Liu Tong, Dogan Inci, Rothe Michael, Reichardt Jana, Knauf Felix, Gollasch Maik, Luft Friedrich C, Gollasch Benjamin
Experimental and Clinical Research Center (ECRC), a Joint Institution of the Charité Medical Faculty and Max Delbrück Center (MDC) for Molecular Medicine, 13125 Berlin, Germany.
Lipidomix, GmbH, Robert-Rössle-Straße 10, 13125 Berlin, Germany.
Metabolites. 2022 Mar 21;12(3):269. doi: 10.3390/metabo12030269.
Long-chain fatty acids (LCFAs) serve as energy sources, components of cell membranes, and precursors for signaling molecules. Uremia alters LCFA metabolism so that the risk of cardiovascular events in chronic kidney disease (CKD) is increased. End-stage renal disease (ESRD) patients undergoing dialysis are particularly affected and their hemodialysis (HD) treatment could influence blood LCFA bioaccumulation and transformation. We investigated blood LCFA in HD patients and studied LCFA profiles in vivo by analyzing arterio-venous (A-V) LFCA differences in upper limbs. We collected arterial and venous blood samples from 12 ESRD patients, before and after HD, and analyzed total LCFA levels in red blood cells (RBCs) and plasma by LC-MS/MS tandem mass spectrometry. We observed that differences in arterial and venous LFCA contents within RBCs (RBC LCFA A-V differences) were affected by HD treatment. Numerous saturated fatty acids (SFA), monounsaturated fatty acids (MUFA), and polyunsaturated fatty acids (PUFA) n-6 showed negative A-V differences, accumulated during peripheral tissue perfusion of the upper limbs, in RBCs before HD. HD reduced these differences. The omega-3 quotient in the erythrocyte membranes was not affected by HD in either arterial or venous blood. Our data demonstrate that A-V differences in fatty acids status of LCFA are present and active in mature erythrocytes and their bioaccumulation is sensitive to single HD treatment.
长链脂肪酸(LCFAs)可作为能量来源、细胞膜的组成成分以及信号分子的前体。尿毒症会改变LCFA代谢,从而增加慢性肾脏病(CKD)患者发生心血管事件的风险。接受透析的终末期肾病(ESRD)患者受影响尤为明显,其血液透析(HD)治疗可能会影响血液中LCFA的生物蓄积和转化。我们对HD患者的血液LCFA进行了研究,并通过分析上肢动静脉(A-V)LCFA差异来研究体内LCFA谱。我们采集了12例ESRD患者HD治疗前后的动脉血和静脉血样本,并通过液相色谱-串联质谱法(LC-MS/MS)分析红细胞(RBC)和血浆中的总LCFA水平。我们观察到,HD治疗会影响RBC内动脉和静脉LCFA含量的差异(RBC LCFA A-V差异)。许多饱和脂肪酸(SFA)、单不饱和脂肪酸(MUFA)和多不饱和脂肪酸(PUFA)n-6在HD前的RBC中,于上肢外周组织灌注期间呈现负A-V差异并发生蓄积。HD降低了这些差异。红细胞膜中的ω-3比值在动脉血和静脉血中均不受HD影响。我们的数据表明,成熟红细胞中存在并活跃着LCFA脂肪酸状态的A-V差异,且其生物蓄积对单次HD治疗敏感。