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Home All issues Volume 41 / No 3 (Mars 2025) Med Sci (Paris), 41 3 (2025) 253-259 References
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Issue
Med Sci (Paris)
Volume 41, Number 3, Mars 2025
Page(s) 253 - 259
Section M/S Revues
DOI https://doi.org/10.1051/medsci/2025024
Published online 21 March 2025
  1. Evans L, Rhodes A, Alhazzani W, et al. Executive summary : surviving sepsis campaign : international guidelines for the management of sepsis and septic shock 2021. Crit Care Med 2021 ; 49 : 1974–82. [Google Scholar]
  2. Fan E, Cheek F, Chlan L, et al. An official american thoracic society clinical practice guideline : the diagnosis of intensive care unit-acquired weakness in adults. Am J Respir Crit Care Med 2014 ; 190 : 1437–46. [PubMed] [Google Scholar]
  3. Chen J, Huang M. Intensive care unit-acquired weakness : Recent insights. J Intensive Med 2024 ; 4 : 73–80. [Google Scholar]
  4. Odden AJ, Rohde JM, Bonham C, et al. Functional outcomes of general medical patients with severe sepsis. BMC Infect Dis 2013 ; 13 : 588. [Google Scholar]
  5. Ali NA, O’Brien JM, Jr., Hoffmann SP, et al. Acquired weakness, handgrip strength, and mortality in critically ill patients. Am J Respir Crit Care Med 2008 ; 178 : 261–8. [PubMed] [Google Scholar]
  6. De Jonghe B, Bastuji-Garin S, Sharshar T, et al. Does ICU-acquired paresis lengthen weaning from mechanical ventilation? Intensive Care Med 2004 ; 30 : 1117–21. [CrossRef] [PubMed] [Google Scholar]
  7. Lecronier M, Jung B, Molinari N, et al. Severe but reversible impaired diaphragm function in septic mechanically ventilated patients. Ann Intensive Care 2022 ; 12 : 34. [PubMed] [Google Scholar]
  8. Yoshihara I, Kondo Y, Okamoto K, Tanaka H. Sepsis-associated muscle wasting : a comprehensive review from bench to bedside. Int J Mol Sci 2023 ; 24 : 5040. [Google Scholar]
  9. Laitano O, Pindado J, Valera I, et al. The impact of hindlimb disuse on sepsis-induced myopathy in mice. Physiol Rep 2021 ; 9 : e14979. [Google Scholar]
  10. Reid MB, Lännergren J, Westerblad H. Respiratory and limb muscle weakness induced by tumor necrosis factor-alpha : involvement of muscle myofilaments. Am J Respir Crit Care Med 2002 ; 166 : 479–84. [PubMed] [Google Scholar]
  11. Supinski GS, Wang L, Schroder EA, Callahan LAP. MitoTEMPOL, a mitochondrial targeted antioxidant, prevents sepsis-induced diaphragm dysfunction. Am J Physiol Lung Cell Mol Physiol 2020 ; 319 : L228–38. [PubMed] [Google Scholar]
  12. Supinski GS, Alimov AP, Wang L, et al. Calcium-dependent phospholipase A2 modulates infection-induced diaphragm dysfunction. Am J Physiol Lung Cell Mol Physiol 2016 ; 310 : L975–84. [PubMed] [Google Scholar]
  13. Okazaki T, Liang F, Li T, et al. Muscle-specific inhibition of the classical nuclear factor-κB pathway is protective against diaphragmatic weakness in murine endotoxemia. Crit Care Med 2014 ; 42 : e501–9. [Google Scholar]
  14. Supinski GS, Alimov AP, Wang L, et al. Neutral sphingomyelinase 2 is required for cytokine-induced skeletal muscle calpain activation. Am J Physiol Lung Cell Mol Physiol 2015 ; 309 : L614–24. [PubMed] [Google Scholar]
  15. Supinski GS, Callahan LA. Calpain activation contributes to endotoxin-induced diaphragmatic dysfunction. Am J Respir Cell Mol Biol 2010 ; 42 : 80–7. [PubMed] [Google Scholar]
