Cold Storage of Liver Microorgans in ViaSpan® and BG35 Solutions. Study of Ammonia Metabolism during normothermic reoxygenation.

PIZARRO M. DOLORES; MEDIAVILLA MARÍA G.; BERARDI FLORENCIA; TIRIBELLI CLAUDIO; RODRIGUEZ JOAQUIN V.; MAMPRIN MARIA E

ANNALS OF HEPATOLOGY

MEXICAN ASSOC HEPATOLOGY

Lugar: Mexico, DF.; Año: 2014 vol. 13 p. 256 - 264

1665-2681

Introduction. This work focuses on ammonia metabolism of Liver Microorgans (LMOs) after cold preserva- tion in a normothermic reoxygenation system (NRS). We have previously reported the development of a no- vel preservation solution, Bes-Gluconate-PEG 35 kDa (BG35) that showed the same efficacy as ViaSpan® to protect LMOs against cold preservation injury. The objective of this work was to study mRNA levels and activities of two key Urea Cycle enzymes, Carbamyl Phosphate Synthetase I (CPSI) and Ornithine Transcar- bamylase (OTC), after preservation of LMOs in BG35 and ViaSpan® and the ability of these tissue slices to detoxify an ammonia overload in a NRS model. Material and methods. After 48 h of cold storage (0°C in BG35 or ViaSpan®) LMOs were rewarmed in KHR containing an ammonium chloride overload (1 mM). We de- termined ammonium detoxification capacity (ADC), urea synthesis and enzyme activities and relative mRNA levels for CPSI and OTC. Results. At the end of reoxygenation LMOs cold preserved in BG35 have ADC and urea synthesis similar to controls. ViaSpan® group demonstrated a lower capacity to detoxify ammonia and to synthesize urea than fresh LMOs during the whole reoxygenation period which correlated with the lower mRNA levels and activities for CPSI and OTC observed for this group. Conclusion. We demonstrate that our preservation conditions (48 hours, BG35 solution, anoxia, 0oC) did not affect ammonia metabolism of cold preserved LMOs maintaining the physiological and biochemical liver functions tested, which allows their future use as biological component of a BAL system.