scholarly journals Identification of a Novel Dihydrolipoyl Dehydrogenase-binding Protein in the Pyruvate Dehydrogenase Complex of the Anaerobic Parasitic Nematode,Ascaris suum

1996 ◽  
Vol 271 (10) ◽  
pp. 5451-5457 ◽  
Author(s):  
Michele M. Klingbeil ◽  
Daniel J. Walker ◽  
Robin Arnette ◽  
Emil Sidawy ◽  
Karen Hayton ◽  
...  
Keyword(s):  
Pyruvate Dehydrogenase ◽  
Parasitic Nematode ◽  
Binding Protein ◽  
Ascaris Suum ◽  
Pyruvate Dehydrogenase Complex ◽  
Dihydrolipoyl Dehydrogenase ◽  
Dehydrogenase Complex

scholarly journals Carbohydrate-response Element-binding Protein Deletion Alters Substrate Utilization Producing an Energy-deficient Liver

2007 ◽  
Vol 283 (3) ◽  
pp. 1670-1678 ◽  
Author(s):  
Shawn C. Burgess ◽  
Katsumi Iizuka ◽  
Nam Ho Jeoung ◽  
Robert A. Harris ◽  
Yoshihiro Kashiwaya ◽  
...  
Keyword(s):  
Fatty Acid ◽  
Fatty Acid Oxidation ◽  
Pyruvate Dehydrogenase ◽  
Binding Protein ◽  
Pyruvate Dehydrogenase Complex ◽  
Substrate Utilization ◽  
Acid Oxidation ◽  
Nadh Ratio ◽  
Element Binding Protein ◽  
Dehydrogenase Complex

Livers from mice lacking the carbohydrate-responsive element-binding protein (ChREBP) were compared with wild type (WT) mice to determine the effect of this transcription factor on hepatic energy metabolism. The pyruvate dehydrogenase complex was considerably more active in ChREBP-/- mice because of diminished pyruvate dehydrogenase kinase activity. Greater pyruvate dehydrogenase complex activity caused a stimulation of lactate and pyruvate oxidation, and it significantly impaired fatty acid oxidation in perfused livers from ChREBP-/- mice. This shift in mitochondrial substrate utilization led to a 3-fold reduction of the free cytosolic [NAD+]/[NADH] ratio, a 1.7-fold increase in the free mitochondrial [NAD+]/[NADH] ratio, and a 2-fold decrease in the free cytosolic [ATP]/[ADP][Pi] ratio in the ChREBP-/- liver compared with control. Hepatic pyruvate carboxylase flux was impaired with ChREBP deletion secondary to decreased fatty acid oxidation, increased pyruvate oxidation, and limited pyruvate availability because of reduced activity of liver pyruvate kinase and malic enzyme, which replenish pyruvate via glycolysis and pyruvate cycling. Overall, the shift from fat utilization to pyruvate and lactate utilization resulted in a decrease in the energy of ATP hydrolysis and a hypo-energetic state in the livers of ChREBP-/- mice.

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