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The Sick and the Weak: Neuropathies/Myopathies in the Critically Ill
Open accessAbstract
Critical illness polyneuropathies (CIP) and myopathies (CIM) are common complications of critical illness. Several weakness syndromes are summarized under the term intensive care unit-acquired weakness (ICUAW). We propose a classification of different ICUAW forms (CIM, CIP, sepsis-induced, steroid-denervation myopathy) and pathophysiological mechanisms from clinical and animal model data. Triggers include sepsis, mechanical ventilation, muscle unloading, steroid treatment, or denervation. Some ICUAW forms require stringent diagnostic features; CIM is marked by membrane hypoexcitability, severe atrophy, preferential myosin loss, ultrastructural alterations, and inadequate autophagy activation while myopathies in pure sepsis do not reproduce marked myosin loss. Reduced membrane excitability results from depolarization and ion channel dysfunction. Mitochondrial dysfunction contributes to energy-dependent processes. Ubiquitin proteasome and calpain activation trigger muscle proteolysis and atrophy while protein synthesis is impaired. Myosin loss is more pronounced than actin loss in CIM. Protein quality control is altered by inadequate autophagy. Ca 2+dysregulation is present through altered Ca 2+homeostasis. We highlight clinical hallmarks, trigger factors, and potential mechanisms from human studies and animal models that allow separation of risk factors that may trigger distinct mechanisms contributing to weakness. During critical illness, altered inflammatory (cytokines) and metabolic pathways deteriorate muscle function. ICUAW prevention/treatment is limited, e.g., tight glycemic control, delaying nutrition, and early mobilization. Future challenges include identification of primary/secondary events during the time course of critical illness, the interplay between membrane excitability, bioenergetic failure and differential proteolysis, and finding new therapeutic targets by help of tailored animal models.
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Items 401–600 of 677
Skeletal muscle apoptosis after burns is associated with activation of proapoptotic signals
Yasuhara, S., Perez, M., Kanakubo, E., Yasuhara, Y., Shin, Y. S., Kaneki, M., Fujita, T., & Martyn, J. A. J. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.279.5.e1114 · Cited by 97
Microcirculatory Changes in Rat Skeletal Muscle in Sepsis
Piper, R. D., PITT-HYDE, M. L., Li, F., Sibbald, W. J., & Potter, R. F. (1996) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.154.4.8887588 · Cited by 96
Incidence and onset of critical illness polyneuropathy in patients with septic shock
Tepper, M. (2000) · The Netherlands Journal of Medicine · doi:10.1016/s0300-2977(00)00019-x · Cited by 96
Endotoxin-induced skeletal muscle contractile dysfunction: contribution of nitric oxide synthases
El-Dwairi, Q. A., Comtois, A. S., Guo, Y., & Hussain, S. N. A. (1998) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1998.274.3.c770 · Cited by 96
Tiao, G. M., Lieberman, M. A., Fischer, J. E., & Hasselgren, P.-O. (1997) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1997.272.3.r849 · Cited by 96
Callahan, L. A., She, Z. W., & Nosek, T. M. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.90.1.45 · Cited by 94
Caspase and calpain activation both contribute to sepsis-induced diaphragmatic weakness
Supinski, G. S., Wang, W., & Callahan, L. A. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00341.2009 · Cited by 94
Transport of interleukin‐1 across cerebromicrovascular endothelial cells
Skinner, R., Gibson, R. M., Rothwell, N. J., Pinteaux, E., & Penny, J. C. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2008.00129.x · Cited by 93
Anabolic resistance in critically ill patients
Rennie, M. J. (2009) · Critical Care Medicine · doi:10.1097/ccm.0b013e3181b6ec1f · Cited by 93
Activity and expression of the 20S proteasome are increased in skeletal muscle during sepsis
Hobler, S. C., Williams, A., Fischer, D., Wang, J. J., Sun, X., Fischer, J. E., Monaco, J. J., & Hasselgren, P.-O. (1999) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1999.277.2.r434 · Cited by 93
Early impairment of oxidative metabolism and energy production in severe sepsis.
Astiz, M. E., Rackow, E. C., Weil, M. H., & SCHUMER, W. (1988) · PubMed · Cited by 91
Effects of prolonged endotoxemia on liver, skeletal muscle and kidney mitochondrial function
Porta, F., Takala, J. A., Weikert, C., Bracht, H., Kolarova, A., Lauterburg, B. H., Borotto, E. E., & Jakob, S. M. (2006) · Critical Care · doi:10.1186/cc5013 · Cited by 91
Smith, I. J., Alamdari, N., O’Neal, P., GONNELLA, P. A., Aversa, Z., & Hasselgren, P.-O. (2010) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2010.01.006 · Cited by 91
Tavernier, B., Mebazaa, A., Matéo, P., Sys, S. U., Ventura‐Clapier, R., & Veksler, V. (2001) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.163.2.2002128 · Cited by 91
Mirzakhani, H., Williams, J.-N., Mello, J., Joseph, S., Meyer, M. J., Waak, K., Schmidt, U. H., Kelly, E. M., & Eikermann, M. (2013) · Anesthesiology · doi:10.1097/aln.0b013e31829373fe · Cited by 91
Role of IGF-I and the TNFα/NF-κB pathway in the induction of muscle atrogenes by acute inflammation
Schakman, O., Dehoux, M., Bouchuari, S., Delaere, S., Lause, P., Decroly, N., Shoelson, S. E., & Thissen, J. P. (2012) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00060.2012 · Cited by 91
Karatzanos, E., Gerovasili, V., Zervakis, D., Tripodaki, E.-S., Apostolou, K., Vasileiadis, I., Papadopoulos, E., Mitsiou, G., Tsimpouki, D., Routsi, C., et al. (2012) · Critical Care Research and Practice · doi:10.1155/2012/432752 · Cited by 90
Critical illness polyneuropathy and myopathy in pediatric intensive care: A review
