Activated Drp1-mediated mitochondrial ROS influence the gut microbiome and intestinal barrier after hemorrhagic shock

Diversity of the Human Intestinal Microbial Flora

Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913 · see citing works

Alterations of the human gut microbiome in multiple sclerosis

Jangi, S., Gandhi, R., Cox, L. M., Li, N., von Glehn, F., Yan, R., Patel, B., Mazzola, M. A., Liu, S., Glanz, B. L., et al. (2016) · Nature Communications · doi:10.1038/ncomms12015 · Cited by 1,307 · see citing works

Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission

Losón, O. C., Song, Z., Chen, H., & Chan, D. C. (2013) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-10-0721 · Cited by 1,235 · see citing works

A community-driven global reconstruction of human metabolism

Thiele, I., Swainston, N., Fleming, R. M. T., Hoppe, A., Sahoo, S., Aurich, M. K., Haraldsdottir, H., Mo, M. L., Rolfsson, O., Stobbe, M. D., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2488 · Cited by 1,019 · see citing works

Interaction between the gut microbiome and mucosal immune system

Shi, N., Li, N., Duan, X., & Niu, H. (2017) · Military Medical Research · doi:10.1186/s40779-017-0122-9 · Cited by 940 · see citing works

Mitochondria as a therapeutic target for common pathologies

Murphy, M. P., & Hartley, R. C. (2018) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2018.174 · Cited by 832 · see citing works

The immune system and the gut microbiota: friends or foes?

Cerf-Bensussan, N., & Gaboriau-Routhiau, V. (2010) · Nature Reviews Immunology · doi:10.1038/nri2850 · Cited by 704 · see citing works

The Putative Drp1 Inhibitor mdivi-1 Is a Reversible Mitochondrial Complex I Inhibitor that Modulates Reactive Oxygen Species

Bordt, E. A., Clerc, P., Roelofs, B. A., Saladino, A. J., Tretter, L., Ádám‐Vizi, V., Cherok, E., Khalil, A., Yadava, N., Ge, S. X., et al. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.02.020 · Cited by 598 · see citing works

Inhibition of mitochondrial fission prevents cell cycle progression in lung cancer

Rehman, J., Zhang, H. J., Tóth, P. T., Zhang, Y., Marsboom, G., Hong, Z., Salgia, R., Husain, A. N., Wietholt, C., & Archer, S. L. (2012) · The FASEB Journal · doi:10.1096/fj.11-196543 · Cited by 594 · see citing works

Twin Study Indicates Loss of Interaction Between Microbiota and Mucosa of Patients With Ulcerative Colitis

Lepage, P., Häsler, R., Spehlmann, M. E., Rehman, A., Žvirblienė, A., Begun, A., Ott, S. J., Kupčinskas, L., Dore, J. M., Raedler, A., et al. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.04.011 · Cited by 592 · see citing works

Benefits of short-chain fatty acids and their receptors in inflammation and carcinogenesis

Sivaprakasam, S., Prasad, P. D., & Singh, N. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.04.007 · Cited by 573 · see citing works

Arsenic Exposure Perturbs the Gut Microbiome and Its Metabolic Profile in Mice: An Integrated Metagenomics and Metabolomics Analysis

Lü, K., Abo, R., Schlieper, K. A., Graffam, M. E., Levine, S. S., Wishnok, J. S., Swenberg, J. A., Tannenbaum, S. R., & Fox, J. G. (2014) · Environmental Health Perspectives · doi:10.1289/ehp.1307429 · Cited by 517 · see citing works

Mitochondrial fission triggered by hyperglycemia is mediated by ROCK1 activation in podocytes and endothelial cells

Wang, W., Wang, Y., Long, J., Wang, J., Haudek, S. B., Overbeek, P., Chang, B. H. J., Schumacker, P. T., & Danesh, F. R. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.01.009 · Cited by 476 · see citing works

Altered intestinal microbiota–host mitochondria crosstalk in new onset Crohn’s disease

Mottawea, W., Chiang, C., Mühlbauer, M., Starr, A. E., Butcher, J., Abujamel, T. S., Deeke, S. A., Brandel, A., Zhou, H., Shokralla, S., et al. (2016) · Nature Communications · doi:10.1038/ncomms13419 · Cited by 444 · see citing works

Gut pathobionts underlie intestinal barrier dysfunction and liver T helper 17 cell immune response in primary sclerosing cholangitis

Nakamoto, N., Sasaki, N., Aoki, R., Miyamoto, K., Suda, W., Teratani, T., Suzuki, T., Koda, Y., Chu, P.-S., Taniki, N., et al. (2019) · Nature Microbiology · doi:10.1038/s41564-018-0333-1 · Cited by 425 · see citing works

Membrane Remodeling Induced by the Dynamin-Related Protein Drp1 Stimulates Bax Oligomerization

Montessuit, S., Somasekharan, S. P., Terrones, O., Lucken‐Ardjomande, S., Herzig, S., Schwarzenbacher, R., Manstein, D. J., Bossy‐Wetzel, E., Basáñez, G., Meda, P., et al. (2010) · Cell · doi:10.1016/j.cell.2010.08.017 · Cited by 422 · see citing works

A Proinflammatory Gut Microbiota Increases Systemic Inflammation and Accelerates Atherosclerosis

Brandsma, E. T., Kloosterhuis, N., Koster, M. H., Dekker, D., Gijbels, M. J., van der Velden, S., Ríos-Morales, M., van Faassen, M. H. J. R., Loreti, M. G., de Bruin, A., et al. (2019) · Circulation Research · doi:10.1161/circresaha.118.313234 · Cited by 376 · see citing works

On the origin of mitochondria: a genomics perspective

Andersson, G., Karlberg, O., Canbäck, B., & Kurland, C. G. (2003) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1193 · Cited by 360 · see citing works

Enhanced translocation of bacteria across metabolically stressed epithelia is reduced by butyrate†

