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1.
PLoS Negl Trop Dis ; 10(5): e0004698, 2016 05.
Artigo em Inglês | MEDLINE | ID: mdl-27145083

RESUMO

Current control strategies for onchocerciasis and lymphatic filariasis (LF) rely on prolonged yearly or twice-yearly mass administration of microfilaricidal drugs. Prospects for near-term elimination or eradication of these diseases would be improved by availability of a macrofilaricide that is highly effective in a short regimen. Flubendazole (FLBZ), a benzimidazole anthelmintic registered for control of human gastrointestinal nematode infections, is a potential candidate for this role. FLBZ has profound and potent macrofilaricidal effects in many experimental animal models of filariases and in one human trial for onchocerciasis after parental administration. Unfortunately, the marketed formulation of FLBZ provides very limited oral bioavailability and parenteral administration is required for macrofilaricidal efficacy. A new formulation that provided sufficient oral bioavailability could advance FLBZ as an effective treatment for onchocerciasis and LF. Short-term in vitro culture experiments in adult filariae have shown that FLBZ damages tissues required for reproduction and survival at pharmacologically relevant concentrations. The current study characterized the long-term effects of FLBZ on adult Brugia malayi by maintaining parasites in jirds for up to eight weeks following brief drug exposure (6-24 hr) to pharmacologically relevant concentrations (100 nM-10 µM) in culture. Morphological damage following exposure to FLBZ was observed prominently in developing embryos and was accompanied by a decrease in microfilarial output at 4 weeks post-exposure. Although FLBZ exposure clearly damaged the parasites, exposed worms recovered and were viable 8 weeks after treatment.


Assuntos
Antinematódeos/farmacologia , Brugia Malayi/efeitos dos fármacos , Mebendazol/análogos & derivados , Animais , Feminino , Gerbillinae , Masculino , Mebendazol/farmacologia , Cavidade Peritoneal/parasitologia
2.
Vet Parasitol ; 202(1-2): 49-53, 2014 Apr 28.
Artigo em Inglês | MEDLINE | ID: mdl-24703077

RESUMO

Cats may be infected by heartworm, Dirofilaria immitis, through mosquito bites. They can develop severe heartworm disease when infective D. immitis larvae migrate and develop into adults in the pulmonary vasculature or other tissues. As there is no curative treatment for feline heartworm infection, the monthly administration of preventative treatment is recommended in endemic areas. Three controlled, blinded laboratory studies were conducted to evaluate the preventative efficacy of BROADLINE(®), a novel combination of fipronil, (S)-methoprene, eprinomectin, and praziquantel against D. immitis in cats. In each study, 28 cats were inoculated with approximately 100 (studies 1 and 2) or 40 (study 3) infective third stage D. immitis larvae by subcutaneous injection, thirty days prior to treatment. The larvae were from recent field isolates from naturally infected dogs from three distinct geographic areas (two in the USA and one in Europe). In each study, the cats were allocated randomly to two study groups of 14 cats each. The control group remained untreated. On Day 0, each cat in the treated group received one topical application of the novel topical formulation, delivering the minimum intended dose of 0.5mg of eprinomectin per kilogram of body weight. At 6 months after infection, all cats were humanely euthanized and examined for adult D. immitis. Across all three studies, 28 (68%) of the 41 untreated cats harbored one or more heartworms, while 100% of the 42 treated cats remained free of heartworm infection, demonstrating the 100% preventive efficacy of BROADLINE(®) against D. immitis in cats. The treatment was well tolerated and no health abnormality was observed in any treated cat.


Assuntos
Antiparasitários/administração & dosagem , Doenças do Gato/tratamento farmacológico , Dirofilariose/prevenção & controle , Animais , Gatos , Dirofilaria immitis/fisiologia , Combinação de Medicamentos , Feminino , Ivermectina/administração & dosagem , Ivermectina/análogos & derivados , Masculino , Metoprene/administração & dosagem , Praziquantel/administração & dosagem , Pirazóis/administração & dosagem , Distribuição Aleatória , Resultado do Tratamento
3.
Vet Parasitol ; 179(4): 335-42, 2011 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-21777736

RESUMO

Healthy, purpose-bred laboratory beagle dogs that had not been exposed to ticks and were seronegative for Borrelia burgdorferi and Anaplasma phagocytophilum were randomly assigned to four groups of eight dogs each. Control group 1 was not treated. Groups 2, 3 and 4 were treated with a single topical application of a new formulation of fipronil, amitraz and (S)-methoprene (CERTIFECT™, Merial Limited, GA, USA) at 28, 21 or 14 days prior to tick infestation, respectively. Each dog was infested with 25 female and 25 male field-collected adult Ixodes scapularis ticks that had infection rates of 66% for B. burgdorferi sensu stricto and 23% for A. phagocytophilum, as determined by polymerase chain reaction. Two and five days after tick infestation, control dogs had an average of 9.5 and 13.9 attached adult female ticks, respectively, whilst the 24 treated dogs remained tick-free aside from a single tick on the 2nd day after infestation. Serial serological tests demonstrated that the ticks successfully infected 8/8 control dogs with B. burgdorferi and co-infected 6/8 with A. phagocytophilum. B. burgdorferi infection also was confirmed in most control dogs by culture (6/8) and PCR (7/8) of skin biopsies. In contrast, CERTIFECT protected all 24 treated dogs against infection by both B. burgdorferi and A. phagocytophilum, as demonstrated by their negative serological tests throughout the study and the absence of any positive skin biopsy culture or PCR in these dogs.


Assuntos
Vetores Aracnídeos/efeitos dos fármacos , Doenças do Cão/prevenção & controle , Inseticidas/uso terapêutico , Ixodes/efeitos dos fármacos , Infestações por Carrapato/veterinária , Administração Tópica , Anaplasma phagocytophilum/fisiologia , Animais , Anticorpos Antibacterianos , Vetores Aracnídeos/microbiologia , Vetores Aracnídeos/fisiologia , Borrelia burgdorferi/fisiologia , Doenças do Cão/tratamento farmacológico , Doenças do Cão/parasitologia , Doenças do Cão/transmissão , Cães , Método Duplo-Cego , Combinação de Medicamentos , Ehrlichiose/parasitologia , Ehrlichiose/prevenção & controle , Ehrlichiose/transmissão , Ehrlichiose/veterinária , Feminino , Inseticidas/farmacologia , Ixodes/microbiologia , Ixodes/fisiologia , Doença de Lyme/parasitologia , Doença de Lyme/prevenção & controle , Doença de Lyme/transmissão , Doença de Lyme/veterinária , Masculino , Metoprene/farmacologia , Metoprene/uso terapêutico , Pirazóis/farmacologia , Pirazóis/uso terapêutico , Rhode Island , Controle de Ácaros e Carrapatos/métodos , Infestações por Carrapato/tratamento farmacológico , Infestações por Carrapato/parasitologia , Infestações por Carrapato/prevenção & controle , Fatores de Tempo , Toluidinas/farmacologia , Toluidinas/uso terapêutico
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