Desowitz R S, Palumbo N E, Perri S F, Sylvester M S
Am J Trop Med Hyg. 1982 Mar;31(2):309-12. doi: 10.4269/ajtmh.1982.31.309.
Lodoxamide ethyl, a new oral anti-allergy drug, was tested for its ability to inhibit the post-treatment adverse reaction to diethylcarbamazine (DEC) in Dirofilaria immitis-infected dogs. Lodoxamide was highly effective, as judged by the absence of both overt signs and characteristic post-DEC changes in platelet numbers, serum fibrinogen level, and serum transaminase (SGOT, SGPT) levels, in blocking the reaction in dogs with a microfilaremia level that would make them moderately reactive. Lodoxamide was less effective in blocking the reaction in dogs with microfilaremias greater than approximately 10,000 mf/ml, a level which is regularly associated with a severe post-DEC adverse reaction. Some dogs with this level of microfilaremia were fully protected, others partially protected, and others were afforded no protection. Two other agents tested, indomethacin and homochlorocyclizine, were found to have comparatively little or no blocking activity.
洛度沙胺乙酯是一种新型口服抗过敏药物,对其抑制感染犬恶丝虫的犬在乙胺嗪(DEC)治疗后出现不良反应的能力进行了测试。通过观察犬在微丝蚴血症水平处于中度反应范围时,洛度沙胺在阻止反应方面高度有效,这表现为既无明显体征,血小板数量、血清纤维蛋白原水平及血清转氨酶(SGOT、SGPT)水平也无乙胺嗪治疗后的特征性变化。对于微丝蚴血症水平高于约10,000条/毫升的犬,洛度沙胺在阻止反应方面效果较差,该水平通常与严重的乙胺嗪治疗后不良反应相关。部分微丝蚴血症处于此水平的犬得到了完全保护,部分得到了部分保护,而其他犬则未获得保护。另外两种受试药物,吲哚美辛和氯环利嗪,发现其阻断活性相对较小或无阻断活性。