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Use of L4 larvae of Nippostrongylus brasiliensis for the in vivo screening of anthelmintic drugs.

Five groups of Wistar rats were subcutaneously infected with 5,000 L3 stage larvae of Nippostrongylus brasiliensis. Four groups were dosed orally with 5, 10, 15, and 20 mg/kg body weight of albendazole at 5 h postinfection, and one group served as an untreated control. The animals were euthanized and the intestines were dissected out 72 h postinfection and were incubated on a Baermann's apparatus to recover L4 stage larvae. No larvae were recovered from the 20 mg/kg albendazole-treated group, and means of 15, 33, and 175 L4 larvae were recovered from the 15, 10, and 5 mg/kg albendazole-treated groups, respectively. Levamisole and fenbendazole were also tested using the same procedure. Means of 100 and 1,887 L4 larvae were obtained from the 50 and 10 mg/kg of levamisole-treated groups respectively; while, 191 and 583 L4 larvae were recovered from rats treated with 50 and 10 mg/kg of fenbendazole, respectively. These results indicate that the L4 stage of N. brasiliensis could be useful for in vivo screening of new nematocide drugs.

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The anthelmintic efficacy of fenbendazole against a mixed nematode infection in sheep.

Fenbendazole (methyl-5-(phenylthio)-2-benzimidazole carbamate) at dose rates of 5 mg/kg and above was 100 per cent effective in eliminating a naturally acquired Dictyocaulus filaria infection in sheep. The drug was 100 per cent effective in eliminating concurrent infections of adult Trichostrongylus axei, Haemonchus contortus, Haemonchus placei, Ostertagia circumcincta, Ostertagia ostertagii, Cooperia oncophora, Cooperia mcmasterii, Nematodirus spathiger, Neumatodirus filcollis, Oesophagostomum venulosum and Chabertia ovina. Fenbendazole was 93 per cent and 97 per cent effective at doses of 5 and 10 mg/kg respectively in removing infection with adult T colubriformis, and post-treatment worm-egg production was completely suppressed in surviving female worms. No adverse side-effects were observed in treated sheep at either of the two dose rates used.

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[Caustic sclerosing cholangitis following injection of anthelmintics into rat bile duct. An experimental study].

It is the purpose of the study to assay the effect of intrabiliary injection of scolicide agents most frequently used in clinical practice. Fifty-five albino rats are divided up into 4 groups according to type of solution injected, as follows: control group A--with physiological saline, B--20 per cent natrium chloratum, C--10 per cent povidone iodine, and D--3 per cent hydrogenium hyperoxidatum. Histological assessment of extrahepatic bile ducts and liver parenchyma are conducted at 10 and 90 days of treatment. Lesions along with cholestatic and reparative changes are documented, most markedly expressed after injecting 20 per cent NaCl, rather weakly--after 10 per cent povidone iodine, and least pronpunced after injecting 3 per cent hydrogen peroxide. Periductal sclerosis is noted in three rats only injected with hypertonic saline. The experimental results are analyzed, and clinically relevant inferences reached.

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Laboratory investigations on pigs with the new anthelmintic fenbendazole.

The efficacy of fenbendazole was investigated in piglets infected artificially with Hyostrongylus rubidus and Oesophagostomum spp. After administration of 3.5 mg/kg, five-day-old stages of H rubidus were reduced by 72.5 per cent; an effect of 78.4 per cent, 96.0 per cent and 100 per cent was achieved against five-day-old, 16-day-old and 42-day-old stages, respectively, of H rubidus using a dose of 5 mg/kg. A 55 per cent effect was obtained against five-day-old stages after the administration of 3.5 mg/kg. A dose of 5 mg/kg reduced five-day-old, 16-day-old and 42-day-old stages of Oesophagotomum spp by 72.6 per cent, 44 per cent and 100 per cent respectively.

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Oxibendazole: critical anthelmintic trials in equids.

The efficacy of oxibendazole against gastrointestinal parasites of horses was evaluated by the critical test method. Naturally infected ponies of various ages were given single oral doses of 5, 10, or 15 mg-kg of bodyweight. The drug was highly effective against adult large strongylids (Strongylus vulgaris, S edentatus, S equins), adult small strongylids (especially species of the genera Cylicostephanus, Cylicocyclus, Cyaathostomum, and Triodontophorus), and adult and larval stages of the large pinworm, Oxyuris equi. There was no apparent dose-related differences in efficacy. Oxibendazole was less effective against fourth-stage small strongylid larvae than it was against adults. The drug was inactive against stomach bots (Gasterophilus spp), tapeworms (Anoplocephala magna and A perfoliata), lungworms (Dictyocaulus arnfieldi), abdominal worms )Setaria equina), and mature or immature nematodes in locations other than the lumen of the gastrointestinal tract.

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