  16. Divangahi M, Demoule A, Danialou G, et al. Impact of IL-10 on diaphragmatic cytokine expression and contractility during Pseudomonas Infection. Am J Respir Cell Mol Biol 2007 ; 36 : 504–12. [PubMed] [Google Scholar]
  17. Friedrich O, Yi B, Edwards JN, et al. IL-1a reversibly inhibits skeletal muscle ryanodine receptor. a novel mechanism for critical illness myopathy? Am J Respir Cell Mol Biol 2014 ; 50 : 1096–106. [PubMed] [Google Scholar]
  18. Delneste Y, Beauvillain C, Jeannin P. Immunité naturelle : structure et fonction des Toll-like receptors. Med Sci (Paris) 2007 ; 23 : 67–73. [Google Scholar]
  19. Thoma A, Lightfoot AP. NF-kB and inflammatory cytokine signalling : role in skeletal muscle atrophy. Advances in experimental medicine and biology 2018; 1088 : 267–79. [Google Scholar]
  20. Cho DS, Schmitt RE, Dasgupta A, et al. Single-cell deconstruction of post-sepsis skeletal muscle and adipose tissue microenvironments. J Cachexia Sarcopenia Muscle 2020 ; 11 : 1351–63. [Google Scholar]
  21. Crowell KT, Lang CH. Contractility and myofibrillar content in skeletal muscle are decreased during post-sepsis recovery, but not during the acute phase of sepsis. Shock 2021 ; 55 : 649–59. [Google Scholar]
  22. Bonaldo P, Sandri M. Cellular and molecular mechanisms of muscle atrophy. Dis Models Mech 2013 ; 6 : 25–39. [Google Scholar]
  23. Gellhaus B, Böker KO, Gsaenger M, et al. Foxo3 knockdown mediates decline of myod1 and myog reducing myoblast conversion to myotubes. Cells 2023 ; 12 : 2167. [Google Scholar]
  24. Sandri M. Autophagy in skeletal muscle. FEBS Lett 2010 ; 584 : 1411–6. [Google Scholar]
  25. Brunet A. Les multiples actions des facteurs de transcription FOXO. Med Sci (Paris) 2004 ; 20 : 856–9. [Google Scholar]
  26. Bertoli C, Copetti T, Lam EWF, et al. Calpain small-1 modulates Akt/ FoxO3A signaling and apoptosis through PP2A. Oncogene 2009 ; 28 : 721–33. [Google Scholar]
  27. Tiao G, Fagan JM, Samuels N, et al. Sepsis stimulates nonlysosomal, energy-dependent proteolysis and increases ubiquitin mRNA levels in rat skeletal muscle. J clin invest 1994 ; 94 : 2255–64. [Google Scholar]
  28. Hobler SC, Tiao G, Fischer JE, et al. Sepsis-induced increase in muscle proteolysis is blocked by specific proteasome inhibitors. Am J Physiol Regul Integr Comp Physiol 1998 ; 274 : R30–R7. [Google Scholar]
  29. Zanders L, Kny M, Hahn A, et al. Sepsis induces interleukin 6, gp130/JAK2/STAT3, and muscle wasting. J Cachexia Sarcopenia Muscle 2022 ; 13 : 713–27. [Google Scholar]
  30. Lapaquette P, Nguyen HTT, Faure M. L’autophagie garante de l’immunité et de l’inflammation. Med Sci (Paris) 2017 ; 33 : 305–11. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  31. Leduc-Gaudet JP, Franco-Romero A, Cefis M, et al. MYTHO is a novel regulator of skeletal muscle autophagy and integrity. Nat Commun 2023 ; 14 : 1199. [PubMed] [Google Scholar]
  32. Leduc-Gaudet JP, Miguez K, Cefis M, et al. Autophagy ablation in skeletal muscles worsens sepsis-induced muscle wasting, impairs whole-body metabolism, and decreases survival. iScience 2023 ; 26 : 107475. [Google Scholar]
  33. Baud L, Fouqueray B, Bellocq A, Peltier J. Les calpaïnes participent au développement de la réaction inflammatoire. Med Sci (Paris) 2003 ; 19 : 71–6. [Google Scholar]
