一些苯并咪唑和阿莫昔酸(Go.9333)对实验性丝虫病感染的比较疗效。

Tropenmedizin und Parasitologie Pub Date : 1983-12-01
A B Reddy, U R Rao, R Chandrashekar, R Shrivastava, D Subrahmanyam
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引用次数: 0

摘要

研究了甲苯达唑、芬苯达唑、氧化苯达唑、氧化苯达唑、阿苯达唑、氟苯达唑和微粉氨苯酸酯(粒径5 ~ 8微米)对马腹螨(Mastomys natalensis)体内caromosoides carinii和Brugia pahangi感染的防治效果,分别采用口服给药(150 mg/kg/d,连续5 d)和皮下给药(100 mg/kg/d,连续5 d)。结果表明,口服苯并咪唑对卡氏乳杆菌和彭氏乳杆菌成虫无显著影响。对于大多数这些化合物,微丝蚴在外周循环中出现不同程度的下降之前都有所上升。口服甲苯达唑(99%)、氟苯达唑(95%)和奥芬达唑(85%)可使卡氏乳杆菌微丝蚴逐渐减少,但效果显著。对pahangi微丝虫未见此效果。在皮下给药时,除非苯达唑外,所有的苯并咪唑对卡氏乳杆菌都有明显的杀丝活性。氧苯达唑、氧苯达唑和苯苯达唑对pahangi成虫无明显的抑制作用。与苯并咪唑相比,口服和皮下给药的Amoscanate均能杀灭L. carinii和B. pahangi两种微丝虫和成虫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative efficacy of some benzimidazoles and amoscanate (Go.9333) against experimental filarial infections.

The comparative efficacy of mebendazole, fenbendazole, oxibendazole, oxfendazole, albendazole, flubendazole and micronized amoscanate (particle size 5-8 micron) against Litomosoides carinii and Brugia pahangi infections in Mastomys natalensis was studied on administration of the compounds per os (150 mg/kg/day for 5 days) and subcutaneous (100 mg/kg/day for 5 days) routes. It was found that benzimidazoles when given by the oral route had no effect on adults of L. carinii and B. pahangi. With most of these compounds there was a rise in microfilariae before registering a fall to varying degrees in the peripheral circulation. There was a gradual but effective reduction of microfilariae of L. carinii in animals treated orally with mebendazole (99%), flubendazole (95%) and oxfendazole (85%). No such effect was seen against B. pahangi microfilariae. On subcutaneous administration, all the benzimidazoles with the exception of fenbendazole exhibited marked macrofilaricidal activity against L. carinii. Such activity was not seen with oxibendazole, oxfendazole and fenbendazole against adults of B. pahangi. Amoscanate exhibited superiority over the benzimidazoles in that the compound eliminated microfilariae and adult worms of both L. carinii and B. pahangi species when given by oral and subcutaneous routes.

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