1. Donor preconditioning with taurine protects kidney grafts from injury after experimental transplantation.
- Author
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Guan X, Dei-Anane G, Liang R, Gross ML, Nickkholgh A, Kern M, Ludwig J, Zeier M, Büchler MW, Schmidt J, and Schemmer P
- Subjects
- Animals, Apoptosis drug effects, Biopsy, Caspase 3 metabolism, Dose-Response Relationship, Drug, Female, Graft Rejection pathology, Graft Rejection prevention & control, HSP72 Heat-Shock Proteins metabolism, Kidney metabolism, Kidney pathology, Kidney Transplantation pathology, Models, Animal, Necrosis pathology, Necrosis prevention & control, Rats, Rats, Sprague-Dawley, Reperfusion Injury pathology, Superoxide Dismutase metabolism, Kidney drug effects, Kidney Transplantation methods, Reperfusion Injury prevention & control, Taurine pharmacology
- Abstract
Background: Ischemia/reperfusion injury is a major problem in clinical transplantation (Tx). Taurine has been shown to protect liver grafts from ischemia/reperfusion injury after Tx. Thus, this study was designed to evaluate its effect on kidney grafts after transplantation., Materials and Methods: Various concentrations of taurine were infused before donor nephrectomy (1.5 mL; 30, 100, 300 mM). Controls were given the same volume of Ringers' solution. Subsequently, grafts were cold-stored for 19 h in histidine-tryptophan-ketoglutarate solution and transplanted. Six hours after Tx, graft function and injury were assessed with blood urea nitrogen/creatinine and aspartate aminotransferase/lactate dehydrogenase. Graft biopsies were taken to evaluate tubular damage, caspase-3, superoxide dismutase, and heat shock protein 72 (HSP-72) to index necrosis, apoptosis, antioxidative capacity, and regeneration, respectively., Results: Taurine significantly decreased blood urea nitrogen, creatinine, aspartate aminotransferase, and lactate dehydrogenase in a dose-dependent manner to up to 71%, 69%, 51%, and 53% of controls, respectively. Further, tubular damage and caspase-3 expression decreased to 44% and 18% of control values (P < 0.01), while superoxide dismutase and heat shock protein 72 expression increased by 95% and 77% of controls, respectively (P < 0.05)., Conclusions: This study demonstrates that donor preconditioning with taurine protects kidney grafts from injury (apoptosis, necrosis), improves graft function, and increases the regenerative potential most likely via mechanisms including antioxidation.
- Published
- 2008
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