Lewis, K. J., Lutgendorff, F., Phan, V., Söderholm, J. D., Sherman, P. M., & McKay, D. M. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21177 · Cited by 338 · see citing works

The Crosstalk between the Gut Microbiota and Mitochondria during Exercise

Clark, A. P., & Mach, N. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00319 · Cited by 338 · see citing works

MAPL SUMOylation of Drp1 Stabilizes an ER/Mitochondrial Platform Required for Cell Death

Prudent, J., Zunino, R., Sugiura, A., Mattie, S., Shore, G. C., & McBride, H. M. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.08.001 · Cited by 321 · see citing works

Mitochondrial function — gatekeeper of intestinal epithelial cell homeostasis

Rath, E., Moschetta, A., & Haller, D. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-018-0021-x · Cited by 306 · see citing works

Drp1-Dependent Mitochondrial Fission Plays Critical Roles in Physiological and Pathological Progresses in Mammals

Hu, C., Huang, Y., & Li, L. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18010144 · Cited by 302 · see citing works

CoCl 2 , a Chemical Inducer of Hypoxia‐Inducible Factor‐1, and Hypoxia Reduce Apoptotic Cell Death in Hepatoma Cell Line HepG2

Piret, J., Mottet, D., Raes, M. J., & Michiels, C. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04680.x · Cited by 258 · see citing works

Critical Role for the Microbiota in CX3CR1+ Intestinal Mononuclear Phagocyte Regulation of Intestinal T Cell Responses

Kim, M., Galan, C., Hill, A. A., Wu, W.-J., Fehlner-Peach, H., Song, H. W., Schady, D., Bettini, M. L., Simpson, K. W., Longman, R. S., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.05.009 · Cited by 202 · see citing works

Mitochondrial fission causes cisplatin resistance under hypoxic conditions via ROS in ovarian cancer cells

Han, Y., Kim, B., Cho, U., Park, I. S., Kim, S. I., Dhanasekaran, D. N., Tsang, B. K., & Song, Y. S. (2019) · Oncogene · doi:10.1038/s41388-019-0949-5 · Cited by 188 · see citing works

Targeting Mitochondria-Derived Reactive Oxygen Species to Reduce Epithelial Barrier Dysfunction and Colitis

Wang, A., Keita, Å. V., Phan, V., McKay, C. M., Schoultz, I., Lee, J., Murphy, M. P., Fernando, M., Ronaghan, N. J., Balce, D. R., et al. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.05.019 · Cited by 177 · see citing works

Intracellular MLCK1 diversion reverses barrier loss to restore mucosal homeostasis

Graham, W. V., He, W., Marchiando, A. M., Zha, J., Singh, G., Li, H.-S., Biswas, A., Ong, M. L. D. M., Jiang, Z.-H., Choi, W., et al. (2019) · Nature Medicine · doi:10.1038/s41591-019-0393-7 · Cited by 176 · see citing works

BIRC5/Survivin enhances aerobic glycolysis and drug resistance by altered regulation of the mitochondrial fusion/fission machinery

Hagenbuchner, J., Kuznetsov, A. V., Obexer, P., & Ausserlechner, M. J. (2012) · Oncogene · doi:10.1038/onc.2012.500 · Cited by 175 · see citing works

A chitosan–glutathione based injectable hydrogel for suppression of oxidative stress damage in cardiomyocytes

Li, J., Shu, Y., Hao, T., Wang, Y., Qian, Y., Duan, C., Sun, H., Lin, Q., & Wang, C. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.08.031 · Cited by 165 · see citing works

Microbial Siderophore Enterobactin Promotes Mitochondrial Iron Uptake and Development of the Host via Interaction with ATP Synthase

Qi, B., & Han, M. (2018) · Cell · doi:10.1016/j.cell.2018.07.032 · Cited by 164 · see citing works

Cdk1, PKCδ and calcineurin-mediated Drp1 pathway contributes to mitochondrial fission-induced cardiomyocyte death

Žaja, I., Bai, X., Liu, Y., Kikuchi, C., Došenović, S., Yan, Y., Canfield, S. G., & Bosnjak, Z. J. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.09.144 · Cited by 156 · see citing works

HKOCl-3: a fluorescent hypochlorous acid probe for live-cell and in vivo imaging and quantitative application in flow cytometry and a 96-well microplate assay

Hu, J. J., Wong, N.-K., Lu, M.-Y., Chen, X., Ye, S., Zhao, A. Q., Gao, P., Kao, R. Y. T., Shen, J., & Yang, D. (2016) · Chemical Science · doi:10.1039/c5sc03855c · Cited by 156 · see citing works

Receptor-mediated Drp1 oligomerization on endoplasmic reticulum

Ji, W.-K., Chakrabarti, R., Fan, X., Schoenfeld, L. W., Strack, S., & Higgs, H. N. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201610057 · Cited by 144 · see citing works

Gastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome

Frye, R. E., Rose, S., Slattery, J. M., & MacFabe, D. F. (2015) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v26.27458 · Cited by 142 · see citing works

The Effect oftert-Butyl Hydroperoxide-Induced Oxidative Stress on Lean and Steatotic Rat HepatocytesIn Vitro

Kučera, O., Endlicher, R., Roušar, T., Lotková, H., Garnol, T., Drahota, Z., & Červinková, Z. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/752506 · Cited by 138 · see citing works

Sex-Specific Effects of Organophosphate Diazinon on the Gut Microbiome and Its Metabolic Functions

Gao, B., Bian, X., Mahbub, R., & Lü, K. (2016) · Environmental Health Perspectives · doi:10.1289/ehp202 · Cited by 125 · see citing works

Mdivi-1 ameliorates early brain injury after subarachnoid hemorrhage via the suppression of inflammation-related blood–brain barrier disruption and endoplasmic reticulum stress-based apoptosis

