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Toxicity and Cell Cycle Effects of Synthetic 8-Prenylnaringenin and Derivatives in Human Cells

2004; Karger Publishers; Volume: 71; Issue: 1 Linguagem: Inglês

10.1159/000076261

1423-0313

Sergey V. Tokalov, Yvonne Henker, Pia Schwab, Peter Metz, Herwig O. Gutzeit,

Powdery Mildew Fungal Diseases

The estrogenic flavanone <i>rac</i>-8-prenylnaringenin (8-PN) and 3 derivatives (<i>rac</i>-7-(O-prenyl)naringenin-4′-acetate (7-O-PN), <i>rac</i>-5-(O-prenyl)naringenin-4′,7-diacetate (5-O-PN), and <i>rac</i>-6-(1,1-dimethylallyl)naringenin (6-DMAN) were prepared by chemical synthesis and analyzed with respect to their toxicity and possible cell cycle effects in human acute myeloid leukemia (HL-60) cells. With the exception of 5-O-PN, all the other naringenins showed only weak toxic effects at concentrations below 50 µmol/l. A cell cycle analysis over several cell generations up to 4 days was carried out using the fluorescent dye carboxyfluorescein diacetate N-succinimidyl ester (CFSE) followed by propidium iodide (PI) staining at the end of the experiment. The well-studied flavonol quercetin was included in the analysis as a reference substance. All flavonoids affected cell proliferation, but the extent and the resulting changes in the proliferation pattern were specific for each substance. In contrast to the radical scavenging activity of quercetin, the tested flavanones showed no anti-oxidative properties using several different test systems. Similarly, the mitochondrial membrane potential (ΔΨm) was hardly effected by these compounds, while both menadione and quercetin strongly reduced the potential after 1 h of treatment. The reported chemical modification of interesting lead substances (like the strongly estrogenic 8-PN) presents a promising approach to modulate the properties of a relevant substance in a pharmacologically desirable way. The low toxicity and weak cytostatic properties of the tested naringenin derivatives is encouraging for further studies on known naringenin target molecules.