Mio M, Izushi K, Tasaka K
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Okayama University, Japan.
Immunopharmacology. 1991 Jul-Aug;22(1):59-66. doi: 10.1016/0162-3109(91)90056-5.
Substance P-induced histamine release and Ca2+ release from the intracellular Ca store of rat peritoneal mast cells were inhibited by both antiallergic drugs and microtubule inhibiting agents. It was found that in the case of antiallergic compounds, histamine release inhibition may be intimately related to the inhibition of Ca2+ release from the intracellular store in which the microtubules play an important role. When mast cells were pretreated with either theophylline or dibutyryl cAMP, the inhibition of histamine release was closely related to the inhibition of Ca2+ release from the intracellular Ca store. Calmodulin inhibitors were also effective in inhibiting histamine release from mast cells induced by substance P. The inhibitory potencies of calmodulin inhibitors on histamine release from mast cells were closely correlated with those exerted on calmodulin activity.
P物质诱导的大鼠腹膜肥大细胞组胺释放及细胞内钙库的钙释放均受到抗过敏药物和微管抑制因子的抑制。研究发现,对于抗过敏化合物而言,组胺释放抑制可能与细胞内钙库钙释放的抑制密切相关,其中微管发挥着重要作用。当肥大细胞用茶碱或二丁酰环磷腺苷预处理时,组胺释放的抑制与细胞内钙库钙释放的抑制密切相关。钙调蛋白抑制剂也能有效抑制P物质诱导的肥大细胞组胺释放。钙调蛋白抑制剂对肥大细胞组胺释放的抑制效力与对钙调蛋白活性的抑制效力密切相关。