Fan, L., He, P., Peng, Y., Du, Q.-H., Ma, Y.-J., Jin, J., Xu, H., Li, J., Wang, Z., Cao, S., et al. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.08.003 · Cited by 117 · see citing works

Mitochondria: A target for bacteria

Lobet, E., Letesson, J., & Arnould, T. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.02.007 · Cited by 115 · see citing works

ATAD3A oligomerization causes neurodegeneration by coupling mitochondrial fragmentation and bioenergetics defects

Zhao, Y., Sun, X., Hu, D., Prosdocimo, D. A., Hoppel, C. L., Jain, M. K., Ramachandran, R., & Qi, X. (2019) · Nature Communications · doi:10.1038/s41467-019-09291-x · Cited by 109 · see citing works

Detoxification of H 2 S by Differentiated Colonic Epithelial Cells: Implication of the Sulfide Oxidizing Unit and of the Cell Respiratory Capacity

Mimoun, S., Andriamihaja, M., Chaumontet, C., Atanasiu, C., Benamouzig, R., Blouin, J. M., Tomé, D., Bouillaud, F., & Blachier, F. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4186 · Cited by 107 · see citing works

Regulation of mitochondrial morphology by APC/CCdh1-mediated control of Drp1 stability

Horn, S. R. G.-V., Thomenius, M. J., Johnson, E. S., Freel, C. D., Wu, J. Q., Coloff, J. L., Yang, C., Tang, W., An, J., Ilkayeva, O., et al. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-07-0567 · Cited by 101 · see citing works

mtDNA haplogroup and single nucleotide polymorphisms structure human microbiome communities

Ma, J., Coarfa, C., Qin, X., Bonnen, P. E., Milosavljevic, A., Versalovic, J. A., & Aagaard, K. M. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-257 · Cited by 99 · see citing works

Host-Directed Antimicrobial Drugs with Broad-Spectrum Efficacy against Intracellular Bacterial Pathogens

Czyż, D. M., Potluri, L., Jain‐Gupta, N., Riley, S. P., Martinez, J. J., Steck, T. L., Crosson, S., Shuman, H. A., & Gabay, J. E. (2014) · mBio · doi:10.1128/mbio.01534-14 · Cited by 95 · see citing works

DRP1 Suppresses Leptin and Glucose Sensing of POMC Neurons

Santoro, A. N., Campolo, M., Liu, C., Sesaki, H., Meli, R., Liu, Z.-W., Kim, J. D., & Diano, S. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.01.003 · Cited by 92 · see citing works

Pyrroloquinoline Quinone, a Redox-Active o -Quinone, Stimulates Mitochondrial Biogenesis by Activating the SIRT1/PGC-1α Signaling Pathway

才原一浩, Kamikubo, R., Ikemoto, K., Uchida, K., & Akagawa, M. (2017) · Biochemistry · doi:10.1021/acs.biochem.7b01185 · Cited by 78 · see citing works

ROS and calcium signaling mediated pathways involved in stress responses of the marine microalgae Dunaliella salina to enhanced UV-B radiation

Zhang, X., Tang, X., Wang, M., Zhang, W., Zhou, B., & Wang, Y. (2017) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2017.05.038 · Cited by 71 · see citing works

Hemorrhagic Shock-Induced Vascular Hyporeactivity in the Rat: Relationship to Gene Expression of Nitric Oxide Synthase, Endothelin-1, and Select Cytokines in Corresponding Organs

Liu, L., & Dubick, M. A. (2005) · Journal of Surgical Research · doi:10.1016/j.jss.2004.12.008 · Cited by 70 · see citing works

ClC-2 chloride secretion mediates prostaglandin-induced recovery of barrier function in ischemia-injured porcine ileum

Moeser, A. J., Haskell, M. M., Shifflett, D. E., Little, D., Schultz, B. D., & Blikslager, A. T. (2004) · Gastroenterology · doi:10.1053/j.gastro.2004.06.004 · Cited by 69 · see citing works

Microbe-mitochondrion crosstalk and health: An emerging paradigm

Bajpai, P., Darra, A., & Agrawal, A. (2017) · Mitochondrion · doi:10.1016/j.mito.2017.08.008 · Cited by 55 · see citing works

Microbiome and Longevity: Gut Microbes Send Signals to Host Mitochondria

Gruber, J., & Kennedy, B. K. (2017) · Cell · doi:10.1016/j.cell.2017.05.048 · Cited by 40 · see citing works

Activation of sirtuin 1/3 improves vascular hyporeactivity in severe hemorrhagic shock by alleviation of mitochondrial damage

Li, P., Meng, X., Bian, H., Burns, N., Zhao, K., & Song, R. (2015) · Oncotarget · doi:10.18632/oncotarget.6076 · Cited by 38 · see citing works

Effects of the Balance in Activity of RhoA and Rac1 on the Shock-Induced Biphasic Change of Vascular Reactivity in Rats

Li, T., Fang, Y., Yang, G., Xu, J., Zhu, Y., & Liu, L. (2011) · Annals of Surgery · doi:10.1097/sla.0b013e3181f9b88b · Cited by 38 · see citing works

Lactobacillus rhamnosus CNCMI-4317 Modulates Fiaf/Angptl4 in Intestinal Epithelial Cells and Circulating Level in Mice

Jacouton, E., Mach, N., Cadiou, J., Lapaque, N., Clément, K., Doré, J., van Hylckama Vlieg, J. E. T., Smokvina, T., & Blottière, H. M. (2015) · PLOS ONE · doi:10.1371/journal.pone.0138880 · Cited by 32 · see citing works

Inhibition of Drp1 after traumatic brain injury provides brain protection and improves behavioral performance in rats

Song, Y., Li, T., Liu, Z., Xu, Z., Zhang, Z., Chi, L., & Liu, Y. (2019) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2019.03.013 · Cited by 31 · see citing works

