Objective: We aim to investigate the role of aldose reductase (AR) in hepatic ischemia-reperfusion injury (IRI) of normal and fatty livers and to explore the underlying mechanisms.
Background: Hepatic IRI is a typical inflammatory response during liver surgery. It contributes to liver graft failure or nonfunction after transplantation. Increasing evidence implicates that AR plays a key role in a number of inflammatory diseases. However, the role of AR in hepatic IRI is still unknown.
Methods: Intragraft AR expression profile and the association with liver graft injury were investigated in both human and rat liver transplantation using normal or fatty graft. The direct role of AR in hepatic IRI was studied in the AR knockout mice IRI model with or without fatty liver. They were further validated by the simulated IRI in vitro model using fatty LO2 cells with or without AR inhibitor zopolrestat and primary peritoneal macrophages isolated from AR knockout and wild-type mice. Gene expression of inflammatory cytokines/chemokines, the infiltration of macrophages/neutrophils, and NF-κB pathway activation were compared among different groups.
Results: AR was overexpressed in liver graft after human and rat liver transplantation and correlated with consequent liver injuries. The knockout of AR significantly attenuated hepatic sinusoidal damage and apoptosis in both normal and fatty livers after IRI. The expression of proinflammatory cytokines/chemokines and neutrophil chemoattractants, infiltration of macrophage and neutrophil, and activation of inflammation-associated NF-κB and JNK pathway were downregulated in AR knockout mice. Furthermore, the inhibition of AR effectively suppressed macrophage migration and decreased lipopolysaccharide (LPS)-induced production of proinflammatory cytokines/chemokines in isolated macrophages.
Conclusions: The deficiency of AR attenuated hepatic IRI in both normal and fatty livers by reducing liver inflammatory responses.
Inflammatory response plays an important role during hepatic ischemia-reperfusion injury (IRI). Aldose reductase (AR), as an important mediator in inflammatory response, is overexpressed after liver IRI, and its deficiency attenuates IRI by decreasing liver inflammatory response in normal/fatty liver. Targeting AR may provide a novel means to attenuate IRI and improve liver surgery outcomes.
Departments of *Surgery and
†Anatomy, Centre for Cancer Research, The University of Hong Kong, Hong Kong, China.
Reprints: Kwan Man, PhD, Department of Surgery, The University of Hong Kong, L9-55, Faculty of Medicine Bldg, 21 Sassoon Rd, Hong Kong, China. E-mail: email@example.com.
Disclosure: Supported by the Collaborative Research Fund (HKU5/CRF/08, HKU3/CRF/11R) and GRF (HKU775011M) of the Research Grant Council, Hong Kong, and seed funding, The University of Hong Kong. The authors declare no conflicts of interest.
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