Williams, S. P., Horrocks, I. A., Ouvrier, R., Gillis, J., & Ryan, M. M. (2007) · Pediatric Critical Care Medicine · doi:10.1097/01.pcc.0000256623.01254.40 · Cited by 90
Acute type II myofiber atrophy in critical illness
Gutmann, L., Blumenthal, D. T., Gutmann, L., & Schochet, S. S. (1996) · Neurology · doi:10.1212/wnl.46.3.819 · Cited by 90
Trumbeckaitė, S., Opalka, J. R., Neuhof, C., Zierz, S., & Gellerich, F. N. (2001) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2001.02012.x · Cited by 89
Hassoun, S. M., Marechal, X., Montaigne, D., Bouazza, Y., Decoster, B., Lancel, S., & Nevière, R. (2008) · Critical Care Medicine · doi:10.1097/ccm.0b013e3181844276 · Cited by 89
Yang, J., Sladky, J. T., Kallen, R. G., & Barchi, R. L. (1991) · Neuron · doi:10.1016/0896-6273(91)90294-a · Cited by 89
Dulhunty, A. F. (1979) · The Journal of Membrane Biology · doi:10.1007/bf01869290 · Cited by 89
Hyperglycemic kidney damage in an animal model of prolonged critical illness
Vanhorebeek, I., Gunst, J., Ellger, B., Boussemaere, M., Lerut, E., Debaveye, Y. A., Rabbani, N., Thornalley, P. J., Schetz, M., & den Berghe, G. V. (2009) · Kidney International · doi:10.1038/ki.2009.217 · Cited by 89
Self-citationEarly type II fiber atrophy in intensive care unit patients with nonexcitable muscle membrane
Bierbrauer, J., Koch, S., Olbricht, C., Hamati, J., Lodka, D., Schneider, J., Luther-Schröder, A., Kleber, C., Faust, K., Wiesener, S., et al. (2012) · Critical Care Medicine · doi:10.1097/ccm.0b013e31823295e6 · Cited by 88
Pancuronium-induced prolonged neuromuscular blockade
Rossiter, A., Souney, P. F., McGOWAN, S., & Carvajal, P. (1991) · Critical Care Medicine · doi:10.1097/00003246-199112000-00023 · Cited by 88
Llovera, M., García-Martínez, C., López-Soriano, J., Agell, N., López-Soriano, F., Garcia, I., & Argilés, J. (1998) · Cancer Letters · doi:10.1016/s0304-3835(98)00137-2 · Cited by 87
Chronic TNF Infusion Causes Anorexia But Not Accelerated Nitrogen Loss
MICHIE, H. R., Sherman, M. L., Spriggs, D. R., CHRISTIE, M., Wilmore, D. W., & Rounds, J. D. (1989) · Annals of Surgery · doi:10.1097/00000658-198901000-00002 · Cited by 87
Changes in Intermediary Metabolism in Severe Surgical Illness
Wolfe, R. R., & Martini, W. Z. (2000) · World Journal of Surgery · doi:10.1007/s002689910105 · Cited by 87
Lynch, G. S., Fary, C., & Williams, D. A. (1997) · Cell Calcium · doi:10.1016/s0143-4160(97)90022-1 · Cited by 87
Bennett, E. S. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.013285 · Cited by 87
Mitochondrial nitric oxide metabolism in rat muscle during endotoxemia
Álvarez, S., & Boveris, A. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.06.034 · Cited by 86
Denervation-induced oxidative stress and autophagy signaling in muscle
O′Leary, M. F. N., & Hood, D. A. (2009) · Autophagy · doi:10.4161/auto.5.2.7391 · Cited by 86
Dulhunty, A. F., Laver, D. R., Gallant, E. M., Casarotto, M. G., Pace, S. M., & Curtis, S. M. (1999) · Biophysical Journal · doi:10.1016/s0006-3495(99)76881-5 · Cited by 86
Modulation of angiogenesis by dithiolethione‐modified NSAIDs and valproic acid
Isenberg, J. S., Jia, Y., Field, L., Ridnour, L. A., Sparatore, A., Soldato, P. D., Sowers, A. L., Yeh, G. C., Moody, T. W., Wink, D. A., et al. (2007) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707198 · Cited by 86
Muscle regeneration occurs to coincide with mitochondrial biogenesis
Wagatsuma, A., Kotake, N., & Yamada, S. (2010) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-010-0668-2 · Cited by 85
Hsieh, P.-F., Liu, J.-Y., Pan, Y., Wu, M.-C., Lin, T., Huang, Y., & Wang, J. (2013) · The Journal of Infectious Diseases · doi:10.1093/infdis/jit384 · Cited by 85
Posterino, G. S., & Lamb, G. D. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00219.x · Cited by 83
Sepsis-induced increase in muscle proteolysis is blocked by specific proteasome inhibitors
Hobler, S. C., Tiao, G. M., Fischer, J. E., Monaco, J. J., & Hasselgren, P.-O. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.274.1.r30 · Cited by 83
Puthucheary, Z., Rawal, J., Ratnayake, G., Harridge, S. D. R., Montgomery, H., & Hart, N. (2012) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201107-1320oe · Cited by 82
Ubiquitin Gene Expression in Skeletal Muscle Is Increased by Tumor Necrosis Factor-α
Garcia‐Martínez, C., Llovera, M., Agell, N., López-Soriano, F. J., & Argilés, J. M. A. (1994) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1994.1754 · Cited by 81
Vanhorebeek, I., Ellger, B., Vos, R. D., Boussemaere, M., Debaveye, Y. A., Perre, S. V., Rabbani, N., Thornalley, P. J., & den Berghe, G. V. (2009) · Critical Care Medicine · doi:10.1097/ccm.0b013e31819cec17 · Cited by 81
Self-citationGoldberg, A. L., Baracos, V. E., Rodemann, P., Waxman, L., & Dinarello, C. A. (1984) · PubMed · Cited by 80
Profiles of Serum Cytokines in Acute Drug-Induced Liver Injury and Their Prognostic Significance
Steuerwald, N., Foureau, D., Norton, H. J., Zhou, J., Parsons, J. C., Chalasani, N., Fontana, R. J., Watkins, P. B., Lee, W. M., Reddy, K. R., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081974 · Cited by 79
Weekers, F., Herck, E. V., Coopmans, W., Michalaki, M. A., Bowers, C. Y., Veldhuis, J. D., & den Berghe, G. V. (2002) · Endocrinology · doi:10.1210/endo.143.3.8664 · Cited by 78
Critical illness polyneuropathy a review of the literature, definition and pathophysiology
Leijten, F. S. S., & de Weerd, A. W. (1994) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(94)90023-x · Cited by 78
The impact of severe burns on skeletal muscle mitochondrial function
Porter, C. C., Herndon, D. N., Sidossis, L. S., & Børsheim, E. (2013) · Burns · doi:10.1016/j.burns.2013.03.018 · Cited by 77
ICU-acquired weakness: what is preventing its rehabilitation in critically ill patients?
