Key result
Addition of the PARP inhibitor 3-aminobenzamide prior to H(2)O(2) exposure delayed cell death beyond 24 hours and increased cell survival by approximately 25%.
Inhibition of PARP-1 with 3-aminobenzamide maintains intracellular ATP levels and shifts H2O2-induced cell death from necrosis to apoptosis, increasing overall cell survival in an in vitro neuronal trauma model.
PARP-1 activation may deplete NAD after neural trauma; hypothesis-generating for oxidative stress therapies, leaves clinical translation open.
Trauma to the nervous system triggers responses that include oxidative stress due to the generation of reactive oxygen species (ROS). DNA is a major macromolecular target of ROS, and ROS-induced DNA strand breaks activate poly(ADP-ribose)polymerase-1 (PARP-1). Upon activation PARP-1 uses NAD(+) as a substrate to catalyze the transfer of ADP-ribose subunits to a host of nuclear proteins. In the face of extensive DNA strand breaks, PARP-1 activation can lead to depletion of intracellular NAD(P)(H) pools, large decreases in ATP, that threaten cell survival. Accordingly, inhibition of PARP-1 activity after acute oxidative injury has been shown to increase cell survival. When NGF-differentiated PC12 cells, an in vitro neuronal model, are exposed to H(2)O(2) there is increased synthesis of poly ADP-ribose and decreases in intracellular NAD(P)(H) and ATP. Addition of the chemical PARP inhibitor 3-aminobenzamide (AB) prior to H(2)O(2) exposure blocks the synthesis of poly ADP-ribose and maintains intracellular NAD(P)(H) and ATP levels. H(2)O(2) injury is characterized by an immediate, necrotic cell death 2h after injury and a delayed apoptotic-like death 12-24h after injury. This apoptotic-like death is characterized by apoptotic membrane changes and apoptotic DNA fragmentation but is not associated with measurable caspase-3 activity. AB delays cell death beyond 24h and increases cell survival by approximately 25%. This protective effect is accompanied by significantly decreased necrosis and the apoptotic-like death associated with H(2)O(2) exposure. AB also restores caspase-3 which can be attributed to the activation of the upstream activator of caspase-3, caspase-9. Thus, the maintenance of intracellular ATP levels associated with PARP-1 inhibition shifts cell death from necrosis to apoptosis and from apoptosis to cell survival. Furthermore, the shift from necrosis to apoptosis may be explained, in part, by an energy-dependent activation of caspase-9.
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Cole et al. (2004) studied Neuronal trauma and oxidative injury. 3-aminobenzamide (AB) vs. H(2)O(2) exposure without AB was evaluated on Cell survival. Addition of the PARP inhibitor 3-aminobenzamide prior to H(2)O(2) exposure delayed cell death beyond 24 hours and increased cell survival by approximately 25%.
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