TY - JOUR
T1 - Methodology for the assessment of lung protection
T2 - Human pulmonary artery endothelial cell preservation using haemaccel
AU - Spaggiari, Lorenzo
AU - Carbognani, Paolo
AU - Rusca, Michele
AU - Alfieri, Roberta
AU - Solli, PierGiorgio
AU - Cattelani, Leonardo
AU - Urbani, Simonetta
AU - Petronini, Piergiorgio
AU - Borghetti, Angelo F.
AU - Bobbio, Paolo
PY - 1995/11/15
Y1 - 1995/11/15
N2 - This investigation was designed to show an original methodology for the assessment of lung preservation and to analyze the efficacy of a low potassium polyge-lin solution (haemaccel [HM]) on isolated human pulmonary artery endothelial cells. The effects of HM were compared with those of low potassium dextran (LPD), Belzer (University of Wisconsin [UWS]), and Ëuro-Collins solutions. The viability of the endothelial cultures was assessed by means of both total protein content and recovery of metabolic cellular function expressed as the protein synthesis rate after 6 hr and 16 hr of incubation at 10°C. Our results failed to show any significant difference in the total protein content for HM, LPD, and UWS, both after 6 and 16 hr of incu-bation; however, the Euro-Collins-preserved sample revealed a significant drop in this parameter as early as 6 hr after the start. This finding was regarded as a clear indication of cellular cytotoxicity. In contrast, the metabolism recovery capacity of the cells varied significantly between HM and UWS at 6 hr and among HM, LPD, and UWS at 16 hr; at 6 hr, however, no significant difference was observed between HM and LPD. In conclusion, HM appears to exert a more significant effect on human pulmonary artery endothelial cell metabolism recovery than do the other fluids, thus suggesting its suitability as a long-term pulmonary perfusate.
AB - This investigation was designed to show an original methodology for the assessment of lung preservation and to analyze the efficacy of a low potassium polyge-lin solution (haemaccel [HM]) on isolated human pulmonary artery endothelial cells. The effects of HM were compared with those of low potassium dextran (LPD), Belzer (University of Wisconsin [UWS]), and Ëuro-Collins solutions. The viability of the endothelial cultures was assessed by means of both total protein content and recovery of metabolic cellular function expressed as the protein synthesis rate after 6 hr and 16 hr of incubation at 10°C. Our results failed to show any significant difference in the total protein content for HM, LPD, and UWS, both after 6 and 16 hr of incu-bation; however, the Euro-Collins-preserved sample revealed a significant drop in this parameter as early as 6 hr after the start. This finding was regarded as a clear indication of cellular cytotoxicity. In contrast, the metabolism recovery capacity of the cells varied significantly between HM and UWS at 6 hr and among HM, LPD, and UWS at 16 hr; at 6 hr, however, no significant difference was observed between HM and LPD. In conclusion, HM appears to exert a more significant effect on human pulmonary artery endothelial cell metabolism recovery than do the other fluids, thus suggesting its suitability as a long-term pulmonary perfusate.
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M3 - Article
C2 - 7491678
AN - SCOPUS:0028875781
VL - 60
SP - 1040
EP - 1043
JO - Transplantation
JF - Transplantation
SN - 0041-1337
IS - 9
ER -