Mio M, Ikeda A, Akagi M, Tasaka K
Agents Actions. 1985 Apr;16(3-4):113-7. doi: 10.1007/BF01983115.
Histamine release from isolated rat peritoneal mast cells induced by compound 48/80 (0.5 microgram/ml) or antigen-antibody reaction was inhibited by lysophosphatidylcholine in a dose-dependent fashion at concentrations up to 4 microM. Within the same range of concentration, lysophosphatidylcholine exhibited a membrane-stabilizing action on the model membrane systems decreasing the permeability of lipid bilayer and the fluidity of liposomal membrane in the liquid crystalline state. At concentrations higher than 8 microM, lysophosphatidylcholine damaged the cell membrane and subsequently histamine was released. It was assumed that lysophosphatidylcholine may act as an endogenous membrane stabilizer inhibiting histamine release in normal mast cells.
化合物48/80(0.5微克/毫升)或抗原-抗体反应诱导的大鼠腹膜肥大细胞组胺释放,在浓度高达4微摩尔时,溶血磷脂酰胆碱呈剂量依赖性抑制。在相同浓度范围内,溶血磷脂酰胆碱对模型膜系统具有膜稳定作用,可降低脂双层的通透性和液晶态脂质体膜的流动性。浓度高于8微摩尔时,溶血磷脂酰胆碱会损伤细胞膜,随后组胺释放。推测溶血磷脂酰胆碱可能作为内源性膜稳定剂抑制正常肥大细胞中的组胺释放。