Entacapone is an Antioxidant More Potent than Vitamin C and Vitamin E for Scavenging of Hypochlorous Acid and Peroxynitrite, and the Inhibition of Oxidative Stress-Induced Cell Death

Chen, A. Y., Lü, J.-M., Yao, Q. C., & Chen, C. (2016) · Medical Science Monitor · doi:10.12659/msm.896462 · Cited by 30 · see citing works

Intestinal microbiota link lymphopenia to murine autoimmunity via PD-1+CXCR5−/dim B-helper T cell induction

Eri, T., Kawahata, K., Kanzaki, T., Imamura, M., Michishita, K., Akahira, L., Bannai, E., Yoshikawa, N., Kimura, Y., Satoh, T., et al. (2017) · Scientific Reports · doi:10.1038/srep46037 · Cited by 25 · see citing works

Regulation of Intestinal Barrier Function by Microbial Metabolites

Ghosh, S., Whitley, C. S., Haribabu, B., & Jala, V. R. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.02.007 · Cited by 835 · see citing works

The role of short-chain fatty acids in intestinal barrier function, inflammation, oxidative stress, and colonic carcinogenesis

Liu, P., Wang, Y., Yang, G., Zhang, Q., Meng, L., Xin, Y., & Jiang, X. M. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105420 · Cited by 787 · see citing works

Activated Drp1 regulates p62-mediated autophagic flux and aggravates inflammation in cerebral ischemia-reperfusion via the ROS-RIP1/RIP3-exosome axis

Zeng, X., Zhang, Y., Ma, R., Chen, Y.-J., Xiang, X., Hou, D., Li, X.-H., Huang, H., Li, T., & Duan, C. (2022) · Military Medical Research · doi:10.1186/s40779-022-00383-2 · Cited by 276 · see citing works

Crataegus pinnatifida polysaccharide alleviates colitis via modulation of gut microbiota and SCFAs metabolism

Guo, C., Wang, Y., Zhang, S., Zhang, X., Du, Z., Li, M., & Ding, K. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.03.137 · Cited by 272 · see citing works

Mdivi-1 attenuates oxidative stress and exerts vascular protection in ischemic/hypoxic injury by a mechanism independent of Drp1 GTPase activity

Duan, C., Wang, L., Zhang, J., Xiang, X., Wu, Y., Zhang, Z., Li, Q., Tian, K. L., Xue, M., Li, T., et al. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101706 · Cited by 106 · see citing works

Commensal microbe-derived SCFA alleviates atrial fibrillation via GPR43/NLRP3 signaling

Zuo, K., Chen, F., Liu, Z., Fu, Y., Liu, Y., Liu, L., Wang, Y., Yin, X., Liu, X., Li, J., et al. (2022) · International Journal of Biological Sciences · doi:10.7150/ijbs.70644 · Cited by 89 · see citing works

Drp1 regulates mitochondrial dysfunction and dysregulated metabolism in ischemic injury via Clec16a-, BAX-, and GSH- pathways

Duan, C., Kuang, L., Xiang, X., Zhang, J., Zhu, Y., Wu, Y., Yan, Q., Liu, L., & Li, T. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2461-9 · Cited by 87 · see citing works

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 84 · see citing works

Mitochondrial Drp1 recognizes and induces excessive mPTP opening after hypoxia through BAX-PiC and LRRK2-HK2

Duan, C., Kuang, L., Hong, C., Xiang, X., Liu, J., Li, Q., Peng, X., Zhou, Y., Wang, H., Liu, L., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04343-x · Cited by 76 · see citing works

Empagliflozin ameliorates type 2 diabetes mellitus-related diabetic nephropathy via altering the gut microbiota

Deng, L., Yang, Y., & Xu, G. (2022) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2022.159234 · Cited by 73 · see citing works

Gut microbiome and attention deficit/hyperactivity disorder: a systematic review

Gkougka, D., Mitropoulos, K., Tzanakaki, G., Panagouli, E., Psaltopoulou, T., Thomaidis, L., Tsolia, M., Sergentanis, T. N., & Tsitsika, A. (2022) · Pediatric Research · doi:10.1038/s41390-022-02027-6 · Cited by 69 · see citing works

Protective Effects of Dexmedetomidine on Sepsis-Induced Vascular Leakage by Alleviating Ferroptosis via Regulating Metabolic Reprogramming

She, H., Hu, Y., Zhou, Y., Tan, L., Zhu, Y., Ma, C., Wu, Y., Chen, W., Wang, L., Zhang, Z., et al. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s340420 · Cited by 66 · see citing works

Targeting mitochondrial quality control: new therapeutic strategies for major diseases

Hong, W., Huang, H., Zeng, X., & Duan, C. (2024) · Military Medical Research · doi:10.1186/s40779-024-00556-1 · Cited by 65 · see citing works

Polysaccharides derived from Shenling Baizhu San improve colitis via modulating tryptophan metabolism in mice

Lv, W., Ma, Y., Huang, J., He, S., Li, S.-P., Lin, J., Chen, R., Lun, J., Liu, J., & Guo, S. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.09.246 · Cited by 59 · see citing works

Alterations of the Gut Microbiota in Response to Total Sleep Deprivation and Recovery Sleep in Rats

Wang, Z., Yuan, K., Ji, Y.-B., Li, S.-X., Shi, L., Wang, Z., Zhou, X.-Y., Bao, Y.-P., Xie, W., Han, Y., et al. (2022) · Nature and Science of Sleep · doi:10.2147/nss.s334985 · Cited by 56 · see citing works

Mitochondrial impairment and repair in the pathogenesis of systemic lupus erythematosus

Zhao, L., Hu, X., Xiao, F., Zhang, X., Zhao, L., & Wang, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.929520 · Cited by 52 · see citing works

Effects of dietary Cetobacterium somerae on the intestinal health, immune parameters and resistance against Nocardia seriolae of largemouth bass, Micropterus salmoides

