Oxygen transport2. Tissue hypoxia
Open accessAbstract
Tissues vary considerably in their sensitivity to hypoxia. Neurological cells tolerate hypoxia for only a few minutes whereas bladder smooth muscle may survive for several days without oxygen. This has important implications in the management of oxygen transport and monitoring of tissue hypoxia in critically ill patients. Regional oxygen transport and cellular use are often neglected but are important in maintaining tissue function and overall survival ### Delivery to organs and tissues The mechanisms controlling oxygen distribution are incompletely understood but involve a series of convective and diffusive processes. Convective oxygen transport refers to the bulk movement of oxygen in air or blood and depends on active, energy consuming processes generating flow in the tracheobronchial tree and circulation. Diffusive transport refers to the passive movement of oxygen down its concentration gradient across tissue barriers, including the alveolar-capillary membrane, and across the extracellular matrix between the tissue capillaries and individual cells to mitochondria. The amount of diffusive oxygen movement depends on the oxygen tension gradient and the diffusion distance. Effect of oxygen tension gradient and diffusion distance on availability of oxygen to cells In many critically ill patients tissue hypoxia is due to disordered regional distribution of blood flow both between and within organs. Regional and microcirculatory distribution of cardiac output is determined by a complex interaction of endothelial, receptor, neural, metabolic, and pharmacological factors working on small resistance arterioles and precapillary sphincters. In critical illness, particularly sepsis, hypotension and loss of normal autoregulation cause shunting and tissue hypoxia in some organs despite high global oxygen delivery and mixed venous saturation. The perfusion pressure is an important determinant of regional perfusion, but adrenaline or noradrenaline given to maintain systemic blood pressure may reduce regional distribution, particularly to the renal and splanchnic capillary beds. Severe tissue hypoxia due to capillary microthrombosis in critically ill patient with meningococcal septicaemia …
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The ERN1 and CAPG genes are involved in the regulation of hypoxia.
“The endoplasmic reticulum to nucleus signaling 1 (ERN1) and capping protein gelsolin-like (CAPG) genes are involved in the regulation of hypoxia (a state of a cell with inadequate or reduced oxygen availability) (Leach and Treacher, 1998).”
From Identification of Candidate Signature Genes and Key Regulators Associated With Trypanotolerance in the Sheko Breed (2019) · cites this paper as Leach and Treacher, 1998
The “When is a tissue hypoxic?” section discusses cellular responses to low oxygen, but does not identify ERN1 or CAPG as regulators. Searches for both gene names and their expanded names found no passage addressing their role in hypoxia. (LLM, conf=0.75)
Experimental — accuracy not yet measuredInflammation-associated hypoxia can result from a combination of factors including accumulation of metabolically active leukocytes, interstitial edema, and elevated temperature.
“Inflammation-associated hypoxia (or inflammatory hypoxia) can result from a combination of factors that result in a shift in metabolic supply and demand.”
From Hypoxia and hypoxia-inducible factors as regulators of T cell development, differentiation, and function (2013) · cites this paper as [3]
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Rius, J., Guma, M., Schachtrup, C., Akassoglou, K., Zinkernagel, A. S., Nizet, V., Johnson, R. S., Haddad, G. G., & Karin, M. (2008) · Nature · doi:10.1038/nature06905 · Cited by 1,614 · see citing works
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McKeown, S. R. (2014) · The British Journal of Radiology · doi:10.1259/bjr.20130676 · Cited by 1,050 · see citing works
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Semba, H., Takeda, N., Isagawa, T., Sugiura, Y., Honda, K., Wake, M., Miyazawa, H., Yamaguchi, Y., Miura, M., Jenkins, D. M. R., et al. (2016) · Nature Communications · doi:10.1038/ncomms11635 · Cited by 378 · see citing works
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McNamee, E. N., Korns Johnson, D., Homann, D., & Clambey, E. T. (2013) · Immunologic Research · doi:10.1007/s12026-012-8349-8 · Cited by 234 · see citing works
Spruessel, A., Steimann, G., Jung, M., Lee, S. A., Carr, T., Fentz, A., Spangenberg, J., Zornig, C., Juhl, H. H., & David, K. A. (2004) · BioTechniques · doi:10.2144/04366rr04 · Cited by 231 · see citing works
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Lippi, G., & Favaloro, E. J. (2017) · Seminars in Thrombosis and Hemostasis · doi:10.1055/s-0037-1607202 · Cited by 92 · see citing works
