Effect of garlic-derived organosulfur compounds on mitochondrial function and integrity in isolated mouse liver mitochondria |
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Authors: | Andres A. Caro Luke W. AdlongSamuel J. Crocker Michael W. GardnerEmily F. Luikart Liz U. Gron |
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Affiliation: | Chemistry Department, Hendrix College, Conway, AR, United States |
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Abstract: | The objectives of this work were to evaluate the direct effects of diallysulfide (DAS) and diallyldisulfide (DADS), two major organosulfur compounds of garlic oil, on mitochondrial function and integrity, by using isolated mouse liver mitochondria in a cell-free system. DADS produced concentration-dependent mitochondrial swelling over the range 125–1000 μM, while DAS was ineffective. Swelling experiments performed with de-energized or energized mitochondria showed similar maximal swelling amplitudes. Cyclosporin A (1 μM), or ethylene glycol-bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid (EGTA, 1 mM) were ineffective in inhibiting DADS-induced mitochondrial swelling. DADS produced a minor (12%) decrease in mitochondrial membrane protein thiols, but did not induce clustering of mitochondrial membrane proteins. Incubation of mitochondria with DADS (but not DAS) produced an increase in the oxidation rate of 2′,7′ dichlorofluorescein diacetate (DCFH-DA), together with depletion of reduced glutathione (GSH) and increased lipid peroxidation. DADS (but not DAS) produced a concentration-dependent dissipation of the mitochondrial membrane potential, but did not induce cytochrome c release. DADS-dependent effects, including mitochondrial swelling, DCFH-DA oxidation, lipid peroxidation and loss of mitochondrial membrane potential, were inhibited by antioxidants and iron chelators. These results suggest that DADS causes direct impairment of mitochondrial function as the result of oxidation of the membrane lipid phase initiated by the GSH- and iron-dependent generation of oxidants. |
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Keywords: | OSCs, organosulfur compounds DAS, diallyl sulfide DADS, diallyl disulfide DATS, diallyl trisulfide EGTA, ethylene glycol-bis(2-aminoethylether)-N,N,N&prime ,N&prime -tetraacetic acid DCFH-DA, 2&prime ,7&prime -dichlorofluorescin diacetate GSH, reduced glutathione GSSG, glutathione disulfide Hepes, N-(2-hydroxyethyl) piperazine-N&prime -(2-ethane sulfonic acid) Trolox, 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid buffer A 125 mM sucrose 65 mM KCl 10 mM N-(2-hydroxyethyl) piperazine-N&prime -(2-ethane sulfonic acid)-KOH 20 μM Ca2+ and pH 7.2 CsA, cyclosporin A MOPS, 3-(N-Morpholino)propanesulfonic acid ROS, reactive oxygen species TBARS, thiobarbituric acid-reactive substances TBA, thiobarbituric acid MDA, malondialdehyde DTNB, 5&prime -dithiobis(2-nitrobenzoid acid) FSC, forward scatter SSC, side scatter NAO, 10-N-nonyl acridine orange Pi, inorganic phosphate PMC, 2,2,5,7,8-pentamethyl-6-chromanol FCCP, 4-(trifluoromethoxy)phenylhydrazone |
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