atractyloside and octanoic-acid

atractyloside has been researched along with octanoic-acid* in 2 studies

Other Studies

2 other study(ies) available for atractyloside and octanoic-acid

ArticleYear
Evidence that the major metabolites accumulating in medium-chain acyl-CoA dehydrogenase deficiency disturb mitochondrial energy homeostasis in rat brain.
    Brain research, 2009, Nov-03, Volume: 1296

    Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is an inherited metabolic disorder of fatty acid oxidation in which the affected patients predominantly present high levels of octanoic (OA) and decanoic (DA) acids and their glycine and carnitine by-products in tissues and body fluids. It is clinically characterized by episodic encephalopathic crises with coma and seizures, as well as by progressive neurological involvement, whose pathophysiology is poorly known. In the present work, we investigated the in vitro effects of OA and DA on various parameters of energy homeostasis in mitochondrial preparations from brain of young rats. We found that OA and DA markedly increased state 4 respiration and diminished state 3 respiration as well as the respiratory control ratio, the mitochondrial membrane potential and the matrix NAD(P)H levels. In addition, DA-elicited increase in oxygen consumption in state 4 respiration was partially prevented by atractyloside, indicating the involvement of the adenine nucleotide translocator. OA and DA also reduced ADP/O ratio, CCCP-stimulated respiration and the activities of respiratory chain complexes. The data indicate that the major accumulating fatty acids in MCADD act as uncouplers of oxidative phosphorylation and as metabolic inhibitors. Furthermore, DA, but not OA, provoked a marked mitochondrial swelling and cytochrome c release from mitochondria, reflecting a permeabilization of the inner mitochondrial membrane. Taken together, these data suggest that OA and DA impair brain mitochondrial energy homeostasis that could underlie at least in part the neuropathology of MCADD.

    Topics: Acyl-CoA Dehydrogenase; Animals; Atractyloside; Brain; Caprylates; Cytochromes c; Decanoic Acids; Electron Transport; Enzyme Inhibitors; Fatty Acids; Homeostasis; Membrane Potential, Mitochondrial; Mitochondria; Mitochondrial ADP, ATP Translocases; Mitochondrial Membranes; NADP; Oxygen Consumption; Rats; Rats, Wistar

2009
Mechanism of the stimulation of respiration by fatty acids in rat liver.
    FEBS letters, 1985, Dec-02, Volume: 193, Issue:2

    The mechanism of stimulation of hepatic respiration by fatty acids was studied in isolated rat hepatocytes. Stimulation of respiration by fatty acids varied from about 35% to about 105% depending on chain length. The stimulatory effect of octanoate (1 mM) or oleate (0.5 mM) was prevented by oligomycin (2 micrograms/ml). With carboxyatractyloside (100 microM) and ouabain (2 mM) the stimulation of respiration was partially inhibited (by 50-70 and 50-60%, respectively). From these results it can be concluded that the increased rate of respiration after addition of fatty acids is coupled to ATP synthesis. A large part (50-60%) of this ATP is utilized by the (Na+ + K+)-ATPase.

    Topics: 2,4-Dinitrophenol; Adenine Nucleotides; Animals; Atractyloside; Caprylates; Dinitrophenols; Energy Metabolism; Fatty Acids; In Vitro Techniques; Liver; Male; Oleic Acid; Oleic Acids; Oligomycins; Ouabain; Oxygen Consumption; Rats; Rats, Inbred Strains

1985