摘要
目的 观察磷脂酶A2 抑制剂氯丙嗪对氧化低密度脂蛋白 (OX LDL)所致人红细胞左旋精氨酸 (L arg)转运变化的影响。方法 取 6例健康成人红细胞 ,制备红细胞悬液。将其分别与OX LDL和氯丙嗪分组孵育。实验分 3组 :对照组、OX LDL组和OX LDL加氯丙嗪组 ,分别测定红细胞3H L arg的转运参数。结果 与对照组比较 ,OX LDL组红细胞L Arg总摄入的最大转运速率 (Vmax值 )较对照组降低 33% (P <0 0 5 ) ,亲和力明显减小 (米氏常数Km值增大 ,P <0 0 5 )。OX LDL加氯丙嗪组与OX LDL组相比 ,红细胞L arg的总转运及经y +载体介导的转运均增加 ,Vmax值分别增加了2 5 %和 37% (P <0 0 1) ,亲和力明显增大 (Km值减小 ,P <0 0 5 ) ;两组间经y +L载体介导的转运Vmax和Km值差异无显著性。结论 OX LDL可抑制红细胞L arg的跨膜转运 ,而氯丙嗪可逆转这一过程。
Objective To observe the influence of chlorderazin on the change of L-arginine transport in human erythrocytes induced by oxidized low density lipoprotein. Methods Human erythrocytes were obtained from six healthy donors. The study included three groups: Gr1 (control)? Gr2 (incubated with OX-LDL) and Gr3 (incubated with OX-LDL and chlorderazin, a PLA 2 inhibitor). The 3H-L-arginine transport was measured.Results Compared with Gr1, the Vmax for the total transport of L-arginine in erythrocytes in Gr2 decreased by 33%, and Km value increased. Compared with Gr2, the Vmax for the total transport and the transport via system y+ of L-arginine in erythrocytes in Gr3 increased by 37% and 25% respectively, and Km values decreased for both. But the change of L-arginine transport by system y+L was not statistically significant.Conclusion OX-LDL could inhibit L-arginine transport in human erythrocytes, which could be reversed by chlorderazin, a nonspecific PLA 2 inhibitor.
出处
《中国介入心脏病学杂志》
2003年第3期152-154,共3页
Chinese Journal of Interventional Cardiology