Abstract
Oxidative and nitrosative stress triggers DNA strand breakage, which then activates the nuclear enzyme poly(ADP-ribose) polymerase (PARP). One of the key triggers of DNA single strand breakage in pathophysiological conditions is peroxynitrite, a reactive species produced from the reaction of nitric oxide and superoxide. Activation of PARP can dramatically lower the intracellular concentration of its substrate, nicotinamide adenine dinucleotide, thus slowing the rate of glycolysis, electron transport and subsequently ATP formation. This process can result in cell dysfunction and cell death. Here we review the role of PARP in various forms of liver injury.
Original language | English (US) |
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Pages (from-to) | 2903-2910 |
Number of pages | 8 |
Journal | Current Pharmaceutical Design |
Volume | 12 |
Issue number | 23 |
DOIs | |
State | Published - Aug 2006 |
Externally published | Yes |
Keywords
- Hepatic
- Liver
- Nitric oxide
- Peroxynitrite
- Reperfusion
- Sepsis
- Superoxide
ASJC Scopus subject areas
- Pharmacology
- Drug Discovery