Zhang, Y., Qi, X., Zhang, Z., Jin, Z., Wang, G., & Ling, F. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.108693 · Cited by 53 · see citing works

Curcumin simultaneously improves mitochondrial dynamics and myocardial cell bioenergy after sepsis via the SIRT1-DRP1/PGC-1α pathway

Hou, D., Liao, H., Hao, S., Liu, R., Huang, H., & Duan, C. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e28501 · Cited by 51 · see citing works

Multifaceted functions of Drp1 in hypoxia/ischemia-induced mitochondrial quality imbalance: from regulatory mechanism to targeted therapeutic strategy

Hao, S., Huang, H., Ma, R., Zeng, X., & Duan, C. (2023) · Military Medical Research · doi:10.1186/s40779-023-00482-8 · Cited by 52 · see citing works

Drp1-mediated mitochondrial fission promotes pulmonary fibrosis progression through the regulation of lipid metabolic reprogramming by ROS/HIF-1α

Tong, Z., Du, X., Zhou, Y., Jing, F., Ma, J., Feng, Y., Lou, S., Wang, Q. A., & Dong, Z. (2024) · Cellular Signalling · doi:10.1016/j.cellsig.2024.111075 · Cited by 42 · see citing works

Potentials of orally supplemented selenium-enriched Lacticaseibacillus rhamnosus to mitigate the lead induced liver and intestinal tract injury

Han, J., Rajoka, M. S. R., Xu, X., Liao, N., Pang, B., Yan, L., Liu, G., Sun, H., Jiang, C., Shao, D., et al. (2022) · Environmental Pollution · doi:10.1016/j.envpol.2022.119062 · Cited by 41 · see citing works

Activated Drp1 Initiates the Formation of Endoplasmic Reticulum‐Mitochondrial Contacts via Shrm4‐Mediated Actin Bundling

Duan, C., Liu, R., Kuang, L., Zhang, Z., Hou, D., Zheng, D., Xiang, X., Huang, H., Liu, L., & Li, T. (2023) · Advanced Science · doi:10.1002/advs.202304885 · Cited by 39 · see citing works

Drp1 activates ROS/HIF-1α/EZH2 and triggers mitochondrial fragmentation to deteriorate hypercalcemia-associated neuronal injury in mouse model of chronic kidney disease

Sun, H., Li, X., Chen, X., Xiong, Y., Cao, Y., & Wang, Z. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02542-7 · Cited by 33 · see citing works

Protective Effects of Dexmedetomidine on the Vascular Endothelial Barrier Function by Inhibiting Mitochondrial Fission via ER/Mitochondria Contact

She, H., Zhu, Y., Deng, H., Kuang, L., He, F., Zhang, Z., Duan, C., Ye, J., Zhang, J., Liu, L., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.636327 · Cited by 33 · see citing works

Protective Effects of Inhibition of Mitochondrial Fission on Organ Function After Sepsis

Zhu, Y., Kuang, L., Wu, Y., Deng, H., She, H., Zhou, Y., Zhang, J., Liu, L., & Li, T. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.712489 · Cited by 33 · see citing works

Akkermansia muciniphila-Nlrp3 is involved in the neuroprotection of phosphoglycerate mutase 5 deficiency in traumatic brain injury mice

Chen, Y., Chen, J., Wei, H., Gong, K., Meng, J., Long, T.-L., Guo, J.-F., Hong, J., Yang, L.-J., Qiu, J., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1172710 · Cited by 23 · see citing works

Deubiquitinase USP16 induces gouty arthritis via Drp1-dependent mitochondrial fission and NLRP3 inflammasome activation

Wang, Q., & Qiu, H. (2023) · Arthritis Research & Therapy · doi:10.1186/s13075-023-03095-7 · Cited by 24 · see citing works

The Intestinal Microbiome after Traumatic Injury

Munley, J. A., Kirkpatrick, S. L., Gillies, G. S., Bible, L. E., Efron, P. A., Nagpal, R., & Mohr, A. M. (2023) · Microorganisms · doi:10.3390/microorganisms11081990 · Cited by 23 · see citing works

Navigating Hemorrhagic Shock: Biomarkers, Therapies, and Challenges in Clinical Care

Monge, K. M., Rosa, C., Sublette, C. M., Pratap, A., Kovacs, E. J., & Idrovo, J. (2024) · Biomedicines · doi:10.3390/biomedicines12122864 · Cited by 22 · see citing works

Oral administration of asparagine and 3-indolepropionic acid prolongs survival time of rats with traumatic colon injury

Cao, B., Zhao, R., Li, H.-H., Xu, X., Cui, H., Deng, H., Chen, L., & Wei, B. (2022) · Military Medical Research · doi:10.1186/s40779-022-00397-w · Cited by 20 · see citing works

Multi-omics revealed anti-fatigue property of polyphenol from areca nut

Zhang, Y., He, Y., Yuan, L., Shi, J., Zhao, J., Tan, C., Liu, Y., & Xu, Y. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155838 · Cited by 19 · see citing works

Magnesium hydride attenuates intestinal barrier injury during hemorrhage shock by regulating neutrophil extracellular trap formation via the ROS/MAPK/PAD4 pathway

Cao, C., Yu, P., Chu, C., Wang, Z., Xu, W., Cheng, F., Zhao, H., & Qiu, Z. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.111688 · Cited by 18 · see citing works

Exosomes: an innovative therapeutic target for cerebral ischemia-reperfusion injury

Yang, Y., Duan, Y., Yue, J., Yin, Y., Ma, Y., Wan, X., & Shao, J. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1552500 · Cited by 15 · see citing works

Effects of Malate Ringer's solution on myocardial injury in sepsis and enforcement effects of TPP@PAMAM-MR

Tan, L., She, H., Zheng, J., Peng, X., Guo, N., Zhang, B., Sun, Y., Ma, C., Xu, S., Bao, D., et al. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03811-y · Cited by 15 · see citing works

