Author/Authors :
Stephen M. Altmann، نويسنده , , Andrey Muryshev، نويسنده , , Elisa Fossale، نويسنده , , Michele M. Maxwell، نويسنده , , Francine N. Norflus، نويسنده , , Jonathan Fox.، نويسنده , , Steven M. Hersch، نويسنده , , Anne B. Young، نويسنده , , Marcy E. MacDonald، نويسنده , , Ruben Abagyan and Jens Schneider-Mergener، نويسنده , , Aleksey G. Kazantsev، نويسنده ,
Abstract :
Poly (ADP-ribose) polymerase (PARP1) is a nuclear protein that, when overactivated by oxidative stress-induced DNA damage, ADP ribosylates target proteins leading to dramatic cellular ATP depletion. We have discovered a biologically active small-molecule inhibitor of PARP1. The discovered compound inhibited PARP1 enzymatic activity in vitro and prevented ATP loss and cell death in a surrogate model of oxidative stress in vivo. We also investigated a new use for PARP1 inhibitors in energy-deficient cells by using Huntingtonʹs disease as a model. Our results showed that insult with the oxidant hydrogen peroxide depleted cellular ATP in mutant cells below the threshold of viability. The protective role of PARP1 inhibitors against oxidative stress has been shown in this model system.