Lee, C. M., & Fan, E. (2012) · BMC Medicine · doi:10.1186/1741-7015-10-115 · Cited by 77
Critical illness polyneuropathy
van Mook, W., & -Evers, R. P. M. G. H. (2002) · Current Opinion in Critical Care · doi:10.1097/00075198-200208000-00006 · Cited by 77
Wei, W., Fareed, M. U., Evenson, A. R., Menconi, M. J., Yang, H., Petkova, V., & Hasselgren, P.-O. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00341.2004 · Cited by 77
Maximum inspiratory pressure, a surrogate parameter for the assessment of ICU-acquired weakness
Tzanis, G., Vasileiadis, I., Zervakis, D. I., Karatzanos, E., Dimopoulos, S. K., Pitsolis, T., Tripodaki, E. S., Gerovasili, V., Routsi, C., & Nanas, S. (2011) · BMC Anesthesiology · doi:10.1186/1471-2253-11-14 · Cited by 77
Effect of Free Radical Scavengers on Endotoxin-induced Respiratory Muscle Dysfunction
Supinski, G. S., Nethery, D. E., & DiMarco, A. F. (1993) · American Review of Respiratory Disease · doi:10.1164/ajrccm/148.5.1318 · Cited by 76
Winkelman, C. (2004) · AACN Clinical Issues Advanced Practice in Acute & Critical Care · doi:10.1097/00044067-200401000-00006 · Cited by 76
Wilcox, P., Milliken, C. E., & Bressler, B. (1996) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.153.5.8630610 · Cited by 75
Zhang, J., Jiang, W., & Zuo, Z. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.12.034 · Cited by 75
Sedation, analgesia, and neuromuscular blockade in sepsis: An evidence-based review
Vender, J. S., Szokol, J. W., Murphy, G. S., & Nitsun, M. (2004) · Critical Care Medicine · doi:10.1097/01.ccm.0000145907.86298.12 · Cited by 75
Long-term functional outcome and health status of patients with critical illness polyneuromyopathy
Intiso, D., Amoruso, L., Zarrelli, M. M., Pazienza, L., Basciani, M., Grimaldi, G., Iarossi, A., & Rienzo, F. D. (2010) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.2010.01414.x · Cited by 75
Calcium transients in single mammalian skeletal muscle fibres.
Delbono, O., & Stefani, E. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019617 · Cited by 74
Friedrich, O., Hund, E., Weber, C., Hacke, W., & Fink, R. (2004) · Journal of Neurology · doi:10.1007/s00415-004-0272-z · Cited by 74
Self-citationPlasma from septic shock patients induces loss of muscle protein
van Hees, H. W. H., Schellekens, W. M., Linkels, M., Leenders, F., Zoll, J., Donders, R., Dekhuijzen, P. R., van der Hoeven, J. G., & Heunks, L. M. A. (2011) · Critical Care · doi:10.1186/cc10475 · Cited by 74
Downregulation of diaphragm electron transport chain and glycolytic enzyme gene expression in sepsis
Callahan, L. A., & Supinski, G. S. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01157.2004 · Cited by 73
Callahan, L. A., Stofan, D. A., Szweda, L. I., Nethery, D. E., & Supinski, G. S. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00454-8 · Cited by 73
Teichmann, M. D. H., von Wegner, F., Fink, R., Chamberlain, J. S., Launikonis, B. S., Martinac, B., & Friedrich, O. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003644 · Cited by 73
Self-citationMAFbx/Atrogin-1 expression is a poor index of muscle proteolysis
Attaix, D., & Baracos, V. E. (2010) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e328338b9a6 · Cited by 73
Altered mitochondrial redox responses in gram negative septic shock in primates.
Simonson, S. G., Welty‐Wolf, K. E., Huang, Y. T., Griebel, J. A., Caplan, M. S., Fracica, P. J., & Piantadosi, C. A. (1994) · PubMed · Cited by 72
Acute hyperglycemia enhances proteolysis in normal man
Flakoll, P. J., Hill, J. O., & Abumrad, N. N. (1993) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1993.265.5.e715 · Cited by 71
Muscle wasting and the temporal gene expression pattern in a novel rat intensive care unit model
Llano‐Diez, M., Gustafson, A., Olsson, C., Göransson, H., & Larsson, L. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-602 · Cited by 71
Self-citationSiegfried, A., Berchtold, S., Manncke, B., Deuschle, E., Reber, J., Ott, T., Weber, M., Kalinke, U., Hofer, M. J., Hatesuer, B., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1203305 · Cited by 70
Resting calcium concentrations in isolated skeletal muscle fibres of dystrophic mice.