Notoginsenoside R1 improves intestinal microvascular functioning in sepsis by targeting Drp1-mediated mitochondrial quality imbalance

Hou, D., Liu, R., Hao, S., Dou, Y., Chen, G., Liu, L., Li, T., Cao, Y., Huang, H., & Duan, C. (2024) · Pharmaceutical Biology · doi:10.1080/13880209.2024.2318349 · Cited by 14 · see citing works

Gut microbiome and metabolome to discover pathogenic bacteria and probiotics in ankylosing spondylitis

Lai, Y., Tang, W., Luo, X., Zheng, H., Zhang, Y., Wang, M., Yu, G., & Yang, M. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1369116 · Cited by 12 · see citing works

Involvement of CD44 and MAPK14-mediated ferroptosis in hemorrhagic shock

Ye, H., He, S., Du, Y., Wang, Y., Hu, Y., Zhao, C., Jin, Y., Liu, F., & Guo, Y. (2023) · APOPTOSIS · doi:10.1007/s10495-023-01894-6 · Cited by 12 · see citing works

Bifidobacterium animalis subsp. lactis MN-Gup protects mice against gut microbiota-related obesity and endotoxemia induced by a high fat diet

Niu, X., Zhang, N., Li, S., Li, N., Wang, R., Zhang, Q., He, J., Sun, E., Kang, X., & Zhan, J. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.992947 · Cited by 11 · see citing works

The role of the “gut microbiota-mitochondria” crosstalk in the pathogenesis of multiple sclerosis

Tian, H., Huang, D., Wang, J., Li, H., Gao, J., Zhong, Y., Xia, L., Zhang, A., Lin, Z., & Ke, X. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1404995 · Cited by 12 · see citing works

PPARγ agonist alleviates calcium oxalate nephrolithiasis by regulating mitochondrial dynamics in renal tubular epithelial cell

Liu, J., Liu, X., Guo, L., Liu, X., Gao, Q., Wang, E., & Dong, Z. (2024) · PLoS ONE · doi:10.1371/journal.pone.0310947 · Cited by 11 · see citing works

ESTROGEN ALLEVIATES POSTHEMORRHAGIC SHOCK MESENTERIC LYMPH-MEDIATED LUNG INJURY THROUGH AUTOPHAGY INHIBITION

Sun, Q., Zhang, H., Du, H.-B., Zhao, Z., Li, C.-J., Chen, S.-J., Li, Y., Zhang, S.-L., Liu, J., Niu, C., et al. (2023) · Shock · doi:10.1097/shk.0000000000002102 · Cited by 11 · see citing works

Drp1-mediated mitochondrial fission exacerbates inflammatory responses in intestinal epithelial cells: A potential therapeutic target for IBD

Kang, Y., & Kang, B. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.152508 · Cited by 8 · see citing works

Effects of Long Noncoding RNA H19 on Isoflurane-Induced Cognitive Dysregulation by Promoting Neuroinflammation

Ge, Y., Lin, D., Cui, B., Zhang, L., Li, S., Wang, Z., & Ma, J. (2021) · NeuroImmunoModulation · doi:10.1159/000519124 · Cited by 8 · see citing works

Melatonin supplementation protects against traumatic colon injury by regulating SERPINA3N protein expression

Cao, B., Gao, J., Zhang, Q., Xu, X., Zhao, R., Li, H.-H., & Wei, B. (2023) · iMeta · doi:10.1002/imt2.141 · Cited by 6 · see citing works

Critical Knowledge Gaps and Future Priorities Regarding the Intestinal Barrier Damage After Traumatic Brain Injury

Guangliang, H., Wang, T., Danxin, W., Liu, L., & Ye, M. (2024) · World Neurosurgery · doi:10.1016/j.wneu.2024.05.105 · Cited by 6 · see citing works

N-Acetyl-L-Cysteine Protects Organ Function After Hemorrhagic Shock Combined With Seawater Immersion in Rats by Correcting Coagulopathy and Acidosis

Liu, Y., Zhu, Y., Zhang, Z., Bao, D., Deng, H., Liu, L., & Li, T. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.831514 · Cited by 5 · see citing works

Gut-brain axis in Attention Deficit Hyperactivity Disorder (ADHD): A narrative review of the links between gut microbiota and ADHD pathophysiology

Luyens, B., Felgueroso-Bueno, F., Everard, A., & Massat, I. (2026) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2026.01.038 · Cited by 4 · see citing works

THE MITOCHONDRIAL DIVISION INHIBITOR MDIVI-1 PROTECTED ORGAN FUNCTION AND EXTENDED THE TREATMENT WINDOW IN RATS WITH UNCONTROLLED HEMORRHAGIC SHOCK

Hu, Y., He, F., Tan, L., She, H., Du, Y., Zhu, Y., Wu, Y., Liu, L., & Li, T. (2024) · Shock · doi:10.1097/shk.0000000000002459 · Cited by 4 · see citing works

SUMOylation in peripheral tissues under low perfusion‐related pathological states

Oliveira, F. R. M. B., Soares, E. S., Harms, C., Cimarosti, H., & Sordi, R. (2022) · Journal of Cellular Biochemistry · doi:10.1002/jcb.30293 · Cited by 4 · see citing works

Effects of Mdivi‐1 on Extending the Golden Treatment Time following Hemorrhagic Shock in Hot Environment in Rats

Wu, Y., Li, Q., Zhu, Y., Zhou, Y., Liu, L., & Li, T. (2023) · Advanced Biology · doi:10.1002/adbi.202300024 · Cited by 3 · see citing works

The inflammation-aging axis: Shared and distinct mechanisms in physiological gut aging and IBD-associated accelerated gut aging.

