Okamoto H, Nakano K
Department of Nutritional Regulation, Nagoya University, Japan.
Immunology. 1990 Jan;69(1):162-5.
The response of mouse peritoneal macrophages to Escherichia coli lipopolysaccharide (LPS) resulted in induction of histidine decarboxylase (HDC) and, consequently, of histamine production. Concanavalin A had no effect on the reactions. Alpha-fluoromethylhistidine, a suicide inhibitor of HDC, attenuated, in a dose-dependent manner, both spontaneous and LPS-stimulated IL-1 synthesis by macrophages. IL-1 production was significantly blocked by either an H1 anti-histamine, diphenhydramine, or H2 anti-histamine ranitidine, in the absence of any exogenous histamine. Addition of exogenous histamine accentuated the IL-1 production by macrophages as a function of its dose. These results suggest that IL-1 production by mouse peritoneal macrophages is regulated by histamine synthesized in the system per se and that the effect of histamine is dependent on both H1 and H2 histamine receptors located on the surface of the cells.
小鼠腹腔巨噬细胞对大肠杆菌脂多糖(LPS)的反应导致组氨酸脱羧酶(HDC)的诱导,进而导致组胺的产生。伴刀豆球蛋白A对这些反应没有影响。α-氟甲基组氨酸是HDC的自杀性抑制剂,它以剂量依赖的方式减弱巨噬细胞自发的和LPS刺激的IL-1合成。在没有任何外源性组胺的情况下,H1抗组胺药苯海拉明或H2抗组胺药雷尼替丁均可显著阻断IL-1的产生。添加外源性组胺可增强巨噬细胞的IL-1产生,且呈剂量依赖性。这些结果表明,小鼠腹腔巨噬细胞产生IL-1受系统自身合成的组胺调节,且组胺的作用依赖于细胞表面的H1和H2组胺受体。