selenide, but not selenite, inhibits 5-lipoxygenase

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  1. Roger

    Roger Guest

    Biochemistry. 1996 Jul 2;35(26):8511-6.

    Selenite incubated with NADPH and mammalian thioredoxin reductase yields selenide, which inhibits
    lipoxygenase and changes the electron spin resonance spectrum of the active site iron.

    Bjornstedt M, Odlander B, Kuprin S, Claesson HE, Holmgren A. Medical Nobel Institute for
    Biochemistry, Karolinska Institutet, Stockholm, Sweden.

    Selenite and selenodiglutathione (GS-Se-SG) efficiently inhibited 5-lipoxygenase activity in
    sonicates of human monoclonal B-lymphocytes. The apparent IC50 of GS-Se-SG was 0.5 microM. The
    inhibitory effect of these compounds was observed within 10 min of incubation. In order to elucidate
    if the mechanism of inhibition by these compounds was result of direct interference with
    lipoxygenase or indirectly mediated by cellular factors, pure 15-lipoxygenase from soybeans was used
    as a model system for enzyme assays and electron spin resonance (ESR) measurements. Incubation of
    15-lipoxygenase with a mixture of human placenta thioredoxin reductase (TR) or calf-thymus TR,
    selenite, and NADPH blocked the activity of the enzyme. Neither TR and NADPH nor selenite inhibited
    soybean lipoxygenase when incubated separately. These results suggest that selenite must be reduced
    to selenide in order to inhibit 5- and 15-lipoxygenase activities. Preincubation anaerobically of
    15-lipoxygenase with chemically generated selenide (6 microM) resulted in a strong inhibition of
    activity, in assays with arachidonic acid in the presence of oxygen. In contrast, selenide exposed
    to air prior to preincubation did not inhibit the enzyme. Since selenide is known to be efficiently
    oxidized by oxygen and to form elemental selenium the results evidence that selenide was the
    inhibitor of lipoxygenase activity in the anaerobic preincubations. After incubation with TR, NADPH,
    and selenite or with chemically generated selenide, the ESR spectrum of 15-lipoxygenase changed: the
    dominant axial component with a peak at g = 6.1 decreased, and a rhombic form with a feature at g =
    4.28 grew. The results suggest that selenide produced by the reduction of selenite reduces the
    active site iron to the ESR invisible state and changes the ligation geometry of the oxidized form.