Lindell Susanne L, Klahn Shawna L, Piazza Timothy M, Mangino Martin J, Torrealba Jose R, Southard James H, Carey Hannah V
Department of Comparative Biosciences, University of Wisconsin, 2015 Linden Dr., Madison WI 53706, USA.
Am J Physiol Gastrointest Liver Physiol. 2005 Mar;288(3):G473-80. doi: 10.1152/ajpgi.00223.2004.
The success of liver grafts is currently limited by the length of time organs are cold preserved before transplant. Novel insights to improve viability of cold-stored organs may emerge from studies with animals that naturally experience low body temperatures (T(b)) for extended periods. In this study, we tested whether livers from hibernating ground squirrels tolerate cold ischemia-warm reperfusion (cold I/R) for longer times and with better quality than livers from rats or summer squirrels. Hibernators were used when torpid (T(b) < 10 degrees C) or aroused (T(b) = 37 degrees C). Livers were stored at 4 degrees C in University of Wisconsin solution for 0-72 h and then reperfused with 37 degrees C buffer in vitro. Lactate dehydrogenase (LDH) release after 60 min was increased 37-fold in rat livers after 72 h cold I/R but only 10-fold in summer livers and approximately three- to sixfold in torpid and aroused hibernator livers, despite twofold higher total LDH content in livers from hibernators compared with rats or summer squirrels. Reperfusion for up to 240 min had the least effect on LDH release in livers from hibernators and the greatest effect in rats. Compared with rats or summer squirrels, livers from hibernators after 72 h cold I/R showed better maintenance of mitochondrial respiration, bile production, and sinusoidal lining cell viability, as well as lower vascular resistance and Kupffer cell phagocytosis. These results demonstrate that the hibernation phenotype in ground squirrels confers superior resistance to liver cold I/R injury compared with rats and summer squirrels. Because hibernation-induced protection is not dependent on animals being in the torpid state, the mechanisms responsible for this effect may provide new strategies for liver preservation in humans.
目前,肝移植的成功率受到移植前器官冷保存时间的限制。对长时间自然经历低体温(Tb)的动物进行的研究,可能会为提高冷保存器官的活力带来新的见解。在本研究中,我们测试了来自冬眠地松鼠的肝脏是否比来自大鼠或夏季松鼠的肝脏更能耐受长时间的冷缺血-热再灌注(冷I/R),且质量更好。当冬眠动物处于蛰伏状态(Tb < 10摄氏度)或苏醒状态(Tb = 37摄氏度)时使用。将肝脏在威斯康星大学溶液中于4摄氏度保存0至72小时,然后在体外用37摄氏度的缓冲液进行再灌注。在72小时冷I/R后,大鼠肝脏在60分钟后的乳酸脱氢酶(LDH)释放增加了37倍,但夏季松鼠肝脏仅增加了10倍,蛰伏和苏醒的冬眠动物肝脏增加了约三至六倍,尽管冬眠动物肝脏中的总LDH含量比大鼠或夏季松鼠高出两倍。长达240分钟的再灌注对冬眠动物肝脏中LDH释放的影响最小,对大鼠的影响最大。与大鼠或夏季松鼠相比,72小时冷I/R后的冬眠动物肝脏在维持线粒体呼吸、胆汁生成和窦状内皮细胞活力方面表现更好,血管阻力和库普弗细胞吞噬作用更低。这些结果表明,与大鼠和夏季松鼠相比,地松鼠的冬眠表型赋予了对肝脏冷I/R损伤的更强抵抗力。由于冬眠诱导的保护不依赖于动物处于蛰伏状态,负责这种效应的机制可能为人类肝脏保存提供新策略。