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1.
Biokhimiia ; 52(5): 715-9, 1987 May.
Article in Russian | MEDLINE | ID: mdl-3593796

ABSTRACT

It was shown that hydrophilic benzo- and naphthoquinones stimulate the cyanide-resistant respiration in liver and muscle mitochondria when succinate or NADH and glutamate or malate are used as oxidation substrates. The substrate-dependent oxygen uptake in the presence of cyanide is initiated by menadione, vicasol, 1.2-naphthoquinone, coenzyme Q0 and duroquinone. Rotenone and antimycin A do not inhibit the cyanide-resistant respiration. Oxidation of glutamate and malate in the course of CN-resistant respiration is inhibited by ortho- and bathophenanthroline and p-chloromercurybenzoate, whereas succinate oxidation by tenoyltrifluoroacetone, carboxin and pentachlorophenol. Superoxide dismutase, Cu2+ and catalase inhibit the CN-resistant respiration in the presence of quinones. Addition of catalase to the experimental cell causes O2 release.


Subject(s)
Cyanides/pharmacology , Mitochondria, Heart/metabolism , Mitochondria, Liver/metabolism , Oxygen Consumption/drug effects , Quinones/pharmacology , Animals , Electron Transport , In Vitro Techniques , Kinetics , Mitochondria, Heart/drug effects , Mitochondria, Liver/drug effects , Oxidation-Reduction , Rats , Stimulation, Chemical
2.
Ukr Biokhim Zh (1978) ; 56(2): 204-7, 1984.
Article in Russian | MEDLINE | ID: mdl-6326357

ABSTRACT

Polycationic peptide antibiotics, polymixins B and M, are studied for their effect on oxygen uptake by rat liver mitochondria. They both inhibit the process at state 3 and 3p according to Chance. Low concentrations of polymixin M do not affect oxygen uptake by mitochondria at state 4, but its high concentrations inhibit it. Concentration dependence of polymixin B effect on mitochondria at state 4 is of a bell-like character. Competitive interrelations are found between polymixins M and B in their effect on mitochondria at state 4. Chromatography reveals differences in peptide mobility in a thin layer. It is supposed that polymixin inhibition of oxygen uptake by mitochondria is associated with a disordering effect of the polymixins on the membrane structure during peptide binding to the lipid phase of the membranes. Low concentrations of polymixin B are likely to promote an increase in membrane permeability of mitochondria at state 4.


Subject(s)
Intracellular Membranes/drug effects , Mitochondria, Liver/drug effects , Oxygen Consumption/drug effects , Polymyxins/pharmacology , Animals , Biological Transport/drug effects , Chemical Phenomena , Chemistry , Depression, Chemical , In Vitro Techniques , Mitochondria, Liver/metabolism , Polymyxin B/pharmacology , Rats
3.
Biofizika ; 27(6): 1057-60, 1982.
Article in Russian | MEDLINE | ID: mdl-7159616

ABSTRACT

Preincubation of mitochondria treated with chelator of non-heme ferrum o-phenanthroline (0,067-0,267) for 20 min at 18 degrees C in the constant magnetic field of 330 mT brings about a decrease of the intensity of their uncoupled respiration with NAD-dependent substrates by 15-20% as compared to similar mitochondria preparations without the magnetic field effect. The latter is not realized during conjugated respiration with NAD-dependent substrates at uncoupled respiration with succinate, and in the absence of o-phenanthroline as well.


Subject(s)
Mitochondria, Liver/metabolism , Oxygen Consumption/drug effects , Phenanthrolines/pharmacology , Animals , Kinetics , Magnetics , Mitochondria, Liver/drug effects , Rats
4.
Biofizika ; 26(6): 1100-2, 1981.
Article in Russian | MEDLINE | ID: mdl-6274432

ABSTRACT

Effect of polymyxin B on the movement of K+ and H+ in polymyxin-sensitive cells of E. coli under different metabolic states has been studied. It was shown that polymyxin B induced the efflux of K+, decreased the efflux of H+ and inhibited the consumption of oxygen in bacterial cells. The effect of antibiotic on ion movement was independent of respiratory conditions. It was suggested that polymyxin B increased ion permeability and destroyed lipid-protein interactions of the respiratory chain simultaneously.


Subject(s)
Cell Membrane Permeability/drug effects , Escherichia coli/metabolism , Polymyxin B/pharmacology , Polymyxins/pharmacology , Escherichia coli/drug effects , Hydrogen-Ion Concentration , Oxygen Consumption/drug effects , Potassium/metabolism
5.
Biofizika ; 26(5): 889-91, 1981.
Article in Russian | MEDLINE | ID: mdl-6274424

ABSTRACT

Effect of polymyxin B on the planar bilayer lipid membranes (BLM) formed from synthetic phosphatidic acid has been studied. The addition of cholesterol to phospholipid in molar ratio 1 : 2 was followed by an increase of BLM conductance from 2 x 10(-8) to 3 x 10(-7) Ohm-1 cm-2. It was suggested that the observed increase of conductance was due to the fluidity of the membrane matrix in the presence of cholesterol. It was shown that 10(-6)--10(-5) M polymyxin slightly affected the conductance of BLM from phosphatidic acid. It was found that polymyxin increased conductance of negatively charged BLM modified by palmitic acid from 10(-8) to 10(-6) Ohm-1 cm-2.


Subject(s)
Ions/metabolism , Lipid Bilayers , Polymyxin B/pharmacology , Polymyxins/pharmacology , Electrochemistry , Palmitic Acid , Palmitic Acids , Permeability , Phosphatidic Acids
6.
Biokhimiia ; 45(9): 1682-4, 1980 Sep.
Article in Russian | MEDLINE | ID: mdl-6264969

ABSTRACT

the mechanism of the effect of the peptide antibiotic polymixin B on respiration of rat liver mitochondria was studied. It was shown that polymixin B at concentrations of (1,6--2,0) . 10(-3) M inhibits mitochondrial respiration in state 3 and 3u irrespective of the oxidation substrate used and activates oxygen consumption in state 4 at lower concentrations. It is assumed that the antibiotic affects mitochondrial respiration by changing the ionic permeability of the membranes.


Subject(s)
Mitochondria, Liver/metabolism , Oxygen Consumption/drug effects , Polymyxin B/pharmacology , Polymyxins/pharmacology , Animals , In Vitro Techniques , Intracellular Membranes/drug effects , Kinetics , Mitochondria, Liver/drug effects , Permeability , Rats
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