett, K. A., Marx, N., & Kappel, B. A. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.648259 · Cited by 87 · see citing works

Current understanding of gut microbiota alterations and related therapeutic intervention strategies in heart failure

Chen, X., Li, H., Hu, X., Zhang, Y., & Zhang, S. (2019) · Chinese Medical Journal · doi:10.1097/cm9.0000000000000330 · Cited by 84 · see citing works

Microbiota in Gut‐Heart Axis: Metabolites and Mechanisms in Cardiovascular Disease

Kondapalli, N. B., Katari, V., Dalal, K. K., Paruchuri, S. M., & Thodeti, C. K. (2025) · Comprehensive physiology · doi:10.1002/cph4.70024 · Cited by 93 · see citing works

Yellow Wine Polyphenolic Compound Protects Against Doxorubicin-Induced Cardiotoxicity by Modulating the Composition and Metabolic Function of the Gut Microbiota

Lin, H., Meng, L., Sun, Z., Shiming, S., Huang, X., Lin, N., Zhang, J., Lu, W., Yang, Q., Chi, J., et al. (2021) · Circulation Heart Failure · doi:10.1161/circheartfailure.120.008220 · Cited by 82 · see citing works

Gastrointestinal Disorders and Metabolic Syndrome: Dysbiosis as a Key Link and Common Bioactive Dietary Components Useful for their Treatment

Filippis, A. D., Ullah, H., Baldi, A., Dacrema, M., Esposito, C., Garzarella, E. U., Santarcangelo, C., Tantipongpiradet, A., & Daglia, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144929 · Cited by 85 · see citing works

Gut microbiota and microbial metabolites for osteoporosis

Zheng, X.-Q., Wang, D.-B., Jiang, Y., & Song, C. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2437247 · Cited by 89 · see citing works

Thyroid hormone receptor-beta agonist HSK31679 alleviates MASLD by modulating gut microbial sphingolipids

Zhang, Y., Xie, R., Dai, C.-S., Gao, H., Zhou, G., Qi, T., Wang, W.-Y., Wang, H., & Yi-min, C. (2024) · Journal of Hepatology · doi:10.1016/j.jhep.2024.08.008 · Cited by 77 · see citing works

Therapeutic Potential of Hydroxysafflor Yellow A on Cardio-Cerebrovascular Diseases

Bai, X., Wang, W.-X., Fu, R., Yue, S., Gao, H., Chen, Y., & Tang, Y. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.01265 · Cited by 75 · see citing works

Gut butyrate-producers confer post-infarction cardiac protection

Chen, H.-C., Liu, Y.-W., Chang, K., Wu, Y., Chen, Y., Chao, Y.-K., You, M.-Y., Lundy, D. J., Lin, C., Hsieh, M. L., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43167-5 · Cited by 81 · see citing works

Role of the microbiota–gut–heart axis between bile acids and cardiovascular disease

Zhang, Z., Lv, T., Wang, X., Wu, M., Zhang, R., Yang, X., Fu, Y., & Liu, Z. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116567 · Cited by 77 · see citing works

Pharmacological Modulation of Cardiac Remodeling after Myocardial Infarction

Zhao, W., Zhao, J., & Rong, J. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/8815349 · Cited by 77 · see citing works

Adding insult to injury - Inflammation at the heart of cardiac fibrosis

Smolgovsky, S. A., Ibeh, U., Tamayo, T. P., & Alcaide, P. (2020) · Cellular Signalling · doi:10.1016/j.cellsig.2020.109828 · Cited by 70 · see citing works

Remodeling of the gut microbiome by Lactobacillus johnsonii alleviates the development of acute myocardial infarction

Zhong, X., Zhao, Y., Huang, L. J., Liu, J., Wang, K., Gao, X., Zhao, X., & Wang, X. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1140498 · Cited by 66 · see citing works

Central and peripheral regulations mediated by short-chain fatty acids on energy homeostasis

Luo, P., Lednovich, K., Xu, K., Nnyamah, C., Layden, B. T., & Xu, P. (2022) · Translational research · doi:10.1016/j.trsl.2022.06.003 · Cited by 62 · see citing works

Alterations in gut microbiota and metabolites associated with altitude-induced cardiac hypertrophy in rats during hypobaric hypoxia challenge