  34. Letavernier E, Baud L. Les calpaïnes : une arme à double tranchant. Med Sci (Paris) 2016 ; 32 : 435–8. [Google Scholar]
  35. Smith IJ, Lecker SH, Hasselgren PO. Calpain activity and muscle wasting in sepsis. Am J Physiol Endocrinol Metab 2008 ; 295 : E762–71. [PubMed] [Google Scholar]
  36. Monzel AS, Enríquez JA, Picard M. Multifaceted mitochondria : moving mitochondrial science beyond function and dysfunction. Nat Metab 2023 ; 5 : 546–62. [Google Scholar]
  37. Willingham TB, Ajayi PT, Glancy B. Subcellular specialization of mitochondrial form and function in skeletal muscle cells. Front Cell Dev Biol 2021 ; 9 : 757305. [CrossRef] [PubMed] [Google Scholar]
  38. Li X, Sun B, Li J, et al. Sepsis leads to impaired mitochondrial calcium uptake and skeletal muscle weakness by reducing the micu1 : mcu protein ratio. Shock 2023 ; 60 : 698–706. [Google Scholar]
  39. Callahan LA, Stofan DA, Szweda LI, et al. Free radicals alter maximal diaphragmatic mitochondrial oxygen consumption in endotoxin-induced sepsis. Free Radic Biol Med 2001 ; 30 : 129–38. [CrossRef] [PubMed] [Google Scholar]
  40. Callahan LA, Supinski GS. Sepsis induces diaphragm electron transport chain dysfunction and protein depletion. Am J Respir Crit Care Med 2005 ; 172 : 861–8. [PubMed] [Google Scholar]
  41. Sheng Z, Yu Z, Wang M, et al. Targeting STAT6 to mitigate sepsis-induced muscle atrophy and weakness : Modulation of mitochondrial dysfunction, ferroptosis, and CHI3L1-Mediated satellite cell loss. Biochem Biophys Rep 2024 ; 37 : 101608. [Google Scholar]
  42. Zheng Y, Dai H, Chen R, et al. Endoplasmic reticulum stress promotes sepsis-induced muscle atrophy via activation of STAT3 and Smad3. J Cell Physiol 2023 ; 238 : 582–96. [Google Scholar]
  43. Zink W, Kaess M, Hofer S, et al. Alterations in intracellular Ca2+-homeostasis of skeletal muscle fibers during sepsis. Crit Care Med 2008 ; 36 : 1559–63. [Google Scholar]
  44. Goossens C, Weckx R, Derde S, et al. Impact of prolonged sepsis on neural and muscular components of muscle contractions in a mouse model. J Cachexia Sarcopenia Muscle 2021 ; 12 : 443–55. [Google Scholar]
  45. Rossignol B, Gueret G, Pennec JP, et al. Effects of chronic sepsis on the voltage-gated sodium channel in isolated rat muscle fibers. Crit Care Med 2007 ; 35 : 351–7. [Google Scholar]
  46. Nardelli P, Khan J, Powers R, et al. Reduced motoneuron excitability in a rat model of sepsis. J Neurophysiol 2013 ; 109 : 1775–81. [Google Scholar]
  47. Nardelli P, Vincent JA, Powers R, et al. Reduced motor neuron excitability is an important contributor to weakness in a rat model of sepsis. Exp Neurol 2016 ; 282 : 1–8. [Google Scholar]
  48. Nardelli P, Powers R, Cope TC, et al. Increasing motor neuron excitability to treat weakness in sepsis. Ann Neurol 2017 ; 82 : 961–71. [PubMed] [Google Scholar]
  49. Schäfers M, Sorkin L. Effect of cytokines on neuronal excitability. Neurosci Lett 2008 ; 437 : 188–93. [Google Scholar]
  50. Bourcier CH, Michel-Flutot P, Emam L, et al. ß1-adrenergic blockers preserve neuromuscular function by inhibiting the production of extracellular traps during systemic inflammation in mice. Front Immunol 2023 ; 14 : 1228374. [Google Scholar]

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