The role of NADPH oxidase and neuronal nitric oxide synthase in zinc-induced poly (ADP-ribose) polymerase activation and cell death in cortical culture

YH Kim, JY Koh - Experimental neurology, 2002 - Elsevier
Experimental neurology, 2002Elsevier
In the present study, we examined the role and the mechanism of poly (ADP-ribose)
polymerase (PARP) and poly (ADP-ribose) glycohydrolase (PARG) activation in zinc-
induced cell death in cortical culture. After brief exposure to 400 μM zinc, cortical cells
exhibited DNA fragmentation, increased poly (ADP-ribosyl) ation, and decreased levels of
nicotinamide adenine dinucleotide (NAD) and ATP and subsequently underwent cell death.
Inhibitors of PARP/PARG attenuated both zinc-induced NAD/ATP depletion and cell death …
In the present study, we examined the role and the mechanism of poly(ADP-ribose) polymerase (PARP) and poly(ADP-ribose) glycohydrolase (PARG) activation in zinc-induced cell death in cortical culture. After brief exposure to 400 μM zinc, cortical cells exhibited DNA fragmentation, increased poly(ADP-ribosyl)ation, and decreased levels of nicotinamide adenine dinucleotide (NAD) and ATP and subsequently underwent cell death. Inhibitors of PARP/PARG attenuated both zinc-induced NAD/ATP depletion and cell death, thereby implicating the PARP/PARG cascade in these processes. The zinc-inducible enzymes NADPH oxidase and neuronal nitric oxide synthase (nNOS) contributed to PARP activation as their inhibitors attenuated zinc-induced poly(ADP-ribosyl)ation. Levels of nitric oxide and nitrites increased following zinc exposure, consistent with NOS activation. In addition, Western blots and RT-PCR analysis revealed that protein and mRNA levels of nNOS specifically increased following zinc exposure in a manner similar to that of NADPH oxidase. The present study demonstrates that induction of NADPH oxidase and nNOS actively contributes to PARP/PARG-mediated NAD/ATP depletion and cell death induced by zinc in cortical culture.
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