Williams, D. A., Head, S. I., Bakker, A. J., & Stephenson, D. G. (1990) · The Journal of Physiology · doi:10.1113/jphysiol.1990.sp018210 · Cited by 70
Stibler, H., Edstr�m, L., Ahlbeck, K., Remahl, S., & Ansved, T. (2003) · Intensive Care Medicine · doi:10.1007/s00134-003-1894-9 · Cited by 70
Impact of Hyperglycemia on Neuropathological Alterations during Critical Illness
Sonneville, R., den Hertog, H. M., Güiza, F., Gunst, J., Derese, I., Wouters, P. J., Brouland, J., Polito, A., Gray, F., Chrétien, F., et al. (2012) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2011-2971 · Cited by 69
Self-citationStrasser, E.-M., Stättner, S., Karner, J., Klimpfinger, M., Freynhofer, M. K., Zaller, V., Graf, A. C., Wessner, B., Bachl, N., Roth, E., et al. (2009) · Annals of Surgery · doi:10.1097/sla.0b013e3181a38e71 · Cited by 68
Molecular aspects of the trophic influence of nerve on muscle
McArdle, J. J. (1983) · Progress in Neurobiology · doi:10.1016/0301-0082(83)90001-1 · Cited by 68
MECHANISM OF IL-1 INDUCED INHIBITION OF PROTEIN SYNTHESIS IN SKELETAL MUSCLE
Cooney, R. N., Maish, G. O., Gilpin, T., Shumate, M. L., Lang, C. H., & Vary, T. C. (1999) · Shock · doi:10.1097/00024382-199904000-00002 · Cited by 68
Effect of proteasome inhibitors on endotoxin-induced diaphragm dysfunction
Supinski, G. S., Vanags, J., & Callahan, L. A. (2009) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.90404.2008 · Cited by 68
Corpeño, R., Dworkin, B. R., Cacciani, N., Salah, H. A., Bergman, H. ‐., Ravara, B., Vitadello, M., Gorza, L., Gustafson, A., Hedström, Y., et al. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.277962 · Cited by 68
Self-citationMelatonin restores the mitochondrial production of ATP in septic mice.
López, L. C., Escames, G., Ortiz, F., Ros, E., & Acuña-Castroviejo, D. (2006) · PubMed · Cited by 67
Bustamante, M., Fernández‐Verdejo, R., Jaimovich, E., & Buvinic, S. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00450.2013 · Cited by 67
Wernerman, J. (2011) · Annals of Intensive Care · doi:10.1186/2110-5820-1-25 · Cited by 67
Effect of Free Radical Scavengers on Diaphragmatic Contractility in Septic Peritonitis
Fujimura, N., Sumita, S., Aimono, M., Masuda, Y., Shichinohe, Y., Narimatsu, E., & Namiki, A. (2000) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.162.6.9912144 · Cited by 66
Mitochondrial death in sepsis: A failed concept
GELLER, E. R., Jankauskas, S., & Kirkpatrick, C. J. (1986) · Journal of Surgical Research · doi:10.1016/0022-4804(86)90225-8 · Cited by 66
Fraysse, B., Desaphy, J., Rolland, J., Pierno, S., Liantonio, A., Giannuzzi, V., Camerino, C., Didonna, M. P., Cocchi, D., Luca, A. D., et al. (2005) · Neurobiology of Disease · doi:10.1016/j.nbd.2005.07.012 · Cited by 65
Fischer, D. R., Sun, X., Williams, A. B., Gang, G., Pritts, T. A., James, H. J., Molloy, M. P., Fischer, J. E., Paul, R. J., & Hasselgren, P.-O. J. (2001) · Shock · doi:10.1097/00024382-200115030-00007 · Cited by 65
Spangenburg, E. E. (2009) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h09-010 · Cited by 65
Boucher, P.-A., Joós, B., & Morris, C. E. (2012) · Journal of Computational Neuroscience · doi:10.1007/s10827-012-0387-7 · Cited by 65
Garcia‐Martínez, C., Llovera, M., Agell, N., López-Soriano, F. J., & Argilés, J. M. A. (1995) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1995.2848 · Cited by 64
Muscle membrane dysfunction in critical illness myopathy assessed by velocity recovery cycles
Z'Graggen, W. J., Brander, L., Tuchscherer, D., Scheidegger, O., Takala, J. A., & Bostock, H. (2010) · Clinical Neurophysiology · doi:10.1016/j.clinph.2010.09.024 · Cited by 63
Brunello, A., Hænggi, M., Wigger, O., Porta, F., Takala, J. A., & Jakob, S. M. (2009) · Intensive Care Medicine · doi:10.1007/s00134-009-1645-7 · Cited by 63
Hurne, A. M., OʼBrien, J., Wingrove, D. E., Cherednichenko, G., Allen, P. D., Beam, K. G., & Pessah, I. N. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m506441200 · Cited by 63
Lin, S., Chen, W., Lee, F., Huang, C., & Sheu, W. H. (2004) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00186.2004 · Cited by 63
Are the Catabolic Effects of Tumor Necrosis Factor Mediated by Glucocorticoids?
Mealy, K. (1990) · Archives of Surgery · doi:10.1001/archsurg.1990.01410130044006 · Cited by 62
Görgens, S. W., Eckardt, K., Elsen, M., Tennagels, N., & Eckel, J. (2014) · Biochemical Journal · doi:10.1042/bj20131151 · Cited by 62
Gene expression and muscle fiber function in a porcine ICU model
Banduseela, V. C., Ochala, J., Chen, Y., Göransson, H., Norman, H. S., Radell, P. J., Eriksson, L. I., Hoffman, E. P., & Larsson, L. (2009) · Physiological Genomics · doi:10.1152/physiolgenomics.00026.2009 · Cited by 62
Self-citationComparison of the effects of endotoxin on limb, respiratory, and cardiac muscles
Supinski, G. S., Nethery, D. E., Stofan, D. A., & DiMarco, A. F. (1996) · Journal of Applied Physiology · doi:10.1152/jappl.1996.81.3.1370 · Cited by 62
Intracellular tetanic calcium signals are reduced in fatigue of whole skeletal muscle
Baker, A. J., Longuemare, M. C., Brandes, R. P., & Weiner, M. W. (1993) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1993.264.3.c577 · Cited by 61
The Use of Neuromuscular Blocking Agents in the ICU: Where Are We Now?
