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机构地区:[1]上海医科大学基础医学院寄生虫学教研室,上海200032
出 处:《中国寄生虫学与寄生虫病杂志》1995年第3期182-184,共3页Chinese Journal of Parasitology and Parasitic Diseases
摘 要:小鼠腹腔接种RH株弓形虫速殖子1万个,2h后分别灌服5%淀粉溶液及蒿甲醚200mg/kg,连续8d,取腹腔液沉淀作电镜酶细胞化学。测定弓形虫虫体胞嘧啶单核苷酸酶(CMP酶)和葡萄糖-6-磷酸酶(G-6-P酶)的定位及用药后2种酶超微结构水平上的变化。结果表明,CMP酶定位于虫体的溶酶体,药物对其无明显影响。G-6-P酶定位于虫体的质膜外及围虫泡内,用药后酶反应减弱,说明药物对该酶的活性有一定影响,这可能是药物抗弓形虫的作用机制之一。Male mice of Kunmlng strain were infected with 10 000 tachyzoites intraperitoneally. 2 hours after infection the mice were divided into 2 groups and administered 5 % of amylurn and 200 mg/kg of artemether by gavage for 8 consecutive days. The ultrastructural enzyme cytochemical studles on cytidine monophosphatase (CMP ase) and glucose-6-phosphatase (G-6-P-ase) of the parasites were carried out. CMP-ase was found scattered in the lysosomes of the parasites as well as in the macrophages. No differences were observed in the localization and intensity of CMP-ase activity between the nontreated and treated with drug parasites. G6-P-ase was found surrounding the parasite membrane and scattered in the parasitophorous vacuole in the nontreated parasites. After treatment with artemether, the intensity of G-6-P-ase activity was decreased compared with nontreated control parasites. It is suggested that artemether may exert some action on the G-6-Patase of T. gondii and thus influence the energy metabolism of the parasite.
分 类 号:R382.5[医药卫生—医学寄生虫学]
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