González J A, Lorente F, Romo A, Muriel M, Palomero B, Salazar V
Allergol Immunopathol (Madr). 1986 May-Jun;14(3):215-20.
The results concerning the action of Ketotifen "in vitro" on the adherence, spontaneous and chemotactic mobility and phagocytosis of neutrophil polymorphonuclear cells (PMNs) of the non-specific immunological system are presented. PMN cells were incubated for 30 min at 37 degrees C prior to the evaluation of different functions, with the following concentrations of Ketotifen: 1, 10 and 100 ng, and 1 and 10 micrograms/ml., final concentration. PMN cell adherence to glass spheres was unaffected by doses of the drug considered to have pharmacological action; however, a statistically significant enhancement was observed in this function from a concentration of 10 ng./ml. onwards. Mobility, both spontaneous and chemotactic was inhibited in the presence of Ketotifen only at high doses; the chemotactic function was more susceptible to the action of the drug at doses of 10 ng./ml. than spontaneous mobility, which required ten-fold greater concentrations for inhibition to take place. Likewise, the phagocytosis of C. albicans was inhibited by the presence of the drug at doses of 10 ng./ml. and higher. In conclusion, Ketotifen in PMN cells at pharmacological doses only induces a slight increase in adherence and a decrease in the functions of mobility and phagocytosis of C. albicans; at least "in vitro", much higher concentrations, which are not found with the doses usually employed, are required for these functions to be altered significantly.
本文展示了酮替芬“体外”对非特异性免疫系统中性多形核白细胞(PMN)的黏附、自发移动性、趋化移动性及吞噬作用的影响结果。在评估不同功能之前,将PMN细胞于37℃孵育30分钟,所用酮替芬的终浓度分别为:1、10和100纳克,以及1和10微克/毫升。被认为具有药理作用的药物剂量对PMN细胞黏附玻璃珠的能力没有影响;然而,从10纳克/毫升的浓度起,该功能出现了统计学上显著的增强。仅在高剂量下,酮替芬才会抑制自发移动性和趋化移动性;在10纳克/毫升的剂量下,趋化功能比自发移动性更容易受到药物作用的影响,自发移动性需要高十倍的浓度才会被抑制。同样,在10纳克/毫升及更高剂量下,药物的存在会抑制白色念珠菌的吞噬作用。总之,药理剂量的酮替芬仅会使PMN细胞的黏附略有增加,并使白色念珠菌的移动性和吞噬功能有所下降;至少在“体外”,需要比通常使用的剂量高得多的浓度才能显著改变这些功能。