Strasser T, Schiffl H
Medizinische Klinik der Universität, München, F.R.G.
Biochim Biophys Acta. 1990 Oct 1;1046(3):326-9. doi: 10.1016/0005-2760(90)90249-w.
Biosynthesis of leukotriene B4 (LTB4) was studied in ten patients with end-stage renal failure undergoing chronic hemodialysis with a cuprophane membrane. As compared to healthy subjects the low basal plasma levels of LTB4 quantified by radioimmunoassay after extraction and purification by HPLC showed no significant difference. The time-course of LTB4 release after contact of the blood with the dialysis membrane without further in vitro stimulation was characterized by a rapid increase by about 500% within the first 10 min, appearing approximately at the same time as the known fall of white blood cell count which reaches its nadir after 20 min. Analysis of further release showed a decline of LTB4 biosynthesis to basal levels at the end of hemodialysis. These results indicate that activation of the 5-lipoxygenase pathway is involved in hemodialysis-associated leukopenia and may contribute to the alterations in neutrophils of patients with chronic dialysis therapy.
对10例终末期肾衰竭患者使用铜仿膜进行慢性血液透析时白三烯B4(LTB4)的生物合成进行了研究。通过高效液相色谱法提取和纯化后,采用放射免疫分析法测定LTB4的基础血浆水平,与健康受试者相比,未显示出显著差异。在未进行进一步体外刺激的情况下,血液与透析膜接触后LTB4释放的时间进程特点是,在最初10分钟内迅速增加约500%,几乎与已知的白细胞计数下降同时出现,白细胞计数在20分钟后降至最低点。进一步释放分析显示,血液透析结束时LTB4生物合成降至基础水平。这些结果表明,5-脂氧合酶途径的激活参与了血液透析相关的白细胞减少,并且可能导致慢性透析治疗患者中性粒细胞的改变。