Greenberg, S. B., & Vender, J. S. (2013) · Critical Care Medicine · doi:10.1097/ccm.0b013e31828ce07c · Cited by 61
NA+‐ and K+‐channels as molecular targets of the alkaloid ajmaline in skeletal muscle fibres
Friedrich, O., von Wegner, F., Wink, M., & Fink, R. (2007) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707194 · Cited by 61
Self-citationGiai, C., Gonzalez, C. D., Ledo, C., Garófalo, A. N., Genaro, M. S. D., Sordelli, D. O., & Gómez, M. I. (2013) · Infection and Immunity · doi:10.1128/iai.00593-13 · Cited by 61
Muscle wasting in animal models of severe illness
Holeček, M. (2012) · International Journal of Experimental Pathology · doi:10.1111/j.1365-2613.2012.00812.x · Cited by 60
Hermans, G., Schrooten, M., Damme, P. V., Berends, N., Bouckaert, B., Vooght, W. D., Robberecht, W., & den Berghe, G. V. (2009) · Critical Care · doi:10.1186/cc7694 · Cited by 60
Self-citationWang, X., Li, Y., Engisch, K. L., Nakanishi, S. T., Dodson, S. E., Miller, G. W., Cope, T. C., Pinter, M. J., & Rich, M. M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3252-04.2005 · Cited by 60
Self-citationAutophagic Cellular Responses to Physical Exercise in Skeletal Muscle
Tam, B. T., & Siu, P. M. (2014) · Sports Medicine · doi:10.1007/s40279-013-0140-z · Cited by 60
Effects of Intermittent Electrical Stimulations on Muscle Catabolism in Intensive Care Patients
Boulétreau, P., Patricot, M. C., Saudin, F., Guiraud, M., & Mathian, B. (1987) · Journal of Parenteral and Enteral Nutrition · doi:10.1177/0148607187011006552 · Cited by 59
Alamdari, N., Smith, I. J., Aversa, Z., & Hasselgren, P.-O. J. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00858.2009 · Cited by 59
Sparing of muscle mass and function by passive loading in an experimental intensive care unit model
Renaud, G., Llano‐Diez, M., Ravara, B., Gorza, L., Feng, H., Jin, J., Cacciani, N., Gustafson, A., Ochala, J., Corpeño, R., et al. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.248724 · Cited by 59
Self-citationOxandrolone in Trauma Patients
Gervasio, J. M., Dickerson, R. N., Swearingen, J., Yates, M. E. D., Yuen, C., Fabian, T. C., Croce, M. A., & Brown, R. O. (2000) · Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy · doi:10.1592/phco.20.17.1328.34889 · Cited by 59
Meesen, R., Dendale, P., Cuypers, K., Berger, J. E., Hermans, A., Thijs, H., & Levin, O. (2010) · Neuromodulation Technology at the Neural Interface · doi:10.1111/j.1525-1403.2010.00294.x · Cited by 59
A Sustained Rat Model for Studying the Long-Lasting Catabolic State of Sepsis
Breuillé, D., Voisin, L., Contrepois, M., Arnal, M., Rose, F., & Obled, C. (1999) · Infection and Immunity · doi:10.1128/iai.67.3.1079-1085.1999 · Cited by 59
Alterations of mitochondrial metabolism and protein concentrations in subacute septicemia
Tavakoli, H., & Mela, L. (1982) · Infection and Immunity · doi:10.1128/iai.38.2.536-541.1982 · Cited by 58
Adductor Pollicis Twitch Tension Assessed by Magnetic Stimulation of the Ulnar Nerve
HARRIS, M. L., Luo, Y. M., Watson, A. C., Rafferty, G. F., Polkey, M. I., Green, M., & Moxham, J. (2000) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.162.1.9902073 · Cited by 58
Bialek, P., Morris, C., Parkington, J., St. Andre, M., Owens, J., Yaworsky, P., Seeherman, H., & Jelinsky, S. A. (2011) · Physiological Genomics · doi:10.1152/physiolgenomics.00247.2010 · Cited by 57 · cited 1×
“However, different models of disuse have suggested differential involvement of either the ubiquitin-proteasome system or autophagy in the associated atrophy (58).”
BackgroundRossignol, B., Guéret, G., Pennec, J., Morel, J., Rannou, F., Giroux‐Metges, M., Talarmin, H., Gioux, M., & Arvieux, C. C. (2008) · Critical Care Medicine · doi:10.1097/ccm.0b013e318176106b · Cited by 57
ECG Changes during Septic Shock
Rich, M. M., McGarvey, M. L., Teener, J. W., & Frame, L. H. (2002) · Cardiology · doi:10.1159/000063120 · Cited by 57
Self-citationOxandrolone Does Not Improve Outcome of Ventilator Dependent Surgical Patients
Bulger, E. M., Jurkovich, G. J., Farver, C. L., Klotz, P., & Maier, R. V. (2004) · Annals of Surgery · doi:10.1097/01.sla.0000137131.22608.e2 · Cited by 57
Increased Store-Operated Ca2+ Entry in Skeletal Muscle with Reduced Calsequestrin-1 Expression
Zhao, X., Min, C. K., Ko, J., Parness, J., Kim, D. H., Weisleder, N. L., & Ma, J. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2010.06.050 · Cited by 57
Zamir, O., Hasselgren, P.-O., von Allmen, D., & Fischer, J. E. (1991) · Journal of Surgical Research · doi:10.1016/0022-4804(91)90045-n · Cited by 57
Calpain Activation Contributes to Endotoxin-Induced Diaphragmatic Dysfunction
Supinski, G. S., & Callahan, L. A. (2009) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2008-0275oc · Cited by 56
Learning of physiological responses: I. Habituation, sensitization, and classical conditioning.
