Pearce F L, Blum U, Poblete-Freundt G, Schmutzler W
Naunyn Schmiedebergs Arch Pharmacol. 1978 Apr;302(2):165-72. doi: 10.1007/BF00517983.
The divalent cation ionophore A23187 was found to produce a dose-dependent release of histamine from isolated mesenteric mast cells of the guinea pig. The process showed a specific requirement for calcium ions and was blocked by inhibitors of glycolysis. The effect of cAMP, theophylline, sympathomimetic amines and DSCG on the histamine release induced by the ionophore or by the antigen-antibody reaction was compared. In both cases, the release was inhibited by Bu2cAMP and by theophylline but higher concentrations were required with the ionophore. Adrenaline, isoprenaline and DSCG were effective only in the anaphylactic system. These results are compared with those previously reported for human leucocytes and rat peritoneal mast cells in which the release produced by the ionophore was found not to be inhibited by cAMP and its analogues. On the basis of these findings, the possible role of cAMP in the modulation of histamine release is discussed.
已发现二价阳离子载体A23187能使豚鼠离体肠系膜肥大细胞组胺呈剂量依赖性释放。该过程对钙离子有特定需求,并被糖酵解抑制剂所阻断。比较了环磷酸腺苷(cAMP)、茶碱、拟交感胺和色甘酸钠(DSCG)对载体或抗原抗体反应诱导的组胺释放的影响。在这两种情况下,释放均被双丁酰环磷腺苷(Bu2cAMP)和茶碱所抑制,但载体所需的浓度更高。肾上腺素、异丙肾上腺素和DSCG仅在过敏反应系统中有效。将这些结果与先前报道的人白细胞和大鼠腹腔肥大细胞的结果进行了比较,在后者中发现载体产生的释放不受cAMP及其类似物的抑制。基于这些发现,讨论了cAMP在组胺释放调节中的可能作用。