Browsing by Author "SOTO, U"

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    DETECTION OF AN ATPASE ACTIVITY IN RAT-LIVER PEROXISOMES
    (1988) DELVALLE, R; SOTO, U; NECOCHEA, C; LEIGHTON, F
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    LARGE CATION-SELECTIVE PORES FROM RAT-LIVER PEROXISOMAL MEMBRANES INCORPORATED TO PLANAR LIPID BILAYERS
    (1986) LABARCA, P; WOLFF, D; SOTO, U; NECOCHEA, C; LEIGHTON, F
    Fusion of a highly purified fraction of rat liver peroxisomal membranes to planar lipid bilayers incorporates large, cation-selective voltage-dependent pores. The PK/PCl ratio of these pores estimated in KCl gradients, is close to 4. The pores display several conductance states and spend most of the time open at voltages near 0 mV, closing at more positive and negative voltages. At voltages near 0 mV the most frequent open state has a conductance of 2.4 nS in 0.3 M KCl. At voltages more positive and more negative than 10 mV the most frequent open state displays a conductance of 1.2 nS in 0.3 M KCl. With these results pore diameters of 3 and 1.5 nm, respectively, can be estimated. We suggest that these pores might account for the unusually high permeability of peroxisomes to low molecular weight solutes. Fusion also incorporates a perfectly anion-selective, two-open states channel with conductances of 50 and 100 pS in 0.1 m KCl.
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    PEROXISOMAL FATTY-ACID OXIDATION AND INHIBITORS OF THE MITOCHONDRIAL CARNITINE PALMITOYLTRANSFERASE-I IN ISOLATED RAT HEPATOCYTES
    (1992) SKORIN, C; NECOCHEA, C; JOHOW, V; SOTO, U; GRAU, AM; BREMER, J; LEIGHTON, F
    Fatty acid oxidation was studied in the presence of inhibitors of carnitinic palmitoyltransferase I (CPT I), in normal and in peroxisome-proliferated rat hepatocytes. The oxidation decreased in mitochondria, as expected, but in peroxisomes it increased. These two effects were seen, in variable proportions, with (+)-decanoylcarnitine, 2-tetradecylglycidic acid (TDGA) and etomoxir. The decrease in mitochondrial oxidation (ketogenesis) affected saturated fatty acids with 12 or more carbon atoms, whereas the increase in peroxisomal oxidation (H2O2 production) affected saturated fatty acids with 8 or more carbon atoms. The peroxisomal increase was sensitive to chlorpromazine, a peroxisomal inhibitor. To study possible mechanisms, palmitoyl-, octanoyl- and acetyl-carnitine acyltransferase activities were measured, in homogenates and in subcellular fractions from control and TDGA-treated cells. The palmitoylcarnitine acyltransferase was inhibited, as expected, but the octanoyltransferase activity also decreased. The CoA derivative of TDGA was synthesized and tentatively identified as being responsible for inhibition of the octanoylcarnitine acyltransferase. These results show that inhibitors of the mitochondrial CPT 1 may also inhibit the peroxisomal octanoyl transferase; they also support the hypothesis that the octanoyltransferase has the capacity to control or regulate peroxisomal fatty acid oxidation.