Fink A, Bibi H, Eliraz A, Schlesinger M, Bentwich Z
Ann Allergy. 1986 Aug;57(2):103-6.
Peripheral blood leukocytes (PBL) from asthmatic individuals lose their former ability to adhere to glass when incubated with leukotriene C4 (LTC4). A modified leukotriene-induced leukocyte adherence inhibition (LAI) assay was therefore used to study the ability of anti-asthmatic drugs to abrogate such activity. Ketotifen, disodium cromoglycate, Verapamil, and dimethpyridene, all at concentrations of 2 X 10(-6) M, were co-cultured with 2 X 10(-7) M LTC4 and their effect on the LTC4-induced LAI determined. Verapamil, Ketotifen, and disodium cromoglycate all inhibited the LTC4 activity while the H1 antagonist, dimethpyridene, did not. These results suggest that the beneficial effect of Verapamil, Ketotifen, and disodium cromoglycate in bronchial asthma is probably as calcium antagonists that cause the inhibition of leukotriene activity.
哮喘患者的外周血白细胞(PBL)在与白三烯C4(LTC4)孵育后,会丧失其先前附着于玻璃的能力。因此,采用一种改良的白三烯诱导的白细胞黏附抑制(LAI)试验来研究抗哮喘药物消除这种活性的能力。将酮替芬、色甘酸二钠、维拉帕米和二甲吡茚,均以2×10⁻⁶ M的浓度与2×10⁻⁷ M的LTC4共同培养,并测定它们对LTC4诱导的LAI的影响。维拉帕米、酮替芬和色甘酸二钠均抑制LTC4活性,而H1拮抗剂二甲吡茚则无此作用。这些结果表明,维拉帕米、酮替芬和色甘酸二钠在支气管哮喘中的有益作用可能是作为钙拮抗剂,从而抑制白三烯活性。