Dworkin, B. R., & Dworkin, S. (1990) · Behavioral Neuroscience · doi:10.1037//0735-7044.104.2.298 · Cited by 56
Dysregulation of sodium channel gating in critical illness myopathy
Teener, J. W., & Rich, M. M. (2006) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-006-9074-5 · Cited by 56
Self-citationMyofilament calcium sensitivity is decreased in skinned cardiac fibres of endotoxin-treated rabbits
Tavernier, B. (1998) · Cardiovascular Research · doi:10.1016/s0008-6363(98)00028-5 · Cited by 56
The measurement of tissue protein turnover
Smith, K., & Rennie, M. J. (1996) · Baillière s Clinical Endocrinology and Metabolism · doi:10.1016/s0950-351x(96)80651-3 · Cited by 55
Fischer, D., Sun, X., Gang, G., Pritts, T. A., & Hasselgren, P.-O. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.1987 · Cited by 55
Role of ubiquitin-proteasome pathway in skeletal muscle wasting in rats with endotoxemia
Chai, J., Wu, Y., & Sheng, Z.-Y. (2003) · Critical Care Medicine · doi:10.1097/01.ccm.0000069728.49939.e4 · Cited by 55
Sepsis-Induced Muscle Proteolysis Is Prevented by a Proteasome Inhibitor in Vivo
Fischer, D., Gang, G., Pritts, T. A., & Hasselgren, P.-O. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2398 · Cited by 55
Tolosa, L., Morlá, M., Iglesias, A., Busquets, X., Lladó, J., & Olmos, G. (2005) · Cellular Signalling · doi:10.1016/j.cellsig.2005.02.001 · Cited by 55
Rofe, A. M., Conyers, R. A. J., Bais, R., Gamble, J. R., & Vadas, M. A. (1987) · Biochemical Journal · doi:10.1042/bj2470789 · Cited by 55
Signs of critical illness polyneuropathy and myopathy can be seen early in the ICU course
Ahlbeck, K., Fredriksson, K., Rooyackers, O., MÅBÄCK, G., Remahl, S., Ansved, T., Eriksson, L. I., & Radell, P. J. (2009) · Acta Anaesthesiologica Scandinavica · doi:10.1111/j.1399-6576.2009.01952.x · Cited by 54
Endotoxin administration alters the force vs. pCa relationship of skeletal muscle fibers
Supinski, G. S., Nethery, D. E., Nosek, T. M., Callahan, L. A., Stofan, D. A., & DiMarco, A. F. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.278.4.r891 · Cited by 54
S100A1 and calmodulin regulation of ryanodine receptor in striated muscle
Prosser, B. L., Hernández‐Ochoa, E. O., & Schneider, M. F. (2011) · Cell Calcium · doi:10.1016/j.ceca.2011.06.001 · Cited by 53
Critical illness myopathy: what is happening?
Friedrich, O. (2006) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/01.mco.0000232900.59168.a0 · Cited by 53
Self-citationBotelho, F. M., Rangel‐Moreno, J., Fritz, D. K., Randall, T. D., Xing, Z., & Richards, C. D. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1203318 · Cited by 52
Authier, F., Mhiri, C., Chazaud, B., et al. (1997) · PubMed · Cited by 52
Control of Capillary Growth and Differentiation by Extracellular Matrix
Ingber, D. E. (1991) · CHEST Journal · doi:10.1378/chest.99.3_supplement.34s · Cited by 52
Signaling Mechanisms of Altered Cellular Responses in Trauma, Burn, and Sepsis
Sayeed, M. M. (2000) · Archives of Surgery · doi:10.1001/archsurg.135.12.1432 · Cited by 52
Monocyte Inflammatory Mediators Impair In Vitro Hamster Diaphragm Contractility
Wilcox, P., Osborne, S., & Bressler, B. (1992) · American Review of Respiratory Disease · doi:10.1164/ajrccm/146.2.462 · Cited by 52
ULTRASTRUCTURAL CHANGES IN SKELETAL MUSCLE MITOCHONDRIA IN GRAM-NEGATIVE SEPSIS
Welty‐Wolf, K. E., Simonson, G., Huang, Y.-C. T., Fracica, P. J., Patterson, J., & Piantadosi, C. A. (1996) · Shock · doi:10.1097/00024382-199605000-00011 · Cited by 52
Ibebunjo, C., & Martyn, J. A. J. (1999) · Critical Care Medicine · doi:10.1097/00003246-199902000-00031 · Cited by 52
Metabolic factors contributing to altered Ca2+ regulation in skeletal muscle fatigue
Steele, D. S., & Duke, A. M. (2003) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2003.01169.x · Cited by 52
Micronutrient supplementation for critically ill adults: A systematic review and meta-analysis
Visser, J., Labadarios, D., & Blaauw, R. (2011) · Nutrition · doi:10.1016/j.nut.2010.12.009 · Cited by 52
Goldhaber, J. I., & Philipson, K. D. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-4756-6_30 · Cited by 51
Neuromuscular disorders in critical illness
Pandit, L., & Agrawal, A. (2006) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2006.04.003 · Cited by 51
Myopathies in Critical Illness: Characterization and Nutritional Aspects
Burnham, E. L., Moss, M., & Ziegler, T. R. (2005) · Journal of Nutrition · doi:10.1093/jn/135.7.1818s · Cited by 50
Thompson, M. T., Kliewer, A. L., Maass, D. L., Becker, L., White, D. J., Bryant, D. D., Arteaga, G. M., Horton, J. W., & Giroir, B. P. (2000) · Pediatric Research · doi:10.1203/00006450-200005000-00019 · Cited by 50
Fram, R. Y., Cree‐Green, M., Wolfe, R. R., Mlcak, R. P., Qian, T., Chinkes, D. L., & Herndon, D. N. (2010) · Critical Care Medicine · doi:10.1097/ccm.0b013e3181de8b9e · Cited by 50
Jespersen, J. G., Nedergaard, A., Reitelseder, S., Mikkelsen, U. R., Dideriksen, K., Agergaard, J., Kreiner, F. F., Pott, F. C., Schjerling, P., & Kjær, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018090 · Cited by 50
Connolly, B., Denehy, L., Brett, S., Elliott, D., & Hart, N. (2012) · Critical Care · doi:10.1186/cc11219 · Cited by 49
Interleukin-6 does not activate protein breakdown in rat skeletal muscle
Garcia‐Martínez, C., López-Soriano, F. J., & Argilés, J. M. A. (1994) · Cancer Letters · doi:10.1016/0304-3835(94)90126-0 · Cited by 49
