[Inhibition of degranulation of human basophils by calcium antagonists].

Journal de pharmacologie Pub Date : 1985-10-01
C Frisch, F Leynadier, A Nassar, J Dry
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Abstract

The human basophil degranulation test (HBDT) quantifies the apparent disappearance of basophils after contact with the sensitizing allergen. The inhibition of degranulation by pharmacological products can be appreciated by incubating beforehand the basophils with the substance concerned during various times. The inhibitory effect is evaluated by the difference of degranulation with or without it. EDTA, sodium cromoglycate, verapamil and bepridil have been tested at different concentrations and at 3 times of basophils preincubation (0,15 and 30 minutes). Results obtained confirm previous reports concerning cromoglycate which didn't inhibit degranulation of basophils. EDTA at 3.4*10(-2)M and 3.4*10(-3)M concentration has an inhibitory effect, not increasing with the time of preincubation. The inhibition with verapamil is of the same order at 1*10(-4)M for the 3 times of incubation and weaker, but significant, at 1*10-M5 after 30 minutes of preincubation. Bepridil inhibits at 1*10(-4)M, but this effect disappears if basophils are preincubated 30 minutes with the drug. The inhibition of the specific basophil degranulation by these drugs is probably du to their calcium antagonist property. However their effect is not quite similar when cells are preincubated at different times with the drug. On the other hand, one can study with HBDT the inhibitory effect of a new product, even if the therapeutic indications would have to be studied afterwards.

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钙拮抗剂对人嗜碱性细胞脱颗粒的抑制作用。
人嗜碱性粒细胞脱颗粒试验(HBDT)量化与致敏过敏原接触后嗜碱性粒细胞的明显消失。通过事先将嗜碱性粒细胞与有关物质在不同时间孵育,可以了解药物产物对脱颗粒的抑制作用。通过有无脱粒效果的差异来评价抑菌效果。EDTA、cromoglycate钠、维拉帕米和bepridil在不同浓度和3倍的嗜碱性粒细胞预孵育(0,15和30分钟)下进行了测试。结果证实了前人关于甘露糖酸不抑制嗜碱性细胞脱颗粒的报道。EDTA在3.4*10(-2)M和3.4*10(-3)M浓度下均有抑制作用,且不随预孵育时间的延长而增加。维拉帕米在1*10(-4)M孵育3次时的抑制程度相同,在1*10- m5孵育30分钟后的抑制程度较弱,但显著。Bepridil的抑制作用为1*10(-4)M,但如果嗜碱性细胞与药物一起预孵育30分钟,这种作用就会消失。这些药物对特异性嗜碱性粒细胞脱颗粒的抑制可能是由于它们的钙拮抗剂特性。然而,当细胞与药物在不同时间预孵育时,它们的效果并不十分相似。另一方面,人们可以用HBDT研究新产品的抑制作用,即使治疗适应症必须在之后研究。
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