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S-Nitroso-N-Acetylcysteine: A Promising Drug for Early Ischemia/Reperfusion Injury in Rat Liver

Authors
Journal
Transplantation Proceedings
0041-1345
Publisher
Elsevier
Publication Date
Volume
42
Issue
10
Identifiers
DOI: 10.1016/j.transproceed.2010.09.152
Disciplines
  • Biology
  • Medicine

Abstract

Abstract Background/Aims Ischemia-reperfusion (I/R) injury is among the major causes of poor graft function early after liver transplantation that adversely influences patient survival. A variety of mediators have been implicated in the pathogenesis of I/R vascular injury, including nitric oxide (NO). Because of the beneficial effects of NO during preconditioning and reperfusion, strategies to prevent or ameliorate I/R injury through the stimulation of hepatic NO production are an area of significant clinical interest. We evaluated the role of S-nitroso- N-acetylcysteine (SNAC) as an NO donor in the prevention of liver I/R injury in an animal model. Methods Adult male Wistar rats were randomly assigned to 3 experimental groups containing 5 animals each: the University of Wisconsin (UW) solution group; SNAC solution group; and SNAC-containing UW solution (SNAC+UW) group. Aspartate aminotransferase (AST), alanine aminotransferase (ALT) and lactate dehydrogenase (LDH) were determined in samples of the cold storage solution at 2, 4, and 6 hours of preservation. After 6 hours of cold storage, We applied a 15-minute reperfusion period. Thereafter, the reperfusion was interrupted with blood samples obtained to measure AST, ALT, LDH, and thiobarbituric acid reactive substances (TBARS). Hepatic fragments were processed for histologic analysis, and to determine of TBARS, catalase, and glutathione levels. Results During cold preservation, AST and LDH were significantly lower among the SNAC than the UW group or the SNAC+UW group ( P = .004 and P = .03, respectively). ALT was comparable among the groups ( P = .3). After reperfusion, serum levels of AST, ALT, and LDH, as well as of hepatic TBARS and catalase showed no differences among the groups. Glutathione concentration was lower in the SNAC and SNAC+UW group ( P < .001) compared with the UW group. We did not observe histologic signs of preservation injury. Conclusion The SNAC solution showed a greater protective effect to preserve rat livers during cold storage, but it was comparable with UW.

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