Authier, F., Mhiri, C., Chazaud, B., Christov, C., Cherin, P., Barlovatz‐Meimon, G., & Gherardi, R. K. (1997) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1997.tb01195.x · Cited by 49
Understanding Critical Illness Myopathy: Approaching the Pathomechanism
Friedrich, O., Fink, R., & Hund, E. (2005) · Journal of Nutrition · doi:10.1093/jn/135.7.1813s · Cited by 48
Self-citationBoucher, P.-A., Joós, B., & Morris, C. E. (2012) · Journal of Computational Neuroscience · doi:10.1007/s10827-012-0415-7 · Cited by 48
O′Leary, M. F. N., & Hood, D. A. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00724.2007 · Cited by 48
Norman, H. S., Nordquist, J., Andersson, P., Ansved, T., Tang, X., Dworkin, B. R., & Larsson, L. (2006) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-006-0110-5 · Cited by 48
Self-citationMitochondrial Fusion, Fission, and Biogenesis in Prolonged Critically Ill Patients
Vanhorebeek, I., Gunst, J., Derde, S., Derese, I., Boussemaere, M., D’Hoore, A. J. L., Wouters, P. J., & den Berghe, G. V. (2011) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2011-1760 · Cited by 47
Self-citationRole of NO and PAF in the impairment of skeletal muscle contractility induced by TNF-α
Alloatti, G., Penna, C. R. R., Mariano, F., & Camussi, G. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.279.6.r2156 · Cited by 47
Regulation of skeletal muscle oxidative phenotype by classical NF-κB signalling
Remels, A. H. V., Gosker, H. R., Bakker, J. A., Guttridge, D. C., Schols, A. M. W. J., & LANGEN, R. C. J. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.03.018 · Cited by 46
Haeseler, G., Foadi, N., Wiegand, E., Ahrens, J., Krampfl, K., Dengler, R., & Leuwer, M. (2008) · Critical Care Medicine · doi:10.1097/ccm.0b013e31816a02cf · Cited by 46
Human skeletal muscle metabolism and morphology after temporary incomplete ischaemia
Sjöstróm, M., Neglen, P. N., Fridén, J. O., & Eklöf, B. (1982) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.1982.tb00941.x · Cited by 46
Moriggi, M., Cassano, P., Vasso, M., Capitanio, D., Fania, C., Musicco, C., Pesce, V., Gadaleta, M. N., & Gelfi, C. (2008) · PROTEOMICS · doi:10.1002/pmic.200701176 · Cited by 46
Immunomodulatory therapies for sepsis: unexpected effects with macrolides
Giamarellos‐Bourboulis, E. J. (2008) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2008.06.004 · Cited by 46
Mitochondrial Dysfunction in Sepsis: Evidence from Bacteraemic Baboons and Endotoxaemic Rabbits
Gellerich, F. N., Trumbeckaitė, S., Opalka, J. R., et al. (2002) · Bioscience Reports · doi:10.1023/a:1016017224003 · Cited by 46
Critical illness polyneuropathy
Bolton, C. F., & Young, G. B. (2000) · Current Treatment Options in Neurology · doi:10.1007/s11940-000-0027-9 · Cited by 45
Frost, R. A., Nystrom, G. J., & Lang, C. H. (2009) · Shock · doi:10.1097/shk.0b013e3181a034d2 · Cited by 45
Hormonal status and ICU-acquired paresis in critically ill patients
Sharshar, T., Bastuji‐Garin, S., Jonghe, B. D., Stevens, R. D., Polito, A., Maxime, V., Rodríguez, P., Cerf, C., Outin, H., Touraine, P. A., et al. (2010) · Intensive Care Medicine · doi:10.1007/s00134-010-1840-6 · Cited by 45
Interleukin-1 receptor antagonist prevents sepsis-induced inhibition of protein synthesis
Cooney, R. N., Owens, E., Jurasinski, C. V., Gray, K., Vannice, J. L., & Vary, T. C. (1994) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1994.267.5.e636 · Cited by 45
Acetylcholine Metabolism in the Inflamed Rat Intestine
Davis, K. A. M., Masella, J., & Blennerhassett, M. G. (1998) · Experimental Neurology · doi:10.1006/exnr.1998.6839 · Cited by 44
Sepsis in mice stimulates muscle proteolysis in the absence of IL-6
Williams, A., Wang, J. J., Wang, L., Sun, X., Fischer, J. E., & Hasselgren, P.-O. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.275.6.r1983 · Cited by 44
Human mitochondrial oxidative capacity is acutely impaired after burn trauma
Cree‐Green, M., Fram, R. Y., Herndon, D. N., Qian, T., Angel, C. A., Green, J. M., Mlcak, R. P., Aarsland, A. A., & Wolfe, R. R. (2008) · The American Journal of Surgery · doi:10.1016/j.amjsurg.2007.09.048 · Cited by 43
Hsp70 prevents disuse muscle atrophy in senescent rats
DODD, S. L., Hain, B. A., & Judge, A. R. (2008) · Biogerontology · doi:10.1007/s10522-008-9203-1 · Cited by 42
Burn injury—induced nicotinic acetylcholine receptor changes on muscle membrane
Ward, J. M., & Martyn, J. A. J. (1993) · Muscle & Nerve · doi:10.1002/mus.880160403 · Cited by 42
Role of skeletal muscle Na+–K+ ATPase activity in increased lactate production in sub–acute sepsis
McCarter, F. D., Nierman, S. R., James, J. H., Wang, L., King, J.-K., Friend, L. A., & Fischer, J. E. (2002) · Life Sciences · doi:10.1016/s0024-3205(02)01475-3 · Cited by 41
Lee, H.-Y., Kaneki, M., Andreas, J., Tompkins, R. G., & Martyn, J. A. J. (2011) · Shock · doi:10.1097/shk.0b013e3182366872 · Cited by 41
Endotoxin-Induced Tumor Necrosis Factor
Oettgen, H. F., Carswell, E. A., Kassel, R., Fiore, N. C., Williamson, B., Hoffmann, M. K., Haranaka, K., & Old, L. J. (1980) · Recent results in cancer research/Recent Results in Cancer Research · doi:10.1007/978-3-642-81491-4_32 · Cited by 40
Skeletal Muscle Electron Transport Chain Dysfunction After Sepsis in Rats
Peruchi, B. B., Petronilho, F. C., Rojas, H. A., Constantino, L. D. S., Mina, F., Vuolo, F. S., Cardoso, M. R., Gonçalves, C. L., Rezin, G. T., STRECK, E. L., et al. (2011) · Journal of Surgical Research · doi:10.1016/j.jss.2010.11.893 · Cited by 40
