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1.
Vet Parasitol ; 69(1-2): 95-102, 1997 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9187034

RESUMO

A series of five controlled studies involving 114 cattle were conducted in Australia, North America and the United Kingdom to examine the effect of simulated rain, coat length and exposure to natural climatic conditions, on the efficacy of a topical formulation of eprinomectin against nematode parasites of cattle. In all trials infections were induced with a range of bovine nematode species and treatment was applied when the majority of nematodes were mature. In one study, simulated rain was applied to cattle ending one hour before treatment or beginning one, three or six hours after treatment. In a second study cattle had short (1 cm) or long (3-6 cm) haircoats at the time of treatment. Three other studies were conducted using cattle housed indoors or exposed to various natural climatic conditions. Nematode counts were determined using standard techniques and the efficacy of treatment was assessed relative to vehicle-treated controls. Regardless of the timing of simulated rain relative to treatment, eprinomectin was at least 99.9% effective (P < 0.01) against Haemonchus placei, Ostertagia ostertagi. Trichostrongylus axei and Cooperia spp. There were also no differences (p > 0.10) in efficacy between treatment administered to dry or wet cattle, or treatment administered before or after simulated rainfall. Efficacies against O. ostertagi, T. axei, Cooperia ancophora and Dictyocaulus viviparus were > 99.5% (p < 0.01) regardless of the length of the haircoat at the application site. Exposure of treated cattle to sunshine and precipitation had no effect on anthelmintic efficacy (p > 0.10) with efficacies of greater than 99.5% being maintained against H. placei, O. ostertagi (adult and fourth-stage larvae), T. axei, Cooperia spp., Nematodirus helvetianus (adult and inhibited fourth-stage larvae) and Oesophagostomum radiatum. These findings indicate that eprinomectin (500 micrograms/kg) in a topical formulation is a safe and highly effective nematocide for cattle regardless of their coat length and this high level of efficacy is maintained in cattle exposed to a wide variety of climatic conditions.


Assuntos
Antinematódeos/administração & dosagem , Doenças dos Bovinos/tratamento farmacológico , Cabelo , Ivermectina/análogos & derivados , Infecções por Strongylida/veterinária , Tempo (Meteorologia) , Administração Tópica , Animais , Antinematódeos/uso terapêutico , Austrália , Bovinos , Doenças dos Bovinos/parasitologia , Clima , Feminino , Umidade , Ivermectina/administração & dosagem , Ivermectina/uso terapêutico , Masculino , Chuva , Infecções por Strongylida/tratamento farmacológico , Infecções por Strongylida/parasitologia , Reino Unido , Estados Unidos
2.
Int J Parasitol ; 26(11): 1237-42, 1996 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-9024867

RESUMO

Eprinomectin (MK-397 or 4"-epi-acetylamino-4"-deoxy-avermectin B1) is a novel avermectin selected for development as a topical endectocide for all cattle, including lactating dairy cows. Herein, we show its anthelmintic, insecticidal and miticidal activity. To determine its anthelmintic capabilities, eprinomectin was tested topically on Jersey calves at 0.08, 0.2, or 0.5 mg kg-1 in a probe formulation against experimental infections of adult Haemonchus placei, ostertagia ostertagi, Trichostrongylus axei, T. colubriformis, Cooperia oncophora, C. punctata, Nematodirus helvetianus, Oesophagostomum radiatum and Dictyocaulus viviparus. Eprinomectin removed > or = 99% and > or = 98% of the adult stage of every species at the 0.5 and 0.2 mg kg-1 dosage levels, respectively. The lowest dosage (0.08 mg kg-1) produced maximal or near maximal efficacy against most of the adult endoparasites with the exception of T. colubriformis (87%) and C. oncophora (88%). In a separate test, eprinomectin was evaluated topically against the immature stages of species at the same dosages. Results showed > or = 99% and > or = 98% removal of the immature stages of each species at the 0.5 and 0.2 mg kg-1 dosage levels, respectively. The 0.08 mg kg-1 dosage maintained > or = 97% efficacy against 6 species with reduced activity against H. placei (42%) and N. helvetianus (66%). For ectoparasites, eprinomectin was tested topically at 0.16, 0.24, 0.32 or 0.5 mg kg-1 on mixed breed cattle naturally infested with the sucking louse, Linognathus vituli. Complete elimination of lice at all dosages was observed by day 14. Topical delivery of eprinomectin at 0.16, 0.24, 0.32 or 0.5 mg kg-1 to Holstein calves experimentally challenged with horn fly, Haematobia irritans, produced 100% efficacy to challenge by week 2 post-treatment in all dosages groups and 94% and 99% efficacy to challenge at the 0.32 and 0.5 mg kg-1 dosage groups, respectively, at week 4. Topical delivery of eprinomectin at 0.16, 0.24 or 0.5 mg kg-1 to Deutsches Fleckvieh cattle infested with mange mites, Chorioptes bovis, produced > or = 95% control at all dosages levels by day 14 post-treatment and was maintained at or near this efficacious level for the 6-week duration of the trial. No adverse reaction was observed in any animal in any of these tests. In summary, these experimental data indicate that eprinomectin is an excellent broad-spectrum endectocide for cattle and is suitable for topical delivery.


Assuntos
Anti-Helmínticos/uso terapêutico , Doenças dos Bovinos , Helmintos/efeitos dos fármacos , Ivermectina/análogos & derivados , Infestações por Ácaros/veterinária , Infecções por Nematoides/veterinária , Doenças dos Ovinos , Administração Tópica , Animais , Anti-Helmínticos/administração & dosagem , Anti-Helmínticos/toxicidade , Bovinos , Dípteros , Desenho de Fármacos , Feminino , Ivermectina/administração & dosagem , Ivermectina/uso terapêutico , Ivermectina/toxicidade , Lactação , Infestações por Ácaros/tratamento farmacológico , Ácaros , Infecções por Nematoides/tratamento farmacológico , Ovinos , Relação Estrutura-Atividade
3.
Am J Vet Res ; 46(1): 163-4, 1985 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-3970422

RESUMO

Twenty calves at each of 2 Arkansas locations were inoculated with infective Fasciola hepatica metacercariae. After 56 days, the calves at each site were randomly assigned by weight to 2 treatment groups of 10 calves/group; vehicle control or clorsulon at the rate of 7 mg/kg of body weight. All treatments were given orally as a suspension. Calves were killed 6 weeks after treatment and F hepatica counts were performed for all animals. At the 2 sites, mean levels of efficacy were 96% and 91%. Adverse reactions to clorsulon or the vehicle were not observed in the calves.


Assuntos
Antiplatelmínticos/uso terapêutico , Doenças dos Bovinos/tratamento farmacológico , Fasciolíase/veterinária , Sulfanilamidas/uso terapêutico , Animais , Bovinos , Doenças dos Bovinos/parasitologia , Fasciolíase/tratamento farmacológico , Fasciolíase/parasitologia , Fígado/parasitologia
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