Abstract
The effects of pyrimido-pyrimidine derivatives (dipyridamole, RA-642, and RA-233) on lipid peroxidation, using d-α-tocopherol as standard, were studied in enriched membrane fractions from human and rat hepatocytes. Equimolar concentrations of ferrous sulfate and ascorbic acid were used to induce lipid peroxidation. The amount of peroxidized lipids observed in membrane fractions from human liver was smaller than in those from rat liver. In both species, however, pyrimido-pyrimidine derivatives, except for RA-233 in rat liver, inhibited lipid peroxidation dose-dependently in the following sequence: RA-642 > dipyridamole > d-α-tocopherol RA-233.
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Abbreviations
- Cyt C:
-
cytochrome C
- ED-50:
-
effective concentration 50%
- FeAs:
-
ferrous sulfate/ascorbic acid
- GMN:
-
glomerulonephritis
- HA:
-
hydroxyl anions
- IC-50:
-
inhibitory concentration, 50%
- MDA:
-
malondialdehyde
- NBT:
-
nitroblue tetrazolium
- ODFR:
-
oxygen-derived free radicals
- PTRA:
-
post-thrombolysis re-perfusion arrhythmias
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de la Cruz, J.P., Carrasco, T., Ortega, G. et al. Inhibition of ferrous-induced lipid peroxidation by pyrimido-pyrimidine derivatives in human liver membranes. Lipids 27, 192–194 (1992). https://doi.org/10.1007/BF02536177
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DOI: https://doi.org/10.1007/BF02536177