Lachachi H, Plantavid M, Simon M F, Chap H, Braquet P, Douste-Blazy L
Biochem Biophys Res Commun. 1985 Oct 30;132(2):460-6. doi: 10.1016/0006-291x(85)91156-8.
Incorporation of 1-[3H]-O-alkyl-2-acetyl-sn-glycero-3-phosphocholine ([3H] PAF-acether) into rabbit platelet phosphatidylcholine (PC) was inhibited by a specific antagonist, BN 52021 (IC50 5.6 X 10(-6) M, maximal effect, i.e 70% inhibition, at 10(-4) M). Under the same conditions, [3H] lyso-PAF-acether incorporation remained 9 fold lower, compared to PAF-acether, without any effect of BN 52021. Upon cell lysis, both phospholipids attained the same rate of metabolic conversion, corresponding to a 1.15-fold and a 12-fold increase for PAF-acether and lyso-PAF-acether, respectively. In none of these cases was BN 52021 effective. It is concluded that transmembrane movement of the two phospholipids represents the limiting step of their metabolism. The higher rate of PAF-acether conversion by intact platelets could involve its binding to a membrane receptor, as suggested by the inhibitory effect of BN 52021, the significance of which is discussed.
1-[3H]-O-烷基-2-乙酰基-sn-甘油-3-磷酸胆碱([3H]血小板活化因子乙醚)掺入兔血小板磷脂酰胆碱(PC)的过程受到特异性拮抗剂BN 52021的抑制(IC50为5.6×10(-6) M,在10(-4) M时达到最大效应,即70%抑制)。在相同条件下,与血小板活化因子乙醚相比,[3H]溶血血小板活化因子乙醚的掺入量低9倍,且不受BN 52021的影响。细胞裂解后,两种磷脂的代谢转化率相同,血小板活化因子乙醚和溶血血小板活化因子乙醚分别增加1.15倍和12倍。在这些情况下,BN 52021均无效。结论是这两种磷脂的跨膜转运是其代谢的限速步骤。完整血小板对血小板活化因子乙醚的转化率较高,这可能涉及其与膜受体的结合,BN 52021的抑制作用表明了这一点,并对其意义进行了讨论。