Krzykawska-Serda, M., Dąbrowski, J. M., Arnaut, L. G., et al. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.05.003 · Cited by 79 · see citing works
Abdelsalam, M., & Cheifetz, I. M. (2010) · Respiratory Care · doi:10.4187/respcare.10551483 · Cited by 68 · see citing works
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Etheridge, T., Atherton, P. J., Wilkinson, D. J., Selby, A., Rankin, D., Webborn, N., Smith, K., & Watt, P. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00276.2011 · Cited by 61 · see citing works
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Nahum, E., Ben‐Ari, J., & Schonfeld, T. M. (2004) · Journal of Intensive Care Medicine · doi:10.1177/0885066603257966 · Cited by 55 · see citing works
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Schober, P. R., & Schwarte, L. A. (2012) · Journal of Clinical Monitoring and Computing · doi:10.1007/s10877-012-9350-4 · Cited by 46 · see citing works
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Ho, K. M., Harding, R., Chamberlain, J., et al. (2008) · Journal of Cardiothoracic and Vascular Anesthesia · doi:10.1053/j.jvca.2007.10.011 · Cited by 45 · see citing works
Shen, S. H., Wertz, D. L., & Klinman, J. P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029270 · Cited by 43 · see citing works
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Zheng, X., Mansouri, S., Krager, A., Grimminger, F., Seeger, W., Pullamsetti, S. S., Wheelock, C. E., & Savai, R. (2020) · European Respiratory Review · doi:10.1183/16000617.0134-2020 · Cited by 41 · see citing works
Patel, J., Schoenfeld, E. R., Parikh, P. B., et al. (2016) · Journal of Intensive Care Medicine · doi:10.1177/0885066616658420 · Cited by 40 · see citing works
Hydrogen peroxide production is affected by oxygen levels in mammalian cell culture
Maddalena, L. A., Selim, S., Fonseca, J., Messner, H. N., McGowan, S., & Stuart, J. A. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.09.037 · Cited by 41 · see citing works
Saleem, S., Teal, P. D., Howe, C. A., Tymko, M. M., Ainslie, P. N., & Tzeng, Y. (2018) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00032.2018 · Cited by 40 · see citing works
Rossi, S., Stocchetti, N., Longhi, L. G., et al. (2001) · Journal of Neurotrauma · doi:10.1089/08977150150502596 · Cited by 39 · see citing works
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Alvord, L. A., Hall, W. J., Keyes, L. D., et al. (2007) · Cornea · doi:10.1097/ico.0b013e31804f5a22 · Cited by 39 · see citing works
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Nami, R., Mondillo, S., Agricola, E., Lenti, S., Ferro, G., Nami, N., Tarantino, M., Glauco, G., Spano, E., & Gennari, C. (2000) · American Journal of Hypertension · doi:10.1016/s0895-7061(99)00265-4 · Cited by 38 · see citing works
Mekonnen, Y. A., Gültas, M., Effa, K., Hanotte, O., & Schmitt, A. O. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.01095 · Cited by 37 · see citing works
“…Rius et al., 2008; Liao et al., 2009; Minchenko et al., 2015; Singh et al., 2016) 48924511–48971838 CAPG CLR 11 Immune tolerance and neurological dysfunction (Leach and Treacher, 1998; Oosthuyse et al., 2001; Rius et al., 2008; Liao et al., 2009; Zhang et al., 2009; Minchenko et al., 2015; Singh…”
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Kang, S., Lee, D. C., Theusch, B. E., et al. (2013) · Wound Repair and Regeneration · doi:10.1111/wrr.12081 · Cited by 37 · see citing works
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Sun, H., Sun, R., Hao, M., Wang, Y., Zhang, X., Liu, Y., & Cong, X. (2015) · Annals of Surgical Oncology · doi:10.1245/s10434-014-4327-9 · Cited by 36 · see citing works
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Khurana, P., Sugadev, R., Jain, J., & Singh, S. B. (2013) · Database · doi:10.1093/database/bat074 · Cited by 36 · see citing works
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MacIntyre, N. R. (2013) · Respiratory Care · doi:10.4187/respcare.02087 · Cited by 32 · see citing works
Corneal oxygenation during contact lens wear: comparison of diffusion and EOP‐based flux models
Brennan, N. A. (2005) · Clinical and Experimental Optometry · doi:10.1111/j.1444-0938.2005.tb06675.x · Cited by 34 · see citing works
Dolt, K. S., Karar, J., Mishra, M. K., et al. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.12.159 · Cited by 34 · see citing works
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Ho, K. M., Harding, R., & Chamberlain, J. (2007) · Shock · doi:10.1097/shk.0b013e318067dec1 · Cited by 33 · see citing works
Retinal oximetry and systemic arterial oxygen levels
Eliasdottir, T. S. (2018) · Acta Ophthalmologica · doi:10.1111/aos.13932 · Cited by 33 · see citing works
“Normally above 1– 3 mmHg of oxygen pressure is required to maintain cellular oxidative metabolism which allows for a large safety margin in animals (Leach & Treacher 1998; Guyton & Hall 2000; Scheufler 2004).”