Yang, L.-C., Jiang, Z., Sun, Q., Karako, K., Yuan, L.-W., & Song, P. (2025) · BioScience Trends · doi:10.5582/bst.2025.01279 · Cited by 3 · see citing works

Metabolomics after trauma in experimental models- a systematic review

Stückelberger, G., Weuster, M., Hana, A., Hübner, C. T., Kalbas, Y., Pape, H., Klingebiel, F. K.-L., & Pfeifer, R. (2026) · Langenbeck s Archives of Surgery · doi:10.1007/s00423-025-03917-z · Cited by 1 · see citing works

An Aedes aegypti seryl-tRNA synthetase paralog controls bacteroidetes growth in the midgutPreprint

Silveira, G. O., Talyuli, O. A. C., Walter‐Nuno, A. B., Crnković, A., Gandara, A. C. P., Gaviraghi, A., Bottino-Rojas, V., Söll, D. G., & Polycarpo, C. R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.25.505225 · Cited by 1 · see citing works

Félix Lope de Vega, Arte nuevo de hacer comedias en este tiempo, Edición políglota: castellano, italiano, portugués, francés, inglés, alemán y polaco

Sâmbrian, O. A. (2010) · Dialnet (Universidad de la Rioja)

Early-stage Hyperglycemia-induced Gut Microbial Changes Are Partially Associated with Mechanical Allodynia in db/db Mice

Wang, X., Wu, J., Qi, S., Huang, R., Wu, X., Tian, L., Wang, P., & Wang, S. (2021) · International Journal of Diabetes and Endocrinology · doi:10.11648/j.ijde.20210604.15

Curcumin synergistically improves mitochondrial dynamics and myocardial cell bioenergy after sepsis through the SIRT1-Drp1/PGC-1α pathwayPreprint

Liu, R., Hao, S., Hou, D., Tian, H., Hong, W., Huang, H., & Duan, C. (2023) · Research Square · doi:10.21203/rs.3.rs-3210579/v1

Probiotics as Chemical Decontamination Candidates

Singh, B., Mal, G., Kalra, R. S., & Marotta, F. (2024) · Springer eBooks · doi:10.1007/978-3-031-65455-8_21

Effect of ultrasound-guided thoracolumbar interfascial plane block on postoperative recovery in patients undergoing posterior lumbar intervertebral fusion: a prospective observational study

Zhang, Y., Lu, Q., Gao, J., Sun, Y., Lu, W., & Luo, Y. (2025) · BMC Musculoskeletal Disorders · doi:10.1186/s12891-025-08871-x

Host stress proteins shape hemorrhagic shock via gut microbiota: evidence from Mendelian randomization and animal models

Deng, G., Wu, L., Xiong, S., Zhou, J., & Li, Z. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-07364-8

Additional file 5 of Effects of Malate Ringer's solution on myocardial injury in sepsis and enforcement effects of TPP@PAMAM-MR

Tan, L., She, H., Zheng, J., Peng, X., Guo, N., Zhang, B., Sun, Y., Ma, C., Xu, S., Daiqin, B., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26553860

Additional file 2 of Effects of Malate Ringer's solution on myocardial injury in sepsis and enforcement effects of TPP@PAMAM-MR

Tan, L., She, H., Zheng, J., Peng, X., Guo, N., Zhang, B., Sun, Y., Ma, C., Xu, S., Daiqin, B., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26553851

Additional file 3 of Deubiquitinase USP16 induces gouty arthritis via Drp1-dependent mitochondrial fission and NLRP3 inflammasome activation

Wang, Q., & Qiu, H. (2023) · Figshare · doi:10.6084/m9.figshare.23740632

Additional file 2 of Deubiquitinase USP16 induces gouty arthritis via Drp1-dependent mitochondrial fission and NLRP3 inflammasome activation

Wang, Q., & Qiu, H. (2023) · Figshare · doi:10.6084/m9.figshare.23740629

Additional file 1 of Activated Drp1 regulates p62-mediated autophagic flux and aggravates inflammation in cerebral ischemia-reperfusion via the ROS-RIP1/RIP3-exosome axis

Zeng, X., Zhang, Y.-D., Ma, R.-Y., Chen, Y.-J., Xinming, X., Hou, D.-Y., Li, X.-H., Huang, H., Li, T., & Duan, C.-Y. (2022) · Figshare · doi:10.6084/m9.figshare.19914898

Additional file 4 of Effects of Malate Ringer's solution on myocardial injury in sepsis and enforcement effects of TPP@PAMAM-MR

Tan, L., She, H., Zheng, J., Peng, X., Guo, N., Zhang, B., Sun, Y., Ma, C., Xu, S., Daiqin, B., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26553857

Additional file 3 of Effects of Malate Ringer's solution on myocardial injury in sepsis and enforcement effects of TPP@PAMAM-MR

Tan, L., She, H., Zheng, J., Peng, X., Guo, N., Zhang, B., Sun, Y., Ma, C., Xu, S., Daiqin, B., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26553854

Additional file 1 of Deubiquitinase USP16 induces gouty arthritis via Drp1-dependent mitochondrial fission and NLRP3 inflammasome activation

Wang, Q., & Qiu, H. (2023) · Figshare · doi:10.6084/m9.figshare.23740626

Additional file 3 of Drp1 activates ROS/HIF-1α/EZH2 and triggers mitochondrial fragmentation to deteriorate hypercalcemia-associated neuronal injury in mouse model of chronic kidney disease

Sun, H., Li, X., Chen, X., Xiong, Y., Cao, Y., & Wang, Z. (2022) · Figshare · doi:10.6084/m9.figshare.20786828

Additional file 4 of Drp1 activates ROS/HIF-1α/EZH2 and triggers mitochondrial fragmentation to deteriorate hypercalcemia-associated neuronal injury in mouse model of chronic kidney disease

Sun, H., Li, X., Chen, X., Xiong, Y., Cao, Y., & Wang, Z. (2022) · Figshare · doi:10.6084/m9.figshare.20786831

