West G B
Int Arch Allergy Appl Immunol. 1982;68(4):399-401. doi: 10.1159/000233134.
The action of ethylenediamine tetraacetic acid (EDTA) on the release of histamine induced by clinical dextran, concanavalin A and compound 48/80 has been studied in rats after intraperitoneal and intrapedial injection as well as in tubes containing isolated peritoneal mast cells. Whereas large doses of EDTA were required for inhibiting histamine release in the whole animal, relatively much smaller concentrations were necessary when the inhibitor was injected locally into the paw or included in the incubation mixture with isolated cells. When dextran was used as the histamine releaser, EDTA was relatively much more effective an inhibitor in vitro than in vivo.
在大鼠腹腔注射和足内注射后以及在含有分离的腹膜肥大细胞的试管中,研究了乙二胺四乙酸(EDTA)对临床右旋糖酐、伴刀豆球蛋白A和化合物48/80诱导的组胺释放的作用。虽然在整个动物体内抑制组胺释放需要大剂量的EDTA,但当抑制剂局部注射到爪中或包含在与分离细胞的孵育混合物中时,所需的浓度相对要小得多。当使用右旋糖酐作为组胺释放剂时,EDTA在体外作为抑制剂比在体内相对更有效。