Niederberger Petra, Farine Emilie, Arnold Maria, Wyss Rahel K, Sanz Maria N, Méndez-Carmona Natalia, Gahl Brigitta, Fiedler Georg M, Carrel Thierry P, Tevaearai Stahel Hendrik T, Longnus Sarah L
Department of Cardiovascular Surgery, Inselspital, Bern University Hospital, University of Bern, Switzerland.
Center of Laboratory Medicine, University Institute of Clinical Chemistry, University Hospital, Inselspital, Bern, Switzerland.
Metabolism. 2017 Jun;71:107-117. doi: 10.1016/j.metabol.2017.03.007. Epub 2017 Mar 15.
Donation after circulatory death (DCD) could improve cardiac graft availability. However, strategies to optimize cardiac graft recovery remain to be established in DCD; these hearts would be expected to be exposed to high levels of circulatory fat immediately prior to the inevitable period of ischemia prior to procurement.
We investigated whether acute exposure to high fat prior to warm, global ischemia affects subsequent hemodynamic and metabolic recovery in an isolated rat heart model of DCD.
Hearts of male Wistar rats underwent 20min baseline perfusion with glucose (11mM) and either high fat (1.2mM palmitate; HF) or no fat (NF), 27min global ischemia (37°C), and 60min reperfusion with glucose only (n=7-8 per group). Hemodynamic recovery was 50% lower in HF vs. NF hearts (34±30% vs. 78±8% (60min reperfusion value of peak systolic pressureheart rate as percentage of mean baseline); p<0.01). During early reperfusion, glycolysis (0.3±0.3 vs. 0.7±0.3μmolming dry, p<0.05), glucose oxidation (0.1±0.03 vs. 0.4±0.2μmolming dry, p<0.01) and pyruvate dehydrogenase activity (1.8±0.6 vs. 3.6±0.5Ug protein, p<0.01) were significantly reduced in HF vs. NF groups, respectively, while lactate release was significantly greater (1.8±0.9 vs. 0.6±0.2μmolg wetmin; p<0.05).
Acute, pre-ischemic exposure to high fat significantly lowers post-ischemic cardiac recovery vs. no fat despite identical reperfusion conditions. These findings support the concept that oxidation of residual fatty acids is rapidly restored upon reperfusion and exacerbates ischemia-reperfusion (IR) injury. Strategies to optimize post-ischemic cardiac recovery should take pre-ischemic fat levels into consideration.
心脏死亡后器官捐献(DCD)可提高心脏移植物的可获得性。然而,在DCD中优化心脏移植物获取的策略仍有待确立;预计这些心脏在获取前不可避免的缺血期之前会立即暴露于高水平的循环脂肪中。
我们在DCD大鼠离体心脏模型中研究了在温暖的全心缺血前急性暴露于高脂肪是否会影响随后的血流动力学和代谢恢复。
雄性Wistar大鼠的心脏先接受20分钟的葡萄糖(11mM)基线灌注,其中一组添加高脂肪(1.2mM棕榈酸;HF),另一组不添加脂肪(NF),然后进行27分钟的全心缺血(37°C),最后仅用葡萄糖进行60分钟的再灌注(每组n = 7 - 8)。与NF组心脏相比,HF组心脏的血流动力学恢复降低了50%(34±30%对78±8%(60分钟再灌注时收缩压峰值心率占平均基线的百分比);p<0.01)。在早期再灌注期间,HF组的糖酵解(0.3±0.3对0.7±0.3μmol分钟克干重,p<0.05)、葡萄糖氧化(0.1±0.03对0.4±0.2μmol分钟克干重,p<0.01)和丙酮酸脱氢酶活性(1.8±0.6对3.6±0.5U克蛋白质,p<0.01)分别显著低于NF组,而乳酸释放则显著更高(1.8±0.9对0.6±0.2μmol克湿重分钟;p<0.05)。
尽管再灌注条件相同,但与无脂肪组相比,缺血前急性暴露于高脂肪会显著降低缺血后心脏的恢复。这些发现支持了这样的概念,即再灌注时残余脂肪酸的氧化会迅速恢复并加剧缺血再灌注(IR)损伤。优化缺血后心脏恢复的策略应考虑缺血前的脂肪水平。