Sterile inflammation in hepatic ischemia/reperfusion injury: Present concepts and potential therapeutics

作者：Rowan F. van Golen, Megan J. Reiniers, Pim B. Olthof, Thomas M. van Gulik, Michal Heger · 发表于：Journal of Gastroenterology and Hepatology · 年份：2012 · DOI：10.1111/jgh.12072 · 被引用次数：162 · 研究领域：Organ Transplantation Techniques and Outcomes、Heme Oxygenase-1 and Carbon Monoxide、Adenosine and Purinergic Signaling

Ischemia and reperfusion (I/R) injury is an often unavoidable consequence of major liver surgery and is characterized by a sterile inflammatory response that jeopardizes the viability of the organ. The inflammatory response results from acute oxidative and nitrosative stress and consequent hepatocellular death during the early reperfusion phase, which causes the release of endogenous self-antigens known as damage-associated molecular patterns (DAMPs). DAMPs, in turn, are indirectly responsible for a second wave of reactive oxygen and nitrogen species (ROS and RNS) production by driving the chemoattraction of various leukocyte subsets that exacerbate oxidative liver damage during the later stages of reperfusion. In this review, the molecular mechanisms underlying hepatic I/R injury are outlined, with emphasis on the interplay between ROS/RNS, DAMPs, and the cell types that either produce ROS/RNS and DAMPs or respond to them. This theoretical background is subsequently used to explain why current interventions for hepatic I/R injury have not been very successful. Moreover, novel therapeutic modalities are addressed, including MitoSNO and nilotinib, and metalloporphyrins on the basis of the updated paradigm of hepatic I/R injury.