Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:1.3.99.3 (acyl-CoA dehydrogenase)
 1,425 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The theory of steady-state flux control was applied to characterize the regulation of beta-oxidation flux in uncoupled rat liver mitochondria oxidizing palmitoylcarnitine in the presence of rotenone, malonate and the beta-hydroxybutyrate/acetoacetate redox buffer. By titrations with inhibitors such as antimycin, myxothiazol, azide and 4-pentenoic acid, the flux control coefficients of the b-c1 complex, cytochrome c oxidase and thiolase, were determined experimentally. The flux control coefficients of carnitine palmitoyltransferase II, ETF:CoQ oxidoreductase and beta-hydroxybutyrate dehydrogenase were determined from elasticity coefficients obtained by measuring the flux dependencies of acyl-CoA and acetyl-CoA+CoASH concentrations, the electron transfer flavoprotein redox state, the CoQ redox state and the NAD redox state. It was found that at low flux rates the flux control was distributed mainly between acyl-CoA dehydrogenase and beta-hydroxyacyl-CoA dehydrogenase (Ci = 0.89). At maximum flux rates, carnitine palmitoyltransferase II (Ci = 0.35) and thiolase (Ci = 0.13) contribute additionally to the flux control. Thus, the phenomena of regulation of mitochondrial beta-oxidation can be described as multistep control.
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PMID:Application of the theory of steady-state flux control to mitochondrial beta-oxidation. 166 35

Tibialis anterior (TA) muscles of four small mammals were subjected to chronic nerve stimulation for 28 days (10 Hz, 10 hours per day). Total cellular activities of phosphofructokinase (PFK), hexokinase (HK), citrate synthase (CS), 3-hydroxy-acyl-CoA dehydrogenase (HADH) and 3-hydroxybutyrate dehydrogenase (HBDH) were measured in the stimulated and unstimulated contralateral muscles. Normal TA muscles displayed ranges of oxidative and glycolytic capacities with rabbit TA showing the lowest and mouse TA the highest oxidative capacity. Chronic stimulation was almost without effect in mouse TA. In all other species, glycolytic capacity was decreased and reference enzymes of aerobic-oxidative pathways were increased. Rabbit TA displayed the highest increment in oxidative capacity with approximately three-fold increases in CS and HADH and eleven-fold increases in HBDH. Different responses were also observed for HK. In some cases, the extent of adaptation appeared to be independent of the initial enzyme activity levels, while in other cases it appeared to follow an order which corresponded to the size of the animals. Thus, there exist species-specific ranges of adaptation and adaptive alterations in one species may not necessarily reflect the adaptive response of another species.
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PMID:Specific effects of low-frequency stimulation upon energy metabolism in tibialis anterior muscles of mouse, rat, guinea pig and rabbit. 297 3