Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model

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Standard

Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model. / Ochala, Julien; Ahlbeck, Karsten; Radell, Peter J.; Eriksson, Lars I.; Larsson, Lars.

I: PLoS ONE, Bind 6, Nr. 6, e20876, 2011.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ochala, J, Ahlbeck, K, Radell, PJ, Eriksson, LI & Larsson, L 2011, 'Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model', PLoS ONE, bind 6, nr. 6, e20876. https://doi.org/10.1371/journal.pone.0020876

APA

Ochala, J., Ahlbeck, K., Radell, P. J., Eriksson, L. I., & Larsson, L. (2011). Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model. PLoS ONE, 6(6), [e20876]. https://doi.org/10.1371/journal.pone.0020876

Vancouver

Ochala J, Ahlbeck K, Radell PJ, Eriksson LI, Larsson L. Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model. PLoS ONE. 2011;6(6). e20876. https://doi.org/10.1371/journal.pone.0020876

Author

Ochala, Julien ; Ahlbeck, Karsten ; Radell, Peter J. ; Eriksson, Lars I. ; Larsson, Lars. / Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model. I: PLoS ONE. 2011 ; Bind 6, Nr. 6.

Bibtex

@article{96ae4bc0a7bf4f239bb1802717d32715,
title = "Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model",
abstract = "The basic mechanisms underlying acquired generalized muscle weakness and paralysis in critically ill patients remain poorly understood and may be related to prolonged mechanical ventilation/immobilization (MV) or to other triggering factors such as sepsis, systemic corticosteroid (CS) treatment and administration of neuromuscular blocking agents (NMBA). The present study aims at exploring the relative importance of these factors by using a unique porcine model. Piglets were all exposed to MV together with different combinations of endotoxin-induced sepsis, CS and NMBA for five days. Peroneal motor nerve conduction velocity and amplitude of the compound muscle action potential (CMAP) as well as biceps femoris muscle biopsy specimens were obtained immediately after anesthesia on the first day and at the end of the 5-day experimental period. Results showed that peroneal nerve motor conduction velocity is unaffected whereas the size of the CMAP decreases independently of the type of intervention, in all groups after 5 days. Otherwise, despite a preserved size, muscle fibre specific force (maximum force normalized to cross-sectional area) decreased dramatically for animals exposed to MV in combination with CS or/and sepsis. These results suggest that the rapid declines in CMAP amplitude and in force generation capacity are triggered by independent mechanisms with significant clinical and therapeutic implications.",
author = "Julien Ochala and Karsten Ahlbeck and Radell, {Peter J.} and Eriksson, {Lars I.} and Lars Larsson",
year = "2011",
doi = "10.1371/journal.pone.0020876",
language = "English",
volume = "6",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "6",

}

RIS

TY - JOUR

T1 - Factors underlying the early limb muscle weakness in acute quadriplegic myopathy using an experimental ICU porcine model

AU - Ochala, Julien

AU - Ahlbeck, Karsten

AU - Radell, Peter J.

AU - Eriksson, Lars I.

AU - Larsson, Lars

PY - 2011

Y1 - 2011

N2 - The basic mechanisms underlying acquired generalized muscle weakness and paralysis in critically ill patients remain poorly understood and may be related to prolonged mechanical ventilation/immobilization (MV) or to other triggering factors such as sepsis, systemic corticosteroid (CS) treatment and administration of neuromuscular blocking agents (NMBA). The present study aims at exploring the relative importance of these factors by using a unique porcine model. Piglets were all exposed to MV together with different combinations of endotoxin-induced sepsis, CS and NMBA for five days. Peroneal motor nerve conduction velocity and amplitude of the compound muscle action potential (CMAP) as well as biceps femoris muscle biopsy specimens were obtained immediately after anesthesia on the first day and at the end of the 5-day experimental period. Results showed that peroneal nerve motor conduction velocity is unaffected whereas the size of the CMAP decreases independently of the type of intervention, in all groups after 5 days. Otherwise, despite a preserved size, muscle fibre specific force (maximum force normalized to cross-sectional area) decreased dramatically for animals exposed to MV in combination with CS or/and sepsis. These results suggest that the rapid declines in CMAP amplitude and in force generation capacity are triggered by independent mechanisms with significant clinical and therapeutic implications.

AB - The basic mechanisms underlying acquired generalized muscle weakness and paralysis in critically ill patients remain poorly understood and may be related to prolonged mechanical ventilation/immobilization (MV) or to other triggering factors such as sepsis, systemic corticosteroid (CS) treatment and administration of neuromuscular blocking agents (NMBA). The present study aims at exploring the relative importance of these factors by using a unique porcine model. Piglets were all exposed to MV together with different combinations of endotoxin-induced sepsis, CS and NMBA for five days. Peroneal motor nerve conduction velocity and amplitude of the compound muscle action potential (CMAP) as well as biceps femoris muscle biopsy specimens were obtained immediately after anesthesia on the first day and at the end of the 5-day experimental period. Results showed that peroneal nerve motor conduction velocity is unaffected whereas the size of the CMAP decreases independently of the type of intervention, in all groups after 5 days. Otherwise, despite a preserved size, muscle fibre specific force (maximum force normalized to cross-sectional area) decreased dramatically for animals exposed to MV in combination with CS or/and sepsis. These results suggest that the rapid declines in CMAP amplitude and in force generation capacity are triggered by independent mechanisms with significant clinical and therapeutic implications.

UR - http://www.scopus.com/inward/record.url?scp=79958808182&partnerID=8YFLogxK

U2 - 10.1371/journal.pone.0020876

DO - 10.1371/journal.pone.0020876

M3 - Journal article

C2 - 21695079

AN - SCOPUS:79958808182

VL - 6

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 6

M1 - e20876

ER -

ID: 245664352