Fayer R, Fetterer R
Parasite Immunobiology Laboratory, Livestock and Poultry Sciences Institute, United States Department of Agriculture, Beltsville, Maryland 20705, USA.
J Parasitol. 1995 Oct;81(5):794-5.
The need for an effective compound for the prevention and treatment of cryptosporidiosis in humans and animals has led to the testing of benzimidazoles based on reports that albendazole was clinically effective against related protozoan parasites causing microsporidiosis in humans. Albendazole and other benzimidazole derivatives were tested for prophylactic efficacy against cryptosporidiosis at dosage levels 1-3x the levels found effective for treatment of cattle or sheep for helminth infections. Daily dosage levels of thiabendazole, parbendazole, oxibendazole, mebendazole, and albendazole, as high as 200, 30, 10, 15, and 15 mg/kg of body weight, respectively, were not efficacious in neonatal mice. Although the number of parasites in histologic sections of intestine from mice mediated with 15 mg albendazole/kg of body weight was significantly lower than in unmedicated control mice, suggesting activity against the parasite, a high percentage of epithelial cells in the medicated mice were infected.
由于需要一种有效的化合物来预防和治疗人和动物的隐孢子虫病,基于阿苯达唑在临床上对引起人类微孢子虫病的相关原生动物寄生虫有效的报道,人们对苯并咪唑进行了测试。阿苯达唑和其他苯并咪唑衍生物在剂量水平为治疗牛或羊蠕虫感染有效剂量的1 - 3倍时,进行了预防隐孢子虫病的功效测试。噻苯达唑、帕苯达唑、奥苯达唑、甲苯达唑和阿苯达唑的每日剂量水平分别高达200、30、10、15和15 mg/kg体重,但对新生小鼠无效。尽管用15 mg阿苯达唑/kg体重处理的小鼠肠道组织切片中的寄生虫数量明显低于未用药的对照小鼠,表明对寄生虫有活性,但用药小鼠中有很高比例的上皮细胞被感染。