TY - JOUR
T1 - The effect of PGE1and temperature on lungfunction following preservation
AU - Ueno, T.
AU - Yokomise, H.
AU - Oka, T.
AU - Puskas, J.
AU - Mayer, E.
AU - Slutsky, A. S.
AU - Patterson, G. Alexander
PY - 1991/10
Y1 - 1991/10
N2 - We studied the effect of a vasodilator (prostaglandin E1) as well as flush (F) and storage (S) temperatures (4°C or 10°C) on lung preservation in an isolated rabbit lung perfusion model. Low-potassium dextran (LPD) or Euro-Collins (E-C) solution was used as flush solution. Six groups of six animals were studied: group 1 (LPD, 4°C F-S), group 2 (LPD with PGE1, 4°C F-S), group 3 (E-C with PGE1, 4°C F-S), group 4 (LPD, 10°C F-S), group 5 (LPD with PGE1, 10°C F-S), group 6 (E-C with PGE1, 10°C F-S). After 18-hr preservation, left lungs alone were ventilated, and reperfused with fresh venous blood. PaO2, PaCO2, pulmonary artery pressure (PAP), tracheal pressure (Pt) during reperfusion, and wet/dry weight (W/D) ratios were measured. PaO2 after LPD with or without PGE1 was significantly higher than after E-C with PGE1 at 4°C (95.8±11.5 mmHg in group 1 or 102.7±8.6 in group 2 vs. 41.8±10.5 in group 3, P<0.01) and at 10°C (119.3±2.3 in group 4 or 131.1± 6.2 in group 5 vs. 54.6±5.2 in group 6, P<0.01). PaCO2, PAP, Pt, and W/D ratios in the LPD groups were lower than in the E-C groups. LPD/PGE1 and LPD alone produced similar pulmonary preservation. PaO2 of lungs flushed with LPD and preserved at 10°C was higher than that of lungs stored at 4°C. We conclude that LPD solution is superior to E-C solution in this ex vivo rabbit lung preservation model, even when PGE1 is used. A moderate dose of PGE1 did not improve the performance of LPD as a flush solution. Pulmonary preservation with LPD at 10°C is superior to preservation at 4°C.
AB - We studied the effect of a vasodilator (prostaglandin E1) as well as flush (F) and storage (S) temperatures (4°C or 10°C) on lung preservation in an isolated rabbit lung perfusion model. Low-potassium dextran (LPD) or Euro-Collins (E-C) solution was used as flush solution. Six groups of six animals were studied: group 1 (LPD, 4°C F-S), group 2 (LPD with PGE1, 4°C F-S), group 3 (E-C with PGE1, 4°C F-S), group 4 (LPD, 10°C F-S), group 5 (LPD with PGE1, 10°C F-S), group 6 (E-C with PGE1, 10°C F-S). After 18-hr preservation, left lungs alone were ventilated, and reperfused with fresh venous blood. PaO2, PaCO2, pulmonary artery pressure (PAP), tracheal pressure (Pt) during reperfusion, and wet/dry weight (W/D) ratios were measured. PaO2 after LPD with or without PGE1 was significantly higher than after E-C with PGE1 at 4°C (95.8±11.5 mmHg in group 1 or 102.7±8.6 in group 2 vs. 41.8±10.5 in group 3, P<0.01) and at 10°C (119.3±2.3 in group 4 or 131.1± 6.2 in group 5 vs. 54.6±5.2 in group 6, P<0.01). PaCO2, PAP, Pt, and W/D ratios in the LPD groups were lower than in the E-C groups. LPD/PGE1 and LPD alone produced similar pulmonary preservation. PaO2 of lungs flushed with LPD and preserved at 10°C was higher than that of lungs stored at 4°C. We conclude that LPD solution is superior to E-C solution in this ex vivo rabbit lung preservation model, even when PGE1 is used. A moderate dose of PGE1 did not improve the performance of LPD as a flush solution. Pulmonary preservation with LPD at 10°C is superior to preservation at 4°C.
UR - http://www.scopus.com/inward/record.url?scp=0025925174&partnerID=8YFLogxK
M3 - Article
C2 - 1718066
AN - SCOPUS:0025925174
SN - 0041-1337
VL - 52
SP - 626
EP - 630
JO - Transplantation
JF - Transplantation
IS - 4
ER -