Pan, Z., Hu, Y., Huang, Z., Han, N., Li, Y., Zhuang, X., Yin, J., Peng, H., Gao, Q., Zhang, W., et al. (2022) · Science China Life Sciences · doi:10.1007/s11427-021-2056-1 · Cited by 63 · see citing works

Gut microbiota protects from triptolide-induced hepatotoxicity: Key role of propionate and its downstream signalling events

Huang, J., Zhao, Q., Dai, M., Xiao, X.-R., Zhang, T., Zhu, W., & Li, F. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.104752 · Cited by 63 · see citing works

Short-Chain Fatty Acids in the Metabolism of Heart Failure – Rethinking the Fat Stigma

Palm, C. L., Nijholt, K. T., Bakker, B. M., & Westenbrink, B. D. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.915102 · Cited by 61 · see citing works

Melatonin alleviates Ochratoxin A-induced liver inflammation involved intestinal microbiota homeostasis and microbiota-independent manner

Xia, D., Yang, L., Li, Y., Chen, J., Zhang, X., Wang, H., Zhai, S., Jiang, X., Meca, G., Wang, S., et al. (2021) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2021.125239 · Cited by 60 · see citing works

The emerging role of gut microbial metabolism on cardiovascular disease

Kasahara, K., & Rey, F. E. (2019) · Current Opinion in Microbiology · doi:10.1016/j.mib.2019.09.007 · Cited by 58 · see citing works

Oral Supplementation With Butyrate Improves Myocardial Ischemia/Reperfusion Injury via a Gut-Brain Neural Circuit

Yu, Z., Han, J., Chen, H., Wang, Y., Zhou, L., Wang, M., Zhang, R., Jin, X., Zhang, G., Wang, C., et al. (2021) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2021.718674 · Cited by 59 · see citing works

Update on gut microbiota in cardiovascular diseases

Qian, B., Zhang, K., Li, Y., & Sun, K. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.1059349 · Cited by 59 · see citing works

Opportunities and challenges of bacterial extracellular vesicles in regenerative medicine

Guo, J., Huang, Z., Wang, Q., Wang, M., Ming, Y., Chen, W., Huang, Y., Tang, Z., Huang, M., Liu, H., et al. (2025) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02935-1 · Cited by 58 · see citing works

Anti-hypertensive and cardioprotective activities of traditional Chinese medicine-derived polysaccharides: A review

Xie, M., Tao, W., Wu, F., Wu, K., Huang, X., Ling, G., Zhao, C., Lv, Q., Wang, Q., Zhou, X., et al. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.07.008 · Cited by 57 · see citing works

Gut microbiome and its meta-omics perspectives: profound implications for cardiovascular diseases

Xu, J., & Yang, Y. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1936379 · Cited by 56 · see citing works

Exploring the Potential Role of the Gut Microbiome in Chemotherapy-Induced Neurocognitive Disorders and Cardiovascular Toxicity

Čierniková, S., Mego, M., & Chovanec, M. (2021) · Cancers · doi:10.3390/cancers13040782 · Cited by 54 · see citing works

Oral-gut microbial transmission promotes diabetic coronary heart disease

Li, Y., Liu, Y., Cui, J., Zhu, M., Wang, W., Chen, K., Huang, L., & Liu, Y. (2024) · Cardiovascular Diabetology · doi:10.1186/s12933-024-02217-y · Cited by 51 · see citing works

Gut microbiota regulates cardiac ischemic tolerance and aortic stiffness in obesity

Battson, M. L., Lee, D. M., Puma, L. C. L., Ecton, K. E., Thomas, K. N., Febvre, H. P., Chicco, A. J., Weir, T. L., & Gentile, C. L. (2019) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00346.2019 · Cited by 51 · see citing works

Hypotension as a marker or mediator of perioperative organ injury: a narrative review

Ackland, G. L., & Abbott, T. E. F. (2022) · British Journal of Anaesthesia · doi:10.1016/j.bja.2022.01.012 · Cited by 50 · see citing works

Exercise ameliorates osteopenia in mice via intestinal microbial-mediated bile acid metabolism pathway

Yu, C., Sun, R., Yang, W., Gu, T., Ying, X., Ye, L., Zheng, Y., Fan, S., Zeng, X., & Yao, S. (2025) · Theranostics · doi:10.7150/thno.104186 · Cited by 49 · see citing works

