Berti F, Rossoni G, Zuccari G, Buschi A, Robuschi M, Villa L M, Caratozzolo O
Department of Pharmacology, Chemotherapy and Medical Toxicology, University of Milan, Italy.
Pulm Pharmacol. 1992 Jun;5(2):115-20. doi: 10.1016/0952-0600(92)90028-f.
The antianaphylactic activity of inhaled frusemide was studied in ovalbumin-sensitized guinea-pigs. The exposure of the animals to frusemide aerosol (1% solution for 20 min) attenuated the respiratory response to ovalbumin challenge (aerosol 1% solution) and was associated with a significant reduction of blood histamine (70%; P less than 0.01) and thromboxane-B2 (35%; P less than 0.01) compared to control animals. Similar results were obtained in isolated lungs perfused via the trachea excised from ovalbumin-sensitized guinea-pigs exposed to frusemide aerosol (1% solution for 20 min). In this series of experiments frusemide significantly prevented the increase in tracheal perfusion pressure (45%; P less than 0.01) and the concomitant release into the pulmonary effluent of both histamine (75%; P less than 0.01) and thromboxane-B2 (39%; P less than 0.01). In another series of experiments, frusemide (1 x 10(-4) M) significantly reduced the immune release of histamine from mast cells of ovalbumin-sensitized rats. The inhibitory activity of frusemide was in the same range of potency (66%; P less than 0.01) as that of disodium cromoglycate (1 x 10(-4) M). These data taken together indicate that frusemide when given by inhalation prevents histamine release secondary to antigen-antibody reaction.
在卵清蛋白致敏的豚鼠中研究了吸入速尿的抗过敏活性。让动物暴露于速尿气雾剂(1%溶液,持续20分钟)可减轻对卵清蛋白激发(1%溶液气雾剂)的呼吸反应,并且与对照组动物相比,血液组胺(降低70%;P<0.01)和血栓素B2(降低35%;P<0.01)显著减少。在从暴露于速尿气雾剂(1%溶液,持续20分钟)的卵清蛋白致敏豚鼠切下的经气管灌注的离体肺中也获得了类似结果。在这一系列实验中,速尿显著阻止了气管灌注压的升高(降低45%;P<0.01)以及组胺(降低75%;P<0.01)和血栓素B2(降低39%;P<0.01)同时释放到肺流出液中。在另一系列实验中,速尿(1×10⁻⁴M)显著减少了卵清蛋白致敏大鼠肥大细胞组胺的免疫释放。速尿的抑制活性与色甘酸钠(1×10⁻⁴M)的抑制活性在相同效力范围内(66%;P<0.01)。这些数据综合起来表明,吸入速尿可防止继发于抗原 - 抗体反应的组胺释放。