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Huynh, P. M., Wang, F., & An, Y. (2024) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjae039 · Cited by 40 · see citing works
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Ouellette, D. R. (2005) · CHEST Journal · doi:10.1378/chest.128.5_suppl_2.576s · Cited by 32 · see citing works
Management of chronic respiratory complications in children and adolescents with sickle cell disease
Arigliani, M., & Gupta, A. K. (2020) · European Respiratory Review · doi:10.1183/16000617.0054-2020 · Cited by 30 · see citing works
Multimodal imaging of cutaneous wound tissue
Zhang, S., Gnyawali, S. C., Huang, J., Ren, W., Gordillo, G. M., Sen, C. K., & Xu, R. X. (2015) · Journal of Biomedical Optics · doi:10.1117/1.jbo.20.1.016016 · Cited by 28 · see citing works
Photoacoustic imaging of 3D-printed vascular networks
Ma, C., Li, W., Li, D., Chen, M., Wang, M., Jiang, L., Mille, L. S., Garciamendez‐Mijares, C. E., Zhao, Z., Zhou, Q., et al. (2022) · Biofabrication · doi:10.1088/1758-5090/ac49d5 · Cited by 27 · see citing works
Energy supply per neuron is constrained by capillary density in the mouse brain
Ventura‐Antunes, L., & Herculano‐Houzel, S. (2022) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2022.760887 · Cited by 26 · see citing works
Rapamycin Rescues Endoplasmic Reticulum Stress–Induced Dry Eye Syndrome in Mice
Cho, B., Hwang, J. S., Shin, Y. J., Kim, J. W., Chung, T.-Y., & Hyon, J. Y. (2019) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.18-25583 · Cited by 26 · see citing works
Páez-Franco, J. C., Maravillas‐Montero, J. L., Mejía‐Domínguez, N. R., Torres-Ruiz, J. J., Tamez-Torres, K. M., Pérez‐Fragoso, A., Germán-Acacio, J. M., Ponce‐de‐León, A., Gómez‐Martín, D., & Ulloa‐Aguirre, A. (2022) · PLoS ONE · doi:10.1371/journal.pone.0274910 · Cited by 25 · see citing works
Петрова, А., & Mehta, R. (2009) · Archives of Disease in Childhood Fetal & Neonatal · doi:10.1136/adc.2009.161604 · Cited by 26 · see citing works
Hemodynamic monitoring in cardiogenic shock
Hamzaoui, O., & Boissier, F. (2022) · Journal of Intensive Medicine · doi:10.1016/j.jointm.2022.10.003 · Cited by 25 · see citing works
Vaini, E., Bari, V., Fantinato, A., Pistuddi, V., Cairo, B., MARIA, B. D., Ranucci, M., & Porta, A. (2019) · Physiological Measurement · doi:10.1088/1361-6579/ab21b1 · Cited by 27 · see citing works
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Shehade, H., Oldenhove, G., & Moser, M. (2014) · European Journal of Immunology · doi:10.1002/eji.201444719 · Cited by 25 · see citing works
Ho, K. M., Harding, R., & Chamberlain, J. (2007) · Anaesthesia and Intensive Care · doi:10.1177/0310057x0703500506 · Cited by 23 · see citing works
Tissue Nutrient Environments and Their Effect on Regulatory T Cell Biology
Blagih, J., Hennequart, M., & Zani, F. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.637960 · Cited by 23 · see citing works
Hemoglobin-Laden Microcapsules for Simulating Oxygen Dynamics of Biological Tissue
Liu, G., Wu, Q., Dwivedi, P., et al. (2018) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.8b00830 · Cited by 23 · see citing works
Hypoxic Culture and Insulin Yield Improvements to Fibrin-Based Engineered Tissue
Bjork, J. W., Meier, L. A., Johnson, S. L., Syedain, Z. H., & Tranquillo, R. T. (2011) · Tissue Engineering Part A · doi:10.1089/ten.tea.2011.0017 · Cited by 21 · see citing works
Pathophysiology of Oxygen Delivery in Respiratory Failure
Levy, M. M. (2005) · CHEST Journal · doi:10.1016/s0012-3692(15)31059-x · Cited by 21 · see citing works
Cajanding, R. J. M. (2022) · AACN Advanced Critical Care · doi:10.4037/aacnacc2022448 · Cited by 20 · see citing works
Essential Role of Hemoglobin βCys93 in Cardiovascular Physiology
Premont, R. T., & Stamler, J. S. (2020) · Physiology · doi:10.1152/physiol.00040.2019 · Cited by 19 · see citing works
Koutlas, A., Smilios, I., Kokkinou, E. M., Myrkos, A., Kounoupis, A., Dipla, K., & Zafeiridis, A. (2024) · Research Quarterly for Exercise and Sport · doi:10.1080/02701367.2022.2159309 · Cited by 18 · see citing works
“Cellular use of oxygen is important in maintaining tissue function and overall survival (Leach & Treacher, 1998).”