Antibiotic-induced gut microbiota depletion exacerbates host hypercholesterolemia

Kappel, B. A., Angelis, L. D., Puetz, A., Ballanti, M., Menghini, R., Marx, N., & Federici, M. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106570 · Cited by 49 · see citing works

The Gut–Heart Axis: Molecular Perspectives and Implications for Myocardial Infarction

Rivera, K., González, L., Bravo, L., Manjarres, L., & Andía, M. E. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212465 · Cited by 50 · see citing works

Gut Microbiome-Based Management of Patients With Heart Failure

Mamic, P., Snyder, M. P., & Tang, W. H. W. (2023) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2023.02.045 · Cited by 50 · see citing works

Tributyrin alleviates gut microbiota dysbiosis to repair intestinal damage in antibiotic-treated mice

Yang, N., Lan, T., Han, Y., Zhao, H., Wang, C., Xu, Z. C., Zhao, C., Tao, M., Li, H., Song, Y., et al. (2023) · PLoS ONE · doi:10.1371/journal.pone.0289364 · Cited by 49 · see citing works

Prophylactic Supplementation with Lactobacillus Reuteri or Its Metabolite GABA Protects Against Acute Ischemic Cardiac Injury

Wang, J., Zhang, H., Yuan, H., Chen, S., Yu, Y., Zhang, X., Gao, Z., Du, H., Li, W., Wang, Y., et al. (2024) · Advanced Science · doi:10.1002/advs.202307233 · Cited by 43 · see citing works

Development of an Efficient and Sensitive Chemical Derivatization-Based LC–MS/MS Method for Quantifying Gut Microbiota-Derived Metabolites in Human Plasma and Its Application in Studying Cardiovascular Disease

Liao, H.-Y., Wang, C., Lee, C.-H., Kao, H., Wu, W., & Kuo, C. (2021) · Journal of Proteome Research · doi:10.1021/acs.jproteome.1c00147 · Cited by 43 · see citing works

Intermingling of gut microbiota with brain: Exploring the role of probiotics in battle against depressive disorders

Tyagi, P., Tasleem, M., Prakash, S., & Chouhan, G. (2020) · Food Research International · doi:10.1016/j.foodres.2020.109489 · Cited by 42 · see citing works

Propionate Alleviates Abdominal Aortic Aneurysm by Modulating Colonic Regulatory T-Cell Expansion and Recirculation

Yang, F., Xia, N., Guo, S., Zhang, J., Liao, Y., Tang, T., Nie, S., Zhang, M., Lv, B., Lu, Y., et al. (2022) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2022.05.001 · Cited by 42 · see citing works

The gut–immune axis during hypertension and cardiovascular diseases

Dinakis, E., O’Donnell, J. A., & Marques, F. Z. (2024) · Acta Physiologica · doi:10.1111/apha.14193 · Cited by 45 · see citing works

Gut and Cutaneous Microbiome Featuring Abundance of Lactobacillus reuteri Protected Against Psoriasis-Like Inflammation in Mice

Chen, H., Zeng, Y.-B., Zhang, Z., Kong, C., Zhang, S., Li, Z., Huang, J., Xu, Y., Mao, Y., Cai, P., et al. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s337031 · Cited by 41 · see citing works

Commensal gut microbiota-derived acetate and propionate enhance heart adaptation in response to cardiac pressure overload in mice

Lin, C., Cheng, Y., Chen, H.-C., Chao, Y.-K., Nicholson, M. W., Yen, C.-L., Kamp, T. J., & Hsieh, P. C. H. (2022) · Theranostics · doi:10.7150/thno.76002 · Cited by 42 · see citing works

Gut Microbiota Involvement in Ventricular Remodeling Post–Myocardial Infarction

McMillan, A., & Hazen, S. L. (2019) · Circulation · doi:10.1161/circulationaha.118.037384 · Cited by 39 · see citing works

Gut Microbiota: A Novel Regulator of Cardiovascular Disease and Key Factor in the Therapeutic Effects of Flavonoids

Li, Q., Gao, B. X., Bateer, S., He, Q., Zhang, R., Meng, X., Naiheng, Z., Li, M., & Li, M. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.651926 · Cited by 40 · see citing works

The short-chain fatty acid propionate improved ventricular electrical remodeling in a rat model with myocardial infarction

