ASSESSMENT OF INJURY IN TRANSPLANTED AND NONTRANSPLANTED LUNGS AFTER 6 H OF COLD-STORAGE WITH GLUTATHIONE

被引:13
作者
BRYAN, CL
PATEFIELD, AJ
COHEN, D
NIELSEN, JL
EMANUEL, B
CALHOON, JH
机构
[1] UNIV TEXAS, AUDIE L MURPHY MEM VET HOSP,HLTH SCI CTR, DEPT SURG,DIV CARDIOTHORAC SURG, SAN ANTONIO, TX 78284 USA
[2] USAF, MED CTR, DEPT MED, SAN ANTONIO, TX 78284 USA
[3] USAF, MED CTR, DEPT PATHOL, SAN ANTONIO, TX 78284 USA
关键词
LUNG INJURY; TRANSPLANTATION; NEUTROPHIL; FREE RADICAL; CANINE; PULMONARY EDEMA; LIPID PEROXIDATION;
D O I
10.1152/jappl.1994.76.3.1232
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Single-lung transplantation after 3 h of hypothermic storage produces bilateral lung injury [pulmonary reimplantation response (PRR)]. We hypothesized that glutathione (GSH) hypothermic storage would protect both lungs from PRR for extended preservation times and that differences in injury and protection would be realized between the graft and the nontransplanted lung. Mongrel dogs underwent left single-lung autotransplantation after preservation for 5-6 h in Euro-Collins (EC) solution, EC plus exogenous GSH (EC + GSH), or Viaspan (VIA) at 4 degrees C. Lung injury was measured in both lungs after 1 h of reperfusion. EC dogs demonstrated significant increases in lung edema, lipid peroxidation, and alveolar neutrophil recruitment in the lung graft and to a less extent in the nontransplanted right lung compared with control dogs (P < 0.05). Edema, lipid peroxidation, and alveolar neutrophils were significantly reduced in both lungs from EC + GSH and VIA dogs compared with lungs from EC dogs (P < 0.05). An increase in large-pore permeability was measured in the lung graft from EC dogs compared with all other lungs. Bronchoalveolar lavage fluid lactate dehydrogenase and total protein concentrations were elevated in both lungs from all three groups of transplanted dogs compared with those of control dogs (P < 0.05). These data suggest that GSH-containing solutions attenuate the PRR after 6 h of ischemic hypothermic storage but that the protection is incomplete. Mechanisms of injury affecting the lung graft during the PRR appear to differ from those affecting the nontransplanted lung.
引用
收藏
页码:1232 / 1241
页数:10
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