Additional file 6 of Effects of Malate Ringer's solution on myocardial injury in sepsis and enforcement effects of TPP@PAMAM-MR

Tan, L., She, H., Zheng, J., Peng, X., Guo, N., Zhang, B., Sun, Y., Ma, C., Xu, S., Daiqin, B., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26553878

Additional file 5 of Drp1 activates ROS/HIF-1α/EZH2 and triggers mitochondrial fragmentation to deteriorate hypercalcemia-associated neuronal injury in mouse model of chronic kidney disease

Sun, H., Li, X., Chen, X., Xiong, Y., Cao, Y., & Wang, Z. (2022) · Figshare · doi:10.6084/m9.figshare.20786834

Additional file 2 of Drp1 activates ROS/HIF-1α/EZH2 and triggers mitochondrial fragmentation to deteriorate hypercalcemia-associated neuronal injury in mouse model of chronic kidney disease

Sun, H., Li, X., Chen, X., Xiong, Y., Cao, Y., & Wang, Z. (2022) · Figshare · doi:10.6084/m9.figshare.20786825

Additional file 1 of Effects of Malate Ringer's solution on myocardial injury in sepsis and enforcement effects of TPP@PAMAM-MR

Tan, L., She, H., Zheng, J., Peng, X., Guo, N., Zhang, B., Sun, Y., Ma, C., Xu, S., Daiqin, B., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26553848

Additional file 1 of Drp1 activates ROS/HIF-1α/EZH2 and triggers mitochondrial fragmentation to deteriorate hypercalcemia-associated neuronal injury in mouse model of chronic kidney disease

Sun, H., Li, X., Chen, X., Xiong, Y., Cao, Y., & Wang, Z. (2022) · Figshare · doi:10.6084/m9.figshare.20786822

Influence of acute blood loss on the dynamics of pro-inflammatory cytokine content in the context of traumatic brain injury, blunt abdominal trauma, and skeletal trauma

Izhytska, N. V., ЛЕВЧУК, Р. Д., Hudyma, А. А., & Антонишин, І. В. (2025) · Polski Merkuriusz Lekarski · doi:10.36740/merkur202506101

Caveolin-1 deficiency exacerbates liver fibrosis by driving lipid metabolic reprogramming in hepatic stellate cells via DRP1-mediated mitochondrial fission.

Wang, Y., Wang, X.-Y., Lin, J., Zhang, W.-H., Sun, Y., Geng, Q., Chen, S., Zhang, C., Jin, L., & Hu, C.-M. (2026) · Free Radical Biology & Medicine · doi:10.1016/j.freeradbiomed.2026.03.063

Polygonatum kingianum polysaccharides delay aging through UPRmt-mediated regulation of mitochondrial function and intestinal homeostasis

Yang, J., Zhao, S.-L., Ma, Y., Jiang, J., & Zhang, X. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.108854

Dynamin-Related Protein 1 (Drp1) in Inflammatory Bowel Disease: Molecular Pathways Connecting Mitochondrial Dynamics with Intestinal Inflammation and Homeostasis

Chi, Y., Zhang, H., Jia, C., Zeng, S., Li, X., Chen, D.-P., & Ma, Y. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27093828

Fuzheng Jiedu Tongluo Granule Alleviates Cerebral Ischemia/reperfusion Injury-induced Inflammation By Inhibiting Drp1-mediated TXNIP/NLRP3 Pathway

Chen, Y., Zhou, C., Gong, M.-Q., Lai, F., Wan, H., & He, Y. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05920-x

Targeting the gut-brain axis: microbial interventions for neurological disorders

Hao, Y.-Y., Zhao, Z., Zhang, L.-M., & Zhao, Z. (2026) · Metabolic Brain Disease · doi:10.1007/s11011-026-01877-x

Probiotics targeting mitochondrial dynamics: advances in enhancing energy metabolism of poultry intestinal epithelial cells

Li, X., & Yang, B. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.109883

Вплив крововтрати на динаміку інтерлейкіну-6 за умов експериментальної механічної травми різної локалізації в різні періоди травматичної хвороби

ЛЕВЧУК, Р. Д., Рудинська, С. М., Hudyma, А. А., & Shekera, O. (2026) · Ukrainian Journal of Military Medicine · doi:10.46847/ujmm.2026.3(7)-170

Role of activated dynamin-related protein 1-mediated glutathione metabolism in regulation of mitochondrial dysfunction after hemorrhagic shock

Chenyang, D., Xinming, X., Lei, K., Liangming, L., & Li, T. (2020) · DOAJ (DOAJ: Directory of Open Access Journals) · doi:10.16016/j.1000-5404.201907139

Role of metabolic changes of mucosal layer in the intestinal barrier dysfunction following trauma/hemorrhagic shock

Zhu, R., & Ma, X. (2018) · Pathology - Research and Practice · doi:10.1016/j.prp.2018.08.023 · Cited by 10 · see citing works

Oxidative modification of the intestinal mucus layer is a critical but unrecognized component of trauma hemorrhagic shock-induced gut barrier failure

Fishman, J. E., Levy, G., Alli, V. V., Sheth, S. U., Qu, L., & Deitch, E. A. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00170.2012 · Cited by 42 · see citing works

Events leading to intestinal barrier failure and systemic inflammation following hemorrhagic shock

Thuijls, G., Derikx, J. P. M., de Haan, J. J., Hadfoune, M., Heineman, E., & Buurman, W. A. (2008) · The FASEB Journal · doi:10.1096/fasebj.22.1_supplement.1120.10

Early intestinal tight junction loss after hemorrhagic shock

Thuijls, G., de Haan, J. J., Derikx, J. P. M., BAMBURG, J., Heineman, E., & Buurman, W. A. (2008) · The FASEB Journal · doi:10.1096/fasebj.22.1_supplement.1120.15