Zhou, M., Li, D., Xie, K., Xu, L., Kong, B., Wang, X., Tang, Y., Liu, Y., & Huang, H. (2021) · Food & Function · doi:10.1039/d1fo02040d · Cited by 39 · see citing works

Endocrine organs of cardiovascular diseases: Gut microbiota

Jia, Q., Xie, Y., Lu, C., Zhang, A., Lu, Y., Lv, S., & Zhang, J. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14164 · Cited by 38 · see citing works

Immunotherapy in liver cancer: overcoming the tolerogenic liver microenvironment

Liu, Y., Yang, H., Li, T. X., & Zhang, N. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1460282 · Cited by 39 · see citing works

Stimulating pro-reparative immune responses to prevent adverse cardiac remodelling: consensus document from the joint 2019 meeting of the ESC Working Groups of cellular biology of the heart and myocardial function

Steffens, S., Linthout, S. V., Sluijter, J. P. G., Tocchetti, C. G., Thum, T., & Madonna, R. (2020) · Cardiovascular Research · doi:10.1093/cvr/cvaa137 · Cited by 37 · see citing works

Circadian influence on the microbiome improves heart failure outcomes

Mistry, P., Reitz, C. J., Khatua, T. N., Rasouli, M., Oliphant, K., Young, M. E., Allen‐Vercoe, E., & Martino, T. A. (2020) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2020.09.006 · Cited by 36 · see citing works

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 · see citing works

Intrinsic and Extrinsic Contributors to the Cardiac Benefits of Exercise

Hastings, M. H., Castro, C., Freeman, R., Kadir, A. A., Lerchenmüller, C., Li, H., Rhee, J., Roh, J. D., Roh, K., Singh, A. P., et al. (2023) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2023.07.011 · Cited by 34 · see citing works

The Emerging Role of Gut Dysbiosis in Cardio-metabolic Risk Factors for Heart Failure

Sata, Y., Marques, F. Z., & Kaye, D. M. (2020) · Current Hypertension Reports · doi:10.1007/s11906-020-01046-0 · Cited by 34 · see citing works

Gastrodin attenuates perfluorooctanoic acid-induced liver injury by regulating gut microbiota composition in mice

Ma, S., Sun, Y., Zheng, X., & Yang, Y. (2021) · Bioengineered · doi:10.1080/21655979.2021.2009966 · Cited by 35 · see citing works

Gut Microbiome-Targeted Modulations Regulate Metabolic Profiles and Alleviate Altitude-Related Cardiac Hypertrophy in Rats

Hu, Y., Pan, Z., Huang, Z., Li, Y., Han, N., Zhuang, X., Peng, H., Gao, Q., Wang, Q., Lee, B. J. Y., et al. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.01053-21 · Cited by 35 · see citing works

Short-Chain Carbon Sources

Challa, A. A., & Lewandowski, E. D. (2022) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2021.12.010 · Cited by 35 · see citing works

Gut microbiota and healthy longevity

Luo, J., Liang, S., & Jin, F. (2024) · Science China Life Sciences · doi:10.1007/s11427-023-2595-5 · Cited by 35 · see citing works

Mutual Interplay of Host Immune System and Gut Microbiota in the Immunopathology of Atherosclerosis

Yeh, C., Chen, Y.-H., Liu, S.-F., Kao, H., Wu, M., Yang, K., & Wu, W. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228729 · Cited by 36 · see citing works

The Gut in Heart Failure: Current Knowledge and Novel Frontiers

Gallo, A., Macerola, N., Favuzzi, A. M. R., Nicolazzi, M. A., Gasbarrini, A., & Montalto, M. (2022) · Medical Principles and Practice · doi:10.1159/000522284 · Cited by 35 · see citing works

Exosomes derived from human placental mesenchymal stem cells ameliorate myocardial infarction via anti-inflammation and restoring gut dysbiosis

Yang, L., Wang, T., Zhang, X., Zhang, H., Yan, N., Zhang, G., Yan, R., Li, Y., Yu, J., He, J., et al. (2022) · BMC Cardiovascular Disorders · doi:10.1186/s12872-022-02508-w · Cited by 34 · see citing works

Beneficial Effects of Essential Oils from the Mediterranean Diet on Gut Microbiota and Their Metabolites in Ischemic Heart Disease and Type-2 Diabetes Mellitus

