Steinhauer H B, Brugger U, Atmanspacher R, Lubrich-Birkner I, Schollmeyer P
Dept. of Internal Medicine, University of Freiburg, F.R. Germany.
Adv Perit Dial. 1992;8:47-52.
The effect of fresh peritoneal dialysis (PD) solution and effluent on the generation of eicosanoids and cytokines by human peritoneal macrophages (PMO) was studied in vitro. PMO, isolated by density gradient separation from patients undergoing intermittent peritoneal dialysis (IPD), were incubated for 2 h with PD effluent after dwell periods of 5 to 240 min or fresh PD solution. Supplemented RPMI-1640 medium served as control. PMO were stimulated by calcium ionophore A23187 (10 M). PD solution significantly inhibited the release of prostanoids (PGE2, TXB2, 6-k-PGF1), leukotrienes (LTB4, LTC4), and cytokines (11-6, TNF) from PMO by 60 to 96% (p < 0.05). Addition of A23187 increased the generation of TXB2, LTB4, and LTC4 in PD solution adjusted to pH 7.4 to 2.7 up to 28.6 times the basal level, but was ineffective in PD fluid at pH 5.2. Incubation of PMO with PD effluent of varying dwell times resulted in a rise of all assayed mediators (p < 0.05). The release of IL-6 increased continuously from 80 +/- 10 pg/10(6) PMO (0 min dwell time) to 440 +/- 104 pg/10(6) PMO (4 h dwell time, mean +/- S.E.M.). TNF generation rose from 6.0 +/- 0.1 pg/10(6) PMO (0 min dwell time) to 162 +/- 54 pg/10(6) PMO after 5 min dwell time and remained constant with effluents of longer dwell times (15 to 240 min). Exposure of PMO to PD effluents after 240 min dwell time tended to decrease the median levels of PGE2, TXB2, and 6-k-PGF1.(ABSTRACT TRUNCATED AT 250 WORDS)
体外研究了新鲜腹膜透析(PD)液和流出液对人腹膜巨噬细胞(PMO)生成类花生酸和细胞因子的影响。通过密度梯度分离从接受间歇性腹膜透析(IPD)的患者中分离出PMO,在5至240分钟的驻留期后,将其与PD流出液或新鲜PD液一起孵育2小时。补充的RPMI-1640培养基用作对照。用钙离子载体A23187(10 μM)刺激PMO。PD液显著抑制PMO中前列腺素(PGE2、TXB2、6-k-PGF1)、白三烯(LTB4、LTC4)和细胞因子(IL-6、TNF)的释放,抑制率为60%至96%(p<0.05)。添加A23187使pH值调至7.4至2.7的PD液中TXB2、LTB4和LTC4的生成增加至基础水平的28.6倍,但在pH 5.2的PD液中无效。用不同驻留时间的PD流出液孵育PMO导致所有检测介质的水平升高(p<0.05)。IL-6的释放从80±10 pg/10⁶ PMO(驻留时间0分钟)持续增加至440±104 pg/10⁶ PMO(驻留时间4小时,平均值±标准误)。TNF的生成从6.0±0.1 pg/10⁶ PMO(驻留时间0分钟)在驻留5分钟后升至162±54 pg/10⁶ PMO,并在较长驻留时间(15至240分钟)的流出液中保持恒定。驻留240分钟后将PMO暴露于PD流出液中倾向于降低PGE2、TXB2和6-k-PGF1的中位数水平。(摘要截断于250字)