Zierenberg O, Odenthal J, Betzing H
Atherosclerosis. 1979 Nov;34(3):259-76.
Radioactive polyenephosphatidycholine (PPC) was injected i.v. in dogs, rats and rabbits. In addition, PPC was administered orally to dogs and rats. The incorporation of the PPC applied into serum lipoproteins was determined. After i.v. injection in dogs approximately 80% of the radioactive dose was transported by HDL. Only around 50% of the dose was found, however, in the HDL fraction of rats and rabbits. Radiochemical analyses provided a quantitative determination of the time course of PPC incorporation into HDL as well as of the metabolites of PPC. After in vitro incubation with rat and human serum PPC was incorporated into HDL by approximately 50% of the applied dose and by 5--14% into LDL, by approximately 15% into VLDL and by 20--30% into other serum constituents. In vitro incubation of PPC with human HDL yielded the complete incorporation into this lipoprotein fraction.
将放射性多烯磷脂酰胆碱(PPC)经静脉注射到犬、大鼠和兔体内。此外,将PPC口服给予犬和大鼠。测定了所给予的PPC在血清脂蛋白中的掺入情况。在犬经静脉注射后,约80%的放射性剂量由高密度脂蛋白(HDL)转运。然而,在大鼠和兔的HDL组分中仅发现约50%的剂量。放射化学分析对PPC掺入HDL的时间进程以及PPC的代谢产物进行了定量测定。在与大鼠和人血清进行体外孵育后,约50%所给予剂量的PPC掺入HDL,5% - 14%掺入低密度脂蛋白(LDL),约15%掺入极低密度脂蛋白(VLDL),20% - 30%掺入其他血清成分。PPC与人HDL进行体外孵育后完全掺入该脂蛋白组分。