Karlsson 2016 Mitochondrion

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Karlsson M, Ehinger JK, Piel S, Sjövall F, Henriksnäs J, Höglund U, Hansson MJ, Elmér E (2016) Changes in energy metabolism due to acute rotenone-induced mitochondrial complex I dysfunction – an in vivo large animal model. Mitochondrion 31:56-62.

» PMID: 27769952

Karlsson M, Ehinger JK, Piel S, Sjoevall F, Henriksnaes J, Hoeglund U, Hansson MJ, Elmer E (2016) Mitochondrion

Abstract: Metabolic crisis is a clinical condition primarily affecting patients with inherent mitochondrial dysfunction in situations of augmented energy demand. To model this, ten pigs received an infusion of rotenone, a mitochondrial complex I inhibitor, or vehicle. Clinical parameters, blood gases, continuous indirect calorimetry, in vivo muscle oxygen tension, ex vivo mitochondrial respiration and metabolomics were assessed. Rotenone induced a progressive increase in blood lactate which was paralleled by an increase in oxygen tension in venous blood and skeletal muscle. There was an initial decrease in whole body oxygen utilization, and there was a trend towards inhibited mitochondrial respiration in platelets. While levels of succinate were decreased, other intermediates of glycolysis and the TCA cycle were increased. This model may be suited for evaluating pharmaceutical interventions aimed at counteracting metabolic changes due to complex I dysfunction.

Keywords: Animal model, Complex I, Energy metabolism, Metabolic crisis, Mitochondria Bioblast editor: Plangger M O2k-Network Lab: SE Lund Elmer E, US PA Philadelphia Kilbaugh T


Labels: MiParea: Respiration 


Organism: Pig  Tissue;cell: Skeletal muscle, Platelet  Preparation: Intact cells 


Coupling state: ET  Pathway: N, ROX  HRR: Oxygraph-2k 

Labels, 2018-09