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Am J Physiol Endocrinol Metab 291: E1044-E1050, 2006. First published June 27, 2006; doi:10.1152/ajpendo.00218.2006
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Derangements in mitochondrial metabolism in intercostal and leg muscle of critically ill patients with sepsis-induced multiple organ failure

Katarina Fredriksson,1 Folke Hammarqvist,2 Karin Strigård,2 Kjell Hultenby,3 Olle Ljungqvist,4 Jan Wernerman,1 and Olav Rooyackers1

1Department of Anesthesiology and Intensive Care, 2Gastrocentrum, Department of Surgery, 3Clinical Research Center at Karolinska University Hospital, Huddinge; and 4Center for Gastrointestinal Disease at Ersta Hospital, CLINTEC, Karolinska Institutet, Stockholm, Sweden

Submitted 8 May 2006 ; accepted in final form 22 June 2006

Critically ill patients treated for multiple organ failure often develop muscle dysfunction. Here we test the hypothesis that mitochondrial and energy metabolism are deranged in leg and intercostal muscle of critically ill patients with sepsis-induced multiple organ failure. Ten critically ill patients suffering from sepsis-induced multiple organ failure and requiring mechanical ventilation were included in the study. A group (n = 10) of metabolically healthy age- and sex-matched patients undergoing elective surgery were used as controls. Muscle biopsies were obtained from the vastus lateralis (leg) and intercostal muscle. The activities of citrate synthase and mitochondrial respiratory chain complexes I and IV and concentrations of ATP, creatine phosphate, and lactate were analyzed. Morphological evaluation of mitochondria was performed by electron microscopy. Activities of citrate synthase and complex I were 53 and 60% lower, respectively, in intercostal muscle of the patients but not in leg muscle compared with controls. The activity of complex IV was 30% lower in leg muscle but not in intercostal muscle. Concentrations of ATP and creatine phosphate were, respectively, 40 and 34% lower, and lactate concentrations were 43% higher in leg muscle but not in intercostal muscle. We conclude that both leg and intercostal muscle show a twofold decrease in mitochondrial content in intensive care unit patients with multiple organ failure, which is associated with lower concentrations of energy-rich phosphates and an increased anaerobic energy production in leg muscle but not in intercostal muscle.

mitochondrial respiratory chain; energy-rich phosphates; skeletal muscle; intensive care unit; oxidative stress



Address for reprint requests and other correspondence: K. Fredriksson, Dept. of Anesthesiology and Intensive Care, Karolinska University Hospital Huddinge, 141 86 Stockholm, Sweden (e-mail: katarina.fredriksson{at}ki.se)




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