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Abstract Details

NADPH Treatment Decreases C6 Glioma Cell Survival by Increasing oxidative stress
Neuro-oncology
IN10 - (-)
007
NADPH (nicotinamide adenine dinucleotide phosphate, reduced form) plays pivotal roles in antioxidation and reductive biosynthesis. However, the effect of NADPH treatment on cell survival is unknown. In this study, we determined the effect of NADPH treatment on the survival of glioma cells.
Lactate dehydrogenase (LDH) assay;Determinations of nuclear condensation;Flow cytometry-based PI staining;Trypan blue Assay;Dihydroethidium (DHE) assay;Data were assessed by one-way ANOVA, followed by Student-Newman-Keuls post hoc test.
Treatment of C6 glioma cells with as low as 1 [mu]M NADPH for 24 hrs induced a significant decrease in the survival of the glioma cells, while NADPH treatment had no effect on the survival of primary astrocyte cultures. We also found that NADPH treatment increased intracellular oxidative stress. Three antioxidants and the NADPH oxidase inhibitor, apocynin, attenuated the effect of NADPH. Poly(ADP-ribose)polymerase (PARP) activation appears to be a downstream effector of the oxidative stress, since PARP inhibitors reduced the effect of NADPH. Calcium chelator, BAPTAAM,also attenuated the effect of NADPH.
Collectively,these data indicate a novel property of NADPH: NADPH decreases glioma cell survival by inducing the NADPH oxidase-dependent increase in oxidative stress and by PARP activation. These results also suggest a potential therapeutic effect of NADPH on gliomas.
Authors/Disclosures

PRESENTER
No disclosure on file
Takeshi Sakata Takeshi Sakata has received personal compensation for serving as an employee of Mitsubishi Tanabe.
No disclosure on file
No disclosure on file
No disclosure on file
John W. Rose, MD, FAAN (Imaging and Neurosciences Center) The institution of Dr. Rose has received research support from National Multiple Sclerosis Society. The institution of Dr. Rose has received research support from Guthy Jackson Charitable Foundation. The institution of Dr. Rose has received research support from NIH . The institution of Dr. Rose has received research support from VA. The institution of Dr. Rose has received research support from Biogen. The institution of Dr. Rose has received research support from Friends of MS. Dr. Rose has received intellectual property interests from a discovery or technology relating to health care.