Maintained Coupling of Oxidative Phosphorylation to Creatine Kinase Activity in Sarcomeric Mitochondrial Creatine Kinase-deficient Mice

1998 ◽  
Vol 30 (5) ◽  
pp. 901-912 ◽  
Author(s):  
E Boehm
2012 ◽  
Vol 590 (21) ◽  
pp. 5475-5486 ◽  
Author(s):  
Christopher G. R. Perry ◽  
Daniel A. Kane ◽  
Eric A. F. Herbst ◽  
Kazutaka Mukai ◽  
Daniel S. Lark ◽  
...  

2006 ◽  
Vol 281 (49) ◽  
pp. 37361-37371 ◽  
Author(s):  
Laudiene Evangelista Meyer ◽  
Lilia Bender Machado ◽  
Ana Paula S. A. Santiago ◽  
Wagner Seixas da-Silva ◽  
Fernanda G. De Felice ◽  
...  

2009 ◽  
Vol 104 (3) ◽  
pp. 247-257 ◽  
Author(s):  
Linda Ebermann ◽  
Cornelia Piper ◽  
Uwe Kühl ◽  
Karin Klingel ◽  
Uwe Schlattner ◽  
...  

2019 ◽  
Vol 317 (2) ◽  
pp. E327-E336
Author(s):  
Nicola Lai ◽  
Chinna Kummitha ◽  
Mitchell Drumm ◽  
Charles Hoppel

High energy expenditure is reported in cystic fibrosis (CF) animal models and patients. Alterations in skeletal muscle oxidative capacity, fuel utilization, and the creatine kinase-phosphocreatine system suggest mitochondrial dysfunction. Studies were performed on congenic C57BL/6J and F508del ( Cftrtm1kth) mice. Indirect calorimetry was used to measure gas exchange to evaluate aerobic capacity during treadmill exercise. The bioenergetic function of skeletal muscle subsarcolemmal (SSM) and interfibrillar mitochondria (IFM) was evaluated using an integrated approach combining measurement of the rate of oxidative phosphorylation by polarography and of electron transport chain activities by spectrophotometry. CF mice have reduced maximal aerobic capacity. In SSM of these mice, oxidative phosphorylation was impaired in the presence of complex I, II, III, and IV substrates except when glutamate was used as substrate. This impairment appeared to be caused by a defect in complex V activity, whereas the oxidative system of the electron transport chain was unchanged. In IFM, oxidative phosphorylation and electron transport chain activities were preserved, whereas complex V activity was reduced, in CF. Furthermore, creatine kinase activity was reduced in both SSM and IFM of CF skeletal muscle. The decreased complex V activity in SSM resulted in reduced oxidative phosphorylation, which could explain the reduced skeletal muscle response to exercise in CF mice. The decrease in mitochondrial creatine kinase activity also contributed to this poor exercise response.


2014 ◽  
Vol 135 (4) ◽  
pp. 871-879 ◽  
Author(s):  
Kenichiro Enooku ◽  
Hayato Nakagawa ◽  
Yoko Soroida ◽  
Ryunosuke Ohkawa ◽  
Yuko Kageyama ◽  
...  

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