PubMed · 1985 · 31 citations · 0 references
Life SciencesMedicinal ChemistryPharmacologyBiochemical PharmacologyExperimental PharmacologyPharmacodynamicsAntioxidant DefenseLipid MetabolismLipid PeroxidationMedicinal PlantsPlatelet PhysiologyAntioxidants In LipidsFree Radical ScavengingMalondialdehyde FormationThiobarbituric Acid Reactive Substances
Sixteen natural phenolics and semisynthetic derivatives thereof, including silymarin, flavonoids, catechines and phenolic acids, together with 6 standard drug substances with anti-inflammatory, antioxidant and peroxide radical scavenging properties have been tested in an in vitro model using human platelets for their inhibitory action against N-ethyl maleimide-induced lipid peroxidation. The malondialdehyde formed during the reaction was estimated by means of the thiobarbituric acid method. In all compounds tested, the inhibitory action was clearly dose-dependent; IC50 values were calculated from the dose-activity curves. The IC50 found ranged from between 1.47 nM and approximately 900 mM.