Dual-mode Imaging of Cutaneous Tissue Oxygenation and Vascular Function
Xu, R. X., Huang, K., Qin, R., et al. (2010) · Journal of Visualized Experiments · doi:10.3791/2095 · Cited by 16 · see citing works
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Koritala, B. S. C., Lee, Y. Y., Bhadri, S. S., Gaspar, L. S., Stanforth, C., Wu, G., Ruben, M. D., Francey, L. J., & Smith, D. F. (2021) · Genes · doi:10.3390/genes12101627 · Cited by 16 · see citing works
Revisiting the role of hyperbaric oxygen therapy in knee injuries: Potential benefits and mechanisms
Leite, C. B. G., Tavares, L. P., Leite, M. S., & Demange, M. K. (2023) · Journal of Cellular Physiology · doi:10.1002/jcp.30947 · Cited by 16 · see citing works
Sato, M. S., Itô, A., Akiyama, H., Kawabe, Y., & Kamihira, M. (2012) · Tissue Engineering Part A · doi:10.1089/ten.tea.2011.0728 · Cited by 15 · see citing works
Zhu, M., Ma, Y., Tang, M., et al. (2022) · Physiological Research · doi:10.33549/physiolres.934930 · Cited by 14 · see citing works
Sánchez-Aparicio, P., Mota‐Rojas, D., Ortega, M. E. T., et al. (2009) · Journal of Applied Animal Research · doi:10.1080/09712119.2009.9707043 · Cited by 14 · see citing works
From the Atmosphere to the Mitochondrion: The Oxygen Cascade
Biro, G. P. (2013) · Springer eBooks · doi:10.1007/978-3-642-40717-8_2 · Cited by 15 · see citing works
“The consequences of pathological failure of the system to deliver sufficient oxygen for the prevailing metabolic needs are reduction in the tissue pO2 or hypoxia(Leach and Treacher 1998).”
Kim, S. Y., Lee, H. J., Lee, J. K., Park, T. Y., Heo, E. Y., Kim, D. K., Chung, H. S., & Lee, H. W. (2022) · Respiratory Research · doi:10.1186/s12931-022-02063-0 · Cited by 16 · see citing works
Dzhalilova, D. S., Zolotova, N. A., Аршакович, М. В., Kosyreva, A. M., Цветков, И. С., Khalansky, A. S., Алексеева, А. И., Fatkhudinov, T., & Makarova, O. V. (2023) · Scientific Reports · doi:10.1038/s41598-023-39914-9 · Cited by 13 · see citing works
Ultrasound evaluation of dialysis access-related distal ischaemia
Pirozzi, N., Alexandris, L. D., Scrivano, J., et al. (2021) · The Journal of Vascular Access · doi:10.1177/1129729820932420 · Cited by 12 · see citing works
Lu, Y., Hua, Y., Wang, B., Zhong, F., Theophanous, A., Tahir, S., Lee, P., & Sigal, I. A. (2024) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.65.5.1 · Cited by 11 · see citing works
“26,59,61,63 28 We settled on a threshold of 38 mm Hg ( ∼ 5% oxygen) for tissue normoxia, as used in McKeown et al. 29 The mild hypoxia was then selected as the intermediate state between normoxia and severe hypoxia.”