Sanchez‐Quintero, M. J., Delgado, J., Vera, D. M., Becerra‐Muñoz, V. M., Queipo‐Ortuño, M. I., Estévez, M., Plaza-Andrades, I. J., Rodríguez‐Capitán, J., Sanchez, P. L., Crespo‐Leiro, M. G., et al. (2022) · Nutrients · doi:10.3390/nu14214650 · Cited by 37 · see citing works

Gut microbiota and myocardial fibrosis

Han, X., Yang, F., & Bao, Z. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.175355 · Cited by 34 · see citing works

Gut Microbial Metabolome and Dysbiosis in Neurodegenerative Diseases: Psychobiotics and Fecal Microbiota Transplantation as a Therapeutic Approach—A Comprehensive Narrative Review

Uceda, S., Echeverry‐Alzate, V., Reiriz, M., Miguel, E. M., Pérez-Curiel, A., Gómez-Senent, S., & Beltrán-Velasco, A. I. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713294 · Cited by 35 · see citing works

Role of gut microbiota in doxorubicin-induced cardiotoxicity: from pathogenesis to related interventions

Huang, C., Li, X., Li, H., Chen, R., Li, Z., Li, D., Xu, X., Zhang, G., Qin, L., Li, B., et al. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05232-5 · Cited by 35 · see citing works

GV-971 prevents severe acute pancreatitis by remodeling the microbiota-metabolic-immune axis

Chen, X., Chen, X., Ding, Y. P., Zhang, N., Fu, W., Wu, M., Ge, F., Wang, J., Li, X., Geng, M., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-52398-z · Cited by 33 · see citing works

Gut microbiota-derived metabolites as immune modulators in aging and age-related chronic inflammatory diseases

Chen, N., Chan, C. K., Khan, F. U., Makhijani, P., Valentino, T. R., Winer, S., Luk, C. T., & Winer, D. A. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103036 · Cited by 35 · see citing works

Gut microbiota-dependent phenylacetylglutamine in cardiovascular disease: current knowledge and new insights

Song, Y., Wei, H., Zhou, Z., Wang, H., Hang, W., Wu, J., & Wang, D. W. (2024) · Frontiers of Medicine · doi:10.1007/s11684-024-1055-9 · Cited by 32 · see citing works

Daily oral administration of probiotics engineered to constantly secrete short-chain fatty acids effectively prevents myocardial injury from subsequent ischaemic heart disease

Pham, Q. H., Bui, T. V. A., Sim, W., Lim, K. H., Law, C. O. K., Tan, W., Kim, R. Y., Chow, K. T., Park, H., Ban, K., et al. (2024) · Cardiovascular Research · doi:10.1093/cvr/cvae128 · Cited by 32 · see citing works

Abstract 148: Gut Microbial Metabolites Modulate Immune Response for Cardiac Repair

Tang, T. W.-H., & Hsieh, P. C. H. (2017) · Circulation Research · doi:10.1161/res.121.suppl_1.148

Dynamic modulation of gut microbiota improves post‐myocardial infarct tissue repair in rats via butyric acid‐mediated histone deacetylase inhibition

Song, T., Guan, X., Wang, X., Qu, S., Zhang, S., Hui, W., Men, L., & Chen, X. (2021) · The FASEB Journal · doi:10.1096/fj.201903129rrr · Cited by 34 · see citing works

Modulating Cardiac-Gut Microbiome Interaction Post-Myocardial Infarction with Engineered BacteriaPreprint

Madaan, T., Nieman, M. L., Rakheja, T., Siddiqui, N., Gherardini, D., Sertorio, M. G., Kamble, N. S., Thomas, S. C., Hartman, A., Koch, S. E., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.10.664025 · Cited by 3 · see citing works

Targeting gut-immune-heart modulate cardiac remodeling after acute myocardial infarction

Yu, J., Zhou, L., Li, G., Chen, Z., Mudabbar, M. S., Li, L., Tang, X., Jiang, M., Zhang, G., & Liu, X. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123606 · Cited by 8 · see citing works

Additional file 2 of Gut microbiome mediates the protective effects of exercise after myocardial infarction

Zhou, Q., Deng, J., Pan, X., Meng, D., Zhu, Y., Bai, Y., Shi, C., Duan, Y., Wang, T., Li, X., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19933082