Apocynin improves diaphragmatic function after endotoxin administration
Supinski, G. S., Stofan, D. A., Nethery, D. E., Szweda, L. I., & DiMarco, A. F. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.2.776 · Cited by 40
Intensive insulin therapy in the ICU—reconciling the evidence
den Berghe, G. V. (2012) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2012.14 · Cited by 39
Spangenburg, E. E., Brown, D. A., Johnson, M. S., & Moore, R. L. (2009) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-009-0195-1 · Cited by 39
Altered Gene Expression in Steroid-Treated Denervated Muscle
Rich, M. M., Kraner, S. D., & Barchi, R. L. (1999) · Neurobiology of Disease · doi:10.1006/nbdi.1999.0257 · Cited by 39
Self-citationExperimental animal models of muscle wasting in intensive care unit patients
Larsson, L. (2007) · Critical Care Medicine · doi:10.1097/01.ccm.0000278055.40121.54 · Cited by 39
Self-citationWagatsuma, A., Kotake, N., Mabuchi, K., & Yamada, S. (2011) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-011-0083-5 · Cited by 39
Mitochondrial function in sepsis: Respiratory versus leg muscle
Fredriksson, K., & Rooyackers, O. (2007) · Critical Care Medicine · doi:10.1097/01.ccm.0000278048.00896.4b · Cited by 39
Myofibrillar protein and gene expression in acute quadriplegic myopathy
Norman, H. S., Zackrisson, H., Hedström, Y., Andersson, P., Nordquist, J., Eriksson, L. I., Libelius, R., & Larsson, L. (2009) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2009.04.041 · Cited by 38
Self-citationOrellana, R. A., Suryawan, A., Wilson, F. A., Gazzaneo, M. C., Fiorotto, M. L., Nguyen, H. V., & Davis, T. A. (2012) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00259.2011 · Cited by 38
Alterations in intracellular Ca2+-homeostasis of skeletal muscle fibers during sepsis*
Zink, W., Kaess, M., Hofer, S., Plachky, J., Zausig, Y. A., Sinner, B., Weigand, M. A., Fink, R., & Graf, B. M. (2008) · Critical Care Medicine · doi:10.1097/ccm.0b013e318170aa97 · Cited by 38
Greenberg, M. J., Mealy, T. R., Jones, M., Szczesna‐Cordary, D., & Moore, J. R. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00566.2009 · Cited by 38
Li, X., Hughes, S. M., Salviati, G., Teresi, A., & Larsson, L. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021513 · Cited by 37
Self-citationHemin prevents cardiac and diaphragm mitochondrial dysfunction in sepsis
Supinski, G. S., & Callahan, L. A. (2005) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2005.09.025 · Cited by 37
Hauptmann, S., Klosterhalfen, B., Weis, J., et al. (1994) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/bf00195781 · Cited by 36
Banduseela, V. C., Chen, Y., Kultima, H. G., Norman, H. S., Aare, S., Radell, P. J., Eriksson, L. I., Hoffman, E. P., & Larsson, L. (2013) · Physiological Genomics · doi:10.1152/physiolgenomics.00141.2012 · Cited by 36
Self-citationSupinski, G. S., Ji, X., & Callahan, L. A. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.90849.2008 · Cited by 36
Baroreflexes of the rat. III. Open-loop gain and electroencephalographic arousal
Dworkin, B. R., & Dworkin, S. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00469.2003 · Cited by 35
Aare, S., Ochala, J., Norman, H. S., Radell, P. J., Eriksson, L. I., Göransson, H., Chen, Y., Hoffman, E. P., & Larsson, L. (2011) · Physiological Genomics · doi:10.1152/physiolgenomics.00116.2011 · Cited by 35
Self-citationValdés, J. A., Gaggero, E., Hidalgo, J., Leal, N. R., Jaimovich, E., & Carrasco, M. A. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00195.2007 · Cited by 35
Hranjec, T., Swenson, B. R., Dossett, L. A., Metzger, R., Flohr, T. R., Popovsky, K. A., Bonatti, H., May, A. K., & Sawyer, R. G. (2010) · Journal of the American College of Surgeons · doi:10.1016/j.jamcollsurg.2009.12.042 · Cited by 35
Menconi, M. J., Arany, Z. P., Alamdari, N., Aversa, Z., GONNELLA, P. A., O’Neal, P., Smith, I. J., Tizio, S., & Hasselgren, P.-O. J. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00596.2009 · Cited by 35
Hall-Angerås, M., Hasselgren, P.-O. J., Dimlich, R. V. W., & Fischer, J. E. (1991) · Metabolism · doi:10.1016/0026-0495(91)90114-c · Cited by 35
B Cell Production of Tumor Necrosis Factor in Response to Pneumocystis murina Infection in Mice
Opata, M. M., Ye, Z., Hollifield, M., & Garvy, B. A. (2013) · Infection and Immunity · doi:10.1128/iai.00744-13 · Cited by 34
Dworkin, B. R., Dworkin, S., & Tang, X. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.279.5.r1910 · Cited by 34
Bertsch, S., Lang, C. H., & Vary, T. C. (2010) · Shock · doi:10.1097/shk.0b013e3181fd068c · Cited by 33
Hosokawa, S., Koseki, H., Nagashima, M., Maeyama, Y., Yomogida, K., Mehr, C. R., Rutledge, M., Greenfeld, H., Kaneki, M., Tompkins, R. G., et al. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00078.2013 · Cited by 33
Acute Quadriplegic Myopathy: An Acquired “Myosinopathy”
Larsson, L. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-84847-1_8 · Cited by 32
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Metadata
- Authors
- Friedrich, O., Reid, M. B., Van den Berghe, G., Vanhorebeek, I., Hermans, G., Rich, M. M., & Larsson, L.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2015-07
- Volume
- 95
- Issue
- 3
- Pages
- 1025-1109
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2131699531
- Cited by
- 396
- References
- 677
- FWCI
- 3.67
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.