Yang, X., Zhang, W., Zhu, Z., et al. (2025) · Acta Pharmacologica Sinica · doi:10.1038/s41401-025-01582-y · Cited by 10 · see citing works
Dzik, J. (2021) · Acta Biochimica Polonica · doi:10.18388/abp.2020_5683 · Cited by 10 · see citing works
Functional Repercussions of Hypoxia-Inducible Factor-2α in Idiopathic Pulmonary Fibrosis
Torres-Soria, A. K., Romero, Y., Balderas-Martínez, Y. I., Velázquez‐Cruz, R., Espíndola, L. M. T., Camarena, Á., Flores‐Soto, E., Solís‐Chagoyán, H., Ruiz, V., Carlos‐Reyes, Á., et al. (2022) · Cells · doi:10.3390/cells11192938 · Cited by 10 · see citing works
Hypoxia promotes Mycobacterium tuberculosis-specific up-regulation of granulysin in human T cells
Zenk, S. F., Vollmer, M., Schercher, E., Kallert, S., Kubis, J., & Stenger, S. (2015) · Medical Microbiology and Immunology · doi:10.1007/s00430-015-0442-x · Cited by 10 · see citing works
Optimization of pancreatic islet spheroid using various concave patterned-films
Hwang, J. W., Kim, M. J., Kim, H. J., et al. (2012) · Macromolecular Research · doi:10.1007/s13233-012-0189-9 · Cited by 9 · see citing works
What Is the Best Way To Measure Cardiac Output?
Caruso, L. J., Layon, A. J., & Gabrielli, A. (2002) · CHEST Journal · doi:10.1378/chest.122.3.771 · Cited by 9 · see citing works
Perioperative oxygenation—what's the stress?
Larvin, J. T., Edwards, M., Martín, D., Feelisch, M., Grocott, M. P. W., & Cumpstey, A. F. (2024) · BJA Open · doi:10.1016/j.bjao.2024.100277 · Cited by 10 · see citing works
Continuous ST-Segment Monitoring in the Intensive Care Unit
Fox, L., Kirkendall, C. A., & Craney, M. (2010) · Critical Care Nurse · doi:10.4037/ccn2010823 · Cited by 7 · see citing works
Arigliani, M., Zheng, S. L., Ruiz, G., Chakravorty, S., Bossley, C. J., Rees, D. C., & Gupta, A. K. (2020) · BMJ Paediatrics Open · doi:10.1136/bmjpo-2020-000690 · Cited by 8 · see citing works
SRIVASTAVA, V., Tripathi, D., & Bég, O. A. (2017) · Journal of Mechanics in Medicine and Biology · doi:10.1142/s0219519417500270 · Cited by 7 · see citing works
Penketh, P. G., Finch, R. A., Sauro, R., et al. (2017) · Chemical Biology & Drug Design · doi:10.1111/cbdd.13057 · Cited by 7 · see citing works
Zhou, D., Stobdan, T., Visk, D., Xue, J., & Haddad, G. G. (2021) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkab038 · Cited by 7 · see citing works
Can Dietary Nitrate Supplements Improve Tolerance to Hypoxia?
Dauncey, S. (2012) · Journal of the Intensive Care Society · doi:10.1177/175114371201300306 · Cited by 7 · see citing works
Penketh, P. G., Williamson, H. S., & Shyam, K. (2020) · Current Drug Delivery · doi:10.2174/1567201817666200427215044 · Cited by 7 · see citing works
Szczygieł, M., Kalinowska, B., Szczygieł, D., Krzykawska-Serda, M., Fiedor, L., Murzyn, A. A., Sopel, J., Matuszak, Z., & Elas, M. (2024) · Molecular Imaging and Biology · doi:10.1007/s11307-023-01886-7 · Cited by 6 · see citing works
Multi-term fractional linear equations modeling oxygen subdiffusion through capillaries
Pata, V., Siryk, S. V., & Vasylyeva, N. (2025) · Applicable Analysis · doi:10.1080/00036811.2025.2533956 · Cited by 6 · see citing works
“The greater is the difference between capillary and cellular oxygen concentration and the shorter is the distance, the faster is the rate of diffusion [29, 50].”
Leiberich, M., Fitte, A., Burroughs, R. E. J., et al. (2023) · Journal of Wildlife Diseases · doi:10.7589/jwd-d-22-00059 · Cited by 6 · see citing works
“…alternative energy supplies, organ damage will occur, particularly in organs that have limited anaerobic capacity or are very metabolically active, such as the brain, heart, liver, kidneys, and exercising skeletal muscles (Beringer et al. 1996; Leach and Treacher 1998; Schober and Schwarte 2012).”
