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   <subfield code="a">Effects of Menadione, Hydrogen Peroxide, and Quercetin on Apoptosis and Delayed Luminescence of Human Leukemia Jurkat T-Cells</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Irina Baran, Constanta Ganea, Agata Scordino, Francesco Musumeci, Vincenza Barresi, Salvatore Tudisco, Simona Privitera, Rosaria Grasso, Daniele Condorelli, Ioan Ursu, Virgil Baran, Eva Katona, Maria-Magdalena Mocanu, Marisa Gulino, Raluca Ungureanu, Mihaela Surcel, Cornel Ursaciuc]</subfield>
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   <subfield code="a">Menadione (MD) is an effective cytotoxic drug able to produce intracellularly large amounts of superoxide anion. Quercetin (QC), a widely distributed bioflavonoid, can exert both antioxidant and pro-oxidant effects and is known to specifically inhibit cell proliferation and induce apoptosis in different cancer cell types. We have investigated the relation between delayed luminescence (DL) induced by UV-laser excitation and the effects of MD, hydrogen peroxide, and QC on apoptosis and cell cycle in human leukemia Jurkat T-cells. Treatments with 500μM H2O2 and 250μM MD for 20min produced 66.0±4.9 and 46.4±8.6% apoptotic cell fractions, respectively. Long-term (24h) pre-exposure to 5μM, but not 0.5μM QC enhanced apoptosis induced by MD, whereas short-term (1h) pre-incubation with 10μM QC offered 50% protection against H2O2-induced apoptosis, but potentiated apoptosis induced by MD. Since physiological levels of QC in the blood are normally less than 10μM, these data can provide relevant information regarding the benefits of flavonoid-combined treatments of leukemia. All the three drugs exerted significant effects on DL. Our data are consistent with (1) the involvement of Complex I of the mitochondrial respiratory chain as an important source of delayed light emission on the 10μs-10ms scale, (2) the ability of superoxide anions to quench DL on the 100μs-10ms scale, probably via inhibition of reverse electron transfer at the Fe/S centers in Complex I, and (3) the relative insensitivity of DL to intracellular OH• and H2O2 levels.</subfield>
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   <subfield code="u">Department of Biophysics, &quot;Carol Davila” University of Medicine and Pharmacy, 8 Eroii Sanitari, 050474, Bucharest, Romania</subfield>
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