Allen T M, Murray L, Alving C R, Moe J
Can J Physiol Pharmacol. 1987 Feb;65(2):185-90. doi: 10.1139/y87-035.
In experiments designed to examine the adverse effects of chronic liposome administration in vivo on the mononuclear phagocyte system (reticuloendothelial system), the presence of drug entrapped in the liposomes may increase the level of reticuloendothelial impairment. We have compared the effects on the mononuclear phagocyte system in mice of chronic administration of empty liposomes with the effects of liposomes containing the anti-leishmanial drug meglumine antimoniate. We have also examined the effect on the mononuclear phagocyte system of continued injections of liposomes containing lipid A, a component of bacterial lipopolysaccharide, which is responsible for macrophage activation. Ten intravenous injections of multilamellar liposomes composed of dipalmitoylphosphatidylcholine and cholesterol (1:0.75 M ratio) were given to ICR mice over a 25-day period. Two individual groups of mice received endotoxin-free liposomes in which meglumine antimoniate was either present or absent. One addition group received liposomes containing lipid A derived from Escherichia coli lipopolysaccharide. A control group received sterile saline injections. In each group, a depression of the phagocytic index, as measured by reduction of uptake of particulate carbon, was observed among some of the individual animals 24 h after the first injection. In many mice a marked splenomegaly was observed. A depressed phagocytic index and splenomegaly were most marked for mice receiving lipid A liposomes. However, there was a large individual variability among mice receiving these preparations and some mice in each group had normal spleen size and a nearly normal phagocytic index. Tissue distribution of liposomes containing [14C]dipalmitoylphosphatidylcholine as a phospholipid marker was examined in all groups in mice 24 h after the last injection.(ABSTRACT TRUNCATED AT 250 WORDS)
在旨在研究体内长期给予脂质体对单核吞噬细胞系统(网状内皮系统)的不良影响的实验中,脂质体中包裹的药物的存在可能会增加网状内皮系统损伤的程度。我们比较了长期给予空脂质体对小鼠单核吞噬细胞系统的影响与给予含有抗利什曼原虫药物葡甲胺锑酸盐的脂质体的影响。我们还研究了持续注射含有脂多糖成分脂多糖A的脂质体对单核吞噬细胞系统的影响,脂多糖A可激活巨噬细胞。在25天的时间里,给ICR小鼠静脉注射10次由二棕榈酰磷脂酰胆碱和胆固醇(比例为1:0.75M)组成的多层脂质体。两组单独的小鼠接受不含内毒素的脂质体,其中一组含有葡甲胺锑酸盐,另一组不含。另外一组接受含有源自大肠杆菌脂多糖的脂多糖A的脂质体。对照组接受无菌盐水注射。在每组中,在首次注射后24小时,一些个体动物中观察到吞噬指数降低,这通过颗粒碳摄取的减少来衡量。在许多小鼠中观察到明显的脾肿大。接受脂多糖A脂质体的小鼠吞噬指数降低和脾肿大最为明显。然而,接受这些制剂的小鼠之间存在很大的个体差异,每组中的一些小鼠脾脏大小正常且吞噬指数几乎正常。在最后一次注射后24小时,在所有组的小鼠中检查了含有[14C]二棕榈酰磷脂酰胆碱作为磷脂标记物的脂质体的组织分布。(摘要截短至250字)