Koibuchi Y, Ichikawa A, Nakagawa M, Tomita K
Eur J Pharmacol. 1985 Sep 24;115(2-3):163-70. doi: 10.1016/0014-2999(85)90687-9.
Compound 48/80 and 14C-labeled compound 48/80 were synthesized, and fractionated by thin-layer chromatography into 14 components (A-N) with various histamine releasing activities and different Ca2+ requirements for their actions. The histamine release induced from rat mast cells in vitro by the most active component, fraction D (molecular weight = 2280, a tridecamer composed of 13 monomer units), was greatly enhanced by extracellular Ca2+, and was partially reduced by pretreatment of the cells with dinitrophenylated ascaris antiserum, an IgE. In contrast, the histamine release induced by fraction H (molecular weight = 1580, a nonamer composed of 9 monomer units), was higher in Ca2+ -free medium than in Ca2+-containing medium, and was partially reduced by pretreatment of mast cells with neurotensin or substance P, Ca2+-independent releasers. Apparently both fractions D and H are useful reagents for investigating the role of Ca2+ in histamine release and releaser binding in mast cells.
合成了化合物48/80和14C标记的化合物48/80,并通过薄层色谱法将其分离为14种组分(A - N),这些组分具有不同的组胺释放活性以及不同的作用所需Ca2+条件。最具活性的组分D(分子量 = 2280,由13个单体单元组成的十三聚体)在体外诱导大鼠肥大细胞释放组胺的过程中,细胞外Ca2+可显著增强该作用,并且用二硝基苯化蛔虫抗血清(一种IgE)对细胞进行预处理可使其部分降低。相比之下,组分H(分子量 = 1580,由9个单体单元组成的九聚体)诱导的组胺释放在无Ca2+培养基中比在含Ca2+培养基中更高,并且用神经降压素或P物质(不依赖Ca2+的释放剂)对肥大细胞进行预处理可使其部分降低。显然,组分D和H都是研究Ca2+在肥大细胞组胺释放和释放剂结合中作用的有用试剂。