Connor H D, Gao W, Nukina S, Lemasters J J, Mason R P, Thurman R G
Department of Pharmacology, University of North Carolina, Chapel Hill 27599.
Transplantation. 1992 Aug;54(2):199-204. doi: 10.1097/00007890-199208000-00002.
The purpose of these studies was to determine whether free radicals were formed as a consequence of reperfusion during orthotopic liver transplantation and whether their formation was related to graft failure. Grafts were stored for 18 hr in Euro-Collins solution or for 48 hr in University of Wisconsin solution (nonsurvival conditions) and reperfused with blood containing the spin trap alpha-phenyl N-tert-butylnitrone (PBN). Venous blood samples (4-5 ml) were collected, and serum was extracted with chloroform and methanol (2:1) and analyzed for radical adducts by electron paramagnetic resonance (EPR) spectroscopy. In samples from livers stored under nonsurvival conditions, EPR spectra were detected indicating the presence of PBN radical adducts. In contrast, radical adduct formation was 3- to 4-fold lower in similar experiments performed with untransplanted livers or with livers stored under survival conditions (1 hr in Ringer's solution or 24 hr in UW solution). Oxygen radicals are more likely involved in the production of radical adducts because formation was nearly completely prevented by superoxide dismutase plus catalase or Carolina rinse, which contains glutathione, desferrioxamine mesylate, and allopurinol. Radical adduct formation was much greater in a blood-free perfusion system where oxygen delivery was high, suggesting that blood elements are not necessary for radical adduct formation. An inverse correlation between survival of livers stored in UW solution and radical adduct signal was observed in this study. Thus, it is concluded that free radicals formed during reperfusion are involved in the mechanism of graft failure following liver transplantation in the rat.
这些研究的目的是确定在原位肝移植再灌注过程中是否会产生自由基,以及自由基的形成是否与移植物功能衰竭有关。将移植物在欧洲柯林斯溶液中保存18小时或在威斯康星大学溶液中保存48小时(非存活条件),然后用含有自旋捕捉剂α-苯基N-叔丁基硝酮(PBN)的血液进行再灌注。采集静脉血样本(4 - 5毫升),用氯仿和甲醇(2:1)提取血清,并通过电子顺磁共振(EPR)光谱分析自由基加合物。在非存活条件下保存的肝脏样本中,检测到EPR光谱,表明存在PBN自由基加合物。相比之下,在对未移植肝脏或在存活条件下保存的肝脏(在林格氏溶液中保存1小时或在UW溶液中保存24小时)进行的类似实验中,自由基加合物的形成要低3至4倍。氧自由基更有可能参与自由基加合物的产生,因为超氧化物歧化酶加过氧化氢酶或含有谷胱甘肽、甲磺酸去铁胺和别嘌呤醇的卡罗来纳冲洗液几乎完全阻止了其形成。在无血灌注系统中,自由基加合物的形成要大得多,因为在该系统中氧输送量很高,这表明血液成分对于自由基加合物的形成不是必需的。在本研究中观察到,在UW溶液中保存的肝脏的存活与自由基加合物信号之间呈负相关。因此,得出结论,再灌注过程中形成的自由基参与了大鼠肝移植后移植物功能衰竭的机制。