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  • 1
    ISSN: 1619-7089
    Keywords: Radiolabeled free fatty acids ; Free radicals ; Myocardial metabolism ; Allopurinol ; Superoxide dismutase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In a canine model of reversible global ischemia, the residual quantity of 123I was assessed following a bolus injection of 15-p-(123I)-iodophenyl pentadecanoic acid (123I-IPPA). This technique was used to assess changes in free fatty acid metabolism following the utilization of three cardioplegic formulations. Cardioplegic arrest was initiated with Tyers' iso-osmolar (IO) solution (Group A); IO+superoxide dismutase (SOD) (Group B) and IO+allopurinol (Group C). Pre and post operative scanning were completed with 2–5 mCi 123I-IPPA. Clearance was assessed by IPPA time activity curve analysis generating t 1/2 (half lives in min) for the early and late phases of the curve. The assessment between groups demonstrated that the elimination of 123I-IPPA products (early phase) was faster from the lateral wall in groups B and C versus group A (14±12 min, 13±9 min and 24±10 min, respectively). The elimination of IPPA (late phase) was also faster from the lateral wall in groups B and C when compared to group A (240±270 min, 132±85 min and 416±238 min). Examining the changes between control and postoperative values for each area of the left ventricle within each group demonstrated no significant, changes for groups B and C. Group A, however, demonstrated significantly increased t 1/2 values for the lateral wall (early and late phases) and the apical wall (late phase). From this study it can be concluded that following 2 h of reversible global ischemia and reperfusion, the assessment of turnover of 123I-IPPA can be used to differentiate the effectiveness of various cardioplegic formulations. It appears that cardioplegic solutions supplemented with allopurinol and SOD (groups B and C) may be better able to protect myocardial fatty acid metabolism compared to Tyers' iso-osmolar solution (group A).
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Cultured bovine adrenocortical cells were previously shown to be functionally deficient in selenium and vitamin E when grown in medium supplemented with fetal bovine serum. In the present experiments, the lack of significant bioavailable amounts of selenium in the medium was demonstrated by the finding of only low levels of glutathione peroxidase in the cultured cells (0.008 U/mg protein compared with 0.045 U/mg protein in fresh adrenocortical tissue). When 20 nM selenium as selenite was added to the cultured adrenocortical cells, glutathione peroxidase activity increased continuously over 72 h, with a total increase of about eightfold over this period. Over the same time-course, the highest concentration of cumene hydroperoxide tolerated by the cells without cell death increased progressively from 10 μM to 50 μM. Addition of 1μM α-tocopherol also increased the amount of cumene hydroperoxide tolerated to 50 μM. Cell death was measured by cloning efficiency after removal of cumene hydroperoxide. Addition of either selenium or α-tocopherol had little effect on the growth rate of the cells over six passages, even when residual vitamin E was removed from the serum by extraction with ether and residual low molecular weight selenium compounds were removed by dialysis. It is concluded that combined deficiency of selenium and vitamin E, at least in the presence of other components of fetal bovine serum, has little effect on the ability of the cells to survive under normal conditions, as evidenced by continued long-term proliferation. However, the low levels of glutathione peroxidase resulting from selenium deficiency cause an increase susceptibility to peroxide-mediated toxicity. The combined deficiency of selenium and vitamin E impairs the ability of cells to survive under adverse conditions, as well as altering mitochondrial functions, as previously demonstrated.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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