Department of Chemical and Biochemical Engineering, Rutgers, State University of New Jersey, Piscataway, New Jersey 08854, USA.
Biotechnol Bioeng. 2011 Dec;108(12):2947-57. doi: 10.1002/bit.23261. Epub 2011 Aug 4.
Isolated liver perfusion systems have been used to characterize intrinsic metabolic changes in liver as a result of various perturbations, including systemic injury, hepatotoxin exposure, and warm ischemia. Most of these studies were done using hyperoxic conditions (95% O(2)) but without the use of oxygen carriers in the perfusate. Prior literature data do not clearly establish the impact of oxygenation, and in particular that of adding oxygen carriers to the perfusate, on the metabolic functions of the liver. Therefore, herein the effects of oxygen delivery in the perfusion system on liver metabolism were investigated by comparing three modes of oxygenation. Rat livers were perfused via the portal and hepatic veins at a constant flow rate of 3 mL/min/g liver in a recirculating perfusion system. In the first group, the perfusate was equilibrated in a membrane oxygenator with room air (21% O(2)) before entering the liver. In the second group, the perfusate was equilibrated with a 95% O(2)/5% CO(2) gas mixture. In the third group, the perfusate was supplemented with washed bovine red blood cells (RBCs) at 10% hematocrit and also equilibrated with the 95% O(2)/5% CO(2) gas mixture. Oxygen and CO(2) gradients across the liver were measured periodically with a blood gas analyzer. The rate of change in the concentration of major metabolites in the perfusate was measured over time. Net extracellular fluxes were calculated from these measurements and applied to a stoichiometric-based optimization problem to determine the intracellular fluxes and active pathways in the perfused livers. Livers perfused with RBCs consumed oxygen at twice the rate observed using hyperoxic (95% O(2)) perfusate without RBCs, and also produced more urea and ketone bodies. At the flow rate used, the oxygen supply in perfusate without RBCs was just sufficient to meet the average oxygen demand of the liver but would be insufficient if it increased above baseline, as is often the case in response to environmental perturbations. Metabolic pathway analysis suggests that significant anaerobic glycolysis occurred in the absence of RBCs even using hyperoxic perfusate. Conversely, when RBCs were used, glucose production from lactate and glutamate, as well as pathways related to energy metabolism were upregulated. RBCs also reversed an increase in PPP fluxes induced by the use of hyperoxic perfusate alone. In conclusion, the use of oxygen carriers is required to investigate the effect of various perturbations on liver metabolism.
离体肝脏灌注系统已被用于研究各种干扰因素(包括全身损伤、肝毒素暴露和热缺血)导致的肝脏内在代谢变化。这些研究大多采用高氧条件(95%O2),但灌注液中未使用氧载体。先前的文献数据并未明确确定氧合作用的影响,特别是添加氧载体对肝脏代谢功能的影响。因此,本文通过比较三种供氧方式,研究了灌注系统中氧输送对肝脏代谢的影响。将大鼠肝脏通过门静脉和肝静脉以 3 mL/min/g 肝脏的恒定流速在循环灌注系统中进行灌注。在第一组中,灌注液在膜式氧合器中用空气(21%O2)平衡,然后进入肝脏。在第二组中,灌注液用 95%O2/5%CO2 气体混合物平衡。在第三组中,灌注液用 10%血细胞比容的洗涤牛红细胞(RBC)补充,并与 95%O2/5%CO2 气体混合物平衡。用血气分析仪定期测量肝脏内外的氧气和 CO2 梯度。随着时间的推移,测量灌注液中主要代谢物浓度的变化率。从这些测量中计算出净细胞外通量,并应用于基于化学计量的优化问题,以确定灌注肝脏中的细胞内通量和活性途径。用 RBC 灌注的肝脏以比无 RBC 时高氧(95%O2)灌注液高两倍的速度消耗氧气,并且还产生更多的尿素和酮体。在使用的流速下,无 RBC 灌注液中的氧气供应仅足以满足肝脏的平均氧气需求,但如果氧气需求增加超过基线,就会不足,这种情况在环境干扰时经常发生。代谢途径分析表明,即使使用高氧灌注液,无 RBC 时也会发生显著的无氧糖酵解。相反,当使用 RBC 时,从乳酸和谷氨酸产生葡萄糖以及与能量代谢相关的途径被上调。RBC 还逆转了仅使用高氧灌注液引起的 PPP 通量增加。总之,需要使用氧载体来研究各种干扰因素对肝脏代谢的影响。