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Siela, D., & Kidd, M. (2017) · Critical Care Nurse · doi:10.4037/ccn2017627 · Cited by 5 · see citing works
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Aubert, V., Kaminski, J., Guillaud, F., Hauet, T., & Hannaert, P. A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20246246 · Cited by 6 · see citing works
Taylor, J. L., Downs, A. K., Danner, C. L., Downs, J. H., Donkor, J., Johnston, J. I., Rozendaal, D., Larsen, P. L., Johnson, B. D., & Summerfield, D. T. (2025) · Physiological Reports · doi:10.14814/phy2.70210 · Cited by 5 · see citing works
The effects of declined oxygen levels on hypoxia symptoms and blood gases: An experimental study
Sugiharto, A. F., Firdausi, R. A., Safitry, O., & Gunanti (2018) · Journal of Physics Conference Series · doi:10.1088/1742-6596/1073/4/042023 · Cited by 5 · see citing works
Güven, H., & Székely, Z. (2025) · Pharmaceutics · doi:10.3390/pharmaceutics17080980 · Cited by 4 · see citing works
“This phenomenon arises due to abnormally developed tumor vasculature, heterogeneous spatial disorganization, and increased dense connective tissue remodeling, all of which impair tissue permeability and oxygen diffusion [19,49].”
Exploring the fractional Volterra-Fredholm integro-differential equation: An iterative approach
Filali, D., Akram, M., & Dilshad, M. (2025) · AIMS Mathematics · doi:10.3934/math.20251042 · Cited by 4 · see citing works
Cui, B., Wen, M., Zhang, C., Zheng, Y., & Jia, Z. (2026) · Advanced Functional Materials · doi:10.1002/adfm.202532131 · Cited by 5 · see citing works
Pollack, B. L., Torrisi, J. S., Hespe, G. E., Ashokan, G., Shin, J., Mehrara, B. J., & Kataru, R. P. (2025) · Biomedicines · doi:10.3390/biomedicines13051026 · Cited by 4 · see citing works
“…possible that lymphatic dysfunction in chronic wounds or during the early phases of wound repair results in the accumulation of interstitial fluid, thereby increasing local tissue swelling and increasing the distance between cells and their blood supply with resultant gradients of hypoxia [60–62].”
Patel, J. C., Singh, A. B., Tulswani, R., et al. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119718 · Cited by 4 · see citing works
Lu, Y., Hua, Y., Wang, B., Tian, Q., Zhong, F., Theophanous, A., Tahir, S., Lee, P., & Sigal, I. A. (2025) · Ophthalmology Science · doi:10.1016/j.xops.2025.100725 · Cited by 5 · see citing works
“23,53 Pathological processes driven by hypoxia involve complex biochemical mechanisms and vary signi fi cantly across different tissues.”
Single-Sided Magnet System for Quantitative MR Relaxometry and Preclinical In-Vivo Monitoring
Thomas, D. G., Tzeng, Y., Galvosas, P., et al. (2022) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2022.3200626 · Cited by 4 · see citing works
- Authors
- Leach, R. M., & Treacher, D. F.
- Venue
- BMJ
- Publisher
- BMJ
- Published
- 1998-11-14
- Volume
- 317
- Issue
- 7169
- Pages
- 1370-1373
- ISSN
- 0007-1447 (ISSN-L)
- 0959-8138
- 1468-5833
- PMC
- PMC1114253
- OpenAlex
- W2770375493
- Cited by
- 155
- References
- 0
- Citations by year
- 2026: 3 · 2025: 14 · 2024: 9 · 2023: 9 · 2022: 13 · 2021: 14 · 2020: 7 · 2019: 4 · 2018: 8 · 2017: 7 · 2016: 4 · 2015: 7 · 2014: 7 · 2013: 5 · 2012: 9
- FWCI
- 0.74
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.bmj.com/company/legal-information/terms-conditions/legal-information/tdm-licencepolicy (tdm)
- Locations
- BMJ (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Hemodynamic Monitoring and Therapy
- Health Sciences › Medicine › Epidemiology › Sepsis Diagnosis and Treatment
- Health Sciences › Medicine › Surgery › Biomedical and Chemical Research
- Keywords
- tissue hypoxia, oxygen transport, regional blood flow distribution, microcirculation, critical illness, sepsis, autoregulation, precapillary sphincters, perfusion pressure, meningococcal sepsis, diffusion distance
- MeSH terms
- Biological Transport, Capillaries, Energy Metabolism, Humans, Oxygen Consumption, Cell Hypoxia
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